Suricata suricatta isolate VVHF042 chromosome 15, meerkat_22Aug2017_6uvM2_HiC, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Laurasiatheria; Carnivora; Feliformia; Herpestidae; Suricata.
REFSEQ INFORMATION: The reference sequence is identical to\nCM016985.1.\nAssembly name: meerkat_22Aug2017_6uvM2_HiC\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the DNA Zoo on 2019/07/03. The\noriginal whole-genome shotgun project has the accession\nVCRZ00000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: DNA Zoo\nAssembly Method :: 3-D DNA Pipeline v. AUGUST-2017\nAssembly Name :: meerkat_22Aug2017_6uvM2_HiC\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 50.0x\nSequencing Technology :: Illumina HiSeq; Illumina X10\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Suricata suricatta Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.2\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
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 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC115278692, 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 1 sample with support for all annotated introns
uncharacterized LOC115278692, transcript variant X1
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
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
protein kinase, DNA-activated, catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
DNA-dependent protein kinase catalytic subunit
COORDINATES: nucleotide motif:Rfam:12.0:RF00091
uncharacterized LOC115278693, transcript variant X1
uncharacterized LOC115278693, transcript variant X2
minichromosome maintenance complex component 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
ubiquitin-conjugating enzyme E2 variant 2
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: 15 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
EF-hand calcium binding domain 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
EF-hand calcium binding domain 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
EF-hand calcium binding domain 1, transcript variant X2
EF-hand calcium binding domain 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
EF-hand calcium-binding domain-containing protein 1
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
snail family transcriptional repressor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
pancreatic progenitor cell differentiation and proliferation factor like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
pancreatic progenitor cell differentiation and proliferation factor like, transcript variant X2
pancreatic progenitor cell differentiation and proliferation factor-like protein isoform X1
pancreatic progenitor cell differentiation and proliferation factor-like protein isoform X2
tigger transposable element-derived protein 1-like, transcript variant X2
tigger transposable element-derived protein 1-like, transcript variant X1
tigger transposable element-derived protein 1-like, transcript variant X4
tigger transposable element-derived protein 1-like, transcript variant X3
tigger transposable element-derived protein 1-like isoform X1
tigger transposable element-derived protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 5 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115279259, transcript variant X1
uncharacterized LOC115279259, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1, transcript variant X6
protein-L-isoaspartate O-methyltransferase domain-containing protein 1 isoform X1
protein-L-isoaspartate O-methyltransferase domain-containing protein 1 isoform X3
protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein-L-isoaspartate O-methyltransferase domain-containing protein 1 isoform X2
uncharacterized LOC115278671, transcript variant X1
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
uncharacterized LOC115278671, 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 3 samples with support for all annotated introns
uncharacterized LOC115279332, transcript variant X2
uncharacterized LOC115279332, transcript variant X1
ST18 C2H2C-type zinc finger transcription factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
suppression of tumorigenicity 18 protein
uncharacterized LOC115279245, transcript variant X2
uncharacterized LOC115279245, transcript variant X1
RB1 inducible coiled-coil 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
RB1 inducible coiled-coil 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
RB1 inducible coiled-coil 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RB1 inducible coiled-coil 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
RB1 inducible coiled-coil 1, transcript variant X1
RB1-inducible coiled-coil protein 1 isoform X5
RB1-inducible coiled-coil protein 1 isoform X3
RB1-inducible coiled-coil protein 1 isoform X4
RB1-inducible coiled-coil protein 1 isoform X2
RB1-inducible coiled-coil protein 1 isoform X1
RB1 inducible coiled-coil 1, transcript variant X6
RB1-inducible coiled-coil protein 1 isoform X6
RB1 inducible coiled-coil 1, transcript variant X7
RB1-inducible coiled-coil protein 1 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
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 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 88% 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: 10 Proteins, and 43% 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, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATPase H+ transporting V1 subunit H, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
ATPase H+ transporting V1 subunit H, transcript variant X3
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 14 samples with support for all annotated introns
ATPase H+ transporting V1 subunit H, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
V-type proton ATPase subunit H isoform X2
V-type proton ATPase subunit H isoform X3
V-type proton ATPase subunit H isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
transcription elongation factor A1, transcript variant X2
transcription elongation factor A1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transcription elongation factor A1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcription elongation factor A protein 1 isoform X2
transcription elongation factor A protein 1 isoform X1
transcription elongation factor A protein 1 isoform X3
transcription elongation factor A1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
transcription elongation factor A protein 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
39S ribosomal protein L15, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115279214, transcript variant X2
uncharacterized LOC115279214, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 1% coverage of the annotated genomic feature by RNAseq alignments
lipoxygenase homology domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00105
uncharacterized LOC115278685, transcript variant X2
uncharacterized LOC115278685, transcript variant X1
uncharacterized LOC115279074, transcript variant X5
uncharacterized LOC115279074, transcript variant X2
uncharacterized LOC115279074, transcript variant X4
uncharacterized LOC115279074, transcript variant X1
uncharacterized LOC115279074, transcript variant X3
uncharacterized LOC115279074, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 68, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protein 68, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transmembrane protein 68, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
transmembrane protein 68, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
transmembrane protein 68, transcript variant X5
transmembrane protein 68, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protein 68, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
trimethylguanosine synthase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
trimethylguanosine synthase 1, transcript variant X2
LYN proto-oncogene, Src family tyrosine kinase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LYN proto-oncogene, Src family tyrosine kinase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LYN proto-oncogene, Src family tyrosine kinase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LYN proto-oncogene, Src family tyrosine kinase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LYN proto-oncogene, Src family tyrosine kinase, transcript variant X1
LYN proto-oncogene, Src family tyrosine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF01277
MOS proto-oncogene, serine/threonine kinase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
proto-oncogene serine/threonine-protein kinase mos
PLAG1 zinc finger, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PLAG1 zinc finger, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PLAG1 zinc finger, transcript variant X1
PLAG1 zinc finger, transcript variant X2
PLAG1 zinc finger, transcript variant X5
PLAG1 zinc finger, transcript variant X6
coiled-coil-helix-coiled-coil-helix domain containing 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
coiled-coil-helix-coiled-coil-helix domain-containing protein 7
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
short chain dehydrogenase/reductase family 16C member 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
short chain dehydrogenase/reductase family 16C member 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
epidermal retinol dehydrogenase 2 isoform X2
epidermal retinol dehydrogenase 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC115278994, transcript variant X1
uncharacterized LOC115278994, transcript variant X2
inositol monophosphatase domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
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: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC115279182, transcript variant X2
uncharacterized LOC115279182, transcript variant X3
uncharacterized LOC115279182, transcript variant X1
family with sequence similarity 110 member B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 8 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
neutral sphingomyelinase activation associated factor, transcript variant X2
neutral sphingomyelinase activation associated factor, transcript variant X1
neutral sphingomyelinase activation associated factor, transcript variant X3
uncharacterized LOC115279034, transcript variant X1
uncharacterized LOC115279034, transcript variant X2
thymocyte selection associated high mobility group box, transcript variant X3
thymocyte selection associated high mobility group box, transcript variant X2
thymocyte selection associated high mobility group box, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
thymocyte selection-associated high mobility group box protein TOX isoform X1
thymocyte selection-associated high mobility group box protein TOX isoform 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 10 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
uncharacterized LOC115279381, transcript variant X1
uncharacterized LOC115279381, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
