Hypomesus transpacificus isolate Combined female chromosome 1, fHypTra1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Stomiati; Osmeriformes; Osmeridae; Hypomesus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM038972.1.\nAssembly name: fHypTra1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Genomic Variation Lab at\nUniversity of California Davis on 2022/02/04. The original\nwhole-genome shotgun project has the accession JAJTOO000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Genomic Variation Lab at University of\n California Davis\nAssembly Date :: 21-APR-2021\nAssembly Method :: IPA v. 1.3.1; scaff10x v. 4.2; SALSA2 v.\n NA; Chromonomer v. 1.13\nAssembly Name :: fHypTra1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 120.0x\nSequencing Technology :: 10X; PacBio Sequel; Hi-C\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Hypomesus transpacificus Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
USA: Fish Conservation and Culture Laboratory, Discovery Bay, California
Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: polyA evidence [ECO:0006239]
SH3 domain containing ring finger 2, 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 17 samples with support for all annotated introns
SH3 domain containing ring finger 2, 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 27 samples with support for all annotated introns
SH3 domain containing ring finger 2, 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 42 samples with support for all annotated introns
SH3 domain containing ring finger 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 9 samples with support for all annotated introns
E3 ubiquitin-protein ligase SH3RF1 isoform X2
E3 ubiquitin-protein ligase SH3RF2 isoform X1
BTB/POZ domain-containing protein KCTD16-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor), transcript variant X1
nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor), transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: putative fibroblast growth factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
sosondowah ankyrin repeat domain family member Ab
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
ankyrin repeat domain-containing protein SOWAHA
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 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: 28 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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
AUP1 lipid droplet regulating VLDL assembly factor, transcript variant X2
AUP1 lipid droplet regulating VLDL assembly factor, transcript variant X1
lipid droplet-regulating VLDL assembly factor AUP1 isoform X2
lipid droplet-regulating VLDL assembly factor AUP1 isoform X1
transient receptor potential cation channel, subfamily C, member 3
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
short transient receptor potential channel 3
protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha
phosphatidylinositol glycan anchor biosynthesis class G, transcript variant X1
GPI ethanolamine phosphate transferase 2 isoform X1
phosphatidylinositol glycan anchor biosynthesis class G, 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 10 samples with support for all annotated introns
phosphatidylinositol glycan anchor biosynthesis class G, transcript variant X3
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
phosphatidylinositol glycan anchor biosynthesis class G, 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 40 samples with support for all annotated introns
GPI ethanolamine phosphate transferase 2 isoform X2
phosphatidylinositol glycan anchor biosynthesis class G, transcript variant X5
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
phosphatidylinositol glycan anchor biosynthesis class G, transcript variant X6
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
GPI ethanolamine phosphate transferase 2 isoform X3
phosphatidylinositol glycan anchor biosynthesis class G, transcript variant X10
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 31 samples with support for all annotated introns
phosphatidylinositol glycan anchor biosynthesis class G, transcript variant X9
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 34 samples with support for all annotated introns
phosphatidylinositol glycan anchor biosynthesis class G, transcript variant X8
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 19 samples with support for all annotated introns
GPI ethanolamine phosphate transferase 2 isoform X6
GPI ethanolamine phosphate transferase 2 isoform X5
phosphatidylinositol glycan anchor biosynthesis class G, transcript variant X7
GPI ethanolamine phosphate transferase 2 isoform X4
potassium channel tetramerization domain containing 8
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: BTB/POZ domain-containing protein KCTD8
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: translation factor Guf1, mitochondrial
gamma-aminobutyric acid receptor subunit alpha-2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gamma-aminobutyric acid type A receptor subunit alpha4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 117 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit alpha-4
adaptor related protein complex 1 associated regulatory protein, transcript variant X5
adaptor related protein complex 1 associated regulatory protein, transcript variant X6
adaptor related protein complex 1 associated regulatory protein, transcript variant X4
adaptor related protein complex 1 associated regulatory protein, transcript variant X2
adaptor related protein complex 1 associated regulatory protein, transcript variant X1
adaptor related protein complex 1 associated regulatory protein, transcript variant X3
AP-1 complex-associated regulatory protein isoform X1
AP-1 complex-associated regulatory protein isoform X2
AP-1 complex-associated regulatory protein isoform X3
AP-1 complex-associated regulatory protein isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% 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: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
eukaryotic translation initiation factor 4E-1A
leucine rich repeat and Ig domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 2
H/ACA ribonucleoprotein complex subunit 1
paired-like homeodomain 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 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 18 samples with support for all annotated introns
paired-like homeodomain 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
paired-like homeodomain 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
elongation of very long chain fatty acids protein 6
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
info leucine-rich repeat, immunoglobulin-like and transmembrane domains 3a
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
leucine-rich repeat, immunoglobulin-like domain and transmembrane domain-containing protein 3a
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 22 samples with support for all annotated introns
ankyrin repeat and SOCS box containing 5a
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 26 samples with support for all annotated introns
nei-like DNA glycosylase 3, transcript variant X1
nei-like DNA glycosylase 3, transcript variant X2
nei-like DNA glycosylase 3, transcript variant X3
aspartylglucosaminidase, transcript variant X5
aspartylglucosaminidase, transcript variant X2
aspartylglucosaminidase, transcript variant X4
aspartylglucosaminidase, transcript variant X3
aspartylglucosaminidase, transcript variant X1
N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase isoform X5
N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase isoform X2
N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase isoform X4
N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase isoform X1
N(4)-(beta-N-acetylglucosaminyl)-L-asparaginase 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 3 samples with support for all annotated introns
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
glutamate receptor, ionotropic, AMPA 2b, transcript variant X1
glutamate receptor, ionotropic, AMPA 2b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
electron transfer flavoprotein dehydrogenase
electron transfer flavoprotein-ubiquinone oxidoreductase, mitochondrial
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
Rap guanine nucleotide exchange factor 2b, transcript variant X3
Rap guanine nucleotide exchange factor 2b, transcript variant X2
Rap guanine nucleotide exchange factor 2b, transcript variant X4
Rap guanine nucleotide exchange factor 2b, transcript variant X5
Rap guanine nucleotide exchange factor 2b, transcript variant X1
rap guanine nucleotide exchange factor 2 isoform X1
rap guanine nucleotide exchange factor 2 isoform X3
rap guanine nucleotide exchange factor 2 isoform X2
rap guanine nucleotide exchange factor 2 isoform X4
rap guanine nucleotide exchange factor 2 isoform X5
Rap guanine nucleotide exchange factor 2b, transcript variant X6
rap guanine nucleotide exchange factor 2 isoform X6
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: 8 Proteins, and 91% 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; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: follistatin-related protein 5
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 24 samples with support for all annotated introns
LIM domain binding 2a, 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 9 samples with support for all annotated introns
LIM domain binding 2a, 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
LIM domain binding 2a, 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
LIM domain binding 2a, 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 35 samples with support for all annotated introns
LIM domain binding 2a, 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 31 samples with support for all annotated introns
LIM domain binding 2a, transcript variant X6
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 26 samples with support for all annotated introns
LIM domain binding 2a, 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 23 samples with support for all annotated introns
LIM domain-binding protein 2a isoform X1
LIM domain-binding protein 2a isoform X2
LIM domain-binding protein 2a isoform X3
LIM domain-binding protein 2a isoform X4
LIM domain-binding protein 2a isoform X5
LIM domain-binding protein 2a isoform X6
LIM domain-binding protein 2a isoform X7
transmembrane anterior posterior transformation 1a, transcript variant X1
transmembrane anterior posterior transformation 1a, transcript variant X2
transmembrane anterior posterior transformation protein 1 homolog isoform X1
transmembrane anterior posterior transformation protein 1 homolog isoform X2
fibroblast growth factor-binding protein 2-like
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 46 samples with support for all annotated introns
fibroblast growth factor binding protein 1a
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
fibroblast growth factor-binding protein 1
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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
SMU1 DNA replication regulator and spliceosomal factor a
carboxypeptidase X (M14 family), member 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
cytochrome c oxidase assembly protein COX18, mitochondrial
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 38 samples with support for all annotated introns
insulin-like growth factor binding protein 7, transcript variant X2
insulin-like growth factor binding protein 7, 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 36 samples with support for all annotated introns
insulin-like growth factor-binding protein 7 isoform X2
insulin-like growth factor-binding protein 7 isoform X1
DNA-directed RNA polymerase II subunit RPB2
DP-Gal:betaGlcNAc beta 1,4- galactosyltransferase, polypeptide 1, like
