Hypomesus transpacificus isolate Combined female chromosome 5, fHypTra1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Stomiati; Osmeriformes; Osmeridae; Hypomesus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM038976.1.\nAssembly name: fHypTra1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Genomic Variation Lab at\nUniversity of California Davis on 2022/02/04. The original\nwhole-genome shotgun project has the accession JAJTOO000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Genomic Variation Lab at University of\n California Davis\nAssembly Date :: 21-APR-2021\nAssembly Method :: IPA v. 1.3.1; scaff10x v. 4.2; SALSA2 v.\n NA; Chromonomer v. 1.13\nAssembly Name :: fHypTra1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 120.0x\nSequencing Technology :: 10X; PacBio Sequel; Hi-C\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Hypomesus transpacificus Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
USA: Fish Conservation and Culture Laboratory, Discovery Bay, California
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
endonuclease domain-containing 1 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
GRB10 interacting GYF protein 1b, transcript variant X1
GRB10 interacting GYF protein 1b, transcript variant X2
GRB10 interacting GYF protein 1b, transcript variant X4
GRB10 interacting GYF protein 1b, transcript variant X3
GRB10-interacting GYF protein 1 isoform X1
GRB10-interacting GYF protein 1 isoform X2
GRB10-interacting GYF protein 1 isoform X4
GRB10-interacting GYF protein 1 isoform X3
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
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 31 samples with support for all annotated introns
period circadian protein homolog 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
period circadian protein homolog 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
period circadian protein homolog 1-like isoform X2
period circadian protein homolog 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
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.
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00096
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
trimethyllysine hydroxylase, epsilon, 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 17 samples with support for all annotated introns
trimethyllysine hydroxylase, epsilon, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
trimethyllysine dioxygenase, mitochondrial isoform X1
trimethyllysine hydroxylase, epsilon, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
trimethyllysine dioxygenase, mitochondrial isoform X2
H/ACA ribonucleoprotein complex subunit DKC1
COORDINATES: nucleotide motif:Rfam:12.0:RF00567
COORDINATES: nucleotide motif:Rfam:12.0:RF00137
COORDINATES: nucleotide motif:Rfam:12.0:RF00340
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 25 samples with support for all annotated introns
V-set and immunoglobulin domain-containing protein 1-like
gamma-aminobutyric acid type A receptor subunit beta4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit beta-4 isoform X1
gamma-aminobutyric acid type A receptor subunit beta4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit beta-4 isoform X2
gamma-aminobutyric acid receptor subunit alpha-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
BRCA1/BRCA2-containing complex, subunit 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
zinc finger protein-like 1, transcript variant X3
zinc finger protein-like 1, transcript variant X2
zinc finger protein-like 1, transcript variant X1
phospholipase A and acyltransferase 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neutral alpha-glucosidase AB-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
neutral alpha-glucosidase AB-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
neutral alpha-glucosidase AB-like isoform X1
neutral alpha-glucosidase AB-like isoform X3
neutral alpha-glucosidase AB-like, 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 19 samples with support for all annotated introns
neutral alpha-glucosidase AB-like isoform X2
solute carrier family 25 member 45, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
solute carrier family 25 member 45, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
vacuolar protein sorting-associated protein 51 homolog
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 41 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
zinc finger HIT domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
ubiquinol-cytochrome-c reductase complex assembly factor 3
cornichon family AMPA receptor auxiliary protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
WD repeat domain 74, transcript variant X1
WD repeat-containing protein 74 isoform X1
WD repeat domain 74, transcript variant X2
WD repeat-containing protein 74 isoform X2
syntaxin 5A, like, transcript variant X1
syntaxin 5A, like, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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; 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: 2 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
estrogen-related receptor alpha, transcript variant X1
estrogen-related receptor alpha, 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 43 samples with support for all annotated introns
BSCL2 lipid droplet biogenesis associated, seipin
guanine nucleotide binding protein (G protein), gamma 3, transcript variant X3
guanine nucleotide binding protein (G protein), gamma 3, transcript variant X2
guanine nucleotide binding protein (G protein), gamma 3, transcript variant X1
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-3
BAF nuclear assembly factor 1, transcript variant X1
BAF nuclear assembly factor 1, transcript variant X2
spliceosome associated factor 1, recruiter of U4/U6.U5 tri-snRNP
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 2
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 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein si:dkey-175m17.7
MAP/microtubule affinity-regulating kinase 2a, transcript variant X1
MAP/microtubule affinity-regulating kinase 2a, transcript variant X3
MAP/microtubule affinity-regulating kinase 2a, transcript variant X7
MAP/microtubule affinity-regulating kinase 2a, transcript variant X4
MAP/microtubule affinity-regulating kinase 2a, transcript variant X6
MAP/microtubule affinity-regulating kinase 2a, transcript variant X5
MAP/microtubule affinity-regulating kinase 2a, transcript variant X9
MAP/microtubule affinity-regulating kinase 2a, transcript variant X12
MAP/microtubule affinity-regulating kinase 2a, transcript variant X2
MAP/microtubule affinity-regulating kinase 2a, transcript variant X8
serine/threonine-protein kinase MARK2 isoform X1
serine/threonine-protein kinase MARK2 isoform X3
serine/threonine-protein kinase MARK2 isoform X7
serine/threonine-protein kinase MARK2 isoform X4
serine/threonine-protein kinase MARK2 isoform X5
serine/threonine-protein kinase MARK2 isoform X9
serine/threonine-protein kinase MARK2 isoform X11
serine/threonine-protein kinase MARK2 isoform X6
serine/threonine-protein kinase MARK2 isoform X2
serine/threonine-protein kinase MARK2 isoform X8
MAP/microtubule affinity-regulating kinase 2a, transcript variant X10
MAP/microtubule affinity-regulating kinase 2a, transcript variant X11
serine/threonine-protein kinase MARK2 isoform X10
uncharacterized protein LOC541358 homolog
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 6 samples with support for all annotated introns
uncharacterized oxidoreductase Mvan_2161
BCL2 associated agonist of cell death a, transcript variant X1
BCL2 associated agonist of cell death a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 1, regulatory (inhibitor) subunit 14Ba, transcript variant X1
protein phosphatase 1, regulatory (inhibitor) subunit 14Ba, transcript variant X2
protein phosphatase 1, regulatory (inhibitor) subunit 14Ba
peptidyl-prolyl cis-trans isomerase FKBP2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
leucine rich repeat and fibronectin type III domain containing 4a
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 25 samples with support for all annotated introns
leucine-rich repeat and fibronectin type-III domain-containing protein 4
pyruvate carboxylase, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
pyruvate carboxylase, mitochondrial-like, 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 6 samples with support for all annotated introns
pyruvate carboxylase, mitochondrial-like
calmodulin 3b (phosphorylase kinase, delta)
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 32 samples with support for all annotated introns
acidic fibroblast growth factor intracellular-binding protein B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 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 33% coverage of the annotated genomic feature by RNAseq alignments
neuronal PAS domain-containing protein 4B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
28S ribosomal protein S12, mitochondrial-like