chromodomain helicase DNA binding protein 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
chromodomain-helicase-DNA-binding protein 7
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aspartate beta-hydroxylase, transcript variant X3
aspartyl/asparaginyl beta-hydroxylase isoform X3
aspartate beta-hydroxylase, transcript variant X1
aspartate beta-hydroxylase, transcript variant X2
aspartyl/asparaginyl beta-hydroxylase isoform X1
aspartyl/asparaginyl beta-hydroxylase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115279516, transcript variant X2
uncharacterized LOC115279516, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 92% 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 Proteins
sodium/potassium transporting ATPase interacting 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
sodium/potassium-transporting ATPase subunit beta-1-interacting protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 61% 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 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
YTH N6-methyladenosine RNA binding protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
YTH N6-methyladenosine RNA binding protein 3, transcript variant X5
YTH N6-methyladenosine RNA binding protein 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
YTH N6-methyladenosine RNA binding protein 3, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
YTH N6-methyladenosine RNA binding protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
YTH N6-methyladenosine RNA binding protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
YTH N6-methyladenosine RNA binding protein 3, transcript variant X4
YTH N6-methyladenosine RNA binding protein 3, transcript variant X6
YTH domain-containing family protein 3 isoform X1
YTH domain-containing family protein 3 isoform X2
YTH N6-methyladenosine RNA binding protein 3, transcript variant X7
YTH domain-containing family protein 3 isoform X3
uncharacterized LOC115279272, transcript variant X3
uncharacterized LOC115279272, transcript variant X5
uncharacterized LOC115279272, transcript variant X8
uncharacterized LOC115279272, transcript variant X7
uncharacterized LOC115279272, transcript variant X10
uncharacterized LOC115279272, transcript variant X2
uncharacterized LOC115279272, transcript variant X11
uncharacterized LOC115279272, transcript variant X6
uncharacterized LOC115279272, transcript variant X1
uncharacterized LOC115279272, transcript variant X12
uncharacterized LOC115279272, transcript variant X4
uncharacterized LOC115279272, transcript variant X9
uncharacterized protein LOC115279272 isoform X5
uncharacterized protein LOC115279272 isoform X4
uncharacterized protein LOC115279272 isoform X7
uncharacterized protein LOC115279272 isoform X1
uncharacterized protein LOC115279272 isoform X3
uncharacterized protein LOC115279272 isoform X6
uncharacterized protein LOC115279272 isoform X8
uncharacterized protein LOC115279272 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
uncharacterized LOC115279352, transcript variant X2
uncharacterized LOC115279352, transcript variant X1
uncharacterized LOC115279132, transcript variant X4
uncharacterized LOC115279132, transcript variant X6
uncharacterized LOC115279132, transcript variant X3
uncharacterized LOC115279132, transcript variant X5
uncharacterized LOC115279132, transcript variant X2
uncharacterized LOC115279132, transcript variant X1
uncharacterized LOC115279132, transcript variant X7
25-hydroxycholesterol 7-alpha-hydroxylase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
25-hydroxycholesterol 7-alpha-hydroxylase isoform X1
25-hydroxycholesterol 7-alpha-hydroxylase, transcript variant X2
25-hydroxycholesterol 7-alpha-hydroxylase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115279169, transcript variant X2
uncharacterized LOC115279169, transcript variant X1
armadillo repeat containing 1, transcript variant X3
armadillo repeat containing 1, transcript variant X4
armadillo repeat containing 1, transcript variant X2
armadillo repeat containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
mitochondrial fission regulator 1, transcript variant X5
mitochondrial fission regulator 1, transcript variant X4
mitochondrial fission regulator 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mitochondrial fission regulator 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
mitochondrial fission regulator 1 isoform X1
mitochondrial fission regulator 1 isoform X2
mitochondrial fission regulator 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
mitochondrial fission regulator 1 isoform X3
phosphodiesterase 7A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
phosphodiesterase 7A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A isoform X2
high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A isoform X4
phosphodiesterase 7A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
phosphodiesterase 7A, transcript variant X5
phosphodiesterase 7A, transcript variant X3
high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A isoform X1
high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A isoform X3
high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A isoform X5
DnaJ heat shock protein family (Hsp40) member C5 beta, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% 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 C5 beta, transcript variant X3
DnaJ heat shock protein family (Hsp40) member C5 beta, transcript variant X2
DnaJ heat shock protein family (Hsp40) member C5 beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 14% coverage of the annotated genomic feature by RNAseq alignments
dnaJ homolog subfamily C member 5B isoform X1
dnaJ homolog subfamily C member 5B isoform X2
DnaJ heat shock protein family (Hsp40) member C5 beta, transcript variant X5
dnaJ homolog subfamily C member 5B isoform X3
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
tripartite motif containing 55, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif containing 55, transcript variant X1
tripartite motif containing 55, transcript variant X5
tripartite motif containing 55, transcript variant X4
tripartite motif containing 55, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif-containing protein 55 isoform X2
tripartite motif-containing protein 55 isoform X5
tripartite motif-containing protein 55 isoform X1
tripartite motif-containing protein 55 isoform X4
tripartite motif-containing protein 55 isoform X3
corticotropin releasing hormone, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
corticotropin releasing hormone, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
ribosome biogenesis regulatory protein homolog
alcohol dehydrogenase iron containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
alcohol dehydrogenase iron containing 1, transcript variant X2
alcohol dehydrogenase iron containing 1, transcript variant X3
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 7 samples with support for all annotated introns
hydroxyacid-oxoacid transhydrogenase, mitochondrial isoform X1
hydroxyacid-oxoacid transhydrogenase, mitochondrial isoform X2
alcohol dehydrogenase iron containing 1, transcript variant X4
hydroxyacid-oxoacid transhydrogenase, mitochondrial isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
valosin containing protein interacting protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
valosin containing protein interacting protein 1, transcript variant X3
valosin containing protein interacting protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
serine/threonine-protein kinase Sgk3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein kinase Sgk3, transcript variant X10
serine/threonine-protein kinase Sgk3, transcript variant X9
serine/threonine-protein kinase Sgk3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine-protein kinase Sgk3, transcript variant X3
serine/threonine-protein kinase Sgk3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein kinase Sgk3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein kinase Sgk3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine/threonine-protein kinase Sgk3, transcript variant X8
serine/threonine-protein kinase Sgk3, transcript variant X4
serine/threonine-protein kinase Sgk3 isoform X1
serine/threonine-protein kinase Sgk3 isoform X3
serine/threonine-protein kinase Sgk3 isoform X2
minichromosome maintenance domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
minichromosome maintenance domain-containing protein 2
COORDINATES: nucleotide motif:Rfam:12.0:RF00439
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 42
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00432
COP9 signalosome subunit 5, transcript variant X1
COP9 signalosome subunit 5, 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 15 samples with support for all annotated introns
COP9 signalosome complex subunit 5 isoform X1
COP9 signalosome complex subunit 5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
centrosome and spindle pole associated protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
centrosome and spindle pole associated protein 1, transcript variant X4
centrosome and spindle pole associated protein 1, transcript variant X5
centrosome and spindle pole associated protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
centrosome and spindle pole associated protein 1, transcript variant X2
centrosome and spindle pole associated protein 1, transcript variant X6
centrosome and spindle pole-associated protein 1 isoform X3
centrosome and spindle pole-associated protein 1 isoform X1
centrosome and spindle pole-associated protein 1 isoform X4
centrosome and spindle pole-associated protein 1 isoform X5
centrosome and spindle pole-associated protein 1 isoform X2
centrosome and spindle pole-associated protein 1 isoform X6
COORDINATES: nucleotide motif:Rfam:12.0:RF00322
ADP ribosylation factor guanine nucleotide exchange factor 1, transcript variant X2
ADP ribosylation factor guanine nucleotide exchange factor 1, transcript variant X1
ADP ribosylation factor guanine nucleotide exchange factor 1, transcript variant X4
brefeldin A-inhibited guanine nucleotide-exchange protein 1 isoform X2
brefeldin A-inhibited guanine nucleotide-exchange protein 1 isoform X1
brefeldin A-inhibited guanine nucleotide-exchange protein 1 isoform X4
ADP ribosylation factor guanine nucleotide exchange factor 1, transcript variant X3
brefeldin A-inhibited guanine nucleotide-exchange protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 148 Proteins
phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2
phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 2 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: 2 Proteins, and 97% 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: uncharacterized protein C8orf34 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 9% 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: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