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 45 samples with support for all annotated introns
probable pancreatic secretory proteinase inhibitor
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 44 samples with support for all annotated introns
nipsnap homolog 3A (C. elegans), 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 32 samples with support for all annotated introns
nipsnap homolog 3A (C. elegans), transcript variant X1
ATP-binding cassette, sub-family A (ABC1), member 1B
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: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: phospholipid-transporting ATPase ABCA1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TBC1 domain family, member 2, transcript variant X2
TBC1 domain family, member 2, transcript variant X1
TBC1 domain family, member 2, 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 40 samples with support for all annotated introns
elongator acetyltransferase complex subunit 1, transcript variant X1
elongator acetyltransferase complex subunit 1, transcript variant X2
ubiquitin-conjugating enzyme E2 D2-like, transcript variant X1
ubiquitin-conjugating enzyme E2 D2-like, transcript variant X2
ubiquitin-conjugating enzyme E2 D2-like isoform X2
ubiquitin-conjugating enzyme E2 D2-like isoform X1
nuclear factor of kappa light polypeptide gene enhancer in B-cells 1
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 2, transcript variant X1
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 2 isoform X1
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 2, transcript variant X2
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 2 isoform X2
SEC24 homolog B, COPII coat complex component, transcript variant X2
SEC24 homolog B, COPII coat complex component, 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 28 samples with support for all annotated introns
SEC24 homolog B, COPII coat complex component, 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 42 samples with support for all annotated introns
protein transport protein Sec24B isoform X1
protein transport protein Sec24B isoform X2
protein transport protein Sec24B isoform X3
testicular haploid expressed gene protein-like, transcript variant X5
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
testicular haploid expressed gene protein-like, transcript variant X3
testicular haploid expressed gene protein-like, transcript variant X4
testicular haploid expressed gene protein-like, 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
testicular haploid expressed gene protein-like, transcript variant X1
testicular haploid expressed gene protein-like isoform X4
testicular haploid expressed gene protein-like isoform X2
testicular haploid expressed gene protein-like isoform X3
testicular haploid expressed gene protein-like isoform X1
signal recognition particle subunit SRP72
leptin receptor overlapping transcript like 1, transcript variant X1
leptin receptor overlapping transcript like 1, transcript variant X2
leptin receptor overlapping transcript-like 1 isoform X2
leptin receptor overlapping transcript-like 1 isoform 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 39 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 32 samples with support for all annotated introns
ankyrin repeat domain 50, transcript variant X4
ankyrin repeat domain 50, transcript variant X2
ankyrin repeat domain 50, transcript variant X1
ankyrin repeat domain 50, transcript variant X3
ankyrin repeat domain-containing protein 50
sprouty homolog 1, antagonist of FGF signaling (Drosophila)
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 53 samples with support for all annotated introns
ATPase family protein 2 homolog, transcript variant X1
ATPase family protein 2 homolog, transcript variant X2
ATPase family protein 2 homolog isoform X1
ATPase family protein 2 homolog 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 3 samples with support for all annotated introns
spermatogenesis associated 5, 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 4 samples with support for all annotated introns
spermatogenesis associated 5, 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 11 samples with support for all annotated introns
nudix (nucleoside diphosphate linked moiety X)-type motif 6
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 41 samples with support for all annotated introns
nucleoside diphosphate-linked moiety X motif 6
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 44 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 5 samples with support for all annotated introns
adenosine deaminase domain containing 1 (testis-specific)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
adenosine deaminase domain-containing protein 1
T cell leukemia homeobox 2, transcript variant X6
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 30 samples with support for all annotated introns
T cell leukemia homeobox 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 24 samples with support for all annotated introns
T cell leukemia homeobox 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 32 samples with support for all annotated introns
T cell leukemia homeobox 2, 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 43 samples with support for all annotated introns
T cell leukemia homeobox 2, 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 32 samples with support for all annotated introns
T cell leukemia homeobox 2, 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 43 samples with support for all annotated introns
T-cell leukemia homeobox protein 2 isoform X1
T-cell leukemia homeobox protein 2 isoform X2
T-cell leukemia homeobox protein 2 isoform X5
T-cell leukemia homeobox protein 2 isoform X4
T-cell leukemia homeobox protein 2 isoform X3
T-cell leukemia homeobox protein 2 isoform X6
fibroblast growth factor 24, 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 21 samples with support for all annotated introns
fibroblast growth factor 24, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
polycomb group ring finger 1, transcript variant X3
polycomb group ring finger 1, transcript variant X4
polycomb group RING finger protein 1 isoform X3
polycomb group RING finger protein 1 isoform X4
polycomb group ring finger 1, transcript variant X2
polycomb group ring finger 1, transcript variant X1
polycomb group RING finger protein 1 isoform X1
polycomb group RING finger protein 1 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 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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
uncharacterized LOC124481446, transcript variant X1
uncharacterized LOC124481446, transcript variant X3
uncharacterized LOC124481446, transcript variant X2
uncharacterized LOC124481553, transcript variant X2
uncharacterized LOC124481553, transcript variant X1
uncharacterized LOC124480944, transcript variant X6
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
uncharacterized LOC124480944, transcript variant X12
uncharacterized LOC124480944, transcript variant X9
uncharacterized LOC124480944, transcript variant X11
uncharacterized LOC124480944, transcript variant X13
uncharacterized LOC124480944, transcript variant X2
uncharacterized LOC124480944, transcript variant X4
uncharacterized LOC124480944, transcript variant X8
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
uncharacterized LOC124480944, transcript variant X5
uncharacterized LOC124480944, transcript variant X7
uncharacterized LOC124480944, transcript variant X10
uncharacterized LOC124480944, transcript variant X1
uncharacterized LOC124480944, 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 9 samples with support for all annotated introns
uncharacterized LOC124480944, transcript variant X14
uncharacterized LOC124478155, 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 1 sample with support for all annotated introns
uncharacterized LOC124478155, 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 2 samples with support for all annotated introns
Ig kappa chain V-VI region NQ6-8.3.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 42% 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 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, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124478261, 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
uncharacterized protein LOC124478261 isoform X2
uncharacterized LOC124478261, 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 1 sample with support for all annotated introns
uncharacterized protein LOC124478261 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC124470411
uncharacterized LOC124468798, 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
uncharacterized LOC124468798, 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 3 samples with support for all annotated introns
uncharacterized protein LOC124468798 isoform X2
uncharacterized protein LOC124468798 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; 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 78% coverage of the annotated genomic feature by RNAseq alignments
myb/SANT-like DNA-binding domain-containing protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
minichromosome maintenance complex component 7
F-box/LRR-repeat protein 12-like, transcript variant X2
F-box/LRR-repeat protein 12-like, transcript variant X1
F-box/LRR-repeat protein 12-like isoform X1
F-box/LRR-repeat protein 12-like isoform X2
phospholipid-transporting ATPase VB-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: phospholipid-transporting ATPase VB-like
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein phosphatase 2A catalytic subunit alpha isoform
ATP synthase peripheral stalk subunit OSCP
uncharacterized protein LOC797133 homolog, 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 47 samples with support for all annotated introns
uncharacterized protein LOC797133 homolog, transcript variant X2
nuclear receptor binding SET domain protein 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
histone-lysine N-methyltransferase, H3 lysine-36 specific
C1q and TNF related 2, 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 4 samples with support for all annotated introns
C1q and TNF related 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 6 samples with support for all annotated introns
complement C1q tumor necrosis factor-related protein 2
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 35 samples with support for all annotated introns
uncharacterized LOC124471311, transcript variant X2
uncharacterized LOC124471311, transcript variant X3
uncharacterized LOC124471311, 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: Gnomon. Supporting evidence includes similarity to: 5 Proteins
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 29 samples with support for all annotated introns
T-cell immunoglobulin and mucin domain-containing protein 4-like
Down syndrome cell adhesion molecule homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
mitogen-activated protein kinase 9, transcript variant X3
mitogen-activated protein kinase 9, transcript variant X2
mitogen-activated protein kinase 9, transcript variant X1
mitogen-activated protein kinase 9 isoform X2
mitogen-activated protein kinase 9 isoform X1
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X2
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like, transcript variant X1
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X2
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like isoform X1
putative monooxygenase p33MONOX, transcript variant X1
putative monooxygenase p33MONOX, transcript variant X2
putative monooxygenase p33MONOX, transcript variant X3
putative monooxygenase p33MONOX isoform X2
putative monooxygenase p33MONOX isoform X3
putative monooxygenase p33MONOX isoform 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 44 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