C-x(9)-C motif containing 4 homolog (S. cerevisiae), transcript variant X1
C-x(9)-C motif containing 4 homolog (S. cerevisiae), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
retinal outer segment membrane protein 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ribosomal protein S6 kinase, polypeptide 4
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 42 samples with support for all annotated introns
beta,beta-carotene 9',10'-oxygenase-like
succinate dehydrogenase [ubiquinone] cytochrome b small subunit A, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
succinate dehydrogenase [ubiquinone] cytochrome b small subunit A, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
succinate dehydrogenase [ubiquinone] cytochrome b small subunit A, mitochondrial-like
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
grass carp reovirus (GCRV)-induced gene 2o
coiled-coil domain containing 61, transcript variant X3
coiled-coil domain containing 61, transcript variant X4
coiled-coil domain containing 61, transcript variant X7
coiled-coil domain containing 61, transcript variant X6
coiled-coil domain containing 61, transcript variant X2
coiled-coil domain containing 61, transcript variant X1
coiled-coil domain containing 61, transcript variant X5
zinc finger protein ubi-d4-like, transcript variant X1
zinc finger protein ubi-d4-like, transcript variant X2
zinc finger protein ubi-d4-like isoform X1
zinc finger protein ubi-d4-like isoform X2
muscarinic acetylcholine receptor M1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins
sodium/potassium/calcium exchanger 3-like
signal-induced proliferation-associated protein 1-like, transcript variant X1
signal-induced proliferation-associated protein 1-like, transcript variant X2
signal-induced proliferation-associated protein 1-like isoform X1
signal-induced proliferation-associated protein 1-like isoform X2
T-box transcription factor 2a, transcript variant X1
T-box transcription factor 2a, transcript variant X2
T-box transcription factor TBX2a isoform X1
T-box transcription factor TBX2a isoform X2
acetyl-CoA carboxylase alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
acetyl-CoA carboxylase alpha, transcript variant 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 35 samples with support for all annotated introns
acetyl-CoA carboxylase alpha, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
acetyl-CoA carboxylase alpha, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
apoptosis antagonizing transcription factor
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 28% 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: LIM/homeobox protein Lhx1b
mitochondrial rRNA methyltransferase 1 homolog (S. cerevisiae), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
mitochondrial rRNA methyltransferase 1 homolog (S. cerevisiae), transcript variant X2
rRNA methyltransferase 1, mitochondrial isoform X1
mitochondrial rRNA methyltransferase 1 homolog (S. cerevisiae), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
rRNA methyltransferase 1, mitochondrial isoform X2
dehydrogenase/reductase SDR family member 13-like
dehydrogenase/reductase (SDR family) member 13a, tandem duplicate 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 13
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 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
unconventional myosin-XVIIIa-like, transcript variant X13
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 14 samples with support for all annotated introns
unconventional myosin-XVIIIa-like isoform X12
unconventional myosin-XVIIIa-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
unconventional myosin-XVIIIa-like, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
unconventional myosin-XVIIIa-like, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
unconventional myosin-XVIIIa-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
unconventional myosin-XVIIIa-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
unconventional myosin-XVIIIa-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 12 samples with support for all annotated introns
unconventional myosin-XVIIIa-like, transcript variant X3
unconventional myosin-XVIIIa-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
unconventional myosin-XVIIIa-like, transcript variant X2
unconventional myosin-XVIIIa-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
unconventional myosin-XVIIIa-like, transcript variant X1
unconventional myosin-XVIIIa-like, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
unconventional myosin-XVIIIa-like, transcript variant X12
unconventional myosin-XVIIIa-like isoform X10
unconventional myosin-XVIIIa-like isoform X13
unconventional myosin-XVIIIa-like isoform X9
unconventional myosin-XVIIIa-like isoform X8
unconventional myosin-XVIIIa-like isoform X5
unconventional myosin-XVIIIa-like isoform X4
unconventional myosin-XVIIIa-like isoform X3
unconventional myosin-XVIIIa-like isoform X7
unconventional myosin-XVIIIa-like isoform X2
unconventional myosin-XVIIIa-like isoform X6
unconventional myosin-XVIIIa-like isoform X1
unconventional myosin-XVIIIa-like isoform X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
vascular endothelial zinc finger 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
vascular endothelial zinc finger 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
vascular endothelial zinc finger 1-like isoform X1
vascular endothelial zinc finger 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
kinase suppressor of ras 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
kinase suppressor of ras 1a, transcript variant X1
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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
uncharacterized LOC124468194, transcript variant X1
uncharacterized LOC124468194, transcript variant X2
nuclear fragile X mental retardation-interacting protein 2
apoptosis inducing factor mitochondrion associated 1, transcript variant X1
apoptosis inducing factor mitochondrion associated 1, transcript variant X4
apoptosis inducing factor mitochondrion associated 1, transcript variant X3
apoptosis inducing factor mitochondrion associated 1, transcript variant X2
apoptosis-inducing factor 1, mitochondrial isoform X4
apoptosis-inducing factor 1, mitochondrial isoform X3
apoptosis-inducing factor 1, mitochondrial isoform X2
apoptosis-inducing factor 1, mitochondrial isoform X1
non-POU domain containing, octamer-binding, transcript variant X1
non-POU domain containing, octamer-binding, transcript variant X2
non-POU domain-containing octamer-binding protein
uncharacterized protein LOC550591 homolog
vacuolar ATPase assembly integral membrane protein vma21
neuronal PAS domain protein 2, transcript variant X1
neuronal PAS domain protein 2, transcript variant X5
neuronal PAS domain protein 2, transcript variant X6
neuronal PAS domain protein 2, transcript variant X2
neuronal PAS domain protein 2, transcript variant X4
neuronal PAS domain protein 2, transcript variant X3
neuronal PAS domain-containing protein 2 isoform X1
neuronal PAS domain-containing protein 2 isoform X2
neuronal PAS domain-containing protein 2 isoform X3
RPA1 related single stranded DNA binding protein
ring finger protein 128a, transcript variant X2
E3 ubiquitin-protein ligase RNF128a isoform X2
ring finger protein 128a, transcript variant X1
E3 ubiquitin-protein ligase RNF128a isoform X1
TBC1 domain family member 8B, transcript variant X3
TBC1 domain family member 8B, transcript variant X1
TBC1 domain family member 8B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
zinc finger MYM-type protein 3-like, transcript variant X1
zinc finger MYM-type protein 3-like, transcript variant X2
zinc finger MYM-type protein 3-like, transcript variant X4
zinc finger MYM-type protein 3-like, transcript variant X3
zinc finger MYM-type protein 3-like isoform X1
zinc finger MYM-type protein 3-like isoform X2
zinc finger MYM-type protein 3-like isoform X4
zinc finger MYM-type protein 3-like isoform X3
gap junction protein beta 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
gap junction protein beta 1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
immunoglobulin (CD79A) binding protein 1
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
StAR-related lipid transfer (START) domain containing 8, transcript variant X4
StAR-related lipid transfer (START) domain containing 8, transcript variant X3
StAR-related lipid transfer (START) domain containing 8, transcript variant X1
StAR-related lipid transfer (START) domain containing 8, transcript variant X2
stAR-related lipid transfer protein 8 isoform X3
stAR-related lipid transfer protein 8 isoform X2
stAR-related lipid transfer protein 8 isoform X1
ectodysplasin A2 receptor, 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 33 samples with support for all annotated introns
ectodysplasin A2 receptor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
