Aythya fuligula isolate bAytFul2 chromosome 15, bAytFul2.pri, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Archosauria; Dinosauria; Saurischia; Theropoda; Coelurosauria; Aves; Neognathae; Galloanserae; Anseriformes; Anatidae; Aythyinae; Aythya.
REFSEQ INFORMATION: The reference sequence is identical to\nCM020314.1.\nAssembly name: bAytFul2.pri\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2019/12/31. The original whole-genome shotgun project has the\naccession WNMM00000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 20-SEP-2019\nAssembly Method :: FALCON v. 2018.31.08-03.06; FALCON-Unzip\n v. 6.0.0.47841; purge_haplotigs v.\n v1.0.3+ 1.Nov.2018; scaff10x v. 4.1.0;\n Bionano Solve DLS v. 3.2.1; Salsa HiC v.\n 2.2; Arrow smrtanalysis Pacbio polishing\n & gap filling v. 6.0.0.47841; longranger\n align v. 2.2.2; freebayes Illumina\n polishing v. 1.3; gEVAL manual curation\n v. 2019-09-20; VGP assembly pipeline\n individual v. 1.5\nAssembly Name :: bAytFul2.pri\nDiploid :: Principal pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 64.03x\nSequencing Technology :: PacBio Sequel I CLR; Illumina NovaSeq;\n Arima Genomics Hi-C; Bionano Genomics DLS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Aythya fuligula Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.3\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Patrik Ellstrom, Mahmoud Naguib, Josef Jarhult
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
unk like zinc finger, 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 3 samples with support for all annotated introns
unk like zinc finger, 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 2 samples with support for all annotated introns
unk like zinc finger, transcript variant X1
unk like zinc finger, 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 3 samples with support for all annotated introns
unk like zinc finger, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
unk like zinc finger, transcript variant X6
putative E3 ubiquitin-protein ligase UNKL isoform X3
putative E3 ubiquitin-protein ligase UNKL isoform X2
putative E3 ubiquitin-protein ligase UNKL isoform X1
putative E3 ubiquitin-protein ligase UNKL isoform X5
putative E3 ubiquitin-protein ligase UNKL isoform X4
putative E3 ubiquitin-protein ligase UNKL isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
N-acetylglucosamine-1-phosphate transferase subunit gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
N-acetylglucosamine-1-phosphotransferase subunit gamma
ribosome biogenesis protein TSR3 homolog
ubiquitin conjugating enzyme E2 I, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ubiquitin conjugating enzyme E2 I, 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 3 samples with support for all annotated introns
uncharacterized LOC116495174, transcript variant X1
uncharacterized LOC116495174, transcript variant X2
potassium channel tetramerization domain containing 5, 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
potassium channel tetramerization domain containing 5, 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 3 samples with support for all annotated introns
potassium channel tetramerization domain containing 5, 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 3 samples with support for all annotated introns
BTB/POZ domain-containing protein KCTD5 isoform X3
BTB/POZ domain-containing protein KCTD5 isoform X2
BTB/POZ domain-containing protein KCTD5 isoform X1
3-phosphoinositide dependent protein kinase 1, 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
3-phosphoinositide dependent protein kinase 1, transcript variant X2
3-phosphoinositide-dependent protein kinase 1 isoform X1
3-phosphoinositide-dependent protein kinase 1 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: interleukin-9 receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
interleukin 4 receptor, transcript variant X2
interleukin 4 receptor, transcript variant X1
interleukin 4 receptor, transcript variant X3
interleukin-4 receptor subunit alpha isoform X2
interleukin-4 receptor subunit alpha isoform X1
interleukin-4 receptor subunit alpha isoform X3
NSE1 homolog, SMC5-SMC6 complex component
non-structural maintenance of chromosomes element 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
bifunctional peptidase and arginyl-hydroxylase JMJD5
heparan sulfate-glucosamine 3-sulfotransferase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 4
heparan sulfate-glucosamine 3-sulfotransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 31
sodium channel epithelial 1 subunit gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
amiloride-sensitive sodium channel subunit gamma
sodium channel epithelial 1 subunit beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
amiloride-sensitive sodium channel subunit beta
conserved oligomeric Golgi complex subunit 7
golgi associated, gamma adaptin ear containing, ARF binding 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 3 samples with support for all annotated introns
ADP-ribosylation factor-binding protein GGA2
glutamyl-tRNA synthetase 2, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments
probable glutamate--tRNA ligase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ubiquitin domain-containing protein UBFD1
endoplasmic reticulum to nucleus signaling 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase/endoribonuclease IRE2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dynactin subunit 5, 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 3 samples with support for all annotated introns
dynactin subunit 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase subunit AB1
trinucleotide repeat containing adaptor 6A, transcript variant X4
trinucleotide repeat containing adaptor 6A, transcript variant X8
trinucleotide repeat containing adaptor 6A, transcript variant X3
trinucleotide repeat containing adaptor 6A, 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 3 samples with support for all annotated introns
trinucleotide repeat containing adaptor 6A, transcript variant X2
trinucleotide repeat containing adaptor 6A, transcript variant X1
trinucleotide repeat containing adaptor 6A, transcript variant X7
trinucleotide repeat containing adaptor 6A, transcript variant X9
trinucleotide repeat containing adaptor 6A, transcript variant X6
trinucleotide repeat-containing gene 6A protein isoform X8
trinucleotide repeat-containing gene 6A protein isoform X7
trinucleotide repeat-containing gene 6A protein isoform X3
trinucleotide repeat-containing gene 6A protein isoform X6
trinucleotide repeat-containing gene 6A protein isoform X5
trinucleotide repeat-containing gene 6A protein isoform X2
trinucleotide repeat-containing gene 6A protein isoform X1
trinucleotide repeat-containing gene 6A protein isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
calcium voltage-gated channel auxiliary subunit gamma 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
voltage-dependent calcium channel gamma-3 subunit
protein kinase C beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein kinase C beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Rho GTPase activating protein 17, transcript variant X1
Rho GTPase activating protein 17, transcript variant X2
Rho GTPase activating protein 17, transcript variant X3