CCR4-NOT transcription complex subunit 6-like, transcript variant 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 42 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 6-like, 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 43 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 6-like, 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 30 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 6-like, transcript variant 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 13 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 6-like, 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 33 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 6-like isoform X1
CCR4-NOT transcription complex subunit 6-like isoform X2
SUMO-interacting motif-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
sodium-dependent phosphate transport protein 2A
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 34 samples with support for all annotated introns
uncharacterized LOC124470576, 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 44 samples with support for all annotated introns
uncharacterized LOC124470576, transcript variant X1
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: 23 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: ADP-ribosylation factor-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1-like, transcript variant X3
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1-like, transcript variant X1
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1-like, transcript variant X2
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1-like
CD74 molecule, major histocompatibility complex, class II invariant chain a
golgin subfamily A member 6-like protein 22
solute carrier family 35 member A4, transcript variant X2
solute carrier family 35 member A4, transcript variant X1
probable UDP-sugar transporter protein SLC35A4 isoform X1
probable UDP-sugar transporter protein SLC35A4 isoform X2
SLC35A4 upstream open reading frame protein-like, 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 18 samples with support for all annotated introns
SLC35A4 upstream open reading frame protein-like, 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 44 samples with support for all annotated introns
SLC35A4 upstream open reading frame protein-like
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
colony stimulating factor 1 receptor, a, transcript variant X4
colony stimulating factor 1 receptor, a, transcript variant X2
colony stimulating factor 1 receptor, a, transcript variant X3
colony stimulating factor 1 receptor, a, transcript variant X1
macrophage colony-stimulating factor 1 receptor isoform X3
macrophage colony-stimulating factor 1 receptor isoform X2
macrophage colony-stimulating factor 1 receptor isoform X1
platelet-derived growth factor receptor, beta polypeptide, transcript variant 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 31 samples with support for all annotated introns
platelet-derived growth factor receptor, beta polypeptide, 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 1 sample with support for all annotated introns
platelet-derived growth factor receptor beta isoform X2
platelet-derived growth factor receptor beta isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
uncharacterized LOC124467673, transcript variant X1
uncharacterized LOC124467673, transcript variant X2
uncharacterized protein LOC124467673 isoform X2
uncharacterized protein LOC124467673 isoform X1
phosphodiesterase 6A, cGMP-specific, rod, alpha
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 1 sample with support for all annotated introns
rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha
peroxisome proliferator-activated receptor gamma, coactivator 1 beta
peroxisome proliferator-activated receptor gamma coactivator 1-beta
Rho guanine nucleotide exchange factor (GEF) 37, transcript variant X3
Rho guanine nucleotide exchange factor (GEF) 37, transcript variant X1
Rho guanine nucleotide exchange factor (GEF) 37, transcript variant X2
Rho guanine nucleotide exchange factor (GEF) 37, transcript variant X5
Rho guanine nucleotide exchange factor (GEF) 37, transcript variant X4
rho guanine nucleotide exchange factor 37 isoform X1
Rho guanine nucleotide exchange factor (GEF) 37, 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 31 samples with support for all annotated introns
rho guanine nucleotide exchange factor 37 isoform X2
family with sequence similarity 13 member B, transcript variant X1
family with sequence similarity 13 member B, transcript variant X2
family with sequence similarity 13 member B, transcript variant X4
family with sequence similarity 13 member B, transcript variant X3
kelch-like family member 3, transcript variant X2
kelch-like family member 3, transcript variant X3
kelch-like family member 3, 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
glycine receptor, alpha 1, transcript variant X1
glycine receptor, alpha 1, 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
glycine receptor, alpha 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycine receptor subunit alphaZ1 isoform X1
glycine receptor subunit alphaZ1 isoform X2
glycine receptor subunit alphaZ1 isoform X3
GTPase activating protein (SH3 domain) binding protein 1, 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 43 samples with support for all annotated introns
GTPase activating protein (SH3 domain) binding protein 1, transcript variant X1
ras GTPase-activating protein-binding protein 1
secreted protein, acidic, cysteine-rich (osteonectin), transcript variant X4
secreted protein, acidic, cysteine-rich (osteonectin), transcript variant X3
secreted protein, acidic, cysteine-rich (osteonectin), transcript variant X2
secreted protein, acidic, cysteine-rich (osteonectin), transcript variant X1
solute carrier family 36 member 1, 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 10 samples with support for all annotated introns
solute carrier family 36 member 1, 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, including 42 samples with support for all annotated introns
coiled-coil domain containing 69, transcript variant X1
coiled-coil domain-containing protein 69 isoform X1
coiled-coil domain containing 69, transcript variant X2
coiled-coil domain-containing protein 69 isoform 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 20 samples with support for all annotated introns
xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7 (galactosyltransferase I), transcript variant X2
xylosylprotein beta 1,4-galactosyltransferase, polypeptide 7 (galactosyltransferase I), transcript variant X1
beta-1,4-galactosyltransferase 7 isoform X2
beta-1,4-galactosyltransferase 7 isoform X1
transmembrane emp24 domain-containing protein 9
lectin, mannose-binding 2, transcript variant X1
lectin, mannose-binding 2, transcript variant X2
vesicular integral-membrane protein VIP36 isoform X2
vesicular integral-membrane protein VIP36 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein A0-like
macrophage erythroblast attacher, E3 ubiquitin ligase
C-terminal binding protein 1, transcript variant X2
C-terminal binding protein 1, transcript variant X1
spondin 2b, extracellular matrix protein
transmembrane emp24 domain-containing protein 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 12% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor receptor like 1a, transcript variant X2
fibroblast growth factor receptor like 1a, transcript variant X1
fibroblast growth factor receptor-like 1a
ring finger protein 4, transcript variant X2
ring finger protein 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 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: 10 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: 36 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
FMRP translational regulator 1, transcript variant X1
FMRP translational regulator 1, transcript variant X2
FMRP translational regulator 1, transcript variant X3
FMRP translational regulator 1, transcript variant X4
synaptic functional regulator FMR1 isoform X1
synaptic functional regulator FMR1 isoform X2
synaptic functional regulator FMR1 isoform X3
synaptic functional regulator FMR1 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 43 samples with support for all annotated introns
uncharacterized protein LOC321250 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 39 samples with support for all annotated introns
LON peptidase N-terminal domain and RING finger protein 3-like, transcript variant X1
LON peptidase N-terminal domain and RING finger protein 3-like, transcript variant X2
LON peptidase N-terminal domain and RING finger protein 3-like isoform X1
LON peptidase N-terminal domain and RING finger protein 3-like isoform X2
family with sequence similarity 199, X-linked
matrin 3-like 1.1, transcript variant X1
matrin 3-like 1.1, transcript variant X3
matrin 3-like 1.1, transcript variant X2
matrin 3-like 1.1, transcript variant X4
matrin 3-like 1.2, transcript variant X1
matrin 3-like 1.2, transcript variant X2
polyadenylate-binding protein-interacting protein 2-like
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 44 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 93% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3
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 42 samples with support for all annotated introns
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 3
StAR-related lipid transfer (START) domain containing 15
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
transforming growth factor, beta-induced
transforming growth factor-beta-induced protein ig-h3
mothers against decapentaplegic homolog 5
synovial apoptosis inhibitor 1, synoviolin
phospholipase D family, member 7, transcript variant X1
phospholipase D family, member 7, transcript variant X4
phospholipase D family, member 7, transcript variant X2
phospholipase D family, member 7, transcript variant X3
DNA-directed RNA polymerase II subunit RPB7
eukaryotic translation elongation factor 1 gamma
neuroblast differentiation-associated protein AHNAK
kelch-like family member 4, transcript variant X2
kelch-like family member 4, 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
TSC22 domain family, member 3, transcript variant X1
TSC22 domain family, member 3, transcript variant X2
TSC22 domain family protein 3 isoform X1
TSC22 domain family protein 3 isoform X2
probable E3 ubiquitin-protein ligase MID2 isoform X1
probable E3 ubiquitin-protein ligase MID2 isoform X2
uncharacterized protein LOC553526 homolog, transcript variant X2
uncharacterized protein LOC553526 homolog, transcript variant X1
uncharacterized protein LOC553526 homolog, transcript variant X3
uncharacterized protein LOC553526 homolog, transcript variant X4
MORC family CW-type zinc finger protein 3 isoform X1
MORC family CW-type zinc finger protein 3 isoform X2
MORC family CW-type zinc finger protein 3 isoform X3
MORC family CW-type zinc finger protein 3 isoform X4
coagulation factor VIII, procoagulant component, transcript variant X1
coagulation factor VIII, procoagulant component, transcript variant X2
solute carrier family 16 member 2, transcript variant X4
solute carrier family 16 member 2, transcript variant X3
solute carrier family 16 member 2, transcript variant X2
solute carrier family 16 member 2, transcript variant X1
thiosulfate sulfurtransferase like domain containing 1
thiosulfate:glutathione sulfurtransferase
DUF4554 domain-containing protein, transcript variant X5
DUF4554 domain-containing protein, 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 1 sample with support for all annotated introns
DUF4554 domain-containing protein, transcript variant X4
DUF4554 domain-containing protein, transcript variant X1
DUF4554 domain-containing protein isoform X2