ectodysplasin A2 receptor, 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 5 samples with support for all annotated introns
tumor necrosis factor receptor superfamily member 27 isoform X1
tumor necrosis factor receptor superfamily member 27 isoform X2
tumor necrosis factor receptor superfamily member 27 isoform X3
G protein-coupled receptor 83, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
G protein-coupled receptor 83, 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 5 samples with support for all annotated introns
G protein-coupled receptor 83, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
G protein-coupled receptor 83, 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 23 samples with support for all annotated introns
probable G-protein coupled receptor 83 isoform X2
probable G-protein coupled receptor 83 isoform X1
Rho GTPase activating protein 20b, transcript variant X1
Rho GTPase activating protein 20b, transcript variant X2
rho GTPase-activating protein 20 isoform X1
rho GTPase-activating protein 20 isoform X2
zinc finger CCCH-type containing 12B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger CCCH-type containing 12B, 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 39 samples with support for all annotated introns
probable ribonuclease ZC3H12B isoform X2
probable ribonuclease ZC3H12B isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
ankyrin repeat and SOCS box-containing 12a
Cdc42 guanine nucleotide exchange factor (GEF) 9a, transcript variant X2
rho guanine nucleotide exchange factor 9 isoform X2
Cdc42 guanine nucleotide exchange factor (GEF) 9a, transcript variant X1
rho guanine nucleotide exchange factor 9 isoform X1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1, transcript variant X4
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1, transcript variant X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1, transcript variant X1
probable global transcription activator SNF2L1 isoform X1
probable global transcription activator SNF2L1 isoform X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1, transcript variant X5
probable global transcription activator SNF2L1 isoform X4
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1, transcript variant X3
probable global transcription activator SNF2L1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
fibrous sheath CABYR-binding protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
fibrous sheath CABYR-binding protein-like, transcript variant X7
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 16 samples with support for all annotated introns
fibrous sheath CABYR-binding protein-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
fibrous sheath CABYR-binding protein-like, transcript variant X5
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 42 samples with support for all annotated introns
fibrous sheath CABYR-binding protein-like, 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 13 samples with support for all annotated introns
fibrous sheath CABYR-binding protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
fibrous sheath CABYR-binding protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
fibrous sheath CABYR-binding protein-like isoform X4
fibrous sheath CABYR-binding protein-like isoform X7
fibrous sheath CABYR-binding protein-like isoform X6
fibrous sheath CABYR-binding protein-like isoform X5
fibrous sheath CABYR-binding protein-like isoform X3
fibrous sheath CABYR-binding protein-like isoform X2
fibrous sheath CABYR-binding protein-like isoform X1
connector enhancer of kinase suppressor of ras 2-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
GTPase IMAP family member 9-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
GTPase IMAP family member 9-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
GTPase IMAP family member 8-like isoform X3
GTPase IMAP family member 5-like isoform X2
GTPase IMAP family member 9-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
GTPase IMAP family member 9-like isoform 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
serrate RNA effector molecule homolog (Arabidopsis), 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 43 samples with support for all annotated introns
serrate RNA effector molecule homolog (Arabidopsis), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
serrate RNA effector molecule homolog (Arabidopsis), transcript variant X1
serrate RNA effector molecule homolog isoform X1
serrate RNA effector molecule homolog isoform X2
serrate RNA effector molecule homolog isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger HIT domain-containing protein 1
serine/arginine repetitive matrix protein 5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 74% 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: serine/arginine repetitive matrix protein 5
ATPase Na+/K+ transporting subunit beta 2b, transcript variant X1
ATPase Na+/K+ transporting subunit beta 2b, transcript variant X2
sodium/potassium-transporting ATPase subunit beta-2b isoform X1
sodium/potassium-transporting ATPase subunit beta-2b isoform X2
glycolipid transfer protein domain containing 2b
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
LOW QUALITY PROTEIN: glycolipid transfer protein domain-containing protein 2
cholinergic receptor, nicotinic, epsilon
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: 40 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
LOW QUALITY PROTEIN: misshapen-like kinase 1
guanine nucleotide binding protein (G protein), beta polypeptide 2
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-2
solute carrier family 12 member 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
solute carrier family 12 member 9, 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 20 samples with support for all annotated introns
hydroxysteroid (20-beta) dehydrogenase 2
uncharacterized protein LOC566600 homolog, transcript variant X2
uncharacterized protein LOC566600 homolog, transcript variant X3
uncharacterized protein LOC566600 homolog, transcript variant X1
E3 ubiquitin-protein ligase RNF144A isoform X1
E3 ubiquitin-protein ligase RNF144A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein U-like 1 like, transcript variant X1
heterogeneous nuclear ribonucleoprotein U-like 1 like, transcript variant X2
heterogeneous nuclear ribonucleoprotein U-like protein 1 isoform X1
heterogeneous nuclear ribonucleoprotein U-like protein 1 isoform X2
uncharacterized protein LOC797998 homolog
uncharacterized protein LOC566129 homolog
ryanodine receptor 1a (skeletal), transcript variant X1
ryanodine receptor 1a (skeletal), transcript variant X2
ryanodine receptor 1a (skeletal), transcript variant X5
ryanodine receptor 1a (skeletal), transcript variant X4
ryanodine receptor 1a (skeletal), transcript variant X7
ryanodine receptor 1a (skeletal), transcript variant X11
ryanodine receptor 1a (skeletal), transcript variant X3
ryanodine receptor 1a (skeletal), transcript variant X6
ryanodine receptor 1a (skeletal), transcript variant X10
ryanodine receptor 1a (skeletal), transcript variant X9
ryanodine receptor 1a (skeletal), transcript variant X15
ryanodine receptor 1a (skeletal), transcript variant X13
ryanodine receptor 1a (skeletal), transcript variant X8
ryanodine receptor 1a (skeletal), transcript variant X12
ryanodine receptor 1a (skeletal), transcript variant X14
ryanodine receptor 1a (skeletal), transcript variant X16
tyrosine-protein kinase receptor UFO-like
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
uncharacterized LOC124468114, 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 6 samples with support for all annotated introns
uncharacterized LOC124468114, transcript variant X2
solute carrier organic anion transporter family member 2B1-like
olfactory receptor 2A12-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
olfactory receptor 2A12-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
olfactory receptor 52N4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
olfactory receptor 52N4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74 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: 82 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
neuronal acetylcholine receptor subunit alpha-10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
nucleoporin 98 and 96 precursor, transcript variant X5
nucleoporin 98 and 96 precursor, transcript variant X3
nucleoporin 98 and 96 precursor, transcript variant X1
nucleoporin 98 and 96 precursor, transcript variant X2
nucleoporin 98 and 96 precursor, transcript variant X4
nucleoporin 98 and 96 precursor, transcript variant X6
nuclear pore complex protein Nup98-Nup96 isoform X1
nucleoporin 98 and 96 precursor, transcript variant X7
nuclear pore complex protein Nup98-Nup96 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein phosphatase 1D-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
protein phosphatase 1D-like, 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 22 samples with support for all annotated introns