Rho GTPase activating protein 17, transcript variant X4
rho GTPase-activating protein 17 isoform X1
rho GTPase-activating protein 17 isoform X4
rho GTPase-activating protein 17 isoform X3
rho GTPase-activating protein 17 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 14% 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 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
zinc finger DHHC-type palmitoyltransferase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 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: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
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
target of rapamycin complex subunit LST8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CASK interacting protein 1, transcript variant X1
CASK interacting protein 1, transcript variant X2
TNF receptor associated factor 7, 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 3 samples with support for all annotated introns
TNF receptor associated factor 7, transcript variant X2
TNF receptor associated factor 7, transcript variant X3
E3 ubiquitin-protein ligase TRAF7 isoform X1
E3 ubiquitin-protein ligase TRAF7 isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00271
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
polycystin 1, transient receptor potential channel interacting
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
TSC complex subunit 2, 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
TSC complex subunit 2, transcript variant X7
TSC complex subunit 2, transcript variant X6
TSC complex subunit 2, transcript variant X5
TSC complex subunit 2, transcript variant X3
TSC complex subunit 2, transcript variant X4
TSC complex subunit 2, transcript variant X1
Na(+)/H(+) exchange regulatory cofactor NHE-RF2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
growth factor, augmenter of liver regeneration
COORDINATES: nucleotide motif:Rfam:12.0:RF01225
NADH:ubiquinone oxidoreductase subunit B10
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
heparan sulfate-glucosamine 3-sulfotransferase 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
heparan sulfate glucosamine 3-O-sulfotransferase 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
meiosis-specific with OB domain-containing protein
fumarylacetoacetate hydrolase domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
hydroxyacylglutathione hydrolase, 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 3 samples with support for all annotated introns
hydroxyacylglutathione hydrolase, mitochondrial isoform X1
hydroxyacylglutathione hydrolase, transcript variant X3
hydroxyacylglutathione hydrolase, transcript variant X2
hydroxyacylglutathione hydrolase, transcript variant X4
hydroxyacylglutathione hydrolase, mitochondrial isoform X2
hydroxyacylglutathione hydrolase-like protein
cytosolic iron-sulfur assembly component 3
RNA pseudouridine synthase domain containing 1
RNA pseudouridylate synthase domain-containing protein 1
chromosome transmission fidelity factor 18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
chromosome transmission fidelity protein 18 homolog
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-13
uncharacterized LOC116495490, transcript variant X1
uncharacterized LOC116495490, transcript variant X2
uncharacterized protein LOC116495490 isoform X1
uncharacterized LOC116495490, 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 1 sample with support for all annotated introns
uncharacterized protein LOC116495490 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
somatostatin receptor 5, transcript variant X1
somatostatin receptor 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
complement C1q tumor necrosis factor-related protein 8
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
calcium voltage-gated channel subunit alpha1 H, transcript variant X1
voltage-dependent T-type calcium channel subunit alpha-1H isoform X1
calcium voltage-gated channel subunit alpha1 H, transcript variant X2
voltage-dependent T-type calcium channel subunit alpha-1H isoform X2
B9 domain containing 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 3 samples with support for all annotated introns
B9 domain-containing protein 1 isoform X1
B9 domain containing 1, transcript variant X2
B9 domain-containing protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
family with sequence similarity 83 member G
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
phosphoribosyl pyrophosphate synthetase associated protein 2
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
phosphoribosyl pyrophosphate synthase-associated protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
serine hydroxymethyltransferase, cytosolic
SMCR8-C9orf72 complex subunit, transcript variant X1
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, including 2 samples with support for all annotated introns
SMCR8-C9orf72 complex subunit, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SMCR8-C9orf72 complex subunit, transcript variant X2
guanine nucleotide exchange protein SMCR8
LLGL scribble cell polarity complex component 1, transcript variant X3
LLGL scribble cell polarity complex component 1, transcript variant X2
LLGL scribble cell polarity complex component 1, transcript variant X1
lethal(2) giant larvae protein homolog 1 isoform X3
lethal(2) giant larvae protein homolog 1 isoform X2
lethal(2) giant larvae protein homolog 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 9% coverage of the annotated genomic feature by RNAseq alignments
developmentally regulated GTP binding protein 2
developmentally-regulated GTP-binding protein 2
glucose-induced degradation protein 4 homolog
ATP synthase mitochondrial F1 complex assembly factor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
target of myb1 like 2 membrane trafficking protein, transcript variant X1
target of myb1 like 2 membrane trafficking protein, transcript variant X2
target of myb1 like 2 membrane trafficking protein, transcript variant X3
sterol regulatory element binding transcription factor 1
sterol regulatory element-binding protein 1
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, including 3 samples with support for all annotated introns
phosphatidylethanolamine N-methyltransferase, transcript variant X5
phosphatidylethanolamine N-methyltransferase, transcript variant X2
phosphatidylethanolamine N-methyltransferase, transcript variant X1
phosphatidylethanolamine N-methyltransferase, transcript variant X3
phosphatidylethanolamine N-methyltransferase isoform X1
phosphatidylethanolamine N-methyltransferase isoform X2
phosphatidylethanolamine N-methyltransferase, transcript variant X4
phosphatidylethanolamine N-methyltransferase isoform X3
ras related dexamethasone induced 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ras related dexamethasone induced 1, transcript variant X1
dexamethasone-induced Ras-related protein 1
mediator of RNA polymerase II transcription subunit 9
5'(3')-deoxyribonucleotidase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
myosin phosphatase Rho interacting protein, transcript variant X7
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
myosin phosphatase Rho interacting protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myosin phosphatase Rho interacting protein, transcript variant X6
