Theropithecus gelada isolate Dixy chromosome 17, Tgel_1.0, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Cercopithecinae; Theropithecus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM009967.1.\nAssembly name: Tgel_1.0\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the University of Washington on\n2018/06/19. The original whole-genome shotgun project has the\naccession QGDE00000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Kenneth Chiou's shared submissions\nAssembly Date :: APR-2018\nAssembly Method :: Supernova v. APR-2018; 3D-DNA v. APR-2018\nAssembly Name :: Tgel_1.0\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 56.0x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Theropithecus gelada Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.1\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Simien Mountains Gelada Research Project
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 1 Protein
39S ribosomal protein L27, mitochondrial pseudogene
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 ESTs, 2 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 113 ESTs, 5 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 114 ESTs, 6 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 112 ESTs, 4 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 115 ESTs, 9 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
disintegrin and metalloproteinase domain-containing protein 21
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 4 ESTs, 7 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 7 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 ESTs, 17 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
PEST proteolytic signal-containing nuclear protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
dachshund family transcription factor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 92 ESTs, 6 Proteins
dachshund family transcription factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 97 ESTs, 6 Proteins
dachshund family transcription factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 112 ESTs, 12 Proteins
heterogeneous nuclear ribonucleoprotein A1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 122 ESTs, 37 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00440
COORDINATES: nucleotide motif:Rfam:12.0:RF00263
COORDINATES: nucleotide motif:Rfam:12.0:RF00411
X-linked retinitis pigmentosa GTPase regulator-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 48 ESTs, 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: X-linked retinitis pigmentosa GTPase regulator-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 196 ESTs, 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 78 ESTs, 6 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein aurora borealis
DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 196 ESTs, 10 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 179 ESTs, 7 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
DIS3 homolog, exosome endoribonuclease and 3'-5' exoribonuclease, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 127 ESTs, 6 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
exosome complex exonuclease RRP44 isoform X1
exosome complex exonuclease RRP44 isoform X2
exosome complex exonuclease RRP44 isoform X3
progesterone immunomodulatory binding factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 133 ESTs, 6 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Kruppel like factor 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 256 ESTs, 15 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Kruppel like factor 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 263 ESTs, 24 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Kruppel like factor 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 243 ESTs, 16 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00066
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
Kruppel like factor 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 191 ESTs, 7 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Kruppel like factor 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 75 ESTs, 7 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Kruppel like factor 12, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 66 ESTs, 15 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 24 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
TBC1 domain family member 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 181 ESTs, 3 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
TBC1 domain family member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 172 ESTs, 3 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
TBC1 domain family member 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 176 ESTs, 4 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
COMM domain containing 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 71 ESTs, 1 Protein, and 74% coverage of the annotated genomic feature by RNAseq alignments
COMM domain containing 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 256 ESTs, 4 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
COMM domain containing 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 40 ESTs, 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
COMM domain containing 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 71 ESTs, 1 Protein, and 43% coverage of the annotated genomic feature by RNAseq alignments
COMM domain-containing protein 6 isoform X1
COMM domain-containing protein 6 isoform X4
COMM domain-containing protein 6 isoform X3
COMM domain-containing protein 6 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 12 ESTs, 9 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase isozyme L3
protein-glutamate O-methyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 ESTs, 7 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 213 ESTs, 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 207 ESTs, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 230 ESTs, 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 199 ESTs, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 201 ESTs, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 213 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 235 ESTs, 4 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: LMO7 downstream neighbor protein
potassium channel tetramerization domain containing 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 636 ESTs, 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
BTB/POZ domain-containing protein KCTD12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 ESTs, 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 249 ESTs, 4 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ceroid-lipofuscinosis neuronal protein 5
F-box and leucine rich repeat protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 405 ESTs, 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
F-box and leucine rich repeat protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 226 ESTs, 12 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
MYC binding protein 2, E3 ubiquitin protein ligase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 353 ESTs, 7 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, and 26% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 ESTs, 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 ESTs, 20 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
SLAIN motif family member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 207 ESTs, 5 Proteins
SLAIN motif family member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 204 ESTs, 6 Proteins
SLAIN motif family member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 199 ESTs, 6 Proteins
SLAIN motif-containing protein 1 isoform X1
SLAIN motif-containing protein 1 isoform X2
SLAIN motif-containing protein 1 isoform X3
SLAIN motif family member 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 191 ESTs, 6 Proteins
SLAIN motif-containing protein 1 isoform X4
SLAIN motif family member 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 165 ESTs, 2 Proteins
SLAIN motif family member 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 191 ESTs, 1 Protein
SLAIN motif family member 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 309 ESTs, 6 Proteins
SLAIN motif family member 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 169 ESTs, 2 Proteins
SLAIN motif-containing protein 1 isoform X5
SLAIN motif-containing protein 1 isoform X7
SLAIN motif-containing protein 1 isoform X6
endothelin receptor type B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 201 ESTs, 25 Proteins
endothelin receptor type B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, 254 ESTs, 22 Proteins
endothelin receptor type B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 87 ESTs, 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins
POU domain, class 4, transcription factor 1
ring finger protein 219, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 164 ESTs, 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ring finger protein 219, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 97 ESTs, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
T-complex protein 1 subunit epsilon pseudogene
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 17 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
RNA binding motif protein 26, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 299 ESTs, 2 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
RNA binding motif protein 26, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 206 ESTs, 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
RNA binding motif protein 26, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 210 ESTs, 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
RNA binding motif protein 26, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 193 ESTs, 4 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Nedd4 family interacting protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 413 ESTs, 11 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Nedd4 family interacting protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 346 ESTs, 3 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
Nedd4 family interacting protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 ESTs, 1 Protein, and 56% coverage of the annotated genomic feature by RNAseq alignments
NEDD4 family-interacting protein 2 isoform X1
NEDD4 family-interacting protein 2 isoform X2
sprouty RTK signaling antagonist 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 143 ESTs, 8 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sprouty RTK signaling antagonist 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 115 ESTs, 8 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
sprouty RTK signaling antagonist 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 121 ESTs, 8 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
sprouty RTK signaling antagonist 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 127 ESTs, 8 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 ESTs, 35 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 22 ESTs, 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 106 ESTs, 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 1 Protein, and 4% coverage of the annotated genomic feature by RNAseq alignments
SLIT and NTRK like family member 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 ESTs, 7 Proteins
SLIT and NTRK like family member 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 40 ESTs, 7 Proteins
SLIT and NTRK like family member 5, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 ESTs, 7 Proteins
SLIT and NTRK like family member 5, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 15 ESTs, 1 Protein
SLIT and NTRK like family member 5, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 37 ESTs, 7 Proteins
SLIT and NTRK like family member 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 ESTs, 7 Proteins
SLIT and NTRK like family member 5, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 19% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00212
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase HUWE1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 16% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 10 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 78 ESTs, 3 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00618
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 193 ESTs, 12 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs
phosphorylated adapter RNA export protein pseudogene
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 4 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
dopachrome tautomerase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 90 ESTs, 3 Proteins, and 1% coverage of the annotated genomic feature by RNAseq alignments
dopachrome tautomerase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 92 ESTs, 3 Proteins, and 1% coverage of the annotated genomic feature by RNAseq alignments
dopachrome tautomerase, transcript variant X5
dopachrome tautomerase, transcript variant X3
dopachrome tautomerase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 189 ESTs, 7 Proteins
dopachrome tautomerase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 181 ESTs, 2 Proteins
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
TDP-glucose 4,6-dehydratase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 109 ESTs, 6 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TDP-glucose 4,6-dehydratase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 81 ESTs, 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
dTDP-D-glucose 4,6-dehydratase isoform X1
dTDP-D-glucose 4,6-dehydratase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 86 ESTs, 2 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 29 ESTs, 113 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 27 ESTs, 109 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 9 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
ATP binding cassette subfamily C member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 199 ESTs, 4 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
ATP binding cassette subfamily C member 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 202 ESTs, 6 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
ATP binding cassette subfamily C member 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 197 ESTs, 3 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
multidrug resistance-associated protein 4 isoform X3
multidrug resistance-associated protein 4 isoform X2
multidrug resistance-associated protein 4 isoform X1
ATP binding cassette subfamily C member 4, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 22 ESTs, and 42% coverage of the annotated genomic feature by RNAseq alignments
ATP binding cassette subfamily C member 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 27 ESTs, 1 Protein, and 45% coverage of the annotated genomic feature by RNAseq alignments
multidrug resistance-associated protein 4 isoform X6
multidrug resistance-associated protein 4 isoform X4
ATP binding cassette subfamily C member 4, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 ESTs, 1 Protein, and 46% coverage of the annotated genomic feature by RNAseq alignments
ATP binding cassette subfamily C member 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 ESTs, 4 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
multidrug resistance-associated protein 4 isoform X7
multidrug resistance-associated protein 4 isoform X5
COORDINATES: nucleotide motif:Rfam:12.0:RF01210