DUF4554 domain-containing protein, transcript variant X3
DUF4554 domain-containing protein isoform X1
DUF4554 domain-containing protein isoform X3
zinc finger and BTB domain containing 3, transcript variant X3
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 41 samples with support for all annotated introns
zinc finger and BTB domain containing 3, 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 43 samples with support for all annotated introns
zinc finger and BTB domain containing 3, 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 9 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 3
cyclic nucleotide-gated cation channel beta-1-like, transcript variant X1
cyclic nucleotide-gated cation channel beta-1-like, transcript variant X2
cyclic nucleotide-gated cation channel beta-1-like isoform X1
cyclic nucleotide-gated cation channel beta-1-like isoform X2
zinc finger DHHC-type containing 24, transcript variant X1
zinc finger DHHC-type containing 24, transcript variant X2
zinc finger DHHC-type containing 24, 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 16 samples with support for all annotated introns
zinc finger DHHC-type containing 24, transcript variant X4
zinc finger DHHC-type containing 24, transcript variant X5
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 9 samples with support for all annotated introns
probable palmitoyltransferase ZDHHC24 isoform X1
probable palmitoyltransferase ZDHHC24 isoform X2
probable palmitoyltransferase ZDHHC24 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
mono-ADP ribosylhydrolase 1, transcript variant X2
mono-ADP ribosylhydrolase 1, transcript variant X1
ADP-ribose glycohydrolase MACROD1 isoform X1
ADP-ribose glycohydrolase MACROD1 isoform X2
fibronectin leucine rich transmembrane protein 1b, transcript variant X4
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
fibronectin leucine rich transmembrane protein 1b, transcript variant 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 2 samples with support for all annotated introns
fibronectin leucine rich transmembrane protein 1b, transcript variant X1
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 8 samples with support for all annotated introns
fibronectin leucine rich transmembrane protein 1b, transcript variant X5
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 3 samples with support for all annotated introns
fibronectin leucine rich transmembrane protein 1b, transcript variant X3
leucine-rich repeat transmembrane protein FLRT1
coiled-coil domain containing 88B, transcript variant X4
coiled-coil domain containing 88B, transcript variant X2
coiled-coil domain containing 88B, transcript variant X1
coiled-coil domain containing 88B, transcript variant X3
coiled-coil domain containing 88A isoform X3
coiled-coil domain containing 88A isoform X1
coiled-coil domain containing 88A isoform X4
coiled-coil domain containing 88A isoform X2
retinal outer segment membrane protein 1b
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
SCY1-like, kinase-like 1, transcript variant X1
SCY1-like, kinase-like 1, transcript variant X2
SCY1-like, kinase-like 1, transcript variant X3
SCY1-like, kinase-like 1, transcript variant X4
N-terminal kinase-like protein isoform X1
N-terminal kinase-like protein isoform X2
N-terminal kinase-like protein isoform X3
N-terminal kinase-like protein isoform X4
phospholipase A and acyltransferase 4-like, transcript variant X2
phospholipase A and acyltransferase 4-like, transcript variant X1
phospholipase A and acyltransferase 4-like
glucosidase II alpha subunit b, transcript variant X1
glucosidase II alpha subunit b, transcript variant X2
glucosidase II alpha subunit b, transcript variant X3
pre-mRNA-processing factor 39, transcript variant X1
pre-mRNA-processing factor 39, transcript variant X2
pre-mRNA-processing factor 39 isoform X1
pre-mRNA-processing factor 39 isoform X2
microtubule-associated protein 1 light chain 3 gamma, like
microtubule-associated proteins 1A/1B light chain 3C
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 38 samples with support for all annotated introns
nudix (nucleoside diphosphate linked moiety X)-type motif 22, 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 24 samples with support for all annotated introns
nudix (nucleoside diphosphate linked moiety X)-type motif 22, 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 24 samples with support for all annotated introns
nudix (nucleoside diphosphate linked moiety X)-type motif 22, 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 44 samples with support for all annotated introns
uridine diphosphate glucose pyrophosphatase NUDT22 isoform X3
uridine diphosphate glucose pyrophosphatase NUDT22 isoform X2
uridine diphosphate glucose pyrophosphatase NUDT22 isoform X1
DnaJ (Hsp40) homolog, subfamily C, member 4, transcript variant X1
DnaJ (Hsp40) homolog, subfamily C, member 4, transcript variant X2
vascular endothelial growth factor Ba, 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 39 samples with support for all annotated introns
vascular endothelial growth factor Ba, transcript variant X2
vascular endothelial growth factor Ba, transcript variant X3
vascular endothelial growth factor A isoform X2
snake venom vascular endothelial growth factor toxin VR-1' isoform X3
uncharacterized protein vegfba isoform X1
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
potassium channel, subfamily K, member 4a
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
transforming growth factor beta-2 proprotein
tRNA methyltransferase activator subunit 11-2
multifunctional methyltransferase subunit TRM112-like protein
autophagy-related protein 2 homolog A-like
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
nuclear RNA export factor 1a, transcript variant X1
nuclear RNA export factor 1a, transcript variant X2
inositol-trisphosphate 3-kinase A, 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 38 samples with support for all annotated introns
inositol-trisphosphate 3-kinase A, 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
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
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
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 23 samples with support for all annotated introns
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
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
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 13 samples with support for all annotated introns
eukaryotic translation initiation factor 1A domain containing, transcript variant X2
eukaryotic translation initiation factor 1A domain containing, 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 42 samples with support for all annotated introns
eukaryotic translation initiation factor 1A domain containing, transcript variant X3
probable RNA-binding protein EIF1AD isoform X1
probable RNA-binding protein EIF1AD isoform X2
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 26 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 10 samples with support for all annotated introns
transcriptional activator protein Pur-alpha
uncharacterized protein LOC436899 homolog
CXXC finger protein 5b, transcript variant 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 8 samples with support for all annotated introns
CXXC finger protein 5b, transcript variant X1
uncharacterized protein LOC541492 homolog
CDGSH iron-sulfur domain-containing protein 1
ubiquitin-conjugating enzyme E2D 2 (UBC4/5 homolog, yeast)
protein phosphatase 3, catalytic subunit, beta isozyme, 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, including 2 samples with support for all annotated introns
protein phosphatase 3, catalytic subunit, beta isozyme, transcript variant X3
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
serine/threonine-protein phosphatase 2B catalytic subunit beta isoform isoform X1
serine/threonine-protein phosphatase 2B catalytic subunit beta isoform isoform X3
protein phosphatase 3, catalytic subunit, beta isozyme, 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 1 sample with support for all annotated introns
protein phosphatase 3, catalytic subunit, beta isozyme, transcript variant X4
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
serine/threonine-protein phosphatase 2B catalytic subunit beta isoform isoform X2
serine/threonine-protein phosphatase 2B catalytic subunit beta isoform isoform X4
stimulator of interferon response cGAMP interactor 1, transcript variant X1
stimulator of interferon response cGAMP interactor 1, transcript variant X2
DNA damage-inducible transcript 4-like protein-like
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 47 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
DND microRNA-mediated repression inhibitor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins
histidyl-tRNA synthetase, transcript variant X3
histidyl-tRNA synthetase, transcript variant X1
histidyl-tRNA synthetase, transcript variant X2
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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 23 samples with support for all annotated introns
saxitoxin and tetrodotoxin-binding protein 2
Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B-like, transcript variant X1
Alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B-like, transcript variant X2
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B-like isoform X2
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B-like isoform X1
short coiled-coil protein b, transcript variant X1
short coiled-coil protein b, transcript variant X2
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 44 samples with support for all annotated introns
SET domain containing 7, histone lysine methyltransferase, transcript variant X2
SET domain containing 7, histone lysine methyltransferase, transcript variant X3
SET domain containing 7, histone lysine methyltransferase, transcript variant X1
histone-lysine N-methyltransferase SETD7 isoform X1
histone-lysine N-methyltransferase SETD7 isoform X2
uncharacterized protein LOC541425 homolog, transcript variant X1
uncharacterized protein LOC541425 homolog, transcript variant X2
uncharacterized protein zgc:113425 isoform X1
uncharacterized protein zgc:113425 isoform 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 44 samples with support for all annotated introns
N-alpha-acetyltransferase 15, NatA auxiliary subunit a, transcript variant X2
N-alpha-acetyltransferase 15, NatA auxiliary subunit a, transcript variant X1
N-alpha-acetyltransferase 15, NatA auxiliary subunit a isoform X2
N-alpha-acetyltransferase 15, NatA auxiliary subunit a isoform X1
NADH:ubiquinone oxidoreductase subunit C1
NADH dehydrogenase [ubiquinone] 1 subunit C1, mitochondrial
mitochondria localized glutamic acid rich protein a, transcript variant X4
mitochondria localized glutamic acid rich protein a, transcript variant X1
mitochondria localized glutamic acid rich protein a, transcript variant X3
mitochondria localized glutamic acid rich protein a, transcript variant X2
fibrous sheath CABYR-binding protein isoform X1
fibrous sheath CABYR-binding protein isoform X3
fibrous sheath CABYR-binding protein isoform X2
E74-like factor 2a (ets domain transcription factor), transcript variant X3
E74-like factor 2a (ets domain transcription factor), transcript variant X4
E74-like factor 2a (ets domain transcription factor), transcript variant X1
E74-like factor 2a (ets domain transcription factor), transcript variant X2
ETS-related transcription factor Elf-2a isoform X1
ETS-related transcription factor Elf-2a isoform X3
ETS-related transcription factor Elf-2a isoform X2
ETS-related transcription factor Elf-2a isoform X4
signal-transducing adaptor protein 1-like, transcript variant X2
signal-transducing adaptor protein 1-like, transcript variant X1
signal-transducing adaptor protein 1-like isoform X2
signal-transducing adaptor protein 1-like isoform X1