myosin phosphatase Rho interacting protein, transcript variant X2
myosin phosphatase Rho interacting protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
myosin phosphatase Rho-interacting protein isoform X6
myosin phosphatase Rho-interacting protein isoform X4
myosin phosphatase Rho-interacting protein isoform X5
myosin phosphatase Rho-interacting protein isoform X2
myosin phosphatase Rho-interacting protein isoform X1
myosin phosphatase Rho interacting protein, transcript variant X4
myosin phosphatase Rho interacting protein, transcript variant X8
myosin phosphatase Rho interacting protein, transcript variant X3
myosin phosphatase Rho-interacting protein isoform X7
myosin phosphatase Rho-interacting protein isoform X3
tumor necrosis factor receptor superfamily member 13B
ubiquitin specific peptidase 22, 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 3 samples with support for all annotated introns
ubiquitin specific peptidase 22, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 22 isoform X2
ubiquitin carboxyl-terminal hydrolase 22 isoform X1
dehydrogenase/reductase 7B, transcript variant X1
dehydrogenase/reductase SDR family member 7B isoform X1
dehydrogenase/reductase 7B, transcript variant X2
dehydrogenase/reductase SDR family member 7B isoform X2
mitogen-activated protein kinase kinase 3, transcript variant X2
dual specificity mitogen-activated protein kinase kinase 3 isoform X2
mitogen-activated protein kinase kinase 3, transcript variant X1
dual specificity mitogen-activated protein kinase kinase 3 isoform X1
potassium inwardly rectifying channel subfamily J member 12, 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 2 samples with support for all annotated introns
potassium inwardly rectifying channel subfamily J member 12, transcript variant X2
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 1 sample with support for all annotated introns
ATP-sensitive inward rectifier potassium channel 12
cleavage and polyadenylation specific factor 4
cleavage and polyadenylation specificity factor subunit 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pentatricopeptide repeat-containing protein 1, mitochondrial
28 kDa heat- and acid-stable phosphoprotein
actin related protein 2/3 complex subunit 1B
actin-related protein 2/3 complex subunit 1B
actin related protein 2/3 complex subunit 1A, transcript variant X1
actin related protein 2/3 complex subunit 1A, transcript variant X2
actin-related protein 2/3 complex subunit 1A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
SMAD specific E3 ubiquitin protein ligase 1, transcript variant X1
SMAD specific E3 ubiquitin protein ligase 1, transcript variant X2
SMAD specific E3 ubiquitin protein ligase 1, transcript variant X3
SMAD specific E3 ubiquitin protein ligase 1, transcript variant X4
E3 ubiquitin-protein ligase SMURF1 isoform X1
E3 ubiquitin-protein ligase SMURF1 isoform X2
E3 ubiquitin-protein ligase SMURF1 isoform X3
E3 ubiquitin-protein ligase SMURF1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 561 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
F-box and leucine rich repeat protein 18, transcript variant X3
F-box and leucine rich repeat protein 18, transcript variant X1
F-box and leucine rich repeat protein 18, 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 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
trinucleotide repeat-containing gene 18 protein
solute carrier family 29 member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 29 member 4, transcript variant X1
equilibrative nucleoside transporter 4 isoform X2
equilibrative nucleoside transporter 4 isoform X1
WD repeat domain, phosphoinositide interacting 2, transcript variant X2
WD repeat domain, phosphoinositide interacting 2, transcript variant X1
WD repeat domain phosphoinositide-interacting protein 2 isoform X2
WD repeat domain phosphoinositide-interacting protein 2 isoform X1
monocyte to macrophage differentiation associated 2
monocyte to macrophage differentiation factor 2
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 65% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ras-associating and dilute domain-containing protein
adaptor related protein complex 5 subunit zeta 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 87% 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: 21 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
cytochrome P450 3A30-like, transcript variant X3
cytochrome P450 3A30-like, transcript variant X1
cytochrome P450 3A30-like, 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 1 sample with support for all annotated introns
sidekick cell adhesion molecule 1, transcript variant X2
sidekick cell adhesion molecule 1, transcript variant X1
sidekick cell adhesion molecule 1, transcript variant X3
caspase recruitment domain family member 11
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
caspase recruitment domain-containing protein 11
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 3 samples with support for all annotated introns
guanine nucleotide-binding protein subunit alpha-12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
BRCA1 associated ATM activator 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
BRCA1 associated ATM activator 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
BRCA1-associated ATM activator 1 isoform X2
BRCA1-associated ATM activator 1 isoform X1
IQ motif containing E, transcript variant X3
IQ motif containing E, transcript variant X2
IQ motif containing E, transcript variant X1
IQ domain-containing protein E isoform X1
IQ domain-containing protein E isoform X3
IQ domain-containing protein E isoform X2
tweety family member 3, transcript variant X3
tweety family member 3, transcript variant X1
tweety family member 3, transcript variant X2
LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
beta-1,3-N-acetylglucosaminyltransferase lunatic fringe
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 70% coverage of the annotated genomic feature by RNAseq alignments
carbohydrate sulfotransferase 12, transcript variant X1
carbohydrate sulfotransferase 12, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
carbohydrate sulfotransferase 12, 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 2 samples with support for all annotated introns
carbohydrate sulfotransferase 12, transcript variant X2
eukaryotic translation initiation factor 3 subunit B
nudix hydrolase 1, transcript variant X1
nudix hydrolase 1, transcript variant X2
mitotic arrest deficient 1 like 1, transcript variant X1
mitotic spindle assembly checkpoint protein MAD1 isoform X1
mitotic arrest deficient 1 like 1, transcript variant X3
mitotic arrest deficient 1 like 1, transcript variant X2
mitotic spindle assembly checkpoint protein MAD1 isoform X2
extracellular leucine rich repeat and fibronectin type III domain containing 1
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
proteasome assembly chaperone 3, transcript variant X1
proteasome assembly chaperone 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
MAF bZIP transcription factor K, transcript variant X1
MAF bZIP transcription factor K, 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 2 samples with support for all annotated introns
lysosomal alpha-glucosidase-like, transcript variant X2