protein phosphatase 1D-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 32-like
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tyrosine kinase receptor Cad96Ca-like
amyloid beta precursor protein binding family B member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
amyloid beta precursor protein binding family B member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
amyloid beta precursor protein binding family B member 1-like isoform X1
amyloid beta precursor protein binding family B member 1-like isoform X2
ubiquitin associated and SH3 domain containing Ba
ubiquitin-associated and SH3 domain-containing protein B
upstream stimulatory factor 1-like, transcript variant X2
upstream stimulatory factor 1-like, transcript variant X1
upstream stimulatory factor 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein si:ch211-215c18.3
LHFPL tetraspan subfamily member 6, transcript variant X2
LHFPL tetraspan subfamily member 6, transcript variant X1
LHFPL tetraspan subfamily member 6 protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
28S ribosomal protein S31, mitochondrial
mannose-P-dolichol utilization defect 1 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
eukaryotic translation initiation factor 4A1B
gamma-aminobutyric acid receptor-associated protein-like
G protein pathway suppressor 2, transcript variant X3
G protein pathway suppressor 2, transcript variant X2
G protein pathway suppressor 2, transcript variant X4
G protein pathway suppressor 2, transcript variant X1
G protein pathway suppressor 2 isoform X1
G protein pathway suppressor 2 isoform X2
G protein pathway suppressor 2 isoform X3
tumor protein p53, transcript variant X3
tumor protein p53, transcript variant X1
tumor protein p53, transcript variant X2
tumor protein p53, transcript variant X4
solute carrier family 25 member 35, transcript variant X2
solute carrier family 25 member 35, transcript variant X1
RAN guanine nucleotide release factor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
RAN guanine nucleotide release factor, transcript variant X2
ran guanine nucleotide release factor isoform X2
ran guanine nucleotide release factor isoform X1
histone-lysine N-methyltransferase 2D-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor (GEF) 15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
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 15 samples with support for all annotated introns
spermidine/spermine N1-acetyltransferase family member 2b
uncharacterized LOC124467716, transcript variant X2
uncharacterized LOC124467716, transcript variant X3
uncharacterized LOC124467716, transcript variant X1
uncharacterized protein LOC124467716 isoform X1
uncharacterized protein LOC124467716 isoform X2
uncharacterized protein LOC124467716 isoform X3
TAF6 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X3
TAF6 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X1
TAF6 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X4
TAF6 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
transcription initiation factor TFIID subunit 6
zona pellucida sperm-binding protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
segment polarity protein dishevelled homolog DVL-2-like
very long-chain specific acyl-CoA dehydrogenase, mitochondrial-like
integrin alpha-X-like, transcript variant X2
integrin alpha-X-like, transcript variant X1
uncharacterized LOC124467761, transcript variant X1
uncharacterized LOC124467761, transcript variant X2
uncharacterized protein LOC124467761 isoform X1
uncharacterized protein LOC124467761 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC793850 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
uncharacterized protein si:ch211-284e13.6
alpha-soluble NSF attachment protein-like, transcript variant X1
alpha-soluble NSF attachment protein-like, transcript variant X2
alpha-soluble NSF attachment protein-like isoform X1
alpha-soluble NSF attachment protein-like isoform X2
zinc finger BED domain-containing protein 4, transcript variant X2
zinc finger BED domain-containing protein 4, transcript variant X3
zinc finger BED domain-containing protein 4, transcript variant X5
zinc finger BED domain-containing protein 4, transcript variant X1
zinc finger BED domain-containing protein 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger BED domain-containing protein 4 isoform X1
zinc finger BED domain-containing protein 4 isoform X2
zinc finger BED domain-containing protein 4 isoform X3
EH domain-containing protein 2-like, transcript variant X2
EH domain-containing protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
EH domain-containing protein 2-like isoform X1
EH domain-containing protein 2-like isoform X2
guanine nucleotide binding protein (G protein), gamma 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-8
nuclear factor related to kappaB binding protein, transcript variant X2
nuclear factor related to kappaB binding protein, transcript variant X1
nuclear factor related to kappaB binding protein, transcript variant X3
nuclear factor related to kappa-B-binding protein isoform X2
nuclear factor related to kappa-B-binding protein isoform X1
ST14 transmembrane serine protease matriptase b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
WD repeat domain 73, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
WD repeat-containing protein 73 isoform X1
WD repeat domain 73, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
WD repeat-containing protein 73 isoform X2
sialidase 3 (membrane sialidase), tandem duplicate 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
X-ray radiation resistance-associated protein 1
polymerase (DNA-directed), delta 3, accessory subunit, 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 27 samples with support for all annotated introns
polymerase (DNA-directed), delta 3, accessory subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
DNA polymerase delta subunit 3 isoform X1
DNA polymerase delta subunit 3 isoform X2
voltage-gated potassium channel subunit beta-3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TNF superfamily member 13, 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
TNF superfamily member 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
TNF superfamily member 13, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
TNF superfamily member 13, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 13 isoform X1
tumor necrosis factor ligand superfamily member 13 isoform X2
tumor necrosis factor ligand superfamily member 13 isoform X3
7SK snRNA methylphosphate capping enzyme
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein kinase PAK 3, transcript variant X1
serine/threonine-protein kinase PAK 3, transcript variant X2
serine/threonine-protein kinase PAK 3 isoform X1
serine/threonine-protein kinase PAK 3 isoform X2
neuronal migration protein doublecortin-like, transcript variant X3
neuronal migration protein doublecortin-like, transcript variant X1
neuronal migration protein doublecortin-like, transcript variant X2
neuronal migration protein doublecortin-like isoform X2
neuronal migration protein doublecortin-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
interleukin 13 receptor, alpha 2, transcript variant X2
interleukin 13 receptor, alpha 2, transcript variant X1
interleukin-13 receptor subunit alpha-2 isoform X2
interleukin-13 receptor subunit alpha-2 isoform X1
interleukin 13 receptor, alpha 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
interleukin-13 receptor subunit alpha-2 isoform X3
interleukin 13 receptor, alpha 2, transcript variant X4
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 42 samples with support for all annotated introns
interleukin-13 receptor subunit alpha-2 isoform X4
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 2, 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 38 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 2, 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 29 samples with support for all annotated introns
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X4
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X3
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X2
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X1
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X5
uncharacterized protein LOC100037380 homolog, transcript variant X1
U2 snRNP-associated SURP motif-containing protein isoform X1
uncharacterized protein LOC100037380 homolog, transcript variant X2
U2 snRNP-associated SURP motif-containing protein isoform X2
WD repeat domain 44, transcript variant X2
WD repeat domain 44, transcript variant X1
WD repeat-containing protein 44 isoform X2
WD repeat-containing protein 44 isoform X1
kelch-like family member 13, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
kelch-like family member 13, transcript variant X4
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 42 samples with support for all annotated introns
kelch-like family member 13, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