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 73 ESTs, 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 69 ESTs, 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 EST
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 132 ESTs, 9 Proteins
DAZ interacting zinc finger protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 136 ESTs, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DAZ interacting zinc finger protein 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 123 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
DAZ interacting zinc finger protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 134 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DAZ interacting zinc finger protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 46 ESTs, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DAZ interacting zinc finger protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 ESTs, 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DAZ interacting zinc finger protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 ESTs, 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DnaJ heat shock protein family (Hsp40) member C3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 337 ESTs, 7 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
UDP-glucose glycoprotein glucosyltransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 124 ESTs, 8 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
UDP-glucose:glycoprotein glucosyltransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 69 ESTs, 14 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 31 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins
oxoglutarate receptor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 4 ESTs, 3 Proteins
oxoglutarate receptor 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 3 ESTs, 3 Proteins
oxoglutarate receptor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 4 ESTs, 3 Proteins
oxoglutarate receptor 1, transcript variant X1
oxoglutarate receptor 1, transcript variant X3
heat shock factor-binding protein 1 pseudogene
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 272 ESTs, 6 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
muscleblind like splicing regulator 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 276 ESTs, 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
muscleblind like splicing regulator 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 385 ESTs, 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
muscleblind like splicing regulator 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 386 ESTs, 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
muscleblind like splicing regulator 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 387 ESTs, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
muscleblind like splicing regulator 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 377 ESTs, 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, and 6% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 380 ESTs, 14 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 999 ESTs, 23 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 911 ESTs, 23 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 422 ESTs, 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
FERM, ARH/RhoGEF and pleckstrin domain protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 363 ESTs, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
FERM, ARH/RhoGEF and pleckstrin domain protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 10 ESTs, 1 Protein, and 38% coverage of the annotated genomic feature by RNAseq alignments
FERM, ARHGEF and pleckstrin domain-containing protein 1 isoform X1
FERM, ARHGEF and pleckstrin domain-containing protein 1 isoform X2
serine/threonine kinase 24, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 409 ESTs, 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine kinase 24, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 458 ESTs, 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine kinase 24, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 449 ESTs, 15 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase 24 isoform X3
serine/threonine-protein kinase 24 isoform X2
serine/threonine-protein kinase 24 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 122 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 15 ESTs, 10 Proteins
dedicator of cytokinesis 9, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 202 ESTs, 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
dedicator of cytokinesis 9, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 199 ESTs, 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
dedicator of cytokinesis 9, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 201 ESTs, 1 Protein, and 83% coverage of the annotated genomic feature by RNAseq alignments
dedicator of cytokinesis 9, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 122 ESTs, 12 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
dedicator of cytokinesis 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 111 ESTs, and 85% coverage of the annotated genomic feature by RNAseq alignments
dedicator of cytokinesis 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 123 ESTs, 12 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
dedicator of cytokinesis 9, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 127 ESTs, 12 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
dedicator of cytokinesis protein 9 isoform X6
dedicator of cytokinesis protein 9 isoform X2
dedicator of cytokinesis protein 9 isoform X1
dedicator of cytokinesis protein 9 isoform X3
dedicator of cytokinesis protein 9 isoform X7
dedicator of cytokinesis protein 9 isoform X4
dedicator of cytokinesis protein 9 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 44 ESTs
UBA domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 645 ESTs, 9 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
UBA domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 423 ESTs, 9 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
UBA domain containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 369 ESTs, 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin-associated domain-containing protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins
ubiquitin-associated domain-containing protein 2 isoform X1
ubiquitin-associated domain-containing protein 2 isoform X3
G protein-coupled receptor 18, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 29 ESTs, 4 Proteins
G protein-coupled receptor 18, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 20 ESTs, 4 Proteins
G protein-coupled receptor 18, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 19 ESTs, 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 138 ESTs, 3 Proteins
transmembrane 9 superfamily member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 970 ESTs, 9 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane 9 superfamily member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 495 ESTs, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane 9 superfamily member 2 isoform X1
transmembrane 9 superfamily member 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 31 ESTs, 3 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00402
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 33 ESTs, 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 106 ESTs, 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
propionyl-CoA carboxylase subunit alpha, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 277 ESTs, 6 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase subunit alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 276 ESTs, 4 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase subunit alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 350 ESTs, 9 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase subunit alpha, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 329 ESTs, 7 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase subunit alpha, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 331 ESTs, 4 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase subunit alpha, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 337 ESTs, 4 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase subunit alpha, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 316 ESTs, 4 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase subunit alpha, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 321 ESTs, 3 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase subunit alpha, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 210 ESTs, 6 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase subunit alpha, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 137 ESTs, 3 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase subunit alpha, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 191 ESTs, 4 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase subunit alpha, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 184 ESTs, 4 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase alpha chain, mitochondrial isoform X1
propionyl-CoA carboxylase alpha chain, mitochondrial isoform X2
propionyl-CoA carboxylase alpha chain, mitochondrial isoform X5
propionyl-CoA carboxylase alpha chain, mitochondrial isoform X3
propionyl-CoA carboxylase alpha chain, mitochondrial isoform X6
propionyl-CoA carboxylase alpha chain, mitochondrial isoform X4
propionyl-CoA carboxylase alpha chain, mitochondrial isoform X7
propionyl-CoA carboxylase alpha chain, mitochondrial isoform X8
propionyl-CoA carboxylase alpha chain, mitochondrial isoform X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 23 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
propionyl-CoA carboxylase alpha chain, mitochondrial isoform X10
propionyl-CoA carboxylase alpha chain, mitochondrial isoform X11
propionyl-CoA carboxylase alpha chain, mitochondrial isoform X12
gamma-glutamylamine cyclotransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 41 ESTs, 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
gamma-glutamylamine cyclotransferase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 43 ESTs, 3 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
gamma-glutamylamine cyclotransferase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 47 ESTs, 3 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
gamma-glutamylamine cyclotransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 48 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gamma-glutamylamine cyclotransferase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 35 ESTs, 3 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
gamma-glutamylamine cyclotransferase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 41 ESTs, 3 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
transmembrane and tetratricopeptide repeat containing 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 135 ESTs, 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
transmembrane and tetratricopeptide repeat containing 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 189 ESTs, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
transmembrane and tetratricopeptide repeat containing 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 196 ESTs, 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane and tetratricopeptide repeat containing 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 185 ESTs, and 92% coverage of the annotated genomic feature by RNAseq alignments
transmembrane and tetratricopeptide repeat containing 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 189 ESTs, 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
transmembrane and TPR repeat-containing protein 4 isoform X4
transmembrane and TPR repeat-containing protein 4 isoform X3
transmembrane and TPR repeat-containing protein 4 isoform X2
transmembrane and TPR repeat-containing protein 4 isoform X1
sodium leak channel, non-selective, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 44 ESTs, 12 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
sodium leak channel, non-selective, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 ESTs, 7 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
sodium leak channel non-selective protein isoform X2
sodium leak channel non-selective protein isoform X1
integrin subunit beta like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 112 ESTs, 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
integrin subunit beta like 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 167 ESTs, 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
integrin subunit beta like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 115 ESTs, 13 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
integrin subunit beta like 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 25 ESTs, 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 82 ESTs, 14 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 80 ESTs, 1 Protein, and 19% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 87 ESTs, 18 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 86 ESTs, 14 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 86 ESTs, 2 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14, transcript variant X15
fibroblast growth factor 14, transcript variant X12
fibroblast growth factor 14, transcript variant X14
fibroblast growth factor 14, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 80 ESTs, 14 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 79 ESTs, 14 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 79 ESTs, 2 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 79 ESTs, 14 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 79 ESTs, 2 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14, transcript variant X11
fibroblast growth factor 14, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 79 ESTs, 2 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 79 ESTs, 2 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 14, transcript variant X10
fibroblast growth factor 14, transcript variant X8
fibroblast growth factor 14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 82 ESTs, 22 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
tripeptidyl peptidase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 323 ESTs, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
tripeptidyl peptidase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 341 ESTs, 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tripeptidyl peptidase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 225 ESTs, 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
methyltransferase like 21C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 18 ESTs, 2 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
methyltransferase like 21C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 17 ESTs, 2 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
protein-lysine methyltransferase METTL21C isoform X1
protein-lysine methyltransferase METTL21C isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 13 ESTs, 5 Proteins
coiled-coil domain-containing protein 168
testis expressed 30, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 91 ESTs, 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
testis expressed 30, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 154 ESTs, 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
testis expressed 30, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 111 ESTs, 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