bifunctional apoptosis regulator-like, transcript variant X1
bifunctional apoptosis regulator-like, transcript variant X2
uncharacterized protein LOC124469449 isoform X1
bifunctional apoptosis regulator-like 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, including 1 sample with support for all annotated introns
zinc finger CCHC domain-containing protein 7-like, 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
zinc finger CCHC domain-containing protein 7-like, 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 39 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 7-like isoform X1
zinc finger CCHC domain-containing protein 7-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
neuronal acetylcholine receptor subunit beta-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 106 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
neuronal acetylcholine receptor subunit alpha-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
neuronal acetylcholine receptor subunit non-alpha-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
neuronal acetylcholine receptor subunit alpha-9-II
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
amyloid beta precursor protein binding family B member 2-like, transcript variant X2
amyloid beta precursor protein binding family B member 2-like, transcript variant X1
amyloid beta precursor protein binding family B member 2-like isoform X2
amyloid beta precursor protein binding family B member 2-like isoform X1
SH3 domain binding glutamate-rich protein like
SH3 domain-binding glutamic acid-rich-like protein
high mobility group nucleosome binding domain 6, transcript variant X4
high mobility group nucleosome binding domain 6, transcript variant X2
high mobility group nucleosome binding domain 6, transcript variant X3
high mobility group nucleosome binding domain 6, transcript variant X1
high mobility group nucleosome binding domain 6 isoform X1
high mobility group nucleosome binding domain 6 isoform X3
high mobility group nucleosome binding domain 6 isoform X2
high mobility group nucleosome binding domain 6 isoform X4
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
charged multivesicular body protein 1b-2
P2Y receptor family member 10, 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 33 samples with support for all annotated introns
P2Y receptor family member 10, transcript variant X2
P2Y receptor family member 10, transcript variant X1
P2Y receptor family member 10, transcript variant 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
lysophosphatidic acid receptor 4, 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, including 41 samples with support for all annotated introns
lysophosphatidic acid receptor 4, 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 13 samples with support for all annotated introns
uncharacterized LOC124467780, transcript variant X1
uncharacterized LOC124467780, transcript variant X3
uncharacterized LOC124467780, transcript variant X2
cysteinyl leukotriene receptor 1, transcript variant X1
cysteinyl leukotriene receptor 1, transcript variant X2
DNA-directed RNA polymerases I and III subunit RPAC2
microtubule associated tumor suppressor 1a, transcript variant X1
microtubule-associated tumor suppressor 1 homolog A isoform X1
microtubule associated tumor suppressor 1a, transcript variant X3
microtubule associated tumor suppressor 1a, transcript variant X2
microtubule-associated tumor suppressor 1 homolog A isoform X2
microtubule-associated tumor suppressor 1 homolog A isoform X3
platelet-derived growth factor receptor-like
platelet-derived growth factor receptor-like protein
solute carrier family 7 member 2, transcript variant X2
solute carrier family 7 member 2, transcript variant X4
solute carrier family 7 member 2, transcript variant X1
solute carrier family 7 member 2, transcript variant X3
cationic amino acid transporter 2 isoform X3
cationic amino acid transporter 2 isoform X2
cationic amino acid transporter 2 isoform X1
myotubularin related protein 7a, transcript variant X2
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 2 samples with support for all annotated introns
myotubularin related protein 7a, 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 3 samples with support for all annotated introns
myotubularin related protein 7a, transcript variant X1
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 11 samples with support for all annotated introns
CCR4-NOT transcription complex, subunit 7
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 40 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 7
zinc finger DHHC-type palmitoyltransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial calcium uptake family, member 3b, transcript variant X1
mitochondrial calcium uptake family, member 3b, transcript variant X2
mitochondrial calcium uptake family, member 3b, transcript variant X3
calcium uptake protein 3, mitochondrial isoform X2
calcium uptake protein 3, mitochondrial isoform X3
calcium uptake protein 3, mitochondrial isoform 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 14 samples with support for all annotated introns
solute carrier family 9 member A6a, transcript variant X1
solute carrier family 9 member A6a, transcript variant X3
solute carrier family 9 member A6a, 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
four and a half LIM domains 1a, transcript variant X2
four and a half LIM domains 1a, transcript variant X1
four and a half LIM domains protein 1a isoform X1
four and a half LIM domains protein 1a isoform X2
MAP7 domain containing 3, transcript variant X7
MAP7 domain containing 3, transcript variant X11
MAP7 domain containing 3, transcript variant X8
MAP7 domain containing 3, transcript variant X3
MAP7 domain containing 3, transcript variant X10
MAP7 domain containing 3, transcript variant X9
MAP7 domain containing 3, transcript variant X4
MAP7 domain containing 3, transcript variant X6
MAP7 domain containing 3, transcript variant X5
MAP7 domain containing 3, transcript variant X2
MAP7 domain containing 3, transcript variant X1
MAP7 domain-containing protein 2 isoform X9
tumor necrosis factor receptor superfamily member 27-like
transcription cofactor vestigial-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
Rac/Cdc42 guanine nucleotide exchange factor (GEF) 6, transcript variant X4
Rac/Cdc42 guanine nucleotide exchange factor (GEF) 6, transcript variant X3
Rac/Cdc42 guanine nucleotide exchange factor (GEF) 6, transcript variant X2
Rac/Cdc42 guanine nucleotide exchange factor (GEF) 6, transcript variant X1
Rac/Cdc42 guanine nucleotide exchange factor (GEF) 6, transcript variant X5
rho guanine nucleotide exchange factor 6 isoform X4
rho guanine nucleotide exchange factor 6 isoform X3
rho guanine nucleotide exchange factor 6 isoform X2
rho guanine nucleotide exchange factor 6 isoform X1
rho guanine nucleotide exchange factor 6 isoform X5
RNA binding motif protein X-linked, transcript variant X2
RNA binding motif protein X-linked, transcript variant X5
RNA binding motif protein X-linked, transcript variant X4
RNA binding motif protein X-linked, transcript variant X3
RNA binding motif protein X-linked, transcript variant X1
RNA-binding motif protein, X chromosome isoform X4
RNA-binding motif protein, X chromosome isoform X3
RNA-binding motif protein, X chromosome isoform X2
RNA-binding motif protein, X chromosome isoform X1
transmembrane 9 superfamily member 2, transcript variant X1
transmembrane 9 superfamily member 2, transcript variant X2
transmembrane 9 superfamily member 2 isoform X1
transmembrane 9 superfamily member 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: probable G-protein coupled receptor 101
zic family member 3 heterotaxy 1 (odd-paired homolog, Drosophila)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 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: 13 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fibroblast growth factor 13a, transcript variant X2
fibroblast growth factor 13a, transcript variant X4
fibroblast growth factor 13a, transcript variant X1
fibroblast growth factor 13a, transcript variant X5
fibroblast growth factor 13a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MCF.2 cell line derived transforming sequence a, transcript variant X1
MCF.2 cell line derived transforming sequence a, transcript variant X3
MCF.2 cell line derived transforming sequence a, transcript variant X2
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 5 samples with support for all annotated introns
zinc finger protein 835-like, 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 42 samples with support for all annotated introns
zinc finger protein 835-like, transcript variant X3
zinc finger protein 835-like, 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 43 samples with support for all annotated introns
zinc finger protein 835-like, transcript variant X1
macrophage migration inhibitory factor-like
ring finger protein 44, transcript variant X2
ring finger protein 44, transcript variant X4
ring finger protein 44, transcript variant X3
ring finger protein 44, 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
leucine rich repeat transmembrane neuronal 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
leucine-rich repeat transmembrane neuronal protein 2
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 43 samples with support for all annotated introns
melanin-concentrating hormone receptor 2
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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
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
TNFAIP3 interacting protein 1, transcript variant X4
TNFAIP3 interacting protein 1, transcript variant X2
TNFAIP3 interacting protein 1, transcript variant X3
TNFAIP3 interacting protein 1, transcript variant X1
TNFAIP3 interacting protein 1, transcript variant X5
TNFAIP3-interacting protein 1 isoform X2
TNFAIP3-interacting protein 1 isoform X4
TNFAIP3-interacting protein 1 isoform X1
TNFAIP3-interacting protein 1 isoform X3
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 44 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
required for meiotic nuclear division 5 homolog B, transcript variant X2
required for meiotic nuclear division 5 homolog B, transcript variant X1
E3 ubiquitin-protein transferase RMND5B isoform X1
E3 ubiquitin-protein transferase RMND5B isoform X2
serine/arginine repetitive matrix protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
heparin-binding EGF-like growth factor a
RUN and FYVE domain containing 1, transcript variant X2
RUN and FYVE domain containing 1, 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 43 samples with support for all annotated introns
RUN and FYVE domain-containing protein 1 isoform X1
RUN and FYVE domain-containing protein 1 isoform X2
heterogeneous nuclear ribonucleoprotein H-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein H-like, transcript variant X4
heterogeneous nuclear ribonucleoprotein H-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein H-like, transcript variant X3
heterogeneous nuclear ribonucleoprotein H-like isoform X2
heterogeneous nuclear ribonucleoprotein H-like isoform X1
heterogeneous nuclear ribonucleoprotein H-like isoform X4
heterogeneous nuclear ribonucleoprotein H-like isoform X3
ankyrin repeat and KH domain-containing protein 1-like
LOW QUALITY PROTEIN: ankyrin repeat and KH domain-containing protein 1-like
HIG1 hypoxia inducible domain family, member 2A
HIG1 domain family member 2A, mitochondrial
clathrin, light chain B, transcript variant X1
clathrin, light chain B, transcript variant X2
PDZ and LIM domain 7, transcript variant X1
PDZ and LIM domain 7, transcript variant X2
PDZ and LIM domain 7, transcript variant X3
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
docking protein 3, 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 22 samples with support for all annotated introns