kelch-like family member 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kelch-like family member 13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
LRRN4 C-terminal-like protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
LRRN4 C-terminal-like protein, transcript variant X1
latent transforming growth factor beta binding protein 3, transcript variant X4
latent transforming growth factor beta binding protein 3, transcript variant X1
latent transforming growth factor beta binding protein 3, transcript variant X2
latent transforming growth factor beta binding protein 3, transcript variant X3
latent-transforming growth factor beta-binding protein 3 isoform X1
latent-transforming growth factor beta-binding protein 3 isoform X2
latent-transforming growth factor beta-binding protein 3 isoform X4
latent-transforming growth factor beta-binding protein 3 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 5 bases in 4 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 5 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: spectrin family protein
CDC42 effector protein (Rho GTPase binding) 2, transcript variant X5
CDC42 effector protein (Rho GTPase binding) 2, transcript variant X1
CDC42 effector protein (Rho GTPase binding) 2, transcript variant X2
CDC42 effector protein (Rho GTPase binding) 2, transcript variant X4
CDC42 effector protein (Rho GTPase binding) 2, transcript variant X3
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00571
COORDINATES: nucleotide motif:Rfam:12.0:RF00277
ras-related protein Rab-34-like, transcript variant X3
ras-related protein Rab-34-like, transcript variant X4
ras-related protein Rab-34-like isoform X3
ras-related protein Rab-34-like isoform X4
ras-related protein Rab-34-like, transcript variant X1
ras-related protein Rab-34-like, transcript variant X2
ras-related protein Rab-34-like isoform X1
ras-related protein Rab-34-like isoform X2
SPT6 homolog, histone chaperone and transcription elongation factor, transcript variant X2
SPT6 homolog, histone chaperone and transcription elongation factor, transcript variant X1
transcription elongation factor SPT6 isoform X2
transcription elongation factor SPT6 isoform 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
NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor b
methyltransferase like 27, 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 2 samples with support for all annotated introns
methyltransferase like 27, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
methyltransferase-like protein 27 isoform X2
methyltransferase-like protein 27 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 161 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 229 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 185 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 220 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
inactive C-alpha-formylglycine-generating enzyme 2
COORDINATES: nucleotide motif:Rfam:12.0:RF00398
COORDINATES: nucleotide motif:Rfam:12.0:RF00414
28S ribosomal protein S17, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 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: 62 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
lissencephaly-1 homolog B, transcript variant X2
lissencephaly-1 homolog B, transcript variant X1
coiled-coil domain-containing protein 92-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
coiled-coil domain-containing protein 92-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 92-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tripartite motif-containing protein 26-like isoform X1
coiled-coil domain-containing protein 92-like isoform X2
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 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
apoptosis inducing factor mitochondria associated 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
chromosome 5 C17orf97 homolog, 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
chromosome 5 C17orf97 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Golgi SNAP receptor complex member 1-like, transcript variant X2
Golgi SNAP receptor complex member 1-like, transcript variant X1
Golgi SNAP receptor complex member 1-like isoform X2
Golgi SNAP receptor complex member 1-like isoform X1
unc-119 homolog b (C. elegans), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
unc-119 homolog b (C. elegans), 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
aldehyde dehydrogenase 3 family, member A2b
aldehyde dehydrogenase family 3 member A2b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
calcitonin gene-related peptide-receptor component protein, transcript variant X1
calcitonin gene-related peptide-receptor component protein, transcript variant X2
DNA-directed RNA polymerase III subunit RPC9 isoform X1
DNA-directed RNA polymerase III subunit RPC9 isoform X2
tyrosylprotein sulfotransferase 1, like, transcript variant X1
tyrosylprotein sulfotransferase 1, like, transcript variant X2
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ST6 beta-galactosamide alpha-2,6-sialyltranferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ST6 beta-galactosamide alpha-2,6-sialyltranferase 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
beta-galactoside alpha-2,6-sialyltransferase 1
heterogeneous nuclear ribonucleoprotein A/B-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein A/B-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein A/B-like isoform X2
heterogeneous nuclear ribonucleoprotein A/B-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
C-terminal-binding protein 2-like, transcript variant X1
C-terminal-binding protein 2-like, transcript variant X2
C-terminal-binding protein 2-like, transcript variant X3
C-terminal-binding protein 2-like isoform X1
C-terminal-binding protein 1-like isoform X2
family with sequence similarity 53 member C
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 23 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
H/ACA ribonucleoprotein complex subunit 2-like protein
nuclear protein 1-like, transcript variant X2
nuclear protein 1-like, transcript variant X1
vitamin K epoxide reductase complex, subunit 1-like 1, transcript variant X1
vitamin K epoxide reductase complex, subunit 1-like 1, transcript variant X2
vitamin K epoxide reductase complex subunit 1-like protein 1
glucuronidase, beta, transcript variant X2
glucuronidase, beta, transcript variant X1
myotubularin related protein 4, transcript variant X3
myotubularin related protein 4, transcript variant X5
myotubularin related protein 4, transcript variant X4
myotubularin related protein 4, transcript variant X6
myotubularin related protein 4, transcript variant X1
myotubularin related protein 4, transcript variant X2
myotubularin related protein 4, transcript variant X7
myotubularin-related protein 4 isoform X2
myotubularin-related protein 4 isoform X1
myotubularin-related protein 4 isoform X3
myotubularin-related protein 4 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
SPT4 homolog, DSIF elongation factor subunit
scavenger receptor cysteine-rich domain-containing group B protein
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
3-monooxygenase/tryptophan 5-monooxygenase activation protein, gamma polypeptide 1
heat shock protein, alpha-crystallin-related, 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
serine/arginine repetitive matrix protein 3
carbohydrate-responsive element-binding protein, 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
carbohydrate-responsive element-binding protein, 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
carbohydrate-responsive element-binding protein-like isoform X2
carbohydrate-responsive element-binding protein-like isoform X1
complement component 1, q subcomponent binding protein
complement component 1 Q subcomponent-binding protein, mitochondrial
DEAH (Asp-Glu-Ala-His) box polypeptide 33, transcript variant X1
DEAH (Asp-Glu-Ala-His) box polypeptide 33, transcript variant X2
ATP-dependent RNA helicase DHX33 isoform X1
ATP-dependent RNA helicase DHX33 isoform X2
purinergic receptor P2X, ligand-gated ion channel, 1, transcript variant X1
purinergic receptor P2X, ligand-gated ion channel, 1, transcript variant X2
calcium/calmodulin-dependent protein kinase kinase 1, alpha a
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: calcium/calmodulin-dependent protein kinase kinase 1
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
sarcoplasmic/endoplasmic reticulum calcium ATPase 1
zinc finger, ZZ-type with EF hand domain 1
LOW QUALITY PROTEIN: zinc finger ZZ-type and EF-hand domain-containing protein 1
ankyrin repeat and FYVE domain containing 1
ubiquitin-conjugating enzyme E2G 1a (UBC7 homolog, yeast)
spinster homolog 3 (Drosophila), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
spinster homolog 3 (Drosophila), transcript variant X3
spinster homolog 3 (Drosophila), transcript variant X2
spinster homolog 2 (Drosophila), transcript variant X2
spinster homolog 2 (Drosophila), transcript variant X1