KDEL motif containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 95 ESTs, 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
KDEL motif containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 ESTs, 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
KDEL motif-containing protein 1 isoform X1
KDEL motif-containing protein 1 isoform X2
basic, immunoglobulin-like variable motif containing, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 123 ESTs, 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
basic, immunoglobulin-like variable motif containing, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 191 ESTs, 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
basic immunoglobulin-like variable motif-containing protein isoform X1
basic immunoglobulin-like variable motif-containing protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 310 ESTs, 11 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
DNA repair protein complementing XP-G cells
putative methyltransferase-like protein 21E pseudogene
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 18 ESTs, 3 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: D-amino acid oxidase activator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 3 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 258 ESTs, 11 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 535 ESTs, 2 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 173 ESTs, 31 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 155 member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 72 ESTs, 2 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00089
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 72 ESTs, 11 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 81 ESTs, 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 ESTs, 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 66 ESTs, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 69 ESTs, 11 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 66 ESTs, 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 66 ESTs, 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 63 ESTs, 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 67 ESTs, 11 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 148 ESTs, 9 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TNF superfamily member 13b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 mRNAs, 61 ESTs, 7 Proteins
TNF superfamily member 13b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 51 ESTs, 1 Protein
tumor necrosis factor ligand superfamily member 13B isoform X1
tumor necrosis factor ligand superfamily member 13B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 ESTs, 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 21 ESTs, 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 22 ESTs, 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 266 ESTs, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
collagen type IV alpha 1 chain, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, 790 ESTs, 29 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
collagen type IV alpha 1 chain, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 26 ESTs, 4 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, 833 ESTs, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 69 ESTs, 3 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NAD(P)HX dehydratase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 549 ESTs, 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NAD(P)HX dehydratase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 290 ESTs, 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
NAD(P)HX dehydratase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 280 ESTs, 2 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
NAD(P)HX dehydratase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 259 ESTs, and 91% coverage of the annotated genomic feature by RNAseq alignments
NAD(P)HX dehydratase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 320 ESTs, 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
NAD(P)HX dehydratase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 277 ESTs, 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform X4
ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform X6
ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform X3
ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform X5
ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform X1
ATP-dependent (S)-NAD(P)H-hydrate dehydratase isoform X2
cysteinyl-tRNA synthetase 2, mitochondrial, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 74 ESTs, and 79% coverage of the annotated genomic feature by RNAseq alignments
cysteinyl-tRNA synthetase 2, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 224 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
probable cysteine--tRNA ligase, mitochondrial isoform X3
probable cysteine--tRNA ligase, mitochondrial isoform X2
cysteinyl-tRNA synthetase 2, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
probable cysteine--tRNA ligase, mitochondrial isoform X1
cysteinyl-tRNA synthetase 2, mitochondrial, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 48 ESTs, 1 Protein, and 67% coverage of the annotated genomic feature by RNAseq alignments
probable cysteine--tRNA ligase, mitochondrial isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 28 ESTs, and 4% coverage of the annotated genomic feature by RNAseq alignments
inhibitor of growth family member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 96 ESTs, 5 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
inhibitor of growth family member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 127 ESTs, 18 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
inhibitor of growth family member 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 100 ESTs, 5 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
inhibitor of growth protein 1 isoform X2
inhibitor of growth family member 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91 ESTs, 5 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
inhibitor of growth family member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 116 ESTs, 10 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
inhibitor of growth family member 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91 ESTs, 5 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
inhibitor of growth family member 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 90 ESTs, 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
inhibitor of growth protein 1 isoform X1
inhibitor of growth protein 1 isoform X3
putative uncharacterized protein encoded by LINC00346
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 1 Protein, and 22% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain 10, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 330 ESTs, 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain 10, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 280 ESTs, 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain-containing protein 10 isoform X1
ankyrin repeat domain 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 183 ESTs, 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain-containing protein 10 isoform X2
Rho guanine nucleotide exchange factor 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 213 ESTs, 10 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 213 ESTs, 12 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Rho guanine nucleotide exchange factor 7, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 204 ESTs, 6 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 102 ESTs, 9 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 107 ESTs, 10 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 100 ESTs, 8 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 234 ESTs, 7 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
rho guanine nucleotide exchange factor 7 isoform X1
rho guanine nucleotide exchange factor 7 isoform X2
rho guanine nucleotide exchange factor 7 isoform X3
rho guanine nucleotide exchange factor 7 isoform X6
rho guanine nucleotide exchange factor 7 isoform X4
Rho guanine nucleotide exchange factor 7, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 203 ESTs, 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 234 ESTs, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 237 ESTs, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 239 ESTs, 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 244 ESTs, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Rho guanine nucleotide exchange factor 7, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 201 ESTs, 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 103 ESTs, 8 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 103 ESTs, 8 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 99 ESTs, 8 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 239 ESTs, 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 7, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 243 ESTs, 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
rho guanine nucleotide exchange factor 7 isoform X5
rho guanine nucleotide exchange factor 7 isoform X8
rho guanine nucleotide exchange factor 7 isoform X7
rho guanine nucleotide exchange factor 7 isoform X9
rho guanine nucleotide exchange factor 7 isoform X11
Rho guanine nucleotide exchange factor 7, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 201 ESTs, 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
rho guanine nucleotide exchange factor 7 isoform X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 2 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00287
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 48 ESTs, 113 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 19 ESTs, 2 Proteins
tubulin gamma complex associated protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 128 ESTs, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
tubulin gamma complex associated protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 175 ESTs, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gamma-tubulin complex component 3 isoform X2
gamma-tubulin complex component 3 isoform X1
tubulin gamma complex associated protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 99 ESTs, 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
gamma-tubulin complex component 3 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 266 ESTs, 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
probable phospholipid-transporting ATPase IH
MCF.2 cell line derived transforming sequence like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 32 ESTs, 7 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
protein Z, vitamin K dependent plasma glycoprotein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 6 ESTs, 3 Proteins
protein Z, vitamin K dependent plasma glycoprotein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 2 Proteins
vitamin K-dependent protein Z isoform X1
vitamin K-dependent protein Z isoform X2
PCI domain containing 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 249 ESTs, 12 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
PCI domain containing 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 298 ESTs, 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
PCI domain containing 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 217 ESTs, 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
PCI domain containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 268 ESTs, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
PCI domain containing 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 142 ESTs, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
PCI domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 ESTs, 4 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
PCI domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 143 ESTs, 4 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
PCI domain containing 2, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 140 ESTs, 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
PCI domain containing 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 144 ESTs, 5 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
PCI domain containing 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 114 ESTs, 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
PCI domain-containing protein 2 isoform X4
PCI domain-containing protein 2 isoform X2
PCI domain-containing protein 2 isoform X3
PCI domain-containing protein 2 isoform X8
PCI domain-containing protein 2 isoform X5
PCI domain-containing protein 2 isoform X7
PCI domain-containing protein 2 isoform X1
PCI domain-containing protein 2 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 384 ESTs, 10 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 372 ESTs, 10 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 395 ESTs, 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 430 ESTs, 26 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 ESTs, 2 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
lysosomal associated membrane protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 768 ESTs, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
lysosomal associated membrane protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 637 ESTs, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
lysosome-associated membrane glycoprotein 1 isoform X1
lysosome-associated membrane glycoprotein 1 isoform X2
growth hormone regulated TBC protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 17 ESTs, 1 Protein
growth hormone regulated TBC protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 53 ESTs, 5 Proteins
growth hormone-regulated TBC protein 1 isoform X2
growth hormone-regulated TBC protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 7 ESTs, 5 Proteins
protein ADP-ribosylarginine hydrolase-like protein 1
defective in cullin neddylation 1 domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 94 ESTs, 14 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane and coiled-coil domain-containing protein 3
transcription factor Dp-1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 303 ESTs, 17 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
transcription factor Dp-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 200 ESTs, 7 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 15 ESTs, 2 Proteins
potassium-transporting ATPase subunit beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 4 ESTs, 3 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 10% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transmembrane protein 255B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 386 ESTs, 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 ESTs
long intergenic non-protein coding RNA 452
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LINC00452
RAS p21 protein activator 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 165 ESTs, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RAS p21 protein activator 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 153 ESTs, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
ras GTPase-activating protein 3 isoform X1
ras GTPase-activating protein 3 isoform X2
cell division cycle 16, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 277 ESTs, 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cell division cycle 16, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 197 ESTs, 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cell division cycle 16, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 234 ESTs, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