extracellular sulfatase Sulf-1 isoform X1
extracellular sulfatase Sulf-1 isoform X3
extracellular sulfatase Sulf-1 isoform X2
solute carrier organic anion transporter family member 5A1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% 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 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115278742, transcript variant X2
uncharacterized LOC115278742, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor coactivator 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nuclear receptor coactivator 2, transcript variant X8
nuclear receptor coactivator 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
nuclear receptor coactivator 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
nuclear receptor coactivator 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear receptor coactivator 2, transcript variant X6
nuclear receptor coactivator 2, transcript variant X7
nuclear receptor coactivator 2, transcript variant X2
nuclear receptor coactivator 2, transcript variant X9
nuclear receptor coactivator 2, transcript variant X11
nuclear receptor coactivator 2, transcript variant X10
nuclear receptor coactivator 2 isoform X2
nuclear receptor coactivator 2 isoform X1
nuclear receptor coactivator 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
translocation associated membrane protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
translocation associated membrane protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
translocation associated membrane protein 1, transcript variant X3
translocating chain-associated membrane protein 1 isoform X2
translocating chain-associated membrane protein 1 isoform X1
translocating chain-associated membrane protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 75% 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 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC115279329, transcript variant X1
uncharacterized LOC115279329, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00429
EYA transcriptional coactivator and phosphatase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel subfamily A member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
potassium voltage-gated channel subfamily B member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 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: 22 Proteins, and 83% 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 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
chromosome 15 C8orf89 homolog, transcript variant X3
chromosome 15 C8orf89 homolog, transcript variant X4
chromosome 15 C8orf89 homolog, transcript variant X1
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 5 samples with support for all annotated introns
chromosome 15 C8orf89 homolog, transcript variant X2
chromosome 15 C8orf89 homolog, transcript variant X5
putative uncharacterized protein C8orf89 homolog isoform X2
putative uncharacterized protein C8orf89 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
staufen double-stranded RNA binding protein 2, transcript variant X6
staufen double-stranded RNA binding protein 2, transcript variant X4
staufen double-stranded RNA binding protein 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
staufen double-stranded RNA binding protein 2, transcript variant X7
staufen double-stranded RNA binding protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
staufen double-stranded RNA binding protein 2, transcript variant X3
staufen double-stranded RNA binding protein 2, transcript variant X1
double-stranded RNA-binding protein Staufen homolog 2 isoform X3
double-stranded RNA-binding protein Staufen homolog 2 isoform X4
double-stranded RNA-binding protein Staufen homolog 2 isoform X2
double-stranded RNA-binding protein Staufen homolog 2 isoform X1
double-stranded RNA-binding protein Staufen homolog 2 isoform X5
ubiquitin conjugating enzyme E2 W, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ubiquitin conjugating enzyme E2 W, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ubiquitin-conjugating enzyme E2 W isoform X1
ubiquitin-conjugating enzyme E2 W isoform X2
uncharacterized LOC115278902, transcript variant X2
uncharacterized LOC115278902, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 50% 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 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins
uncharacterized LOC115279000, transcript variant X1
uncharacterized LOC115279000, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115279000, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% 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 3 bases in 2 codons; 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: 32 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
ganglioside induced differentiation associated protein 1, transcript variant X1
ganglioside-induced differentiation-associated protein 1 isoform X1
ganglioside induced differentiation associated protein 1, transcript variant X2
ganglioside induced differentiation associated protein 1, transcript variant X3
ganglioside-induced differentiation-associated protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% 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, and 46% coverage of the annotated genomic feature by RNAseq alignments
cysteine rich secretory protein LCCL domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
cysteine-rich secretory protein LCCL domain-containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115278698, transcript variant X1
uncharacterized LOC115278698, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
peroxisomal biogenesis factor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
peroxisomal biogenesis factor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
peroxisomal biogenesis factor 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
peroxisomal biogenesis factor 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
peroxisomal biogenesis factor 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
cAMP-dependent protein kinase inhibitor alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cAMP-dependent protein kinase inhibitor alpha, transcript variant X2
cAMP-dependent protein kinase inhibitor alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 94% 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: zinc finger C2HC domain-containing protein 1A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
hes related family bHLH transcription factor with YRPW motif 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
hairy/enhancer-of-split related with YRPW motif protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
28S ribosomal protein S28, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115278976, transcript variant X1
uncharacterized LOC115278976, transcript variant X3
uncharacterized LOC115278976, transcript variant X2
uncharacterized LOC115278976, transcript variant X4
zinc finger and BTB domain containing 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain-containing protein 10 isoform X2
zinc finger and BTB domain containing 10, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 10 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phosphoprotein membrane anchor with glycosphingolipid microdomains 1, transcript variant X1
phosphoprotein membrane anchor with glycosphingolipid microdomains 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
phosphoprotein membrane anchor with glycosphingolipid microdomains 1, transcript variant X3
phosphoprotein associated with glycosphingolipid-enriched microdomains 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
myelin P2 protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
myelin P2 protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myelin P2 protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
fatty acid binding protein 12, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fatty acid binding protein 12, transcript variant X1
fatty acid binding protein 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 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: inserted 7 bases in 5 codons; deleted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 72% 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 7 bases in 5 codons; deleted 4 bases in 2 codons; substituted 7 bases at 7 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: sodium/bile acid cotransporter 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% 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 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 70% 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: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
RALY RNA binding protein like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RALY RNA binding protein like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RALY RNA binding protein like, transcript variant X1
RALY RNA binding protein like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RALY RNA binding protein like, transcript variant X6
RALY RNA binding protein like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RALY RNA binding protein like, transcript variant X3
RNA-binding Raly-like protein isoform X3
RNA-binding Raly-like protein isoform X1
RNA-binding Raly-like protein isoform X2
RALY RNA binding protein like, transcript variant X7
RNA-binding Raly-like protein isoform X4
uncharacterized LOC115279267, transcript variant X2
uncharacterized LOC115279267, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
leucine rich repeat and coiled-coil centrosomal protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
leucine rich repeat and coiled-coil centrosomal protein 1, transcript variant X2
leucine-rich repeat and coiled-coil domain-containing protein 1 isoform X1
leucine-rich repeat and coiled-coil domain-containing protein 1 isoform X2
leucine rich repeat and coiled-coil centrosomal protein 1, transcript variant X3
leucine-rich repeat and coiled-coil domain-containing protein 1 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00156
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 76% coverage of the annotated genomic feature by RNAseq alignments
E2F transcription factor 5, transcript variant X2
E2F transcription factor 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC115279275, transcript variant X2
uncharacterized LOC115279275, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
carbonic anhydrase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
carbonic anhydrase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
ATPase H+ transporting V0 subunit d2, transcript variant X2
ATPase H+ transporting V0 subunit d2, transcript variant X1
V-type proton ATPase subunit d 2 isoform X1
V-type proton ATPase subunit d 2 isoform X2
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, and 19% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: solute carrier family 7 member 13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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: 47 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