finTRIM family, member 83, transcript variant X1
finTRIM family, member 83, transcript variant X2
finTRIM family, member 82, transcript variant X2
finTRIM family, member 82, transcript variant X3
finTRIM family, member 82, transcript variant X1
intraflagellar transport 22 homolog (Chlamydomonas)
intraflagellar transport protein 22 homolog
ATP synthase, H+ transporting, mitochondrial F0 complex, subunit g
PDZ domain containing 3b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
PDZ domain containing 3b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
PDZ domain containing 3b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ATP-binding cassette, sub-family G (WHITE), member 4a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ATP-binding cassette, sub-family G (WHITE), member 4a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
ATP-binding cassette sub-family G member 4
CUB and sushi domain-containing protein 3
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 40 samples with support for all annotated introns
dolichyl-phosphate (UDP-N-acetylglucosamine) N-acetylglucosaminephosphotransferase 1 (GlcNAc-1-P transferase)
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 44 samples with support for all annotated introns
UDP-N-acetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase
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 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
phospholipid transfer protein C2CD2L isoform X1
phospholipid transfer protein C2CD2L 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: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: porphobilinogen deaminase-like
porphobilinogen deaminase-like, transcript variant X2
porphobilinogen deaminase-like, transcript variant X1
porphobilinogen deaminase-like isoform X2
porphobilinogen deaminase-like isoform X1
pleckstrin homology-like domain, family B, member 1a, transcript variant X1
pleckstrin homology-like domain family B member 1 isoform X1
pleckstrin homology-like domain, family B, member 1a, transcript variant X6
pleckstrin homology-like domain, family B, member 1a, transcript variant X7
pleckstrin homology-like domain, family B, member 1a, transcript variant X9
pleckstrin homology-like domain, family B, member 1a, transcript variant X4
pleckstrin homology-like domain, family B, member 1a, transcript variant X10
pleckstrin homology-like domain, family B, member 1a, transcript variant X5
pleckstrin homology-like domain, family B, member 1a, transcript variant X3
pleckstrin homology-like domain family B member 1 isoform X3
pleckstrin homology-like domain, family B, member 1a, transcript variant X2
pleckstrin homology-like domain family B member 1 isoform X2
pleckstrin homology-like domain family B member 1 isoform X5
pleckstrin homology-like domain family B member 1 isoform X6
pleckstrin homology-like domain family B member 1 isoform X7
pleckstrin homology-like domain family B member 1 isoform X9
pleckstrin homology-like domain family B member 1 isoform X4
pleckstrin homology-like domain family B member 1 isoform X10
pleckstrin homology-like domain, family B, member 1a, transcript variant X8
pleckstrin homology-like domain family B member 1 isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
serine/threonine kinase 36 (fused homolog, Drosophila)
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
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: 44 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger protein 239-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 157 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
uncharacterized protein C11orf53 homolog
A disintegrin and metalloproteinase with thrombospondin motifs 8-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
A disintegrin and metalloproteinase with thrombospondin motifs 8-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 8-like
ADAM metallopeptidase with thrombospondin type 1 motif, 15a
A disintegrin and metalloproteinase with thrombospondin motifs 15a
sorting nexin 19a, transcript variant X1
sorting nexin 19a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sorting nexin 19a, transcript variant X3
sorting nexin 19a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sorting nexin 19a, transcript variant X2
inositol-trisphosphate 3-kinase Ca, transcript variant X1
inositol-trisphosphate 3-kinase C isoform X1
inositol-trisphosphate 3-kinase Ca, transcript variant X2
inositol-trisphosphate 3-kinase Ca, transcript variant X3
inositol-trisphosphate 3-kinase C isoform X2
inositol-trisphosphate 3-kinase C isoform X3
signal-induced proliferation-associated 1-like protein 3
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
glutaminyl-peptide cyclotransferase-like b
glutaminyl-peptide cyclotransferase-like protein
succinate dehydrogenase complex assembly factor 1
succinate dehydrogenase assembly factor 1, mitochondrial
potassium channel, subfamily K, member 12 like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
potassium channel, subfamily K, member 12 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium channel, subfamily K, member 12 like, transcript variant X1
protein phosphatase, Mg2+/Mn2+ dependent, 1Nb (putative)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
diablo, IAP-binding mitochondrial protein b
TLR adapter interacting with SLC15A4 on the lysosome, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
TLR adapter interacting with SLC15A4 on the lysosome, transcript variant X2
TLR adapter interacting with SLC15A4 on the lysosome isoform X1
TLR adapter interacting with SLC15A4 on the lysosome isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
DnaJ heat shock protein family (Hsp40) member B13
39S ribosomal protein L48, mitochondrial
RAB6A, member RAS oncogene family, transcript variant X4
RAB6A, member RAS oncogene family, transcript variant X3
RAB6A, member RAS oncogene family, transcript variant X2
RAB6A, member RAS oncogene family, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
nuclear factor of kappa light polypeptide gene enhancer in B-cells inhibitor, beta
zinc finger and SCAN domain-containing protein 12-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 34 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 12-like, transcript variant X1
zinc finger and SCAN domain-containing protein 12-like
tubulin polymerization-promoting protein family member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00288
ORAI calcium release-activated calcium modulator 2
branched chain ketoacid dehydrogenase kinase, transcript variant X2
branched chain ketoacid dehydrogenase kinase, transcript variant X1
3-methyl-2-oxobutanoate dehydrogenase [lipoamide] kinase, mitochondrial
leucine-rich repeats and WD repeat domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
leucine-rich repeats and WD repeat domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
leucine-rich repeats and WD repeat domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
leucine-rich repeat and WD repeat-containing protein 1 isoform X2
leucine-rich repeat and WD repeat-containing protein 1 isoform X1
alpha-ketoglutarate-dependent dioxygenase alkB homolog 4
DNA-directed RNA polymerase II subunit RPB11-a
Cbl proto-oncogene, E3 ubiquitin protein ligase
cell surface glycoprotein MUC18-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
cell surface glycoprotein MUC18-like, transcript variant X1
cell surface glycoprotein MUC18-like isoform X1
cell surface glycoprotein MUC18-like isoform X2
E3 ubiquitin-protein ligase RNF26-like, transcript variant X2
E3 ubiquitin-protein ligase RNF26-like, transcript variant X1
E3 ubiquitin-protein ligase RNF26-like isoform X1
E3 ubiquitin-protein ligase RNF26-like isoform X2
protein MIS12 homolog, transcript variant X1
protein MIS12 homolog, 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 26 samples with support for all annotated introns
glutamate receptor ionotropic, kainate 1-like
map3k7 C-terminal like, transcript variant X2
map3k7 C-terminal like, transcript variant X1
MAP3K7 C-terminal-like protein isoform X1
MAP3K7 C-terminal-like protein isoform X2
BTB and CNC homology 1, basic leucine zipper transcription factor 1 b
chaperonin containing TCP1, subunit 8 (theta), transcript variant X1
chaperonin containing TCP1, subunit 8 (theta), transcript variant X2
T-complex protein 1 subunit theta isoform X2
T-complex protein 1 subunit theta isoform X1
C-type mannose receptor 2-like, transcript variant X3
C-type mannose receptor 2-like, transcript variant X1
C-type mannose receptor 2-like isoform X1
C-type mannose receptor 2-like, transcript variant X2
secretory phospholipase A2 receptor-like isoform X2
listerin E3 ubiquitin protein ligase 1, transcript variant X2
listerin E3 ubiquitin protein ligase 1, transcript variant X1
E3 ubiquitin-protein ligase listerin isoform X1
E3 ubiquitin-protein ligase listerin isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 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: 46 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC124468117, transcript variant X2