docking protein 3, 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 16 samples with support for all annotated introns
docking protein 3, 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 40 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX41
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 44 samples with support for all annotated introns
family with sequence similarity 193 member B
MAX dimerization protein 3, 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 16 samples with support for all annotated introns
MAX dimerization protein 3, 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 44 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 11 samples with support for all annotated introns
fms related receptor tyrosine kinase 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
fms related receptor tyrosine kinase 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
fms related receptor tyrosine kinase 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
vascular endothelial growth factor receptor 3 isoform X1
vascular endothelial growth factor receptor 3 isoform X2
vascular endothelial growth factor receptor 3 isoform X3
endoplasmic reticulum-golgi intermediate compartment 1
endoplasmic reticulum-Golgi intermediate compartment protein 1
dual specificity phosphatase 1, transcript variant X1
dual specificity phosphatase 1, transcript variant X2
dual specificity protein phosphatase 1 isoform X1
dual specificity protein phosphatase 1 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 40 samples with support for all annotated introns
neuralized E3 ubiquitin protein ligase 1B, 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 17 samples with support for all annotated introns
neuralized E3 ubiquitin protein ligase 1B, transcript variant 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 38 samples with support for all annotated introns
E3 ubiquitin-protein ligase NEURL1B isoform X1
E3 ubiquitin-protein ligase NEURL1B isoform X2
serine protease inhibitor Kazal-type 1-like
biorientation of chromosomes in cell division 1-like 1, transcript variant X1
biorientation of chromosomes in cell division 1-like 1, transcript variant X2
biorientation of chromosomes in cell division protein 1-like 1 isoform X1
biorientation of chromosomes in cell division protein 1-like 1 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 44 samples with support for all annotated introns
RAB28, member RAS oncogene family, transcript variant X1
RAB28, member RAS oncogene family, 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 14 samples with support for all annotated introns
heparan sulfate (glucosamine) 3-O-sulfotransferase 1, transcript variant X1
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 44 samples with support for all annotated introns
heparan sulfate (glucosamine) 3-O-sulfotransferase 1, transcript variant X2
heparan sulfate (glucosamine) 3-O-sulfotransferase 1, transcript variant X3
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 36 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 1
B-cell linker protein, transcript variant X2
B-cell linker protein, 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 26 samples with support for all annotated introns
B-cell linker protein, 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 19 samples with support for all annotated introns
B-cell linker protein, transcript variant X4
solute carrier family 30 member 9, transcript variant X2
solute carrier family 30 member 9, transcript variant X3
solute carrier family 30 member 9, transcript variant X1
glutaredoxin and cysteine rich domain containing 1 a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 57% coverage of the annotated genomic feature by RNAseq alignments
glutaredoxin domain-containing cysteine-rich protein 1
ATPase phospholipid transporting 8A1, transcript variant X2
ATPase phospholipid transporting 8A1, transcript variant X3
ATPase phospholipid transporting 8A1, transcript variant X1
ATPase phospholipid transporting 8A1, transcript variant X6
ATPase phospholipid transporting 8A1, transcript variant X4
probable phospholipid-transporting ATPase IA isoform X2
probable phospholipid-transporting ATPase IA isoform X3
phospholipid-transporting ATPase IA isoform X1
phospholipid-transporting ATPase IA isoform X6
phospholipid-transporting ATPase IA isoform X4
ATPase phospholipid transporting 8A1, transcript variant X5
phospholipid-transporting ATPase IA isoform X5
shisa family member 3, 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 10 samples with support for all annotated introns
shisa family member 3, transcript variant X2
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 40 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 22 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 40 samples with support for all annotated introns
histone-lysine N-trimethyltransferase SMYD5
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
uncharacterized LOC124473427, 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 43 samples with support for all annotated introns
uncharacterized LOC124473427, transcript variant X1
solute carrier family 4 member 11-like, transcript variant X1
solute carrier family 4 member 11-like isoform X1
solute carrier family 4 member 11-like, 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 43 samples with support for all annotated introns
solute carrier family 4 member 11-like isoform X3
solute carrier family 4 member 11-like, 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 36 samples with support for all annotated introns
solute carrier family 4 member 11-like isoform X2
ecto-NOX disulfide-thiol exchanger 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LOW QUALITY PROTEIN: ecto-NOX disulfide-thiol exchanger 2-like
ecto-NOX disulfide-thiol exchanger 2-like, transcript variant X1
ecto-NOX disulfide-thiol exchanger 2-like, transcript variant X2
ecto-NOX disulfide-thiol exchanger 2-like isoform X1
ecto-NOX disulfide-thiol exchanger 2-like isoform X2
ATP-binding cassette sub-family C member 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 12
methionyl-tRNA synthetase 2, mitochondrial
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 39 samples with support for all annotated introns
uncharacterized protein LOC494104 homolog, transcript variant X1
uncharacterized protein LOC494104 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Bruton agammaglobulinemia tyrosine kinase, transcript variant X1
Bruton agammaglobulinemia tyrosine kinase, transcript variant X2
translocase of inner mitochondrial membrane 8 homolog A (yeast)
mitochondrial import inner membrane translocase subunit Tim8 A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
diaphanous-related formin 2, 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 30 samples with support for all annotated introns
diaphanous-related formin 2, 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 32 samples with support for all annotated introns
diaphanous-related formin 2, 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 37 samples with support for all annotated introns
diaphanous-related formin 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
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
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
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 21 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 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
E74-like ETS transcription factor 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 42 samples with support for all annotated introns
ETS-related transcription factor Elf-1 isoform X3
E74-like ETS transcription factor 1, transcript variant X2
E74-like ETS transcription factor 1, transcript variant X8
E74-like ETS transcription factor 1, transcript variant X4
E74-like ETS transcription factor 1, transcript variant X1
E74-like ETS transcription factor 1, transcript variant X6
E74-like ETS transcription factor 1, transcript variant X7
E74-like ETS transcription factor 1, transcript variant X3
ETS-related transcription factor Elf-1 isoform X4
ETS-related transcription factor Elf-1 isoform X2
ETS-related transcription factor Elf-1 isoform X1
ETS-related transcription factor Elf-1 isoform X6
ETS-related transcription factor Elf-1 isoform X5
NFKB repressing factor, transcript variant X2
NFKB repressing factor, transcript variant X1
PTTG1 regulator of sister chromatid separation, securin, transcript variant X1
PTTG1 regulator of sister chromatid separation, securin, transcript variant X2
sosondowah ankyrin repeat domain family d, 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 36 samples with support for all annotated introns
sosondowah ankyrin repeat domain family d, 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 10 samples with support for all annotated introns
ankyrin repeat domain-containing protein SOWAHD
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00265
UPF3B regulator of nonsense mediated mRNA decay
NADH:ubiquinone oxidoreductase subunit A1
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 1
zinc finger and BTB domain containing 33, transcript variant X1
zinc finger and BTB domain containing 33, transcript variant X2
transcriptional regulator Kaiso isoform X1
transcriptional regulator Kaiso isoform X2
transmembrane protein 255A, 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 18 samples with support for all annotated introns
transmembrane protein 255A, 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 9 samples with support for all annotated introns
transmembrane protein 255A, 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 8 samples with support for all annotated introns
ATPase Na+/K+ transporting subunit beta 4
lysosomal-associated membrane protein 2, transcript variant X1
lysosome-associated membrane glycoprotein 2 isoform X1
lysosomal-associated membrane protein 2, transcript variant X2
lysosome-associated membrane glycoprotein 2 isoform 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 42 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, including 2 samples with support for all annotated introns
chloride intracellular channel protein 2
protein eva-1 homolog C, transcript variant X1
protein eva-1 homolog C, transcript variant X2
OCRL inositol polyphosphate-5-phosphatase, transcript variant X1
OCRL inositol polyphosphate-5-phosphatase, transcript variant X3
OCRL inositol polyphosphate-5-phosphatase, transcript variant X2
OCRL inositol polyphosphate-5-phosphatase, transcript variant X4
OCRL inositol polyphosphate-5-phosphatase, transcript variant X5
inositol polyphosphate 5-phosphatase OCRL isoform X1
inositol polyphosphate 5-phosphatase OCRL isoform X3
inositol polyphosphate 5-phosphatase OCRL isoform X2
inositol polyphosphate 5-phosphatase OCRL isoform X4
inositol polyphosphate 5-phosphatase OCRL isoform X5
X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound
SAM and SH3 domain containing 3, transcript variant X2
SAM and SH3 domain containing 3, transcript variant X1
SAM and SH3 domain containing 3, transcript variant X3
SAM and SH3 domain containing 3, transcript variant X4
SAM and SH3 domain-containing protein 3 isoform X1
SAM and SH3 domain-containing protein 3 isoform X2
SAM and SH3 domain-containing protein 3 isoform X3
SAM and SH3 domain-containing protein 3 isoform X4
SAM and SH3 domain containing 3, transcript variant X5
SAM and SH3 domain-containing protein 3 isoform X5
zinc finger DHHC-type palmitoyltransferase 9
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tRNA wybutosine-synthesizing protein 2 homolog
synaptotagmin-like 4, transcript variant X1
synaptotagmin-like 4, transcript variant X4
synaptotagmin-like 4, transcript variant X3
synaptotagmin-like 4, transcript variant X2
sushi-repeat containing protein X-linked 2