WW domain containing E3 ubiquitin protein ligase 1, transcript variant X2
WW domain containing E3 ubiquitin protein ligase 1, transcript variant X5
WW domain containing E3 ubiquitin protein ligase 1, transcript variant X4
WW domain containing E3 ubiquitin protein ligase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
WW domain containing E3 ubiquitin protein ligase 1, transcript variant X1
NEDD4-like E3 ubiquitin-protein ligase WWP1 isoform X3
NEDD4-like E3 ubiquitin-protein ligase WWP1 isoform X1
NEDD4-like E3 ubiquitin-protein ligase WWP1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
regulator of microtubule dynamics 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
regulator of microtubule dynamics 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
regulator of microtubule dynamics 1, transcript variant X3
regulator of microtubule dynamics protein 1 isoform X2
regulator of microtubule dynamics protein 1 isoform X1
regulator of microtubule dynamics protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 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: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cyclic nucleotide gated channel subunit beta 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
cyclic nucleotide-gated cation channel beta-3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
cyclic nucleotide-binding domain-containing protein 1-like, transcript variant X2
cyclic nucleotide-binding domain-containing protein 1-like, transcript variant X4
cyclic nucleotide-binding domain-containing protein 1-like, transcript variant X1
cyclic nucleotide-binding domain-containing protein 1-like, transcript variant X3
cyclic nucleotide-binding domain-containing protein 1-like isoform X2
cyclic nucleotide-binding domain-containing protein 1-like isoform X4
cyclic nucleotide-binding domain-containing protein 1-like isoform X1
cyclic nucleotide-binding domain-containing protein 1-like isoform X3
cyclic nucleotide-binding domain-containing protein 1-like, transcript variant X5
uncharacterized LOC115279279, transcript variant X2
uncharacterized LOC115279279, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115279280, transcript variant X5
uncharacterized LOC115279280, transcript variant X1
uncharacterized LOC115279280, transcript variant X3
uncharacterized LOC115279280, transcript variant X4
uncharacterized LOC115279280, transcript variant X2
receptor interacting serine/threonine kinase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
receptor-interacting serine/threonine-protein kinase 2
oxidative stress induced growth inhibitor family member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
oxidative stress-induced growth inhibitor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
2,4-dienoyl-CoA reductase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
2,4-dienoyl-CoA reductase, mitochondrial isoform X2
2,4-dienoyl-CoA reductase 1, transcript variant X1
2,4-dienoyl-CoA reductase, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115279270, transcript variant X1
uncharacterized LOC115279270, transcript variant X2
N-terminal EF-hand calcium binding protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56% coverage of the annotated genomic feature by RNAseq alignments
N-terminal EF-hand calcium-binding protein 1
phosphatidylinositol-4,5-bisphosphate 4-phosphatase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
type 2 phosphatidylinositol 4,5-bisphosphate 4-phosphatase
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 16 samples with support for all annotated introns
OTU domain containing 6B, transcript variant X2
OTU domain containing 6B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
OTU domain containing 6B, transcript variant X3
leucine rich repeat containing 69, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine rich repeat containing 69, transcript variant X3
leucine rich repeat containing 69, transcript variant X2
leucine-rich repeat-containing protein 69 isoform X1
leucine-rich repeat-containing protein 69 isoform X3
leucine-rich repeat-containing protein 69 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
RUNX1 partner transcriptional co-repressor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RUNX1 partner transcriptional co-repressor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RUNX1 partner transcriptional co-repressor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RUNX1 partner transcriptional co-repressor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC115278676, transcript variant X1
uncharacterized LOC115278676, transcript variant X2
uncharacterized LOC115279511, transcript variant X1
uncharacterized LOC115279511, transcript variant X2
uncharacterized LOC115279043, transcript variant X2
uncharacterized LOC115279043, transcript variant X1
uncharacterized LOC115279188, transcript variant X2
uncharacterized LOC115279188, transcript variant X3
uncharacterized LOC115279188, transcript variant X1
family with sequence similarity 92 member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments
RNA binding motif protein 12B, transcript variant X2
RNA binding motif protein 12B, transcript variant X3
RNA binding motif protein 12B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
RNA binding motif protein 12B, transcript variant X4
pyruvate dehyrogenase phosphatase catalytic subunit 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
pyruvate dehyrogenase phosphatase catalytic subunit 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
pyruvate dehyrogenase phosphatase catalytic subunit 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
pyruvate dehyrogenase phosphatase catalytic subunit 1 isoform X1
pyruvate dehyrogenase phosphatase catalytic subunit 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
GTP binding protein overexpressed in skeletal muscle, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
GTP binding protein overexpressed in skeletal muscle, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
DNA repair and recombination protein RAD54B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
vir like m6A methyltransferase associated, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
vir like m6A methyltransferase associated, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
epithelial splicing regulatory protein 1, transcript variant X1
epithelial splicing regulatory protein 1, transcript variant X3
epithelial splicing regulatory protein 1, transcript variant X5
epithelial splicing regulatory protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
epithelial splicing regulatory protein 1, transcript variant X4
epithelial splicing regulatory protein 1 isoform X3
epithelial splicing regulatory protein 1 isoform X5
epithelial splicing regulatory protein 1 isoform X1
epithelial splicing regulatory protein 1 isoform X2
epithelial splicing regulatory protein 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
probable C-mannosyltransferase DPY19L4 isoform X1
probable C-mannosyltransferase DPY19L4 isoform X2
probable C-mannosyltransferase DPY19L4 isoform X5
probable C-mannosyltransferase DPY19L4 isoform X6
probable C-mannosyltransferase DPY19L4 isoform X3
probable C-mannosyltransferase DPY19L4 isoform X4
integrator complex subunit 8, transcript variant X2
integrator complex subunit 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
tumor protein p53 inducible nuclear protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
tumor protein p53-inducible nuclear protein 1 isoform X1
tumor protein p53 inducible nuclear protein 1, transcript variant X2
tumor protein p53-inducible nuclear protein 1 isoform X2
NADH:ubiquinone oxidoreductase complex assembly factor 6, transcript variant X6
NADH:ubiquinone oxidoreductase complex assembly factor 6, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
NADH:ubiquinone oxidoreductase complex assembly factor 6, transcript variant X1
NADH:ubiquinone oxidoreductase complex assembly factor 6, transcript variant X2
NADH:ubiquinone oxidoreductase complex assembly factor 6, transcript variant X3
NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 isoform X1
NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 isoform X2
NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 isoform X3
NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 isoform X5
NADH:ubiquinone oxidoreductase complex assembly factor 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
NADH:ubiquinone oxidoreductase complex assembly factor 6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
NADH dehydrogenase (ubiquinone) complex I, assembly factor 6 isoform X4
pleckstrin homology and FYVE domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
pleckstrin homology and FYVE domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
pleckstrin homology and FYVE domain containing 2, transcript variant X6
pleckstrin homology and FYVE domain containing 2, transcript variant X4
pleckstrin homology and FYVE domain containing 2, transcript variant X3
pleckstrin homology and FYVE domain containing 2, transcript variant X5
pleckstrin homology domain-containing family F member 2
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
chromosome 15 C8orf37 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
chromosome 15 C8orf37 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial transcription termination factor 3
transcription termination factor 3, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
carboxypeptidase Q, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
carboxypeptidase Q, transcript variant X2
uncharacterized LOC115279296, transcript variant X1
uncharacterized LOC115279296, transcript variant X2
uncharacterized LOC115279296, transcript variant X3
testis-specific Y-encoded-like protein 5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
testis-specific Y-encoded-like protein 5 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
LOW QUALITY PROTEIN: lysosomal-associated transmembrane protein 4B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00139
reactive intermediate imine deaminase A homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
2-iminobutanoate/2-iminopropanoate deaminase
POP1 homolog, ribonuclease P/MRP subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ribonucleases P/MRP protein subunit POP1
uncharacterized LOC115279335, transcript variant X2
uncharacterized LOC115279335, transcript variant X1
uncharacterized LOC115279335, transcript variant X3
potassium voltage-gated channel modifier subfamily S member 2
potassium voltage-gated channel subfamily S member 2
serine/threonine kinase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
serine/threonine kinase 3, transcript variant X1
serine/threonine-protein kinase 3 isoform X2
serine/threonine-protein kinase 3 isoform X1
odd-skipped related transciption factor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