uncharacterized LOC124468117, transcript variant X1
uncharacterized protein LOC124468117 isoform X2
uncharacterized protein LOC124468117 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00150
COORDINATES: nucleotide motif:Rfam:12.0:RF00266
uncharacterized LOC124468117, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
uncharacterized protein LOC124468117 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 89 member B
EH domain binding protein 1-like 1b, transcript variant X1
EH domain binding protein 1-like 1b, transcript variant X3
EH domain binding protein 1-like 1b, transcript variant X7
EH domain binding protein 1-like 1b, transcript variant X4
EH domain binding protein 1-like 1b, transcript variant X8
EH domain binding protein 1-like 1b, transcript variant X10
EH domain binding protein 1-like 1b, transcript variant X5
EH domain binding protein 1-like 1b, transcript variant X2
EH domain binding protein 1-like 1b, transcript variant X6
EH domain binding protein 1-like 1b, transcript variant X9
nascent polypeptide-associated complex subunit alpha, muscle-specific form isoform X1
nascent polypeptide-associated complex subunit alpha, muscle-specific form isoform X3
nascent polypeptide-associated complex subunit alpha, muscle-specific form isoform X4
microtubule-associated protein futsch isoform X5
nascent polypeptide-associated complex subunit alpha, muscle-specific form isoform X2
microtubule-associated protein futsch isoform X9
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 45 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
acetyl-CoA acetyltransferase, mitochondrial
transmembrane serine protease 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
transmembrane serine protease 2, 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 16 samples with support for all annotated introns
transmembrane serine protease 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
transmembrane serine protease 2, transcript variant X4
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 23 samples with support for all annotated introns
protein FAM3B-like, transcript variant X2
protein FAM3B-like, transcript variant X4
protein FAM3B-like, transcript variant X3
protein FAM3B-like, transcript variant X1
protein FAM3B-like, transcript variant X5
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: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: Down syndrome cell adhesion molecule a
Purkinje cell protein 4a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
Purkinje cell protein 4a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
calmodulin regulator protein PCP4a isoform X2
calmodulin regulator protein PCP4a isoform X1
immunoglobulin superfamily, member 5a, transcript variant X3
immunoglobulin superfamily, member 5a, transcript variant X2
immunoglobulin superfamily, member 5a, transcript variant X1
immunoglobulin superfamily member 5 isoform X2
immunoglobulin superfamily member 5 isoform X1
guided entry of tail-anchored proteins factor 1-like
non-histone chromosomal protein HMG-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, including 13 samples with support for all annotated introns
tumor necrosis factor receptor superfamily member 19-like, transcript variant X1
tumor necrosis factor receptor superfamily member 19-like, transcript variant X4
tumor necrosis factor receptor superfamily member 19-like, transcript variant X2
tumor necrosis factor receptor superfamily member 19-like isoform X1
tumor necrosis factor receptor superfamily member 19-like isoform X3
tumor necrosis factor receptor superfamily member 19-like isoform X2
tumor necrosis factor receptor superfamily member 19-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
beta-1,3-glucuronyltransferase 1 (glucuronosyltransferase P) b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
galactosylgalactosylxylosylprotein 3-beta-glucuronosyltransferase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
EI24 autophagy associated transmembrane protein
STT3 oligosaccharyltransferase complex catalytic subunit A
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit STT3A
cytoskeleton-associated protein 2, transcript variant X1
cytoskeleton-associated protein 2, transcript variant X2
cytoskeleton-associated protein 2 isoform X1
cytoskeleton-associated protein 2 isoform 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 42 samples with support for all annotated introns
uncharacterized protein si:dkey-250d21.1
wingless-type MMTV integration site family, member 11
UV radiation resistance-associated gene protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
microtubule-associated protein 6 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain containing 21, transcript variant X1
zinc finger and BTB domain containing 21, transcript variant X2
zinc finger and BTB domain-containing protein 21 isoform X1
zinc finger and BTB domain-containing protein 21 isoform X2
C2 domain-containing protein 2, transcript variant X1
C2 domain-containing protein 2, transcript variant X2
C2 domain-containing protein 2 isoform X1
C2 domain-containing protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
receptor-interacting serine-threonine kinase 4
receptor-interacting serine/threonine-protein kinase 4
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, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
coxsackievirus and adenovirus receptor homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: proline and serine-rich protein 1
vacuolar protein-sorting-associated protein 36
thrombospondin type-1 domain-containing protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
thrombospondin type-1 domain-containing protein 1, transcript variant X2
thrombospondin type-1 domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transmembrane phosphatase with tensin homology, transcript variant X2
transmembrane phosphatase with tensin homology, transcript variant X1
transmembrane phosphatase with tensin homology, transcript variant X3
transmembrane phosphatase with tensin homology, transcript variant X4
putative tyrosine-protein phosphatase TPTE isoform X1
putative tyrosine-protein phosphatase TPTE isoform X2
transmembrane phosphatase with tensin homology, transcript variant X5
putative tyrosine-protein phosphatase TPTE isoform X3
translocase of inner mitochondrial membrane 10 homolog B (yeast)
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 44 samples with support for all annotated introns
mitochondrial import inner membrane translocase subunit Tim10 B
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons
LOW QUALITY PROTEIN: histidine N-acetyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples 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
tricarboxylate transport protein A, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC124467742, transcript variant X2
uncharacterized LOC124467742, transcript variant X1
uncharacterized LOC124467742, 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 23 samples with support for all annotated introns
inositol polyphosphate-5-phosphatase Kb, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
inositol polyphosphate-5-phosphatase Kb, transcript variant X1
inositol polyphosphate-5-phosphatase Kb, transcript variant X2
inositol polyphosphate 5-phosphatase K isoform X3
inositol polyphosphate 5-phosphatase K isoform X2
inositol polyphosphate 5-phosphatase K isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 46 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
ribosomal protein S6 kinase-related protein
phosphatidylinositol glycan anchor biosynthesis, class S
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
HEAT repeat containing 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
HEAT repeat containing 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
HEAT repeat-containing protein 6 isoform X1
HEAT repeat-containing protein 6 isoform X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 52
probable ATP-dependent RNA helicase DDX52
meprin A subunit beta-like, transcript variant X2
meprin A subunit beta-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC124468231, transcript variant X2
uncharacterized LOC124468231, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
baculoviral IAP repeat containing 2, transcript variant X2
baculoviral IAP repeat containing 2, transcript variant X3
baculoviral IAP repeat containing 2, transcript variant X4
baculoviral IAP repeat containing 2, transcript variant X1
baculoviral IAP repeat containing 2, transcript variant X5
baculoviral IAP repeat-containing protein 2
transcriptional coactivator YAP1-like, transcript variant X1
transcriptional coactivator YAP1-like, transcript variant X2
cilia and flagella associated protein 300
cilia- and flagella-associated protein 300
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 37 samples with support for all annotated introns