lysosomal alpha-glucosidase-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 2 samples with support for all annotated introns
lysosomal alpha-glucosidase-like, transcript variant X1
lysosomal alpha-glucosidase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
zinc finger AN1-type containing 2A, transcript variant X1
zinc finger AN1-type containing 2A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
AN1-type zinc finger protein 2A isoform X1
AN1-type zinc finger protein 2A isoform X2
G protein-coupled receptor 146, transcript variant X2
G protein-coupled receptor 146, transcript variant X3
G protein-coupled receptor 146, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 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: 31 Proteins
cytochrome c oxidase assembly protein COX19, transcript variant X2
cytochrome c oxidase assembly protein COX19, transcript variant X1
cytochrome c oxidase assembly protein COX19
arf-GAP with dual PH domain-containing protein 1
guided entry of tail-anchored proteins factor 4
Sad1 and UNC84 domain containing 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Sad1 and UNC84 domain containing 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Sad1 and UNC84 domain containing 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Sad1 and UNC84 domain containing 1, transcript variant X1
Sad1 and UNC84 domain containing 1, transcript variant X8
Sad1 and UNC84 domain containing 1, transcript variant X3
Sad1 and UNC84 domain containing 1, transcript variant X2
Sad1 and UNC84 domain containing 1, transcript variant X4
SUN domain-containing protein 1 isoform X3
SUN domain-containing protein 1 isoform X4
SUN domain-containing protein 1 isoform X2
SUN domain-containing protein 1 isoform X1
SUN domain-containing protein 1 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein kinase cAMP-dependent type I regulatory subunit beta, transcript variant X1
protein kinase cAMP-dependent type I regulatory subunit beta, transcript variant X2
cAMP-dependent protein kinase type I-beta regulatory subunit
platelet derived growth factor subunit A, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
platelet derived growth factor subunit A, transcript variant X3
platelet derived growth factor subunit A, transcript variant X1
platelet derived growth factor subunit A, transcript variant X6
platelet derived growth factor subunit A, transcript variant X4
platelet derived growth factor subunit A, transcript variant X2
platelet derived growth factor subunit A, transcript variant X7
platelet derived growth factor subunit A, transcript variant X8
platelet derived growth factor subunit A, transcript variant X10
platelet derived growth factor subunit A, transcript variant X9
platelet-derived growth factor subunit A isoform X1
platelet-derived growth factor subunit A isoform X3
platelet-derived growth factor subunit A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
FAM20C golgi associated secretory pathway kinase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
extracellular serine/threonine protein kinase FAM20C
transformation/transcription domain associated protein, transcript variant X4
transformation/transcription domain associated protein, transcript variant X2
transformation/transcription domain associated protein, transcript variant X3
transformation/transcription domain associated protein, transcript variant X1
transformation/transcription domain-associated protein isoform X4
transformation/transcription domain-associated protein isoform X2
transformation/transcription domain-associated protein isoform X3
transformation/transcription domain-associated protein isoform X1
BAR/IMD domain containing adaptor protein 2 like 1
brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 1
tectonin beta-propeller repeat containing 1, transcript variant X3
tectonin beta-propeller repeat containing 1, transcript variant X2
tectonin beta-propeller repeat containing 1, transcript variant X4
tectonin beta-propeller repeat containing 1, transcript variant X5
tectonin beta-propeller repeat containing 1, transcript variant X1
tectonin beta-propeller repeat-containing protein 1
basic helix-loop-helix family member a15
class A basic helix-loop-helix protein 15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
CCZ1 homolog, vacuolar protein trafficking and biogenesis associated
radial spoke head 10 homolog B2-like, transcript variant X2
radial spoke head 10 homolog B2-like, transcript variant X3
radial spoke head 10 homolog B2-like, transcript variant X1
radial spoke head 10 homolog B2-like isoform X2
radial spoke head 10 homolog B2-like isoform X1
PMS1 homolog 2, mismatch repair system component
aminoacyl tRNA synthetase complex interacting multifunctional protein 2
aminoacyl tRNA synthase complex-interacting multifunctional protein 2
eukaryotic translation initiation factor 2 alpha kinase 1
eukaryotic translation initiation factor 2-alpha kinase 1
ubiquitin specific peptidase 42, transcript variant X1
ubiquitin specific peptidase 42, transcript variant X4
ubiquitin specific peptidase 42, transcript variant X3
ubiquitin specific peptidase 42, transcript variant X5
ubiquitin specific peptidase 42, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 42 isoform X1
ubiquitin carboxyl-terminal hydrolase 42 isoform X2
ubiquitin carboxyl-terminal hydrolase 42 isoform 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 2 samples with support for all annotated introns
Rac family small GTPase 1, transcript variant X1
ras-related C3 botulinum toxin substrate 1 isoform X1
small integral membrane protein 10-like protein 2A
Rac family small GTPase 1, transcript variant X2
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, including 3 samples with support for all annotated introns
ras-related C3 botulinum toxin substrate 1 isoform X2
KDEL endoplasmic reticulum protein retention receptor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
methyltransferase like 9, transcript variant X2
methyltransferase like 9, transcript variant X1
methyltransferase-like protein 9 isoform X2
methyltransferase-like protein 9 isoform X1
immunoglobulin superfamily member 6, transcript variant X2
immunoglobulin superfamily member 6, transcript variant X1
immunoglobulin superfamily member 6 isoform X1
immunoglobulin superfamily member 6 isoform X2
transmembrane protein 180-like, transcript variant X1
transmembrane protein 180-like, transcript variant X2
cerebellar degeneration related protein 2, transcript variant X1
cerebellar degeneration-related protein 2 isoform X1
cerebellar degeneration related protein 2, transcript variant X2
cerebellar degeneration-related protein 2 isoform X2
DNA-directed RNA polymerase III subunit RPC5
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
eukaryotic elongation factor 2 kinase, transcript variant X2
eukaryotic elongation factor 2 kinase, transcript variant X3
eukaryotic elongation factor 2 kinase, transcript variant X1
eukaryotic elongation factor 2 kinase isoform X2
eukaryotic elongation factor 2 kinase isoform X3
eukaryotic elongation factor 2 kinase isoform X1
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
putative short-chain dehydrogenase/reductase family 42E member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