odd-skipped related transciption factor 2, transcript variant X3
odd-skipped related transciption factor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein odd-skipped-related 2 isoform X1
protein odd-skipped-related 2 isoform X2
vacuolar protein sorting 13 homolog B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
vacuolar protein sorting 13 homolog B, transcript variant X2
vacuolar protein sorting 13 homolog B, transcript variant X3
vacuolar protein sorting 13 homolog B, transcript variant X4
vacuolar protein sorting 13 homolog B, transcript variant X5
vacuolar protein sorting 13 homolog B, transcript variant X6
vacuolar protein sorting 13 homolog B, transcript variant X7
vacuolar protein sorting 13 homolog B, transcript variant X8
vacuolar protein sorting 13 homolog B, transcript variant X9
vacuolar protein sorting 13 homolog B, transcript variant X10
vacuolar protein sorting-associated protein 13B isoform X1
vacuolar protein sorting-associated protein 13B isoform X2
vacuolar protein sorting-associated protein 13B isoform X3
vacuolar protein sorting-associated protein 13B isoform X4
vacuolar protein sorting-associated protein 13B isoform X5
vacuolar protein sorting-associated protein 13B isoform X6
vacuolar protein sorting-associated protein 13B isoform X7
vacuolar protein sorting-associated protein 13B isoform X8
vacuolar protein sorting-associated protein 13B isoform X9
vacuolar protein sorting-associated protein 13B isoform X10
uncharacterized LOC115279291, transcript variant X2
uncharacterized LOC115279291, transcript variant X1
uncharacterized LOC115279290, transcript variant X2
uncharacterized LOC115279290, transcript variant X1
cytochrome c oxidase subunit 6C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
cytochrome c oxidase subunit 6C, transcript variant X2
regulator of G protein signaling 22, transcript variant X3
regulator of G protein signaling 22, transcript variant X5
regulator of G protein signaling 22, transcript variant X1
regulator of G protein signaling 22, transcript variant X2
regulator of G protein signaling 22, transcript variant X4
regulator of G-protein signaling 22 isoform X3
regulator of G-protein signaling 22 isoform X5
regulator of G-protein signaling 22 isoform X1
regulator of G-protein signaling 22 isoform X4
regulator of G-protein signaling 22 isoform X2
regulator of G protein signaling 22, transcript variant X6
regulator of G-protein signaling 22 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
RNA polymerase II subunit K, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
RNA polymerase II subunit K, transcript variant X1
RNA polymerase II subunit K, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
DNA-directed RNA polymerases I, II, and III subunit RPABC4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 19A, RBR E3 ubiquitin protein ligase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain 46, transcript variant X3
ankyrin repeat domain-containing protein 46 isoform X2
ankyrin repeat domain 46, transcript variant X2
ankyrin repeat domain 46, transcript variant X1
ankyrin repeat domain-containing protein 46 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein zeta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger protein 706, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
zinc finger protein 706, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 706, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
zinc finger protein 706, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 24 Proteins
neurocalcin delta, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
neurocalcin delta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neurocalcin delta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
neurocalcin delta, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neurocalcin delta, transcript variant X5
ribonucleotide reductase regulatory TP53 inducible subunit M2B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ribonucleotide reductase regulatory TP53 inducible subunit M2B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ribonucleoside-diphosphate reductase subunit M2 B
ubiquitin protein ligase E3 component n-recognin 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115279519, transcript variant X3
uncharacterized LOC115279519, transcript variant X1
uncharacterized LOC115279519, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
antizyme inhibitor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 25 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
antizyme inhibitor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 25 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
antizyme inhibitor 1, transcript variant X6
antizyme inhibitor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
antizyme inhibitor 1, transcript variant X5
antizyme inhibitor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
antizyme inhibitor 1, transcript variant X7
uncharacterized LOC115278732, transcript variant X3
uncharacterized LOC115278732, transcript variant X1
uncharacterized LOC115278732, transcript variant X2
ATPase H+ transporting V1 subunit C1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ATPase H+ transporting V1 subunit C1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
brain and acute leukemia cytoplasmic protein
uncharacterized LOC115279321, transcript variant X2
uncharacterized LOC115279321, transcript variant X1
uncharacterized LOC115279320, transcript variant X1
uncharacterized LOC115279320, transcript variant X3
uncharacterized LOC115279320, transcript variant X2
collagen triple helix repeat containing 1
collagen triple helix repeat-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
mitochondrial folate transporter/carrier
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
regulating synaptic membrane exocytosis 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis protein 2
regulating synaptic membrane exocytosis protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
dendrocyte expressed seven transmembrane protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dendritic cell-specific transmembrane protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
LDL receptor related protein 12, transcript variant X2
LDL receptor related protein 12, transcript variant X3
LDL receptor related protein 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
low-density lipoprotein receptor-related protein 12 isoform X2
low-density lipoprotein receptor-related protein 12 isoform X1
uncharacterized LOC115279310, transcript variant X2
uncharacterized LOC115279310, transcript variant X1
uncharacterized LOC115279145, transcript variant X1
uncharacterized LOC115279145, 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 8 samples with support for all annotated introns
zinc finger protein, FOG family member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
oxidation resistance 1, transcript variant X1
oxidation resistance 1, transcript variant X2
oxidation resistance 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
oxidation resistance 1, transcript variant X4
uncharacterized LOC115279524, transcript variant X2
uncharacterized LOC115279524, transcript variant X1
oxidation resistance protein 1 isoform X1
oxidation resistance protein 1 isoform X2
oxidation resistance protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
oxidation resistance 1, transcript variant X6
oxidation resistance protein 1 isoform X5
oxidation resistance 1, transcript variant X5
oxidation resistance protein 1 isoform X4
oxidation resistance 1, transcript variant X8
oxidation resistance 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
oxidation resistance protein 1 isoform X7
oxidation resistance protein 1 isoform X6
uncharacterized LOC115279264, transcript variant X1
uncharacterized LOC115279264, transcript variant X3
uncharacterized LOC115279264, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC115279452, transcript variant X1
uncharacterized LOC115279452, transcript variant X3
uncharacterized LOC115279452, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 3 subunit E
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
ER membrane protein complex subunit 2, transcript variant X3
ER membrane protein complex subunit 2, transcript variant X2
ER membrane protein complex subunit 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
ER membrane protein complex subunit 2, transcript variant X4
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 11 samples with support for all annotated introns
ER membrane protein complex subunit 2 isoform X1
ER membrane protein complex subunit 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 18% 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 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
ENY2 transcription and export complex 2 subunit, transcript variant X2
ENY2 transcription and export complex 2 subunit, transcript variant X1
ENY2 transcription and export complex 2 subunit, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
transcription and mRNA export factor ENY2 isoform X3
transcription and mRNA export factor ENY2 isoform X1
transcription and mRNA export factor ENY2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
estrogen receptor binding site associated antigen 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
estrogen receptor binding site associated antigen 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
receptor-binding cancer antigen expressed on SiSo cells isoform X1
receptor-binding cancer antigen expressed on SiSo cells isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
potassium voltage-gated channel modifier subfamily V member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
potassium voltage-gated channel subfamily V member 1
COORDINATES: nucleotide motif:Rfam:12.0:RF00275
CUB and Sushi multiple domains 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 74% coverage of the annotated genomic feature by RNAseq alignments
CUB and Sushi multiple domains 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
CUB and Sushi multiple domains 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
CUB and sushi domain-containing protein 3 isoform X3
CUB and sushi domain-containing protein 3 isoform X2
CUB and sushi domain-containing protein 3 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00598
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins
uncharacterized LOC115279089, transcript variant X1
uncharacterized LOC115279089, transcript variant X2
transcriptional repressor GATA binding 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transcriptional repressor GATA binding 1, transcript variant X6
transcriptional repressor GATA binding 1, transcript variant X1
transcriptional repressor GATA binding 1, transcript variant X2
transcriptional repressor GATA binding 1, transcript variant X7
transcriptional repressor GATA binding 1, transcript variant X5
transcriptional repressor GATA binding 1, transcript variant X3