cell division cycle protein 16 homolog isoform X1
cell division cycle protein 16 homolog isoform X2
cell division cycle 16, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 213 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cell division cycle protein 16 homolog isoform X3
UPF3A, regulator of nonsense mediated mRNA decay, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 179 ESTs, 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
UPF3A, regulator of nonsense mediated mRNA decay, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs, 1 Protein, and 52% coverage of the annotated genomic feature by RNAseq alignments
UPF3A, regulator of nonsense mediated mRNA decay, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 190 ESTs, 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
UPF3A, regulator of nonsense mediated mRNA decay, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 190 ESTs, 5 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
UPF3A, regulator of nonsense mediated mRNA decay, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 187 ESTs, 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulator of nonsense transcripts 3A isoform X1
regulator of nonsense transcripts 3A isoform X2
regulator of nonsense transcripts 3A isoform X3
regulator of nonsense transcripts 3A isoform X4
chromosome alignment maintaining phosphoprotein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 192 ESTs, 7 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
chromosome alignment maintaining phosphoprotein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 156 ESTs, 7 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
chromosome alignment maintaining phosphoprotein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 155 ESTs, 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
chromosome alignment-maintaining phosphoprotein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 14 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 3 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 131 ESTs, 2 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
spindle and kinetochore associated complex subunit 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 81 ESTs, 8 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
spindle and kinetochore-associated protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 912 ESTs, 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
histone deacetylase complex subunit SAP18
COORDINATES: nucleotide motif:Rfam:12.0:RF00086
large tumor suppressor kinase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 185 ESTs, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
large tumor suppressor kinase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 168 ESTs, 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 184 ESTs, 12 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
EEF1A lysine methyltransferase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 63 ESTs, 3 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
EEF1A lysine methyltransferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 68 ESTs, 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
EEF1A lysine methyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 ESTs, 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 107 ESTs, 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 108 ESTs, 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 ESTs, 12 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
intraflagellar transport protein 88 homolog
crystallin lambda 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 241 ESTs, 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
crystallin lambda 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 124 ESTs, 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
gap junction protein beta 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 44 ESTs, 51 Proteins
gap junction protein beta 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 48 ESTs, 51 Proteins
gap junction protein beta 6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 40 ESTs, 51 Proteins
gap junction protein beta 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 40 ESTs, 51 Proteins
gap junction protein beta 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 84 ESTs, 51 Proteins
gap junction protein beta 6, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 39 ESTs, 51 Proteins
gap junction protein beta 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 183 ESTs, 50 Proteins
gap junction protein beta 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 154 ESTs, 50 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 12 ESTs, 4 Proteins
zinc finger MYM-type containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 320 ESTs, 5 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYM-type containing 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 324 ESTs, 15 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYM-type containing 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 326 ESTs, 15 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYM-type containing 2, transcript variant X7
zinc finger MYM-type containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 343 ESTs, 15 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYM-type containing 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 330 ESTs, 15 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYM-type containing 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 324 ESTs, 15 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYM-type containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 334 ESTs, 15 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYM-type containing 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 318 ESTs, and 75% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYM-type protein 2 isoform X1
zinc finger MYM-type protein 2 isoform X2
zinc finger MYM-type containing 2, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 102 ESTs, 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYM-type protein 2 isoform X3
zinc finger MYM-type containing 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 ESTs, 2 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
zinc finger MYM-type containing 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 2 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger MYM-type protein 5 isoform X1
zinc finger MYM-type protein 5 isoform X2
paraspeckle component 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 411 ESTs, 17 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
paraspeckle component 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 404 ESTs, 17 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
paraspeckle component 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 332 ESTs, 17 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
paraspeckle component 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 411 ESTs, 17 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
paraspeckle component 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 343 ESTs, 17 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
paraspeckle component 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 400 ESTs, 25 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
paraspeckle component 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 174 ESTs, 25 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
paraspeckle component 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 154 ESTs, 17 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
M-phase phosphoprotein 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 239 ESTs, 2 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
M-phase phosphoprotein 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 248 ESTs, 7 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 5 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 ESTs, and 13% coverage of the annotated genomic feature by RNAseq alignments
transmembrane phosphoinositide 3-phosphatase and tensin homolog 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 21 ESTs, 6 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
transmembrane phosphoinositide 3-phosphatase and tensin homolog 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 ESTs, 16 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase TPTE2 isoform X1
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase TPTE2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins
zinc finger DHHC-type containing 20, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 213 ESTs, 4 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger DHHC-type containing 20, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 206 ESTs, 4 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger DHHC-type containing 20, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 214 ESTs, 6 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger DHHC-type containing 20, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 213 ESTs, 5 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
zinc finger DHHC-type containing 20, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 197 ESTs, 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 ESTs, 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 56 ESTs, 12 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 11 ESTs
sarcoglycan gamma, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 15 ESTs, 4 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
sarcoglycan gamma, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 ESTs, 4 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
sacsin molecular chaperone, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 192 ESTs, 8 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
sacsin molecular chaperone, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 184 ESTs, 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
sacsin molecular chaperone, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 180 ESTs, 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
TNF receptor superfamily member 19, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 146 ESTs, 5 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
TNF receptor superfamily member 19, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 104 ESTs, 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
TNF receptor superfamily member 19, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 37 ESTs, 9 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TNF receptor superfamily member 19, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 126 ESTs, 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tumor necrosis factor receptor superfamily member 19 isoform X2
tumor necrosis factor receptor superfamily member 19 isoform X1
tumor necrosis factor receptor superfamily member 19 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 155 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
complement C1q and tumor necrosis factor-related protein 9A-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 3 Proteins
LOW QUALITY PROTEIN: complement C1q and tumor necrosis factor-related protein 9A-like
spermatogenesis associated 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 232 ESTs, 18 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
spermatogenesis associated 13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 222 ESTs, 9 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
spermatogenesis-associated protein 13 isoform X1
spermatogenesis-associated protein 13 isoform X2
spermatogenesis associated 13, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 221 ESTs, 6 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
spermatogenesis associated 13, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 236 ESTs, 9 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
spermatogenesis associated 13, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 211 ESTs, 4 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
spermatogenesis-associated protein 13 isoform X3
spermatogenesis-associated protein 13 isoform X4
spermatogenesis-associated protein 13 isoform X5
complement C1q and tumor necrosis factor-related protein 9A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 57 ESTs, 5 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
complement C1q and tumor necrosis factor-related protein 9A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 56 ESTs, 5 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
complement C1q and tumor necrosis factor-related protein 9A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 57 ESTs, 5 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
complement C1q and tumor necrosis factor-related protein 9A
ATPase H+/K+ transporting non-gastric alpha2 subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 29 ESTs, 22 Proteins
potassium-transporting ATPase alpha chain 2
ring finger protein 17, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 33 ESTs, 4 Proteins
ring finger protein 17, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 31 ESTs, 3 Proteins
centromere protein J, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 75 ESTs, 1 Protein, and 41% coverage of the annotated genomic feature by RNAseq alignments
centromere protein J, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 81 ESTs, 10 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
centromere protein J, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 77 ESTs, 2 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
poly(ADP-ribose) polymerase family member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 230 ESTs, 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
poly(ADP-ribose) polymerase family member 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 156 ESTs, 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
poly(ADP-ribose) polymerase family member 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 211 ESTs, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
poly [ADP-ribose] polymerase 4 isoform X1
poly [ADP-ribose] polymerase 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 32 ESTs, and 4% coverage of the annotated genomic feature by RNAseq alignments
poly(A) binding protein cytoplasmic 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 148 ESTs, 5 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
poly(A) binding protein cytoplasmic 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 946 ESTs, 40 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
poly(A) binding protein cytoplasmic 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 344 ESTs, 12 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
poly(A) binding protein cytoplasmic 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 349 ESTs, 5 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
poly(A) binding protein cytoplasmic 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 209 ESTs, 6 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
poly(A) binding protein cytoplasmic 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 632 ESTs, 3 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
polyadenylate-binding protein 3 isoform X5
polyadenylate-binding protein 3 isoform X1
polyadenylate-binding protein 3 isoform X3
polyadenylate-binding protein 3 isoform X2
polyadenylate-binding protein 3 isoform X4
polyadenylate-binding protein 3 isoform X6
APC membrane recruitment protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 54 ESTs, 4 Proteins
APC membrane recruitment protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 ESTs, 4 Proteins