von Willebrand factor A domain containing 3A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
von Willebrand factor A domain-containing protein 3A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytochrome b-c1 complex subunit 2, mitochondrial
ketimine reductase mu-crystallin isoform X1
ketimine reductase mu-crystallin isoform X2
ankyrin repeat and sterile alpha motif domain containing 4B
ankyrin repeat and SAM domain-containing protein 4B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
melanin-concentrating hormone receptor 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
LOW QUALITY PROTEIN: melanin-concentrating hormone receptor 1-like
transmembrane protein 159, transcript variant X2
transmembrane protein 159, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
LYR motif containing 1, transcript variant X2
LYR motif containing 1, transcript variant X1
defective in cullin neddylation 1 domain containing 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
defective in cullin neddylation 1 domain containing 3, transcript variant X2
defective in cullin neddylation 1 domain containing 3, transcript variant X1
defective in cullin neddylation 1 domain containing 3, transcript variant X4
RNA exonuclease 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RNA exonuclease 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
acyl-coenzyme A synthetase ACSM3, mitochondrial-like, transcript variant X5
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 2 samples with support for all annotated introns
acyl-coenzyme A synthetase ACSM3, mitochondrial-like, transcript variant X1
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 3 samples with support for all annotated introns
acyl-coenzyme A synthetase ACSM3, mitochondrial-like, transcript variant X4
acyl-coenzyme A synthetase ACSM3, mitochondrial-like, transcript variant X2
acyl-coenzyme A synthetase ACSM3, mitochondrial-like, transcript variant X3
acyl-coenzyme A synthetase ACSM3, mitochondrial-like isoform X1
acyl-coenzyme A synthetase ACSM3, mitochondrial-like isoform X2
THUMP domain containing 1, transcript variant X1
THUMP domain containing 1, transcript variant X2
THUMP domain-containing protein 1 isoform X1
THUMP domain-containing protein 1 isoform X2
acyl-coenzyme A synthetase ACSM4, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
acyl-coenzyme A synthetase ACSM4, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acyl-coenzyme A synthetase ACSM4, mitochondrial-like, transcript variant X2
acyl-coenzyme A synthetase ACSM4, mitochondrial-like isoform X1
acyl-coenzyme A synthetase ACSM4, mitochondrial-like, transcript variant X3
acyl-coenzyme A synthetase ACSM4, mitochondrial-like isoform X2
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 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 1 sample with support for all annotated introns
acyl-coenzyme A synthetase ACSM4, mitochondrial-like, transcript variant X4
acyl-coenzyme A synthetase ACSM3, mitochondrial-like isoform X3
protein disulfide isomerase like, testis expressed
protein disulfide-isomerase-like protein of the testis
G protein-coupled receptor class C group 5 member B, transcript variant X1
G protein-coupled receptor class C group 5 member B, transcript variant X3
G protein-coupled receptor class C group 5 member B, transcript variant X2
G-protein coupled receptor family C group 5 member B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lysine rich nucleolar protein 1, transcript variant X2
lysine-rich nucleolar protein 1 isoform X2
lysine rich nucleolar protein 1, transcript variant X1
lysine-rich nucleolar protein 1 isoform X1
VPS35 endosomal protein sorting factor like, transcript variant X1
VPS35 endosomal protein sorting factor like, transcript variant X2
VPS35 endosomal protein sorting factor like, transcript variant X3
VPS35 endosomal protein sorting factor-like isoform X1
VPS35 endosomal protein sorting factor-like isoform X2
centriolar coiled-coil protein 110, transcript variant X2
centriolar coiled-coil protein 110, transcript variant X1
centriolar coiled-coil protein 110, transcript variant X3
centriolar coiled-coil protein of 110 kDa
glycerophosphodiester phosphodiesterase 1, transcript variant X3
glycerophosphodiester phosphodiesterase 1, transcript variant X1
glycerophosphodiester phosphodiesterase 1 isoform X1
glycerophosphodiester phosphodiesterase 1, transcript variant X2
glycerophosphodiester phosphodiesterase 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
5-demethoxyubiquinone hydroxylase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
inositol 1,4,5-trisphosphate receptor-interacting protein-like 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 66% coverage of the annotated genomic feature by RNAseq alignments
SMG1 nonsense mediated mRNA decay associated PI3K related kinase, transcript variant X1
serine/threonine-protein kinase SMG1 isoform X1
SMG1 nonsense mediated mRNA decay associated PI3K related kinase, transcript variant X3
serine/threonine-protein kinase SMG1 isoform X3
SMG1 nonsense mediated mRNA decay associated PI3K related kinase, transcript variant X2
serine/threonine-protein kinase SMG1 isoform X2
ADP ribosylation factor like GTPase 6 interacting protein 1
ADP-ribosylation factor-like protein 6-interacting protein 1
xylosyltransferase 1, transcript variant X1
xylosyltransferase 1, transcript variant X2
multidrug resistance-associated protein 6-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
multidrug resistance-associated protein 1, transcript variant X2
multidrug resistance-associated protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
multidrug resistance-associated protein 1 isoform X2
multidrug resistance-associated protein 1 isoform X1
centrosomal protein 20, transcript variant X1
centrosomal protein 20, transcript variant X3
centrosomal protein 20, transcript variant X2
lisH domain-containing protein FOPNL isoform X1
lisH domain-containing protein FOPNL isoform X2
lisH domain-containing protein FOPNL isoform X3
myosin heavy chain 11, transcript variant X1
myosin heavy chain 11, transcript variant X2
nudE neurodevelopment protein 1, transcript variant X2
nudE neurodevelopment protein 1, transcript variant X4
nudE neurodevelopment protein 1, transcript variant X1
nudE neurodevelopment protein 1, transcript variant X3
nuclear distribution protein nudE homolog 1
meiosis regulator and mRNA stability factor 1, transcript variant X1
meiosis regulator and mRNA stability factor 1, transcript variant X2
meiosis regulator and mRNA stability factor 1 isoform X1
meiosis regulator and mRNA stability factor 1 isoform X2
MPV17 mitochondrial inner membrane protein like
pyridoxal dependent decarboxylase domain containing 1, transcript variant X2
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X2
pyridoxal dependent decarboxylase domain containing 1, transcript variant X1
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X1
pyridoxal dependent decarboxylase domain containing 1, transcript variant X3
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X3
protein N-terminal asparagine amidohydrolase
RRN3 homolog, RNA polymerase I transcription factor
RNA polymerase I-specific transcription initiation factor RRN3
ribosomal L1 domain-containing protein 1