transcriptional repressor GATA binding 1, transcript variant X4
zinc finger transcription factor Trps1 isoform X3
zinc finger transcription factor Trps1 isoform X1
zinc finger transcription factor Trps1 isoform X2
zinc finger transcription factor Trps1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 3 subunit H
UTP23 small subunit processome component
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
RAD21 cohesin complex component, transcript variant X2
RAD21 cohesin complex component, transcript variant X1
double-strand-break repair protein rad21 homolog isoform X2
double-strand-break repair protein rad21 homolog isoform X1
alanine and arginine rich domain containing protein
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: alanine and arginine-rich domain-containing protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 50% 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, and 86% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 30
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
sterile alpha motif domain containing 12
sterile alpha motif domain-containing protein 12
uncharacterized LOC115278926, transcript variant X3
uncharacterized LOC115278926, transcript variant X1
uncharacterized LOC115278926, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor receptor superfamily member 11B
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X7
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X2
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X1
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X4
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ectonucleotide pyrophosphatase/phosphodiesterase 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X7
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X6
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X5
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X4
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X2
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X3
ectonucleotide pyrophosphatase/phosphodiesterase family member 2 isoform X1
TATA-box binding protein associated factor 2, transcript variant X2
TATA-box binding protein associated factor 2, transcript variant X3
TATA-box binding protein associated factor 2, transcript variant X1
transcription initiation factor TFIID subunit 2 isoform X2
transcription initiation factor TFIID subunit 2 isoform X3
transcription initiation factor TFIID subunit 2 isoform X1
TATA-box binding protein associated factor 2, transcript variant X13
TATA-box binding protein associated factor 2, transcript variant X4
transcription initiation factor TFIID subunit 2 isoform X4
TATA-box binding protein associated factor 2, transcript variant X14
TATA-box binding protein associated factor 2, transcript variant X5
TATA-box binding protein associated factor 2, transcript variant X7
TATA-box binding protein associated factor 2, transcript variant X6
transcription initiation factor TFIID subunit 2 isoform X6
transcription initiation factor TFIID subunit 2 isoform X5
TATA-box binding protein associated factor 2, transcript variant X9
TATA-box binding protein associated factor 2, transcript variant X8
TATA-box binding protein associated factor 2, transcript variant X12
TATA-box binding protein associated factor 2, transcript variant X11
TATA-box binding protein associated factor 2, transcript variant X10
transcription initiation factor TFIID subunit 2 isoform X8
transcription initiation factor TFIID subunit 2 isoform X7
DNA replication and sister chromatid cohesion 1, transcript variant X3
DNA replication and sister chromatid cohesion 1, transcript variant X1
sister chromatid cohesion protein DCC1 isoform X3
sister chromatid cohesion protein DCC1 isoform X1
DNA replication and sister chromatid cohesion 1, transcript variant X2
sister chromatid cohesion protein DCC1 isoform X2
DNA replication and sister chromatid cohesion 1, transcript variant X4
sister chromatid cohesion protein DCC1 isoform X4
DEP domain containing MTOR interacting protein
DEP domain-containing mTOR-interacting protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial ribosomal protein L13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
39S ribosomal protein L13, mitochondrial isoform X1
mitochondrial ribosomal protein L13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
39S ribosomal protein L13, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC115279305, transcript variant X2
uncharacterized LOC115279305, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
zinc fingers and homeoboxes 2, transcript variant X1
zinc fingers and homeoboxes 2, transcript variant X2
uncharacterized LOC115278679, transcript variant X1
uncharacterized LOC115278679, transcript variant X2
TBC1 domain family member 31, transcript variant X1
TBC1 domain family member 31, transcript variant X2
TBC1 domain family member 31, transcript variant X4
TBC1 domain family member 31, transcript variant X5
TBC1 domain family member 31, transcript variant X3
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
family with sequence similarity 83 member A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 83 member A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 80% coverage of the annotated genomic feature by RNAseq alignments
chromosome 15 C8orf76 homolog, transcript variant X2
chromosome 15 C8orf76 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized protein C8orf76 homolog isoform X2
uncharacterized protein C8orf76 homolog isoform X1
zinc fingers and homeoboxes 1, transcript variant X2
zinc fingers and homeoboxes 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ATPase family AAA domain-containing protein 2
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 17 samples with support for all annotated introns
WDYHV motif containing 1, transcript variant X1
WDYHV motif containing 1, transcript variant X3
WDYHV motif containing 1, transcript variant X4
WDYHV motif containing 1, transcript variant X2
WDYHV motif containing 1, transcript variant X5
protein N-terminal glutamine amidohydrolase isoform X1
protein N-terminal glutamine amidohydrolase isoform X2
protein N-terminal glutamine amidohydrolase isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
family with sequence similarity 91 member A1, transcript variant X1
family with sequence similarity 91 member A1, transcript variant X2
family with sequence similarity 91 member A1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: fer-1-like protein 6
transmembrane protein 65, transcript variant X1
transmembrane protein 65, transcript variant X2
tRNA wybutosine-synthesizing protein 2 homolog
TatD DNase domain containing 1, transcript variant X3
TatD DNase domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
TatD DNase domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
TatD DNase domain containing 1, transcript variant X6
TatD DNase domain containing 1, transcript variant X5
TatD DNase domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
putative deoxyribonuclease TATDN1 isoform X3
putative deoxyribonuclease TATDN1 isoform X1
putative deoxyribonuclease TATDN1 isoform X2
putative deoxyribonuclease TATDN1 isoform X4
NADH:ubiquinone oxidoreductase subunit B9
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9
MTSS I-BAR domain containing 1, transcript variant X4
MTSS I-BAR domain containing 1, transcript variant X2
MTSS I-BAR domain containing 1, transcript variant X3
MTSS I-BAR domain containing 1, transcript variant X1
zinc finger protein 572, transcript variant X3
zinc finger protein 572, transcript variant X2
zinc finger protein 572, transcript variant X1
zinc finger protein 572, transcript variant X4
NSE2 (MMS21) homolog, SMC5-SMC6 complex SUMO ligase, transcript variant X3
NSE2 (MMS21) homolog, SMC5-SMC6 complex SUMO ligase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
NSE2 (MMS21) homolog, SMC5-SMC6 complex SUMO ligase, transcript variant X4
NSE2 (MMS21) homolog, SMC5-SMC6 complex SUMO ligase, transcript variant X5
NSE2 (MMS21) homolog, SMC5-SMC6 complex SUMO ligase, transcript variant X6
NSE2 (MMS21) homolog, SMC5-SMC6 complex SUMO ligase, transcript variant X1
NSE2 (MMS21) homolog, SMC5-SMC6 complex SUMO ligase, transcript variant X7
tribbles pseudokinase 1, transcript variant X2
tribbles pseudokinase 1, transcript variant X1
uncharacterized LOC115279085, transcript variant X1
uncharacterized LOC115279085, transcript variant X2
uncharacterized LOC115279085, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115278973, transcript variant X2
uncharacterized LOC115278973, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115279146, transcript variant X7
uncharacterized LOC115279146, transcript variant X2
uncharacterized LOC115279146, transcript variant X4
uncharacterized LOC115279146, transcript variant X6
uncharacterized LOC115279146, transcript variant X1
uncharacterized LOC115279146, transcript variant X3
uncharacterized LOC115279146, transcript variant X5
uncharacterized LOC115279072, transcript variant X1
uncharacterized LOC115279072, transcript variant X2
MYC proto-oncogene, bHLH transcription factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC115279408, transcript variant X5
uncharacterized LOC115279408, transcript variant X6
uncharacterized LOC115279408, transcript variant X1
uncharacterized LOC115279408, transcript variant X2
uncharacterized LOC115279408, transcript variant X7
uncharacterized LOC115279408, transcript variant X3
uncharacterized LOC115279408, transcript variant X4
uncharacterized LOC115279408, transcript variant X8
uncharacterized LOC115279412, transcript variant X1
uncharacterized LOC115279412, transcript variant X2
uncharacterized LOC115279409, transcript variant X1
uncharacterized LOC115279409, transcript variant X5
uncharacterized LOC115279409, transcript variant X4
uncharacterized LOC115279409, transcript variant X2
uncharacterized LOC115279409, transcript variant X3
uncharacterized LOC115279409, transcript variant X6
uncharacterized LOC115278736, transcript variant X1
uncharacterized LOC115278736, transcript variant X2
uncharacterized LOC115278662, transcript variant X1
uncharacterized LOC115278662, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 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: 1 Protein, and 21% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 49 member B, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
family with sequence similarity 49 member B, transcript variant X12
family with sequence similarity 49 member B, transcript variant X8
family with sequence similarity 49 member B, transcript variant X2
family with sequence similarity 49 member B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
family with sequence similarity 49 member B, transcript variant X11
family with sequence similarity 49 member B, transcript variant X4
family with sequence similarity 49 member B, transcript variant X10
family with sequence similarity 49 member B, transcript variant X1