BCL6 corepressor-like 1, 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 20 samples with support for all annotated introns
BCL6 corepressor-like 1, transcript variant X1
BCL6 corepressor-like 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 7 samples with support for all annotated introns
BCL6 corepressor-like 1, 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 7 samples with support for all annotated introns
BCL-6 corepressor-like protein 1 isoform X2
BCL-6 corepressor-like protein 1 isoform X1
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cleavage stimulation factor, 3' pre-RNA, subunit 2, transcript variant X1
cleavage stimulation factor, 3' pre-RNA, subunit 2, transcript variant X2
cleavage stimulation factor, 3' pre-RNA, subunit 2, transcript variant X3
cleavage stimulation factor, 3' pre-RNA, subunit 2, transcript variant X4
cleavage stimulation factor, 3' pre-RNA, subunit 2, transcript variant X5
cleavage stimulation factor, 3' pre-RNA, subunit 2, transcript variant X6
cleavage stimulation factor subunit 2 isoform X1
cleavage stimulation factor subunit 2 isoform X2
cleavage stimulation factor subunit 2 isoform X3
cleavage stimulation factor subunit 2 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 1 sample with support for all annotated introns
ADP-ribosylation factor-like protein 13A
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 28 samples with support for all annotated introns
dystrophin related protein 2, 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 16 samples with support for all annotated introns
dystrophin related protein 2, 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 27 samples with support for all annotated introns
TAF7 RNA polymerase II, TATA box binding protein (TBP)-associated factor
transcription initiation factor TFIID subunit 7
motile sperm domain containing 1, transcript variant X2
motile sperm domain containing 1, transcript variant X1
motile sperm domain-containing protein 1
PABIR family member 2, transcript variant X2
PABIR family member 2, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF01233
hypoxanthine phosphoribosyltransferase 1, transcript variant X1
hypoxanthine phosphoribosyltransferase 1, transcript variant X2
hypoxanthine-guanine phosphoribosyltransferase isoform X2
hypoxanthine-guanine phosphoribosyltransferase isoform X1
PHD finger protein 6, 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 41 samples with support for all annotated introns
PHD finger protein 6, transcript variant X1
PHD finger protein 6, transcript variant X2
calcium binding protein 39, like 1, transcript variant X2
calcium binding protein 39, like 1, transcript variant X1
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
heparan sulfate 6-O-sulfotransferase 2, transcript variant X1
heparan sulfate 6-O-sulfotransferase 2, transcript variant X2
heparan-sulfate 6-O-sulfotransferase 2 isoform X1
heparan-sulfate 6-O-sulfotransferase 2 isoform X2
muscleblind-like splicing regulator 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
muscleblind-like splicing regulator 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
muscleblind-like splicing regulator 3, transcript variant X1
muscleblind-like splicing regulator 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
muscleblind-like splicing regulator 3, transcript variant X5
muscleblind-like splicing regulator 3, transcript variant X8
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 12 samples with support for all annotated introns
muscleblind-like splicing regulator 3, 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 43 samples with support for all annotated introns
muscleblind-like splicing regulator 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
uncharacterized protein LOC436733 homolog
UDP-N-acetylglucosamine transferase subunit ALG13 homolog
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 20 samples with support for all annotated introns
sorting nexin-12-like, 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 44 samples with support for all annotated introns
sorting nexin-12-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 45 samples with support for all annotated introns
sorting nexin-12-like, transcript variant X1
solute carrier family 7 member 3b, transcript variant X1
solute carrier family 7 member 3b, transcript variant X2
Yip1 interacting factor homolog A (S. cerevisiae)
FOS like 1, AP-1 transcription factor subunit a, transcript variant X1
FOS like 1, AP-1 transcription factor subunit a, transcript variant X2
coiled-coil domain-containing protein 85B
fibroblast growth factor (acidic) intracellular binding protein a, transcript variant X1
fibroblast growth factor (acidic) intracellular binding protein a, transcript variant X2
fibroblast growth factor (acidic) intracellular binding protein a isoform X1
fibroblast growth factor (acidic) intracellular binding protein a isoform X2
EGF containing fibulin extracellular matrix protein 2a
EGF-containing fibulin-like extracellular matrix protein 2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
neuronal PAS domain-containing protein 4A
mitochondrial ribosomal protein L11, transcript variant X1
mitochondrial ribosomal protein L11, transcript variant X2
39S ribosomal protein L11, mitochondrial
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
solute carrier family 25 member 43, transcript variant X1
solute carrier family 25 member 43, transcript variant X2
solute carrier family 25 member 43 isoform X1
solute carrier family 25 member 43 isoform X2
ligand of numb-protein X 2b, 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 43 samples with support for all annotated introns
ligand of numb-protein X 2b, 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 41 samples with support for all annotated introns
ligand of numb-protein X 2b, transcript variant X3
cysteine-rich hydrophobic domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
vascular endothelial growth factor receptor kdr-like
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
discs, large homolog 3 (Drosophila), transcript variant X2
discs, large homolog 3 (Drosophila), transcript variant X4
discs, large homolog 3 (Drosophila), transcript variant X3
discs, large homolog 3 (Drosophila), transcript variant X1
discs, large homolog 3 (Drosophila), transcript variant X6
discs, large homolog 3 (Drosophila), transcript variant X5
glycerophosphodiester phosphodiesterase domain containing 2, transcript variant X1
glycerophosphoinositol inositolphosphodiesterase GDPD2
glycerophosphodiester phosphodiesterase domain containing 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 33 samples with support for all annotated introns
PDZ domain containing 11, transcript variant X3
PDZ domain containing 11, transcript variant X4
PDZ domain containing 11, transcript variant X1
PDZ domain containing 11, transcript variant X2
RAB41, member RAS oncogene family, transcript variant X4
RAB41, member RAS oncogene family, transcript variant X2
RAB41, member RAS oncogene family, transcript variant X1
RAB41, member RAS oncogene family, transcript variant X6
RAB41, member RAS oncogene family, transcript variant X3
RAB41, member RAS oncogene family, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
inositol polyphosphate phosphatase-like 1b, 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 27 samples with support for all annotated introns
inositol polyphosphate phosphatase-like 1b, 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 39 samples with support for all annotated introns
inositol polyphosphate phosphatase-like 1b isoform X1
inositol polyphosphate phosphatase-like 1b isoform X2
pyrimidinergic receptor P2Y4, transcript variant X1
pyrimidinergic receptor P2Y4, 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 5 samples with support for all annotated introns
uncharacterized LOC124466763, transcript variant X2
uncharacterized LOC124466763, 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 4 samples with support for all annotated introns
histamine receptor H2a, 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 2 samples with support for all annotated introns
histamine receptor H2a, 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 20 samples with support for all annotated introns
histamine receptor H2a, transcript variant X5
histamine receptor H2a, transcript variant X3
histamine receptor H2a, transcript variant X4
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 8 samples with support for all annotated introns
histamine receptor H2a, 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 32 samples with support for all annotated introns
histamine receptor H2a, transcript variant X1
zinc finger, C4H2 domain containing, transcript variant X1
zinc finger, C4H2 domain containing, transcript variant X2
zinc finger C4H2 domain-containing protein isoform X1
zinc finger C4H2 domain-containing protein isoform X2
uncharacterized protein C8orf48-like, 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 30 samples with support for all annotated introns
uncharacterized protein C8orf48-like, 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 17 samples with support for all annotated introns
uncharacterized protein C8orf48-like, 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 41 samples with support for all annotated introns
uncharacterized protein C8orf48-like, transcript variant X1
uncharacterized protein C8orf48-like isoform X2
uncharacterized protein C8orf48-like isoform X4
uncharacterized protein C8orf48-like isoform X3
uncharacterized protein C8orf48-like isoform X1
ankyrin repeat and SOCS box protein 12-like, transcript variant X1
ankyrin repeat and SOCS box protein 12-like, transcript variant X2
ankyrin repeat and SOCS box protein 12-like
uncharacterized LOC124464866, transcript variant X6
uncharacterized LOC124464866, transcript variant X5
uncharacterized LOC124464866, transcript variant X1
uncharacterized LOC124464866, transcript variant X2
uncharacterized protein LOC124464866 isoform X6
uncharacterized protein LOC124464866 isoform X5
uncharacterized protein LOC124464866 isoform X2
uncharacterized protein LOC124464866 isoform X1
uncharacterized LOC124464866, 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 13 samples with support for all annotated introns
uncharacterized LOC124464866, 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 29 samples with support for all annotated introns
uncharacterized protein LOC124464866 isoform X3
uncharacterized protein LOC124464866 isoform 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 1 sample with support for all annotated introns
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 13 samples with support for all annotated introns
connector enhancer of kinase suppressor of ras 2-like
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
uncharacterized LOC124466089, transcript variant X4
uncharacterized LOC124466089, transcript variant X3
uncharacterized LOC124466089, transcript variant X2
uncharacterized LOC124466089, transcript variant X1
uncharacterized protein LOC124466089 isoform X3
uncharacterized protein LOC124466089 isoform X2
uncharacterized protein LOC124466089 isoform X1
uncharacterized protein LOC124466089 isoform X4
serine/threonine-protein kinase pim-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain containing 142, transcript variant X1
coiled-coil domain containing 142, transcript variant X2
uncharacterized protein ccdc142 isoform X1
uncharacterized protein ccdc142 isoform X2
NK1 transcription factor related 2-like,b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
NK1 transcription factor-related protein 1
SIL1 nucleotide exchange factor, transcript variant X1
SIL1 nucleotide exchange factor, transcript variant X2
trypsin inhibitor ClTI-1-like, transcript variant X2
trypsin inhibitor ClTI-1-like, transcript variant X1
casein kinase 1, alpha 1, transcript variant X1
casein kinase 1, alpha 1, transcript variant X3