eukaryotic peptide chain release factor GTP-binding subunit ERF3A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor receptor superfamily member 17
calcineurin like phosphoesterase domain containing 1, transcript variant X1
calcineurin like phosphoesterase domain containing 1, transcript variant X2
calcineurin like phosphoesterase domain containing 1, transcript variant X3
serine/threonine-protein phosphatase CPPED1 isoform X1
serine/threonine-protein phosphatase CPPED1 isoform X2
serine/threonine-protein phosphatase CPPED1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 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: 3 Proteins
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
germ cell-specific gene 1-like protein isoform X1
germ cell-specific gene 1-like protein isoform X2
KIAA0556 ortholog, transcript variant X2
KIAA0556 ortholog, transcript variant X3
KIAA0556 ortholog, transcript variant X4
KIAA0556 ortholog, transcript variant X1
KIAA0556 ortholog, transcript variant X5
general transcription factor IIIC subunit 1, transcript variant X1
general transcription factor IIIC subunit 1, transcript variant X2
general transcription factor 3C polypeptide 1 isoform X1
general transcription factor 3C polypeptide 1 isoform X2
DNA-directed RNA polymerase III subunit RPC10
small nuclear ribonucleoprotein U11/U12 subunit 25, transcript variant X1
small nuclear ribonucleoprotein U11/U12 subunit 25, transcript variant X3
small nuclear ribonucleoprotein U11/U12 subunit 25, transcript variant X2
U11/U12 small nuclear ribonucleoprotein 25 kDa protein
rhomboid 5 homolog 1, 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 1 sample with support for all annotated introns
rhomboid 5 homolog 1, transcript variant X2
rhomboid 5 homolog 1, transcript variant X3
N-methylpurine DNA glycosylase, transcript variant X1
N-methylpurine DNA glycosylase, transcript variant X3
N-methylpurine DNA glycosylase, transcript variant X2
NPR3 like, GATOR1 complex subunit, transcript variant X1
NPR3 like, GATOR1 complex subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 286 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 271 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: 288 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
post-glycosylphosphatidylinositol attachment to proteins 6
post-GPI attachment to proteins factor 6
39S ribosomal protein L28, mitochondrial
protein disulfide isomerase family A member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
regulator of G protein signaling 11, transcript variant X1
regulator of G protein signaling 11, transcript variant X2
regulator of G-protein signaling 11 isoform X1
regulator of G-protein signaling 11 isoform X2
family with sequence similarity 234 member A, transcript variant X2
family with sequence similarity 234 member A, transcript variant X1
putative RNA-binding protein Luc7-like 1 isoform X2
putative RNA-binding protein Luc7-like 1 isoform X1
proline and glutamate rich with coiled coil 1
enoyl-CoA delta isomerase 1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
N-alpha-acetyltransferase 60, NatF catalytic subunit, 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 2 samples with support for all annotated introns
N-alpha-acetyltransferase 60, NatF catalytic subunit, transcript variant X2
nudix hydrolase 16 like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nudix hydrolase 16 like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tudor-interacting repair regulator protein isoform X2
tudor-interacting repair regulator protein isoform X1
mahogunin ring finger 1, transcript variant X1
E3 ubiquitin-protein ligase MGRN1 isoform X1
mahogunin ring finger 1, transcript variant X2
E3 ubiquitin-protein ligase MGRN1 isoform X2
cell death inducing p53 target 1, transcript variant X1
cell death inducing p53 target 1, transcript variant X6
cell death inducing p53 target 1, transcript variant X4
cell death inducing p53 target 1, transcript variant X3
cell death inducing p53 target 1, transcript variant X5
cell death inducing p53 target 1, transcript variant X2
cell death-inducing p53-target protein 1 isoform X1
cell death-inducing p53-target protein 1 isoform X2
zinc finger protein 501-like, transcript variant X1
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 2 samples with support for all annotated introns
zinc finger protein 501-like, transcript variant X2
SLX4 structure-specific endonuclease subunit, transcript variant X2
SLX4 structure-specific endonuclease subunit, transcript variant X1
structure-specific endonuclease subunit SLX4 isoform X2
structure-specific endonuclease subunit SLX4 isoform X1
heat shock protein 75 kDa, mitochondrial
CREB binding protein, transcript variant X6
CREB binding protein, transcript variant X4
CREB binding protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CREB binding protein, transcript variant X2
CREB binding protein, transcript variant X7
CREB binding protein, transcript variant X3
CREB binding protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
presequence translocase associated motor 16
mitochondrial import inner membrane translocase subunit TIM16
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 75% 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 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
DnaJ heat shock protein family (Hsp40) member A3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dnaJ homolog subfamily A member 3, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
nmrA-like family domain-containing protein 1
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: 5 Proteins
LOW QUALITY PROTEIN: NLR family CARD domain-containing protein 3
clusterin associated protein 1, transcript variant X2
clusterin associated protein 1, transcript variant X1
clusterin-associated protein 1 isoform X2
clusterin-associated protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and sterile alpha motif domain containing 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 1 sample with support for all annotated introns
ankyrin repeat and SAM domain-containing protein 3 isoform X1
ankyrin repeat and sterile alpha motif domain containing 3, transcript variant X2
ankyrin repeat and SAM domain-containing protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C16orf71 homolog
SH3 domain binding kinase 1, transcript variant X1
SH3 domain binding kinase 1, transcript variant X2
SH3 domain binding kinase 1, transcript variant X3
serine/threonine-protein kinase SBK1 isoform X1
serine/threonine-protein kinase SBK1 isoform X2
serine/threonine-protein kinase SBK1 isoform X3
nucleoside diphosphate kinase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
2,4-dienoyl-CoA reductase 2, transcript variant X2
2,4-dienoyl-CoA reductase 2, transcript variant X1
peroxisomal 2,4-dienoyl-CoA reductase isoform X1
peroxisomal 2,4-dienoyl-CoA reductase isoform X2
RAB11 family interacting protein 3, transcript variant X1
RAB11 family interacting protein 3, transcript variant X2
RAB11 family interacting protein 3, transcript variant X3
rab11 family-interacting protein 3 isoform X1
rab11 family-interacting protein 3 isoform X3
rab11 family-interacting protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
myeloid-associated differentiation marker-like
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