family with sequence similarity 49 member B, transcript variant X7
family with sequence similarity 49 member B, transcript variant X5
family with sequence similarity 49 member B, transcript variant X9
COORDINATES: nucleotide motif:Rfam:12.0:RF00045
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X1
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X2
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X4
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X3
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X4
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X3
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X2
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X1
adenylate cyclase 8, transcript variant X3
adenylate cyclase 8, transcript variant X2
adenylate cyclase 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily Q member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily KQT member 3
uncharacterized LOC115279111, transcript variant X1
uncharacterized LOC115279111, transcript variant X2
leucine rich repeat containing 6, transcript variant X2
leucine rich repeat containing 6, transcript variant X1
transmembrane protein 71, transcript variant X6
transmembrane protein 71, transcript variant X3
transmembrane protein 71, transcript variant X2
transmembrane protein 71, transcript variant X1
transmembrane protein 71, transcript variant X4
transmembrane protein 71, transcript variant X5
PHD finger protein 20 like 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
PHD finger protein 20 like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
PHD finger protein 20 like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
PHD finger protein 20-like protein 1 isoform X1
PHD finger protein 20-like protein 1 isoform X2
PHD finger protein 20-like protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 37% 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, and 83% coverage of the annotated genomic feature by RNAseq alignments
WNT1-inducible-signaling pathway protein 1
N-myc downstream regulated 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
N-myc downstream regulated 1, transcript variant X2
ST3 beta-galactoside alpha-2,3-sialyltransferase 1, transcript variant X4
ST3 beta-galactoside alpha-2,3-sialyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ST3 beta-galactoside alpha-2,3-sialyltransferase 1, transcript variant X2
ST3 beta-galactoside alpha-2,3-sialyltransferase 1, transcript variant X3
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 1
uncharacterized LOC115278747, transcript variant X2
uncharacterized LOC115278747, transcript variant X1
uncharacterized LOC115278747, transcript variant X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00211
uncharacterized LOC115279114, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins
uncharacterized LOC115279114, transcript variant X1
uncharacterized LOC115279397, transcript variant X2
uncharacterized LOC115279397, transcript variant X1
uncharacterized LOC115279397, transcript variant X4
uncharacterized LOC115279397, transcript variant X3
zinc finger and AT-hook domain containing, transcript variant X1
zinc finger and AT-hook domain containing, transcript variant X2
uncharacterized LOC115279057, transcript variant X2
uncharacterized LOC115279057, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00554
uncharacterized LOC115279140, transcript variant X2
uncharacterized LOC115279140, transcript variant X1
uncharacterized LOC115279129, transcript variant X1
uncharacterized LOC115279129, transcript variant X2
KH RNA binding domain containing, signal transduction associated 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
KH domain-containing, RNA-binding, signal transduction-associated protein 3
uncharacterized LOC115279171, transcript variant X1
uncharacterized LOC115279171, transcript variant X2
uncharacterized LOC115279171, transcript variant X3
family with sequence similarity 135 member B, transcript variant X2
family with sequence similarity 135 member B, transcript variant X1
family with sequence similarity 135 member B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments
potassium two pore domain channel subfamily K member 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
trafficking protein particle complex subunit 9
chromatin accessibility complex subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
chromatin accessibility complex protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine kinase 2, transcript variant X22
protein tyrosine kinase 2, transcript variant X16
protein tyrosine kinase 2, transcript variant X14
protein tyrosine kinase 2, transcript variant X13
protein tyrosine kinase 2, transcript variant X10
protein tyrosine kinase 2, transcript variant X12
protein tyrosine kinase 2, transcript variant X11
protein tyrosine kinase 2, transcript variant X15
protein tyrosine kinase 2, transcript variant X8
protein tyrosine kinase 2, transcript variant X9
protein tyrosine kinase 2, transcript variant X5
protein tyrosine kinase 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein tyrosine kinase 2, transcript variant X7
protein tyrosine kinase 2, transcript variant X6
protein tyrosine kinase 2, transcript variant X3
protein tyrosine kinase 2, transcript variant X1
protein tyrosine kinase 2, transcript variant X2
protein tyrosine kinase 2, transcript variant X18
protein tyrosine kinase 2, transcript variant X20
protein tyrosine kinase 2, transcript variant X19
protein tyrosine kinase 2, transcript variant X21
protein tyrosine kinase 2, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 45 member 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
solute carrier family 45 member 4, transcript variant X2
solute carrier family 45 member 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
maestro heat-like repeat family member 5
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, and 89% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: maestro heat-like repeat family member 5
uncharacterized LOC115279173, transcript variant X1
uncharacterized LOC115279173, transcript variant X2
t-SNARE domain containing 1, transcript variant X5
t-SNARE domain containing 1, transcript variant X4
t-SNARE domain containing 1, transcript variant X3
t-SNARE domain containing 1, transcript variant X2
t-SNARE domain containing 1, transcript variant X6
t-SNARE domain containing 1, transcript variant X1
t-SNARE domain-containing protein 1 isoform X5
t-SNARE domain-containing protein 1 isoform X4
t-SNARE domain-containing protein 1 isoform X3
t-SNARE domain-containing protein 1 isoform X2
t-SNARE domain-containing protein 1 isoform X6
t-SNARE domain-containing protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
activity regulated cytoskeleton associated protein
activity-regulated cytoskeleton-associated protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 59% 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, 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 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
secreted LY6/PLAUR domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
secreted LY6/PLAUR domain containing 2, transcript variant X1
secreted Ly-6/uPAR domain-containing protein 2 isoform X2
secreted Ly-6/uPAR domain-containing protein 2 isoform X1
ly-6/neurotoxin-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
ly-6/neurotoxin-like protein 1, transcript variant X3
ly-6/neurotoxin-like protein 1, transcript variant X2
glycosylphosphatidylinositol anchored molecule like
glycosyl-phosphatidylinositol-anchored molecule-like protein
lymphocyte antigen 6 family member K, transcript variant X2
lymphocyte antigen 6 family member K, transcript variant X3
lymphocyte antigen 6 family member K, transcript variant X1
cytochrome P450 11B2, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
cytochrome P450 11B2, mitochondrial-like isoform X2
cytochrome P450 11B2, mitochondrial-like, transcript variant X1
cytochrome P450 11B2, mitochondrial-like isoform X1
lymphocyte antigen 6 family member E, transcript variant X1
lymphocyte antigen 6 family member E, transcript variant X2
uncharacterized LOC115278944, transcript variant X2
uncharacterized LOC115278944, transcript variant X1
uncharacterized LOC115278944, transcript variant X3
uncharacterized protein LOC115278944 isoform X1
uncharacterized protein LOC115278944 isoform X2
uncharacterized LOC115278944, transcript variant X5
uncharacterized LOC115278944, transcript variant X4
uncharacterized protein LOC115278944 isoform X3
uncharacterized protein LOC115278944 isoform X4
lymphocyte antigen 6 family member L, transcript variant X3
lymphocyte antigen 6 family member L, transcript variant X1
lymphocyte antigen 6 family member L, transcript variant X2
glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1
glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1
ZFP41 zinc finger protein, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ZFP41 zinc finger protein, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ZFP41 zinc finger protein, transcript variant X1
ZFP41 zinc finger protein, transcript variant X5
ZFP41 zinc finger protein, transcript variant X3
ZFP41 zinc finger protein, transcript variant X6
ZFP41 zinc finger protein, transcript variant X7
ZFP41 zinc finger protein, transcript variant X4
ZFP41 zinc finger protein, transcript variant X2
ZFP41 zinc finger protein, transcript variant X10
GLI family zinc finger 4, transcript variant X2
GLI family zinc finger 4, transcript variant X4
GLI family zinc finger 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
GLI family zinc finger 4, transcript variant X5
GLI family zinc finger 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
rhophilin Rho GTPase binding protein 1, transcript variant X2
rhophilin Rho GTPase binding protein 1, transcript variant X1
rhophilin Rho GTPase binding protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
zinc finger CCCH domain-containing protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
maestro heat like repeat family member 6, transcript variant X5
maestro heat like repeat family member 6, transcript variant X4
maestro heat like repeat family member 6, transcript variant X3
maestro heat-like repeat-containing protein family member 6 isoform X4
maestro heat-like repeat-containing protein family member 6 isoform X3
maestro heat like repeat family member 6, transcript variant X6
maestro heat like repeat family member 6, transcript variant X1
maestro heat-like repeat-containing protein family member 6 isoform X1
maestro heat-like repeat-containing protein family member 6 isoform X5
maestro heat like repeat family member 6, transcript variant X2
maestro heat-like repeat-containing protein family member 6 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
eukaryotic translation elongation factor 1 delta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
tigger transposable element-derived protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