APC membrane recruitment protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 ESTs, 4 Proteins
APC membrane recruitment protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 ESTs, 4 Proteins
APC membrane recruitment protein 2 isoform X2
APC membrane recruitment protein 2 isoform X1
myotubularin related protein 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 401 ESTs, 12 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myotubularin related protein 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 384 ESTs, 2 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
myotubularin-related protein 6 isoform X2
myotubularin-related protein 6 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 251 ESTs, 2 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 488 ESTs, 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 313 ESTs, 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
ATPase phospholipid transporting 8A2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 149 ESTs, 4 Proteins
phospholipid-transporting ATPase IB isoform X1
ATPase phospholipid transporting 8A2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 148 ESTs, 1 Protein
phospholipid-transporting ATPase IB isoform X2
inorganic pyrophosphatase 2, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 ESTs, 4 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 5 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ring finger protein 6, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 167 ESTs, 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 6, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 168 ESTs, 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 230 ESTs, 8 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 172 ESTs, 8 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 253 ESTs, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ring finger protein 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 169 ESTs, and 92% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 171 ESTs, and 92% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase RNF6 isoform X3
E3 ubiquitin-protein ligase RNF6 isoform X2
E3 ubiquitin-protein ligase RNF6 isoform X1
E3 ubiquitin-protein ligase RNF6 isoform X4
ring finger protein 6, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 45 ESTs, 2 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase RNF6 isoform X5
cyclin dependent kinase 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 120 ESTs, 11 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
cyclin dependent kinase 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 117 ESTs, 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cyclin dependent kinase 8, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 113 ESTs, 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
cyclin dependent kinase 8, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 112 ESTs, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
WAS protein family member 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 216 ESTs, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins
WAS protein family member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 208 ESTs, 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
wiskott-Aldrich syndrome protein family member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 45 ESTs, 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 171 ESTs, 23 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 12
ribosomal protein L21, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 ESTs, 13 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ribosomal protein L21, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 12 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ribosomal protein L21, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 ESTs, 12 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00187
COORDINATES: nucleotide motif:Rfam:12.0:RF00443
RAS like family 11 member A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 21 ESTs, 5 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ras-like protein family member 11A isoform X1
RAS like family 11 member A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 ESTs, 1 Protein, and 43% coverage of the annotated genomic feature by RNAseq alignments
ras-like protein family member 11A isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 296 ESTs, 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transcription factor IIIA
mitochondrial translational initiation factor 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 ESTs, 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial translational initiation factor 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 122 ESTs, 5 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
translation initiation factor IF-3, mitochondrial isoform X1
translation initiation factor IF-3, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 76 ESTs, 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 238 ESTs, 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
DNA-directed RNA polymerases I and III subunit RPAC2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 164 ESTs, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 375 ESTs, 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 146 ESTs, 99 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 21 ESTs, 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 8 ESTs
caudal type homeobox 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 33 ESTs, 2 Proteins
caudal type homeobox 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 49 ESTs, 9 Proteins
ureidoimidazoline (2-oxo-4-hydroxy-4-carboxy-5-) decarboxylase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins
putative 2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase
fms related tyrosine kinase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 18 ESTs, 1 Protein
fms related tyrosine kinase 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 18 ESTs, 7 Proteins
receptor-type tyrosine-protein kinase FLT3 isoform X2
receptor-type tyrosine-protein kinase FLT3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91 Proteins
poly(A) specific ribonuclease subunit PAN3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 149 ESTs, 6 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
PAN2-PAN3 deadenylation complex subunit PAN3
fms related tyrosine kinase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 129 ESTs, 16 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
vascular endothelial growth factor receptor 1 isoform X1
fms related tyrosine kinase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 86 ESTs, 5 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
vascular endothelial growth factor receptor 1 isoform X2
fms related tyrosine kinase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 66 ESTs, 3 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
vascular endothelial growth factor receptor 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 672 ESTs, 2 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 480 ESTs, 7 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 125 ESTs, 8 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
microtubule associated scaffold protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 ESTs, 6 Proteins
microtubule-associated tumor suppressor candidate 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 280 ESTs, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 381 ESTs, 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
high affinity cationic amino acid transporter 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 601 ESTs, 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 ESTs, and 91% coverage of the annotated genomic feature by RNAseq alignments
katanin catalytic subunit A1 like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 32 ESTs, 13 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
katanin catalytic subunit A1 like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 23 ESTs, 13 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
katanin p60 ATPase-containing subunit A-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 ESTs, 5 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin conjugating enzyme E2 L5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 ESTs, 15 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin conjugating enzyme E2 L5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 ESTs, 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin-conjugating enzyme E2 L5 isoform X1
ubiquitin-conjugating enzyme E2 L5 isoform X2
high mobility group box 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 710 ESTs, 40 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
high mobility group box 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 696 ESTs, 40 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
high mobility group box 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 719 ESTs, 40 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
high mobility group box 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 621 ESTs, 40 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
high mobility group box 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 612 ESTs, 40 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
high mobility group box 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 639 ESTs, 40 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
high mobility group box 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 629 ESTs, 40 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
tyrosine-protein phosphatase non-receptor type 2 pseudogene
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, and 65% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin specific peptidase like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 146 ESTs, 9 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin specific peptidase like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 150 ESTs, 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
SUMO-specific isopeptidase USPL1 isoform X1
SUMO-specific isopeptidase USPL1 isoform X2
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
arachidonate 5-lipoxygenase activating protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 147 ESTs, 10 Proteins
arachidonate 5-lipoxygenase-activating protein isoform X1
arachidonate 5-lipoxygenase activating protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 153 ESTs, 9 Proteins
arachidonate 5-lipoxygenase-activating protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 ESTs
mesenteric estrogen dependent adipogenesis
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 101 ESTs, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mesenteric estrogen-dependent adipogenesis protein
testis expressed 26, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 16 ESTs, 4 Proteins
testis expressed 26, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 ESTs, 1 Protein
testis expressed 26, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 ESTs, 1 Protein
testis expressed 26, transcript variant X4
heat shock protein family H (Hsp110) member 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 351 ESTs, 2 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
heat shock protein family H (Hsp110) member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 393 ESTs, 6 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
heat shock protein family H (Hsp110) member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 758 ESTs, 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
heat shock protein family H (Hsp110) member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 673 ESTs, 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 74 ESTs, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
relaxin family peptide receptor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 ESTs, 1 Protein
relaxin family peptide receptor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 ESTs, 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 11 Proteins
FRY microtubule binding protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 150 ESTs, 2 Proteins, and 1% coverage of the annotated genomic feature by RNAseq alignments
FRY microtubule binding protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 156 ESTs, 7 Proteins, and 1% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 3 ESTs, 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 mRNAs, 59 ESTs, 49 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
breast cancer type 2 susceptibility protein
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 ESTs, 7 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: NEDD4-binding protein 2-like 1
small nucleolar RNA SNORA16B/SNORA16A family
COORDINATES: nucleotide motif:Rfam:12.0:RF00190
NEDD4 binding protein 2 like 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 133 ESTs, 4 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
NEDD4 binding protein 2 like 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 42 ESTs, 3 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
NEDD4 binding protein 2 like 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 42 ESTs, 4 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
NEDD4-binding protein 2-like 2 isoform X2
NEDD4-binding protein 2-like 2 isoform X1
NEDD4-binding protein 2-like 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein
NEDD4 binding protein 2 like 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 325 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NEDD4-binding protein 2-like 2 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 20 Proteins
PDS5 cohesin associated factor B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 187 ESTs, 6 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
PDS5 cohesin associated factor B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 193 ESTs, 9 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
sister chromatid cohesion protein PDS5 homolog B isoform X1
sister chromatid cohesion protein PDS5 homolog B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 68 ESTs, 5 Proteins
StAR related lipid transfer domain containing 13, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 121 ESTs, 5 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
StAR related lipid transfer domain containing 13, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 126 ESTs, 5 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
StAR related lipid transfer domain containing 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 138 ESTs, 10 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
StAR related lipid transfer domain containing 13, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 135 ESTs, 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
StAR related lipid transfer domain containing 13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 122 ESTs, 7 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
stAR-related lipid transfer protein 13 isoform X4
stAR-related lipid transfer protein 13 isoform X3
stAR-related lipid transfer protein 13 isoform X1
stAR-related lipid transfer protein 13 isoform X2
stAR-related lipid transfer protein 13 isoform X5
StAR related lipid transfer domain containing 13, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 10 ESTs, 1 Protein, and 61% coverage of the annotated genomic feature by RNAseq alignments
stAR-related lipid transfer protein 13 isoform X6
developmentally-regulated GTP-binding protein 1 pseudogene