casein kinase 1, alpha 1, transcript variant X2
casein kinase 1, alpha 1, transcript variant X6
casein kinase 1, alpha 1, transcript variant X4
casein kinase 1, alpha 1, transcript variant X5
casein kinase 1, alpha 1, transcript variant X7
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
fibroblast growth factor receptor like 1b
fibroblast growth factor receptor-like 1b
COORDINATES: nucleotide motif:Rfam:12.0:RF00090
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
LOW QUALITY PROTEIN: stress-70 protein, mitochondrial
F-BAR and double SH3 domains protein 1-like
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 34 samples with support for all annotated introns
vacuolar ATPase assembly integral membrane protein vma21-like
gap junction alpha-3 protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
gap junction alpha-3 protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
gap junction alpha-3 protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 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: 60 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor ligand superfamily member 13B-like, 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 24 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 13B-like, transcript variant X2
transforming growth factor beta activator LRRC32-like isoform X1
transforming growth factor beta activator LRRC32-like isoform X2
tumor necrosis factor ligand superfamily member 13B-like, transcript variant X4
tumor necrosis factor ligand superfamily member 13B-like, transcript variant X3
tumor necrosis factor ligand superfamily member 13B-like isoform X4
tumor necrosis factor ligand superfamily member 13B-like isoform X3
ectodysplasin-A-like, transcript variant X1
ectodysplasin-A-like, transcript variant X2
ectodysplasin-A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 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: 45 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
small integral membrane protein 19, transcript variant X1
small integral membrane protein 19, transcript variant X2
small integral membrane protein 19 isoform X1
small integral membrane protein 19 isoform X2
uncharacterized protein LOC568697 homolog
uncharacterized protein si:ch211-175m2.5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 96% 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: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
integrator complex subunit 10, transcript variant X2
integrator complex subunit 10, transcript variant X1
integrator complex subunit 10, transcript variant X3
integrator complex subunit 10 isoform X2
integrator complex subunit 10 isoform X1
integrator complex subunit 10 isoform X3
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
LOW QUALITY PROTEIN: mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51-like
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 20 samples with support for all annotated introns
translocase of outer mitochondrial membrane 5 homolog (yeast), transcript variant X1
translocase of outer mitochondrial membrane 5 homolog (yeast), transcript variant X2
mitochondrial import receptor subunit TOM5 homolog isoform X2
mitochondrial import receptor subunit TOM5 homolog isoform X1
glyoxylate reductase/hydroxypyruvate reductase a
glyoxylate reductase/hydroxypyruvate reductase
39S ribosomal protein L18, mitochondrial
uncharacterized LOC124464118, 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
uncharacterized LOC124464118, transcript variant X4
uncharacterized LOC124464118, transcript variant X5
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 26 samples with support for all annotated introns
uncharacterized LOC124464118, transcript variant X1
uncharacterized LOC124464118, transcript variant X2
uncharacterized protein LOC124464118 isoform X3
uncharacterized protein LOC124464118 isoform X1
uncharacterized protein LOC124464118 isoform X2
uncharacterized protein LOC124464118 isoform X4
uncharacterized protein LOC124464118 isoform X5
V-type proton ATPase 116 kDa subunit a3-like, transcript variant X2
V-type proton ATPase 116 kDa subunit a3-like, transcript variant X1
V-type proton ATPase 116 kDa subunit a3-like
uncharacterized LOC124469526, transcript variant X2
uncharacterized LOC124469526, transcript variant X1
uncharacterized LOC124469933, transcript variant X2
uncharacterized LOC124469933, transcript variant X7
uncharacterized LOC124469933, transcript variant X8
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 27 samples with support for all annotated introns
uncharacterized LOC124469933, transcript variant X3
uncharacterized LOC124469933, transcript variant X4
uncharacterized LOC124469933, transcript variant X1
uncharacterized LOC124469933, transcript variant X5
uncharacterized LOC124469933, transcript variant X9
uncharacterized LOC124469933, transcript variant X6
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 28 samples with support for all annotated introns
uncharacterized LOC124469933, transcript variant X10
uncharacterized LOC124476665, transcript variant X1
uncharacterized LOC124476665, transcript variant X2
ring finger protein 20, E3 ubiquitin protein ligase, transcript variant X2
ring finger protein 20, E3 ubiquitin protein ligase, transcript variant X6
ring finger protein 20, E3 ubiquitin protein ligase, transcript variant X5
ring finger protein 20, E3 ubiquitin protein ligase, transcript variant X4
ring finger protein 20, E3 ubiquitin protein ligase, transcript variant X3
ring finger protein 20, E3 ubiquitin protein ligase, transcript variant X1
E3 ubiquitin-protein ligase BRE1A isoform X5
E3 ubiquitin-protein ligase BRE1A isoform X4
E3 ubiquitin-protein ligase BRE1A isoform X3
E3 ubiquitin-protein ligase BRE1A isoform X2
E3 ubiquitin-protein ligase BRE1A isoform 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 6 samples with support for all annotated introns
trafficking protein particle complex subunit 11-like, 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 11 samples with support for all annotated introns
trafficking protein particle complex subunit 11-like, 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 41 samples with support for all annotated introns
trafficking protein particle complex subunit 11-like, transcript variant X3
uncharacterized protein LOC124468285 isoform X1
trafficking protein particle complex subunit 11-like, transcript variant X5
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 31 samples with support for all annotated introns
trafficking protein particle complex subunit 11-like, transcript variant X6
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 21 samples with support for all annotated introns
trafficking protein particle complex subunit 11-like, transcript variant X4
trafficking protein particle complex subunit 11-like isoform X2
trafficking protein particle complex subunit 11-like, transcript variant X7
serine/threonine-protein kinase prk-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC799862 homolog
membrane-spanning 4-domains subfamily A member 4A
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 26 samples with support for all annotated introns
transmembrane and coiled-coil domain-containing protein 6
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 20 samples with support for all annotated introns
fibrinogen-like 1, 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 19 samples with support for all annotated introns
fibrinogen-like 1, 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, including 15 samples with support for all annotated introns
cyclic nucleotide-gated cation channel-like, transcript variant X2
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
cyclic nucleotide-gated cation channel-like, transcript variant X1
cyclic nucleotide-gated cation channel-like isoform X2
cyclic nucleotide-gated olfactory channel-like isoform X1
chromosome 1 C4orf47 homolog, 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 1 sample with support for all annotated introns
chromosome 1 C4orf47 homolog, transcript variant X2
sorbin and SH3 domain-containing protein 2-like, transcript variant X2
sorbin and SH3 domain-containing protein 2-like, transcript variant X4
sorbin and SH3 domain-containing protein 2-like, transcript variant X3
sorbin and SH3 domain-containing protein 2-like, transcript variant X1
sorbin and SH3 domain-containing protein 2-like isoform X3
sorbin and SH3 domain-containing protein 2-like isoform X2
sorbin and SH3 domain-containing protein 2-like 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 38 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 11 samples with support for all annotated introns
interferon regulatory factor 2, transcript variant X1
interferon regulatory factor 2, transcript variant X2
interferon regulatory factor 2 isoform X1
interferon regulatory factor 2 isoform X2
interferon regulatory factor 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
interferon regulatory factor 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 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 38 samples with support for all annotated introns
long-chain-fatty-acid--CoA ligase 1-like
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
ectonucleotide pyrophosphatase/phosphodiesterase 6
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 36 samples with support for all annotated introns
glycerophosphocholine cholinephosphodiesterase ENPP6
storkhead-box protein 2-like, transcript variant X1
storkhead-box protein 2-like, transcript variant X2
storkhead-box protein 2-like, transcript variant X3
uncharacterized LOC124463471, transcript variant X2
uncharacterized LOC124463471, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 22 member 4-like, transcript variant X2
solute carrier family 22 member 4-like, 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
solute carrier family 22 member 4-like isoform X1
solute carrier family 22 member 5-like isoform X2
solute carrier family 22 member 4-like, 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 27 samples with support for all annotated introns
solute carrier family 22 member 4-like isoform X3
solute carrier family 22 member 4-like, transcript variant X4
solute carrier family 22 member 4-like isoform X4
trafficking protein particle complex subunit 11, 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 11 samples with support for all annotated introns
trafficking protein particle complex subunit 11, transcript variant X3
trafficking protein particle complex subunit 11, 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 8 samples with support for all annotated introns
trafficking protein particle complex subunit 11, transcript variant X1
trafficking protein particle complex subunit 11
inner membrane protein, mitochondrial (mitofilin), transcript variant X2
inner membrane protein, mitochondrial (mitofilin), transcript variant X4
inner membrane protein, mitochondrial (mitofilin), transcript variant X1
inner membrane protein, mitochondrial (mitofilin), transcript variant X3
pentatricopeptide repeat domain 3, transcript variant X2
pentatricopeptide repeat domain 3, transcript variant X1
pentatricopeptide repeat domain-containing protein 3, mitochondrial isoform X1
pentatricopeptide repeat domain-containing protein 3, mitochondrial isoform X2
DNA-directed RNA polymerase I subunit RPA1
ST3 beta-galactoside alpha-2,3-sialyltransferase 5
lactosylceramide alpha-2,3-sialyltransferase
transmembrane protein 129, E3 ubiquitin protein ligase, transcript variant X2
E3 ubiquitin-protein ligase TM129 isoform X2
transmembrane protein 129, E3 ubiquitin protein ligase, transcript variant X1
E3 ubiquitin-protein ligase TM129 isoform X1
stem-loop binding protein, transcript variant X1
stem-loop binding protein, transcript variant X2
histone RNA hairpin-binding protein isoform X1
histone RNA hairpin-binding protein isoform X2