tissue specific transplantation antigen P35B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 166
mitogen-activated protein kinase 15, transcript variant X2
mitogen-activated protein kinase 15, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
mitogen-activated protein kinase 15 isoform X1
mitogen-activated protein kinase 15 isoform X2
family with sequence similarity 83 member H
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC115278766, transcript variant X4
uncharacterized LOC115278766, transcript variant X3
uncharacterized LOC115278766, transcript variant X2
uncharacterized LOC115278766, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
poly(U) binding splicing factor 60, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
poly(U) binding splicing factor 60, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
poly(U) binding splicing factor 60, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
poly(U) binding splicing factor 60, transcript variant X4
poly(U) binding splicing factor 60, transcript variant X2
poly(U) binding splicing factor 60, transcript variant X1
poly(U)-binding-splicing factor PUF60 isoform X4
poly(U)-binding-splicing factor PUF60 isoform X3
poly(U)-binding-splicing factor PUF60 isoform X2
poly(U)-binding-splicing factor PUF60 isoform X1
poly(U)-binding-splicing factor PUF60 isoform X6
poly(U)-binding-splicing factor PUF60 isoform X5
nuclear receptor binding protein 2, transcript variant X3
nuclear receptor binding protein 2, transcript variant X2
nuclear receptor binding protein 2, transcript variant X1
nuclear receptor-binding protein 2 isoform X3
nuclear receptor-binding protein 2 isoform X2
nuclear receptor-binding protein 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
glutamate ionotropic receptor NMDA type subunit associated protein 1
spermatogenesis and centriole associated 1, transcript variant X3
spermatogenesis and centriole associated 1, transcript variant X4
spermatogenesis and centriole associated 1, transcript variant X1
spermatogenesis and centriole associated 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
5-oxoprolinase, ATP-hydrolysing, transcript variant X2
5-oxoprolinase, ATP-hydrolysing, transcript variant X1
5-oxoprolinase, ATP-hydrolysing, transcript variant X3
glycosylphosphatidylinositol anchor attachment 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
glycosylphosphatidylinositol anchor attachment 1 protein
cytochrome c1, heme protein, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
SHANK associated RH domain interactor, transcript variant X2
SHANK associated RH domain interactor, transcript variant X1
MAF1 homolog, negative regulator of RNA polymerase III, transcript variant X2
MAF1 homolog, negative regulator of RNA polymerase III, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
repressor of RNA polymerase III transcription MAF1 homolog isoform X1
repressor of RNA polymerase III transcription MAF1 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
testis-specific serine/threonine-protein kinase 5-like
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: 3 Proteins, and 84% 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 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: testis-specific serine/threonine-protein kinase 5-like
maestro heat like repeat family member 1, transcript variant X4
maestro heat like repeat family member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
maestro heat like repeat family member 1, transcript variant X2
maestro heat like repeat family member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
maestro heat like repeat family member 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
maestro heat like repeat family member 1, transcript variant X6
maestro heat like repeat family member 1, transcript variant X7
maestro heat like repeat family member 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
maestro heat like repeat family member 1, transcript variant X10
maestro heat-like repeat-containing protein family member 1 isoform X1
maestro heat-like repeat-containing protein family member 1 isoform X2
maestro heat-like repeat-containing protein family member 1 isoform X3
maestro heat-like repeat-containing protein family member 1 isoform X4
maestro heat-like repeat-containing protein family member 1 isoform X5
maestro heat-like repeat-containing protein family member 1 isoform X7
maestro heat like repeat family member 1, transcript variant X9
maestro heat-like repeat-containing protein family member 1 isoform X6
heat shock transcription factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
heat shock transcription factor 1, transcript variant X3
heat shock transcription factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
heat shock transcription factor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
scratch family transcriptional repressor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 52 member 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
solute carrier family 52 member 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
solute carrier family 52 member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
solute carrier family 52 member 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
solute carrier family 52 member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
solute carrier family 52, riboflavin transporter, member 2 isoform X2
solute carrier family 52, riboflavin transporter, member 2 isoform X1
aarF domain containing kinase 5, transcript variant X3
aarF domain containing kinase 5, transcript variant X5
aarF domain containing kinase 5, transcript variant X4
aarF domain containing kinase 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
aarF domain containing kinase 5, transcript variant X2
uncharacterized aarF domain-containing protein kinase 5 isoform X1
uncharacterized aarF domain-containing protein kinase 5 isoform X3
uncharacterized aarF domain-containing protein kinase 5 isoform X2
uncharacterized aarF domain-containing protein kinase 5 isoform X4
cleavage and polyadenylation specific factor 1
cleavage and polyadenylation specificity factor subunit 1
solute carrier family 39 member 4, transcript variant X1
solute carrier family 39 member 4, transcript variant X2
VPS28 subunit of ESCRT-I, transcript variant X1
VPS28 subunit of ESCRT-I, transcript variant X2
vacuolar protein sorting-associated protein 28 homolog
tonsoku like, DNA repair protein, transcript variant X2
tonsoku like, DNA repair protein, transcript variant X1
tonsoku like, DNA repair protein, transcript variant X3
cysteine and histidine rich 1, transcript variant X2
cysteine and histidine rich 1, transcript variant X1
cysteine and histidine-rich protein 1 isoform X1
cysteine and histidine-rich protein 1 isoform X2
kinesin family member C2, transcript variant X3
kinesin family member C2, transcript variant X2
kinesin family member C2, transcript variant X1
kinesin family member C2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 1 regulatory subunit 16A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
major facilitator superfamily domain containing 3
major facilitator superfamily domain-containing protein 3
RecQ like helicase 4, transcript variant X4
RecQ like helicase 4, transcript variant X3
RecQ like helicase 4, transcript variant X2
RecQ like helicase 4, transcript variant X1
ATP-dependent DNA helicase Q4 isoform X4
ATP-dependent DNA helicase Q4 isoform X3
ATP-dependent DNA helicase Q4 isoform X2
ATP-dependent DNA helicase Q4 isoform X1
RecQ like helicase 4, transcript variant X5
RecQ like helicase 4, transcript variant X6
ATP-dependent DNA helicase Q4 isoform X5
ATP-dependent DNA helicase Q4 isoform X6
RecQ like helicase 4, transcript variant X7
ATP-dependent DNA helicase Q4 isoform X7
leucine rich repeat containing 14, transcript variant X6
leucine rich repeat containing 14, transcript variant X4
leucine rich repeat containing 14, transcript variant X1
leucine rich repeat containing 14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
leucine-rich repeat-containing protein 14 isoform X3
leucine-rich repeat-containing protein 14 isoform X1
leucine rich repeat containing 14, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
leucine rich repeat containing 14, transcript variant X5
leucine-rich repeat-containing protein 14 isoform X2
leucine-rich repeat-containing protein 14 isoform X4
leucine rich repeat containing 24, transcript variant X3
leucine rich repeat containing 24, transcript variant X2
leucine rich repeat containing 24, transcript variant X4
leucine rich repeat containing 24, transcript variant X5
leucine rich repeat containing 24, transcript variant X1
leucine-rich repeat-containing protein 24 isoform X2
leucine-rich repeat-containing protein 24 isoform X1
chromosome 15 C8orf82 homolog, transcript variant X2
chromosome 15 C8orf82 homolog, transcript variant X1
UPF0598 protein C8orf82 homolog isoform X2
UPF0598 protein C8orf82 homolog isoform X1
Rho GTPase activating protein 39, transcript variant X2
Rho GTPase activating protein 39, transcript variant X1
Rho GTPase activating protein 39, transcript variant X4
rho GTPase-activating protein 39 isoform X1
rho GTPase-activating protein 39 isoform X2
Rho GTPase activating protein 39, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
COMM domain containing 5, transcript variant X1
COMM domain containing 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
zinc finger protein 7, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger protein 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 7, transcript variant X6
zinc finger protein 7, transcript variant X2
zinc finger protein 7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 40% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
zinc finger protein 34, transcript variant X1
zinc finger protein 34, transcript variant X2
zinc finger protein 250, transcript variant X9
zinc finger protein 250, transcript variant X3
zinc finger protein 250, transcript variant X1
zinc finger protein 250, transcript variant X4
zinc finger protein 250, transcript variant X5
zinc finger protein 250, transcript variant X6
zinc finger protein 250, transcript variant X7
zinc finger protein 250, transcript variant X2
zinc finger protein 250, transcript variant X8
zinc finger protein 16, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
zinc finger protein 16, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
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 12 samples with support for all annotated introns
zinc finger protein 252-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 252-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 252-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 252-like, transcript variant X3
chromosome 15 C8orf33 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
chromosome 15 C8orf33 homolog, transcript variant X1
UPF0488 protein C8orf33 homolog isoform X2
UPF0488 protein C8orf33 homolog isoform X1