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 209 ESTs, 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 271 ESTs, 10 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 169 ESTs, 15 Proteins, and 1% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 166 ESTs, 9 Proteins, and 1% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 86 ESTs, 12 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 115 ESTs, 5 Proteins, and 3% coverage of the annotated genomic feature by RNAseq alignments
doublecortin like kinase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 205 ESTs, 12 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
doublecortin like kinase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 211 ESTs, 12 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
doublecortin like kinase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 199 ESTs, 9 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
doublecortin like kinase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 321 ESTs, 7 Proteins
doublecortin like kinase 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 309 ESTs, 3 Proteins
serine/threonine-protein kinase DCLK1 isoform X1
serine/threonine-protein kinase DCLK1 isoform X3
serine/threonine-protein kinase DCLK1 isoform X2
serine/threonine-protein kinase DCLK1 isoform X4
spermatogenesis and oogenesis specific basic helix-loop-helix 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 31 ESTs, 4 Proteins
spermatogenesis- and oogenesis-specific basic helix-loop-helix-containing protein 2 isoform X1
spermatogenesis and oogenesis specific basic helix-loop-helix 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 ESTs, 1 Protein
spermatogenesis- and oogenesis-specific basic helix-loop-helix-containing protein 2 isoform X2
coiled-coil domain containing 169, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 ESTs, 2 Proteins
coiled-coil domain containing 169, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 23 ESTs, 2 Proteins
coiled-coil domain containing 169, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 14 ESTs, 4 Proteins
coiled-coil domain-containing protein 169 isoform X1
coiled-coil domain-containing protein 169 isoform X2
coiled-coil domain-containing protein 169 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 264 ESTs, 8 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 352 ESTs, 8 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 308 ESTs, 8 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 73 ESTs, 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 76 ESTs, 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 55 ESTs, 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 64 ESTs, 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 61 ESTs, 6 Proteins
serine rich and transmembrane domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 ESTs, 6 Proteins
serine-rich and transmembrane domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 5 Proteins
regulatory factor X associated protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 61 ESTs, 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulatory factor X associated protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 ESTs, and 85% coverage of the annotated genomic feature by RNAseq alignments
regulatory factor X-associated protein isoform X1
regulatory factor X-associated protein isoform X2
SMAD family member 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 92 ESTs, 26 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
SMAD family member 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 91 ESTs, 21 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
mothers against decapentaplegic homolog 9 isoform X2
mothers against decapentaplegic homolog 9 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
ALG5, dolichyl-phosphate beta-glucosyltransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 108 ESTs, 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
ALG5, dolichyl-phosphate beta-glucosyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 199 ESTs, 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ALG5, dolichyl-phosphate beta-glucosyltransferase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 103 ESTs, 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
dolichyl-phosphate beta-glucosyltransferase isoform X2
dolichyl-phosphate beta-glucosyltransferase isoform X3
dolichyl-phosphate beta-glucosyltransferase isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 180 ESTs, 5 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
SPT20 homolog, SAGA complex component, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 256 ESTs, 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
SPT20 homolog, SAGA complex component, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 271 ESTs, 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
SPT20 homolog, SAGA complex component, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 211 ESTs, 7 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
SPT20 homolog, SAGA complex component, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 189 ESTs, 7 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
SPT20 homolog, SAGA complex component, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 197 ESTs, 7 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
SPT20 homolog, SAGA complex component, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 166 ESTs, 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
transcription factor SPT20 homolog isoform X3
transcription factor SPT20 homolog isoform X1
transcription factor SPT20 homolog isoform X2
transcription factor SPT20 homolog isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 10 Proteins
casein kinase 1 alpha 1 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 ESTs, 39 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
casein kinase 1 alpha 1 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 22 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 ESTs, 17 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 520 ESTs, 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 524 ESTs, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 529 ESTs, 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 527 ESTs, 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 546 ESTs, 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 546 ESTs, 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 529 ESTs, 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 537 ESTs, 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 537 ESTs, 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel subfamily C member 4, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 42 ESTs, 3 Proteins
transient receptor potential cation channel subfamily C member 4, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 45 ESTs, 2 Proteins
transient receptor potential cation channel subfamily C member 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 45 ESTs, 2 Proteins
transient receptor potential cation channel subfamily C member 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 46 ESTs, 4 Proteins
transient receptor potential cation channel subfamily C member 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 44 ESTs, 9 Proteins
transient receptor potential cation channel subfamily C member 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 48 ESTs, 5 Proteins
transient receptor potential cation channel subfamily C member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 37 ESTs, 16 Proteins
short transient receptor potential channel 4 isoform X6
short transient receptor potential channel 4 isoform X5
short transient receptor potential channel 4 isoform X4
short transient receptor potential channel 4 isoform X3
short transient receptor potential channel 4 isoform X2
short transient receptor potential channel 4 isoform X1
short transient receptor potential channel 4 isoform X7
ubiquitin fold modifier 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 254 ESTs, 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ubiquitin fold modifier 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 201 ESTs, 1 Protein, and 73% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin fold modifier 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 208 ESTs, 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
FRAS1 related extracellular matrix protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 ESTs, 5 Proteins
FRAS1-related extracellular matrix protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 17 ESTs, 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 13 ESTs, 11 Proteins
proline and serine rich 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 237 ESTs, 6 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
proline and serine rich 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 224 ESTs, 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
proline and serine-rich protein 1 isoform X2
proline and serine-rich protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, and 90% coverage of the annotated genomic feature by RNAseq alignments
NHL repeat containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 119 ESTs, 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
NHL repeat containing 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 52 ESTs, 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
LHFPL tetraspan subfamily member 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 326 ESTs, 5 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LHFPL tetraspan subfamily member 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 134 ESTs, 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LHFPL tetraspan subfamily member 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 133 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LHFPL tetraspan subfamily member 6 protein isoform X1
LHFPL tetraspan subfamily member 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 196 ESTs, and 75% coverage of the annotated genomic feature by RNAseq alignments
LHFPL tetraspan subfamily member 6 protein isoform X2
component of oligomeric golgi complex 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 114 ESTs, 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
component of oligomeric golgi complex 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 230 ESTs, 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 6 isoform X1
conserved oligomeric Golgi complex subunit 6 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00108
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 293 ESTs, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 ESTs, 10 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 205 ESTs, 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
28S ribosomal protein S31, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 38 ESTs, 9 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 ESTs, and 3% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC112611079, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, and 18% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC112611079, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E74 like ETS transcription factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 273 ESTs, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E74 like ETS transcription factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 273 ESTs, 5 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
WW domain binding protein 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 174 ESTs, 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
WW domain binding protein 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 95 ESTs, 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 16 Proteins
kelch repeat and BTB domain containing 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 128 ESTs, and 87% coverage of the annotated genomic feature by RNAseq alignments
kelch repeat and BTB domain containing 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 292 ESTs, 12 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
kelch repeat and BTB domain-containing protein 6 isoform X1
kelch repeat and BTB domain-containing protein 6 isoform X2
kelch repeat and BTB domain containing 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 204 ESTs, 15 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
kelch repeat and BTB domain containing 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 126 ESTs, 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
kelch repeat and BTB domain-containing protein 7 isoform X2
kelch repeat and BTB domain-containing protein 7 isoform X1
mitochondrial translation release factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 ESTs, 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial translation release factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 24 ESTs, 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial translation release factor 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 43 ESTs, 5 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial translation release factor 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 41 ESTs, 5 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial translation release factor 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 42 ESTs, 5 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial translation release factor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 41 ESTs, 5 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial translation release factor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 47 ESTs, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
peptide chain release factor 1, mitochondrial isoform X1
peptide chain release factor 1, mitochondrial isoform X3
peptide chain release factor 1, mitochondrial isoform X2
N(alpha)-acetyltransferase 16, NatA auxiliary subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 90 ESTs, 15 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
N(alpha)-acetyltransferase 16, NatA auxiliary subunit, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 37 ESTs, 1 Protein, and 67% coverage of the annotated genomic feature by RNAseq alignments
N(alpha)-acetyltransferase 16, NatA auxiliary subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 36 ESTs, 1 Protein, and 62% coverage of the annotated genomic feature by RNAseq alignments
N-alpha-acetyltransferase 16, NatA auxiliary subunit isoform X1
N-alpha-acetyltransferase 16, NatA auxiliary subunit isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 255 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
von Willebrand factor A domain containing 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 109 ESTs, 4 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
von Willebrand factor A domain-containing protein 8
diacylglycerol kinase eta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 ESTs, 2 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
diacylglycerol kinase eta, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 24 ESTs, 7 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
diacylglycerol kinase eta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 20 ESTs, 6 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
diacylglycerol kinase eta, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 135 ESTs, 1 Protein, and 73% coverage of the annotated genomic feature by RNAseq alignments
diacylglycerol kinase eta, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 19 ESTs, 2 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
diacylglycerol kinase eta, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 19 ESTs, 4 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