cytoplasmic phosphatidylinositol transfer protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytoplasmic phosphatidylinositol transfer protein 1-like, transcript variant X1
cytoplasmic phosphatidylinositol transfer protein 1-like
MSS51 mitochondrial translational activator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
putative protein MSS51 homolog, mitochondrial
cilia and flagella associated protein 70
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 75% coverage of the annotated genomic feature by RNAseq alignments
cilia- and flagella-associated protein 70
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 99% coverage of the annotated genomic feature by RNAseq alignments
STIP1 homology and U-box containing protein 1
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, including 3 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 92% coverage of the annotated genomic feature by RNAseq alignments
F-box and leucine rich repeat protein 16, transcript variant X2
F-box and leucine rich repeat protein 16, transcript variant X1
meteorin, glial cell differentiation regulator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
adenine nucleotide translocase lysine methyltransferase
adenine nucleotide translocase lysine N-methyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 78
insulin like growth factor binding protein acid labile subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
insulin-like growth factor-binding protein complex acid labile subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
cytosolic Fe-S cluster assembly factor NUBP2
splA/ryanodine receptor domain and SOCS box containing 3, transcript variant X1
splA/ryanodine receptor domain and SOCS box containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SPRY domain-containing SOCS box protein 3
essential meiotic structure-specific endonuclease subunit 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable crossover junction endonuclease EME2
NME/NM23 nucleoside diphosphate kinase 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and fibronectin type-III domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% coverage of the annotated genomic feature by RNAseq alignments
tubulin epsilon and delta complex protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
inactive serine/threonine-protein kinase VRK3
ATP binding cassette subfamily A member 3
ATP-binding cassette sub-family A member 3
MAPK regulated corepressor interacting protein 2
transfer RNA glycine (anticodon CCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 1
phosphatidylinositol glycan anchor biosynthesis class Q
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q
NADH:ubiquinone oxidoreductase subunit B6
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 6
eukaryotic elongation factor 2 lysine methyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein-lysine N-methyltransferase EEF2KMT
ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
chitobiosyldiphosphodolichol beta-mannosyltransferase
chromosome 15 C16orf89 homolog, transcript variant X2
chromosome 15 C16orf89 homolog, transcript variant X1
N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
SEC14 like lipid binding 5, transcript variant X1
SEC14 like lipid binding 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
TBC1 domain family member 24, transcript variant X1
TBC1 domain family member 24, transcript variant X2
V-type proton ATPase 16 kDa proteolipid subunit
N-acetylglucosamine-6-phosphate deacetylase
UPF0488 protein C8orf33 homolog, transcript variant X3
UPF0488 protein C8orf33 homolog, transcript variant X7
UPF0488 protein C8orf33 homolog, transcript variant X6
UPF0488 protein C8orf33 homolog, transcript variant X8
UPF0488 protein C8orf33 homolog, transcript variant X1
UPF0488 protein C8orf33 homolog, transcript variant X2
UPF0488 protein C8orf33 homolog, transcript variant X5
UPF0488 protein C8orf33 homolog, transcript variant X4
transcription initiation factor TFIID subunit 4-like
RNA binding protein with serine rich domain 1, transcript variant X2
RNA-binding protein with serine-rich domain 1 isoform X2
RNA binding protein with serine rich domain 1, transcript variant X1
RNA-binding protein with serine-rich domain 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
telomere length regulation protein TEL2 homolog
intraflagellar transport 140, transcript variant X2
intraflagellar transport 140, transcript variant X1
intraflagellar transport protein 140 homolog isoform X2
intraflagellar transport protein 140 homolog isoform X1
cramped chromatin regulator homolog 1, transcript variant X1
cramped chromatin regulator homolog 1, transcript variant X2
Jupiter microtubule associated homolog 2
calcium regulated heat stable protein 1, transcript variant X4
calcium regulated heat stable protein 1, transcript variant X3
calcium regulated heat stable protein 1, transcript variant X1
calcium regulated heat stable protein 1, transcript variant X2
calcium regulated heat stable protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
4-aminobutyrate aminotransferase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
4-aminobutyrate aminotransferase, transcript variant X2
4-aminobutyrate aminotransferase, transcript variant X1
4-aminobutyrate aminotransferase, mitochondrial
methyltransferase like 22, transcript variant X3
methyltransferase like 22, transcript variant X2
methyltransferase like 22, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
RNA binding fox-1 homolog 1, transcript variant X5
RNA binding fox-1 homolog 1, transcript variant X2
RNA binding fox-1 homolog 1, transcript variant X4
RNA binding fox-1 homolog 1, transcript variant X18
RNA binding fox-1 homolog 1, transcript variant X21
RNA binding fox-1 homolog 1, transcript variant X9
RNA binding fox-1 homolog 1, transcript variant X15
RNA binding fox-1 homolog 1, transcript variant X3
RNA binding fox-1 homolog 1, transcript variant X24
RNA binding fox-1 homolog 1, transcript variant X17
RNA binding fox-1 homolog 1, transcript variant X12
RNA binding fox-1 homolog 1, transcript variant X23
RNA binding fox-1 homolog 1, transcript variant X1
RNA binding fox-1 homolog 1, transcript variant X10
RNA binding fox-1 homolog 1, transcript variant X6
RNA binding fox-1 homolog 1, transcript variant X7
RNA binding fox-1 homolog 1, transcript variant X19
RNA binding fox-1 homolog 1, transcript variant X13
RNA binding fox-1 homolog 1, transcript variant X8
RNA binding fox-1 homolog 1, transcript variant X20
RNA binding fox-1 homolog 1, transcript variant X22
RNA binding fox-1 homolog 1, transcript variant X16
RNA binding protein fox-1 homolog 1 isoform X13
RNA binding protein fox-1 homolog 1 isoform X3
RNA binding protein fox-1 homolog 1 isoform X18
RNA binding protein fox-1 homolog 1 isoform X5
RNA binding protein fox-1 homolog 1 isoform X2
RNA binding protein fox-1 homolog 1 isoform X4
RNA binding protein fox-1 homolog 1 isoform X14
RNA binding protein fox-1 homolog 1 isoform X15
RNA binding protein fox-1 homolog 1 isoform X9
RNA binding protein fox-1 homolog 1 isoform X8
RNA binding protein fox-1 homolog 1 isoform X1
RNA binding protein fox-1 homolog 1 isoform X17
RNA binding protein fox-1 homolog 1 isoform X6
RNA binding protein fox-1 homolog 1 isoform X12
RNA binding protein fox-1 homolog 1 isoform X16