diacylglycerol kinase eta, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 14 ESTs, 3 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 242 ESTs, 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
TNF superfamily member 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 7 ESTs, 2 Proteins
TNF superfamily member 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 10 ESTs, 5 Proteins
tumor necrosis factor ligand superfamily member 11 isoform X1
tumor necrosis factor ligand superfamily member 11 isoform X2
family with sequence similarity 216 member B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 ESTs, 3 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
epithelial-stromal interaction protein 1
DnaJ heat shock protein family (Hsp40) member C15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 254 ESTs, 7 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 ESTs, and 38% coverage of the annotated genomic feature by RNAseq alignments
ecto-NOX disulfide-thiol exchanger 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 60 ESTs, 12 Proteins
ecto-NOX disulfide-thiol exchanger 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 55 ESTs, 12 Proteins
ecto-NOX disulfide-thiol exchanger 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 55 ESTs, 13 Proteins
ecto-NOX disulfide-thiol exchanger 1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 63 ESTs, 2 Proteins
ecto-NOX disulfide-thiol exchanger 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 85 ESTs, 12 Proteins
ecto-NOX disulfide-thiol exchanger 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 64 ESTs, 12 Proteins
ecto-NOX disulfide-thiol exchanger 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 56 ESTs, 12 Proteins
ecto-NOX disulfide-thiol exchanger 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 56 ESTs, 12 Proteins
ecto-NOX disulfide-thiol exchanger 1, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 54 ESTs, 2 Proteins
ecto-NOX disulfide-thiol exchanger 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 57 ESTs, 12 Proteins
ecto-NOX disulfide-thiol exchanger 1 isoform X1
ecto-NOX disulfide-thiol exchanger 1 isoform X2
ecto-NOX disulfide-thiol exchanger 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 3 Proteins
coiled-coil domain-containing protein 122
laccase domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 ESTs, 7 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
laccase domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 21 ESTs, 7 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
small integral membrane protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 5 ESTs, 1 Protein
small integral membrane protein 2 isoform X2
small integral membrane protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 ESTs, 1 Protein
small integral membrane protein 2 isoform X1
stress associated endoplasmic reticulum protein family member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 ESTs, 2 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
stress associated endoplasmic reticulum protein family member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 43 ESTs, 2 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
stress-associated endoplasmic reticulum protein 2 isoform X1
stress-associated endoplasmic reticulum protein 2 isoform X2
TSC22 domain family member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1002 ESTs, 10 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
TSC22 domain family member 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 899 ESTs, 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
TSC22 domain family member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 938 ESTs, 15 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
TSC22 domain family member 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 899 ESTs, 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
TSC22 domain family member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 mRNAs, 1737 ESTs, 15 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TSC22 domain family member 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 945 ESTs, 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
TSC22 domain family protein 1 isoform X1
TSC22 domain family protein 1 isoform X2
TSC22 domain family protein 1 isoform X4
TSC22 domain family protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 ESTs, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 9 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 91 ESTs, 4 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
nuclear fragile X mental retardation-interacting protein 1
GPALPP motifs containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 35 ESTs, 3 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
GPALPP motifs containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 75 ESTs, 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
GPALPP motifs-containing protein 1 isoform X1
GPALPP motifs-containing protein 1 isoform X2
general transcription factor IIF subunit 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 138 ESTs, 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
general transcription factor IIF subunit 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 177 ESTs, 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
general transcription factor IIF subunit 2 isoform X1
general transcription factor IIF subunit 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 12 Proteins
potassium channel tetramerization domain containing 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 40 ESTs, 7 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00322
tumor protein, translationally-controlled 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 2004 ESTs, 18 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tumor protein, translationally-controlled 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1859 ESTs, 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
tumor protein, translationally-controlled 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1962 ESTs, 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tumor protein, translationally-controlled 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 382 ESTs, 1 Protein, and 87% coverage of the annotated genomic feature by RNAseq alignments
tumor protein, translationally-controlled 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 325 ESTs, and 87% coverage of the annotated genomic feature by RNAseq alignments
translationally-controlled tumor protein isoform X3
translationally-controlled tumor protein isoform X2
translationally-controlled tumor protein isoform X4
translationally-controlled tumor protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 ESTs, and 11% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 25 member 30, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 91 ESTs, 15 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 25 member 30, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 25 ESTs, 15 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 25 member 30, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 ESTs, 3 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
kidney mitochondrial carrier protein 1 isoform X1
kidney mitochondrial carrier protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 255 ESTs, 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
conserved oligomeric Golgi complex subunit 3
spermatid associated, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 64 ESTs, 3 Proteins
spermatid associated, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 41 ESTs, 1 Protein
spermatid associated, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 58 ESTs, 1 Protein
siah E3 ubiquitin protein ligase family member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 2 Proteins
zinc finger CCCH-type containing 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 320 ESTs, 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
zinc finger CCCH domain-containing protein 13 isoform X1
zinc finger CCCH-type containing 13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 189 ESTs, 6 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
zinc finger CCCH domain-containing protein 13 isoform X2
carboxypeptidase B2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 56 ESTs, 1 Protein
carboxypeptidase B2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 73 ESTs, 4 Proteins
lymphocyte cytosolic protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 1021 ESTs, 30 Proteins
lymphocyte cytosolic protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 721 ESTs, 30 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 11 ESTs, 2 Proteins
leucine-rich repeat-containing protein 63
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 4 Proteins
RUN and cysteine rich domain containing beclin 1 interacting protein like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 85 ESTs, 2 Proteins
RUN and cysteine rich domain containing beclin 1 interacting protein like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 86 ESTs, 4 Proteins
RUN and cysteine rich domain containing beclin 1 interacting protein like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 90 ESTs, 7 Proteins
RUN and cysteine rich domain containing beclin 1 interacting protein like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 80 ESTs, 5 Proteins
RUN and cysteine rich domain containing beclin 1 interacting protein like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 81 ESTs, 2 Proteins
RUN and cysteine rich domain containing beclin 1 interacting protein like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 82 ESTs, 3 Proteins
RUN and cysteine rich domain containing beclin 1 interacting protein like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 82 ESTs, 5 Proteins
leucine rich repeats and calponin homology domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 118 ESTs, 10 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
leucine rich repeats and calponin homology domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 36 ESTs, 6 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
leucine rich repeats and calponin homology domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 39 ESTs, 5 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X3
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X1
leucine-rich repeat and calponin homology domain-containing protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 252 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
5-hydroxytryptamine receptor 2A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 35 ESTs, 12 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
5-hydroxytryptamine receptor 2A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 21 ESTs, 3 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
5-hydroxytryptamine receptor 2A isoform X2
5-hydroxytryptamine receptor 2A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 15 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
succinate-CoA ligase ADP-forming beta subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 378 ESTs, 14 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
succinate-CoA ligase ADP-forming beta subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 406 ESTs, 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
succinate-CoA ligase ADP-forming beta subunit, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 62 ESTs, 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial isoform X1
succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 35 ESTs, 4 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
nucleotide triphosphate diphosphatase NUDT15
mediator complex subunit 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 122 ESTs, and 88% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 4 isoform X2
mediator complex subunit 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 121 ESTs, and 84% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 4 isoform X1
mediator complex subunit 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 269 ESTs, 1 Protein, and 64% coverage of the annotated genomic feature by RNAseq alignments
mediator complex subunit 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 356 ESTs, 13 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs, and 53% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 4 isoform X3
mediator of RNA polymerase II transcription subunit 4 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, 2038 ESTs, 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 250 ESTs, 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 14 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 mRNAs, 222 ESTs, 10 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 96 ESTs, 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 145 ESTs, 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 111 ESTs, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RCC1 and BTB domain containing protein 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 156 ESTs, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 158 ESTs, 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 168 ESTs, 19 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RCC1 and BTB domain containing protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 45 ESTs, 19 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 46 ESTs, 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 43 ESTs, 19 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain-containing protein 2 isoform X1
RCC1 and BTB domain-containing protein 2 isoform X2
RCC1 and BTB domain-containing protein 2 isoform X3
RCC1 and BTB domain-containing protein 2 isoform X4
cysteinyl leukotriene receptor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 15 ESTs, 3 Proteins
cysteinyl leukotriene receptor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 ESTs, 3 Proteins
fibronectin type III domain containing 3A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 450 ESTs, 13 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
fibronectin type III domain containing 3A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 404 ESTs, 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
fibronectin type-III domain-containing protein 3A isoform X1
fibronectin type III domain containing 3A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 409 ESTs, 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
fibronectin type-III domain-containing protein 3A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 ESTs, and 15% coverage of the annotated genomic feature by RNAseq alignments
cytidine and dCMP deaminase domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 87 ESTs, 12 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
cytidine and dCMP deaminase domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 70 ESTs, 5 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
cytidine and dCMP deaminase domain-containing protein 1 isoform X2
cytidine and dCMP deaminase domain-containing protein 1 isoform X1
calcium binding protein 39 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 128 ESTs, 14 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
calcium binding protein 39 like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 61 ESTs, 7 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
calcium binding protein 39 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 62 ESTs, 7 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
SET domain bifurcated 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 43 ESTs, 5 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
SET domain bifurcated 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 83 ESTs, 3 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
SET domain bifurcated 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 63 ESTs, 2 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
histone-lysine N-methyltransferase SETDB2 isoform X1
histone-lysine N-methyltransferase SETDB2 isoform X2
histone-lysine N-methyltransferase SETDB2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 141 ESTs, 5 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RCC1 and BTB domain containing protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 275 ESTs, 18 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 208 ESTs, 18 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 204 ESTs, 18 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 199 ESTs, 18 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 200 ESTs, 18 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 247 ESTs, 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain containing protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 198 ESTs, 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RCC1 and BTB domain-containing protein 1 isoform X1
RCC1 and BTB domain-containing protein 1 isoform X3
RCC1 and BTB domain containing protein 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 103 ESTs, 2 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
RCC1 and BTB domain-containing protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 13 ESTs, 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 104 ESTs, 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
emopamil-binding protein-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
emopamil-binding protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 450 ESTs, 19 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
endoplasmic reticulum export factor CTAGE5-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 13 Proteins
LOW QUALITY PROTEIN: endoplasmic reticulum export factor CTAGE5-like
SPRY domain containing 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 98 ESTs, 7 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SPRY domain containing 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 48 ESTs, 2 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
SPRY domain-containing protein 7 isoform X2
SPRY domain-containing protein 7 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, and 33% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif containing 13, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 116 ESTs, 12 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif containing 13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 151 ESTs, 12 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif containing 13, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 133 ESTs, 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tripartite motif containing 13, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 116 ESTs, 12 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tripartite motif containing 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 106 ESTs, 13 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif containing 13, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 113 ESTs, 12 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif containing 13, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 117 ESTs, 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase TRIM13 isoform X1
E3 ubiquitin-protein ligase TRIM13 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 30 ESTs, 2 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: potassium channel regulatory protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 43 ESTs, and 9% coverage of the annotated genomic feature by RNAseq alignments
leukemia-associated protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 2 ESTs, and 27% coverage of the annotated genomic feature by RNAseq alignments
leukemia-associated protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 ESTs, and 32% coverage of the annotated genomic feature by RNAseq alignments
leukemia-associated protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 63 ESTs, and 91% coverage of the annotated genomic feature by RNAseq alignments
leukemia-associated protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 56 ESTs, 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
leukemia-associated protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 ESTs, and 59% coverage of the annotated genomic feature by RNAseq alignments
deleted in lymphocytic leukemia, 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 8 ESTs, 2 Proteins
leukemia-associated protein 7 isoform X2
deleted in lymphocytic leukemia, 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 ESTs, 4 Proteins
leukemia-associated protein 7 isoform X1
ribonuclease H2 subunit B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 ESTs, 7 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
ribonuclease H2 subunit B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 ESTs, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ribonuclease H2 subunit B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 ESTs, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
guanylate cyclase soluble subunit beta-2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: guanylate cyclase soluble subunit beta-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 ESTs, 1 Protein
uncharacterized protein C13orf42 homolog
family with sequence similarity 124 member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 109 ESTs, 3 Proteins, and 1% coverage of the annotated genomic feature by RNAseq alignments
integrator complex subunit 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 86 ESTs, 15 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
integrator complex subunit 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 56 ESTs, 6 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
integrator complex subunit 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 26 ESTs, 7 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
integrator complex subunit 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, and 59% coverage of the annotated genomic feature by RNAseq alignments
integrator complex subunit 6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 68 ESTs, 1 Protein, and 37% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 7 ESTs, and 9% coverage of the annotated genomic feature by RNAseq alignments
40S ribosomal protein S4, X isoform-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 202 ESTs, 5 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
WD repeat and FYVE domain-containing protein 2
heterogeneous nuclear ribonucleoprotein A1-like 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 37 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: heterogeneous nuclear ribonucleoprotein A1-like 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 ESTs, 3 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: dehydrogenase/reductase SDR family member 12
transmembrane protein 272, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 17 ESTs, 2 Proteins
transmembrane protein 272, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 12 ESTs, 1 Protein
transmembrane protein 272, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 14 ESTs, 3 Proteins
coiled-coil domain containing 70, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 23 ESTs, 5 Proteins
coiled-coil domain containing 70, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 30 ESTs, 5 Proteins
coiled-coil domain-containing protein 70
endoplasmic reticulum export factor CTAGE5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 14 ESTs, 30 Proteins, and 2% coverage of the annotated genomic feature by RNAseq alignments
endoplasmic reticulum export factor CTAGE5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 6 Proteins, and 3% coverage of the annotated genomic feature by RNAseq alignments
endoplasmic reticulum export factor CTAGE5-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 1 Protein
endoplasmic reticulum export factor CTAGE5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 6 Proteins
endoplasmic reticulum export factor CTAGE5-like isoform X4
endoplasmic reticulum export factor CTAGE5-like isoform X2
endoplasmic reticulum export factor CTAGE5-like isoform X3
endoplasmic reticulum export factor CTAGE5-like isoform X1
ATPase copper transporting beta, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 88 ESTs, 5 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
ATPase copper transporting beta, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 80 ESTs, 4 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
ATPase copper transporting beta, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 85 ESTs, 4 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
ATPase copper transporting beta, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 85 ESTs, 4 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
ATPase copper transporting beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 85 ESTs, 3 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
ATPase copper transporting beta, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 84 ESTs, 3 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
ATPase copper transporting beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 90 ESTs, 7 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 263 ESTs, 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
GDP-Man:Man(3)GlcNAc(2)-PP-Dol alpha-1,2-mannosyltransferase
UTP14C, small subunit processome component, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 227 ESTs, 5 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
UTP14C, small subunit processome component, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 153 ESTs, 3 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
U3 small nucleolar RNA-associated protein 14 homolog C isoform X1
U3 small nucleolar RNA-associated protein 14 homolog C isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 3 Proteins
NIMA related kinase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 85 ESTs, 5 Proteins, and 2% coverage of the annotated genomic feature by RNAseq alignments
NIMA related kinase 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 ESTs, 4 Proteins, and 3% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase Nek3 isoform X2
serine/threonine-protein kinase Nek3 isoform X1
phosphatidylinositol 3,4,5-trisphosphate 3-phosphatase TPTE2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 54% coverage of the annotated genomic feature by RNAseq alignments
SGT1 homolog, MIS12 kinetochore complex assembly cochaperone, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 ESTs, 3 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
SGT1 homolog, MIS12 kinetochore complex assembly cochaperone, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 65 ESTs, 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SGT1 homolog, MIS12 kinetochore complex assembly cochaperone, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 ESTs, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 42 ESTs, 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 43 ESTs, 4 Proteins
leukocyte cell-derived chemotaxin 1 isoform X2
leukocyte cell-derived chemotaxin 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 34 ESTs, 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 36 ESTs, 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 460 ESTs, 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 313 ESTs, 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 ESTs, 6 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
26S proteasome non-ATPase regulatory subunit 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 297 ESTs, 22 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 177 ESTs, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 156 ESTs, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 ESTs, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/arginine-rich splicing factor 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 124 ESTs, 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 14 Proteins
diaphanous related formin 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 51 ESTs, 2 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
diaphanous related formin 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 51 ESTs, 2 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
diaphanous related formin 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 52 ESTs, 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments
diaphanous related formin 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 60 ESTs, 5 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
diaphanous related formin 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 28 ESTs, 3 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs, and 15% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 13 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
tudor domain containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 204 ESTs, 4 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
tudor domain containing 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 204 ESTs, 5 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
tudor domain-containing protein 3 isoform X1
tudor domain containing 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 186 ESTs, 2 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
tudor domain-containing protein 3 isoform X2
tudor domain-containing protein 3 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 64 ESTs, 6 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 22 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
cytoskeleton associated protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 210 ESTs, 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytoskeleton associated protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 260 ESTs, 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytoskeleton associated protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 188 ESTs, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
cytoskeleton-associated protein 2 isoform X2
cytoskeleton-associated protein 2 isoform X1
cytoskeleton-associated protein 2 isoform X3
cytoskeleton associated protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 113 ESTs, 3 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytoskeleton-associated protein 2 isoform X4
vacuolar protein sorting 36 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 218 ESTs, 2 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
vacuolar protein sorting 36 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 252 ESTs, 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
vacuolar protein sorting 36 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 212 ESTs, 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
vacuolar protein-sorting-associated protein 36 isoform X1
vacuolar protein-sorting-associated protein 36 isoform X2
vacuolar protein-sorting-associated protein 36 isoform X3
thrombospondin type 1 domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 167 ESTs, 5 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
thrombospondin type 1 domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 162 ESTs, 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
thrombospondin type 1 domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 125 ESTs, 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
thrombospondin type-1 domain-containing protein 1 isoform X1
thrombospondin type-1 domain-containing protein 1 isoform X2