RNA binding fox-1 homolog 1, transcript variant X14
RNA binding protein fox-1 homolog 1 isoform X11
RNA binding fox-1 homolog 1, transcript variant X11
RNA binding protein fox-1 homolog 1 isoform X10
RNA binding protein fox-1 homolog 1 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
rogdi atypical leucine zipper, transcript variant X2
rogdi atypical leucine zipper, transcript variant X1
glyoxylate reductase 1 homolog, transcript variant X3
glyoxylate reductase 1 homolog, transcript variant X2
glyoxylate reductase 1 homolog, transcript variant X1
putative oxidoreductase GLYR1 isoform X3
putative oxidoreductase GLYR1 isoform X2
putative oxidoreductase GLYR1 isoform X1
28S ribosomal protein S34, mitochondrial
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X23
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X19
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X21
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X16
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X9
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X24
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X22
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X17
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X14
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X7
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X4
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X20
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X10
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X12
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X5
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X15
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X11
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X8
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X6
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X3
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X2
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X13
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X1
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X18
C-Jun-amino-terminal kinase-interacting protein 3 isoform X23
C-Jun-amino-terminal kinase-interacting protein 3 isoform X19
C-Jun-amino-terminal kinase-interacting protein 3 isoform X21
C-Jun-amino-terminal kinase-interacting protein 3 isoform X16
C-Jun-amino-terminal kinase-interacting protein 3 isoform X9
C-Jun-amino-terminal kinase-interacting protein 3 isoform X24
C-Jun-amino-terminal kinase-interacting protein 3 isoform X22
C-Jun-amino-terminal kinase-interacting protein 3 isoform X17
C-Jun-amino-terminal kinase-interacting protein 3 isoform X14
C-Jun-amino-terminal kinase-interacting protein 3 isoform X7
C-Jun-amino-terminal kinase-interacting protein 3 isoform X4
C-Jun-amino-terminal kinase-interacting protein 3 isoform X20
C-Jun-amino-terminal kinase-interacting protein 3 isoform X10
C-Jun-amino-terminal kinase-interacting protein 3 isoform X18
C-Jun-amino-terminal kinase-interacting protein 3 isoform X12
C-Jun-amino-terminal kinase-interacting protein 3 isoform X5
C-Jun-amino-terminal kinase-interacting protein 3 isoform X15
C-Jun-amino-terminal kinase-interacting protein 3 isoform X11
C-Jun-amino-terminal kinase-interacting protein 3 isoform X8
C-Jun-amino-terminal kinase-interacting protein 3 isoform X6
C-Jun-amino-terminal kinase-interacting protein 3 isoform X3
C-Jun-amino-terminal kinase-interacting protein 3 isoform X2
C-Jun-amino-terminal kinase-interacting protein 3 isoform X13
C-Jun-amino-terminal kinase-interacting protein 3 isoform X1
glutamate ionotropic receptor NMDA type subunit 2A, transcript variant X2
glutamate receptor ionotropic, NMDA 2A isoform X2
glutamate ionotropic receptor NMDA type subunit 2A, 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 3 samples with support for all annotated introns
glutamate receptor ionotropic, NMDA 2A isoform X1
epithelial membrane protein 2, transcript variant X1
epithelial membrane protein 2, transcript variant X3
epithelial membrane protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
cytosolic Fe-S cluster assembly factor NUBP1
trans-golgi network vesicle protein 23 homolog A, transcript variant X2
trans-golgi network vesicle protein 23 homolog A, transcript variant X1
Golgi apparatus membrane protein TVP23 homolog A isoform X2
Golgi apparatus membrane protein TVP23 homolog A isoform X1
class II major histocompatibility complex transactivator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
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.
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
recQ-mediated genome instability protein 2
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: 1 Protein
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; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein LOC116495373
lipopolysaccharide induced TNF factor, transcript variant X1
lipopolysaccharide induced TNF factor, transcript variant X4
lipopolysaccharide induced TNF factor, transcript variant X2
lipopolysaccharide induced TNF factor, transcript variant X3
lipopolysaccharide induced TNF factor, transcript variant X5
lipopolysaccharide-induced tumor necrosis factor-alpha factor isoform X1
lipopolysaccharide-induced tumor necrosis factor-alpha factor isoform 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: thioredoxin domain-containing protein 11
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 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger CCCH domain-containing protein 7A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
bifunctional apoptosis regulator, transcript variant X2
bifunctional apoptosis regulator, transcript variant X1
poly(A)-specific ribonuclease, transcript variant X1
poly(A)-specific ribonuclease, transcript variant X2
poly(A)-specific ribonuclease PARN isoform X1
poly(A)-specific ribonuclease PARN isoform X2
poly(A)-specific ribonuclease, transcript variant X5
poly(A)-specific ribonuclease, transcript variant X3
poly(A)-specific ribonuclease PARN isoform X3
poly(A)-specific ribonuclease, transcript variant X6
poly(A)-specific ribonuclease, transcript variant X4
poly(A)-specific ribonuclease PARN isoform X4
poly(A)-specific ribonuclease PARN isoform X5
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
myocardin related transcription factor B, transcript variant X6
myocardin related transcription factor B, transcript variant X5
myocardin related transcription factor B, transcript variant X4
myocardin related transcription factor B, transcript variant X7
myocardin related transcription factor B, transcript variant X9
myocardin related transcription factor B, transcript variant X1
myocardin related transcription factor B, transcript variant X3
myocardin related transcription factor B, transcript variant X2
myocardin related transcription factor B, transcript variant X8
myocardin-related transcription factor B isoform X2
myocardin-related transcription factor B isoform X4
myocardin-related transcription factor B isoform X1
myocardin-related transcription factor B isoform X3
myocardin related transcription factor B, transcript variant X10
myocardin-related transcription factor B isoform X5
ERCC excision repair 4, endonuclease catalytic subunit, transcript variant X1
ERCC excision repair 4, endonuclease catalytic subunit, transcript variant X2