transient receptor potential cation channel, subfamily C, member 6a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
transient receptor potential cation channel, subfamily C, member 6a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
short transient receptor potential channel 6a isoform X1
short transient receptor potential channel 6a isoform X2
C-type lectin domain family 4 member G-like
complement C1q subcomponent subunit B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
V-set and immunoglobulin domain-containing protein 10-like 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44% coverage of the annotated genomic feature by RNAseq alignments
checkpoint kinase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
checkpoint kinase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
dihydrolipoamide S-acetyltransferase (E2 component of pyruvate dehydrogenase complex)
dihydrolipoyllysine-residue acetyltransferase component of pyruvate dehydrogenase complex, mitochondrial
DIX domain containing 1b, transcript variant X3
DIX domain containing 1b, transcript variant X1
DIX domain containing 1b, transcript variant X2
uncharacterized protein LOC569781 homolog
heat shock protein, alpha-crystallin-related, b2
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 43 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
melanoma-derived growth regulatory protein
BICD family like cargo adaptor 2, transcript variant X2
BICD family like cargo adaptor 2, transcript variant X1
BICD family-like cargo adapter 2 isoform X1
BICD family-like cargo adapter 2 isoform X2
cytokine receptor family member B12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
cytokine receptor family member B12, 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 43 samples with support for all annotated introns
cytokine receptor family member B12 isoform X2
cytokine receptor family member B12 isoform X1
uncharacterized protein LOC569883 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC569883 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC569883 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein LOC569883 homolog, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC569883 homolog, transcript variant X1
mitochondrial import receptor subunit TOM40B isoform X1
mitochondrial import receptor subunit TOM40B isoform X2
ubiquitin-fold modifier conjugating enzyme 1
ubiquitin-fold modifier-conjugating enzyme 1
collagen alpha-1(XXVI) chain, transcript variant X1
collagen alpha-1(XXVI) chain, transcript variant X2
collagen alpha-1(XXVI) chain, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
potassium channel tetramerization domain containing 7
RAB guanine nucleotide exchange factor (GEF) 1, transcript variant X1
RAB guanine nucleotide exchange factor (GEF) 1, transcript variant X2
protein phosphatase, Mg2+/Mn2+ dependent, 1E
inactive serine/threonine-protein kinase TEX14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71% coverage of the annotated genomic feature by RNAseq alignments
spindle and kinetochore associated complex subunit 2, transcript variant X1
spindle and kinetochore associated complex subunit 2, transcript variant X2
spindle and kinetochore-associated protein 2 isoform X1
spindle and kinetochore-associated protein 2 isoform X2
malate dehydrogenase 2, NAD (mitochondrial)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
ras-like protein family member 10B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ras-like protein family member 10B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
adaptor related protein complex 2 subunit beta 1, transcript variant X2
adaptor related protein complex 2 subunit beta 1, transcript variant X1
zinc finger, HIT-type containing 3, transcript variant X1
zinc finger, HIT-type containing 3, transcript variant X2
zinc finger HIT domain-containing protein 3 isoform X1
zinc finger HIT domain-containing protein 3 isoform X2
unconventional myosin-XIX, transcript variant X1
unconventional myosin-XIX, transcript variant X2
phosphatidylinositol glycan anchor biosynthesis, class W
phosphatidylinositol-glycan biosynthesis class W protein
gametogenetin binding protein 2, transcript variant X1
gametogenetin binding protein 2, transcript variant X2
gametogenetin-binding protein 2 isoform X1
gametogenetin-binding protein 2 isoform X2
dehydrogenase/reductase SDR family member 11a
sodium- and chloride-dependent GABA transporter ine
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Era-like 12S mitochondrial rRNA chaperone 1
family with sequence similarity 222 member Ba, transcript variant X1
family with sequence similarity 222 member Ba, transcript variant X5
family with sequence similarity 222 member Ba, transcript variant X6
family with sequence similarity 222 member Ba, transcript variant X3
family with sequence similarity 222 member Ba, transcript variant X2
family with sequence similarity 222 member Ba, transcript variant X4
transient receptor potential cation channel, subfamily V, member 1, transcript variant X2
transient receptor potential cation channel, subfamily V, member 1, transcript variant X4
transient receptor potential cation channel, subfamily V, member 1, transcript variant X3
transient receptor potential cation channel, subfamily V, member 1, transcript variant X1
transient receptor potential cation channel, subfamily V, member 1, transcript variant X5
transient receptor potential cation channel subfamily V member 1 isoform X3
transient receptor potential cation channel subfamily V member 1 isoform X2
transient receptor potential cation channel subfamily V member 1 isoform X1
transient receptor potential cation channel subfamily V member 1 isoform X4
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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
purinergic receptor P2X, ligand-gated ion channel, 5
uncharacterized LOC124467661, transcript variant X2
uncharacterized LOC124467661, transcript variant X1
uncharacterized LOC124467661, transcript variant X3
uncharacterized LOC124467661, transcript variant X4
phosphatidylinositol glycan anchor biosynthesis, class L
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 33 samples with support for all annotated introns
N-acetylglucosaminyl-phosphatidylinositol de-N-acetylase
nuclear receptor corepressor 1-like, transcript variant X1
nuclear receptor corepressor 1-like, transcript variant X2
nuclear receptor corepressor 1-like isoform X1
nuclear receptor corepressor 1-like isoform X2
sodium- and chloride-dependent GABA transporter 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide 2, transcript variant X6
procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide 2, transcript variant X1
procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide 2, transcript variant X4
procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide 2, transcript variant X2
procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide 2, transcript variant X5
procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha polypeptide 2, transcript variant X3
prolyl 4-hydroxylase subunit alpha-2 isoform X2
prolyl 4-hydroxylase subunit alpha-2 isoform X3
prolyl 4-hydroxylase subunit alpha-2 isoform X1
LOW QUALITY PROTEIN: nuclear receptor corepressor 1
serine/threonine-protein kinase 32A-like
dihydropyrimidinase like 3, transcript variant X1
dihydropyrimidinase like 3, transcript variant X2
dihydropyrimidinase-related protein 3 isoform X1
dihydropyrimidinase-related protein 3 isoform X2
janus kinase and microtubule interacting protein 2
janus kinase and microtubule-interacting protein 2
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
SH3 and PX domains 2B, transcript variant X2
SH3 and PX domains 2B, transcript variant X1
SH3 and PX domain-containing protein 2B isoform X2
SH3 and PX domain-containing protein 2B isoform X1
gamma-aminobutyric acid receptor subunit beta-2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid type A receptor subunit alpha6b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit alpha-6
gamma-aminobutyric acid type A receptor subunit alpha1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gamma-aminobutyric acid type A receptor subunit alpha1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit alpha-1 isoform X1
gamma-aminobutyric acid type A receptor subunit alpha1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gamma-aminobutyric acid receptor subunit alpha-1 isoform X2
gamma-aminobutyric acid type A receptor subunit gamma2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit gamma-2
ankyrin repeat domain-containing protein SOWAHA-like
shroom family member 1, transcript variant X3
shroom family member 1, transcript variant X1
shroom family member 1, transcript variant X2
AF4/FMR2 family, member 4, transcript variant X4
AF4/FMR2 family, member 4, transcript variant X2
AF4/FMR2 family, member 4, transcript variant X1
AF4/FMR2 family, member 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
AF4/FMR2 family, member 4, transcript variant X3
zinc finger CCHC domain-containing protein 10
zinc finger, SWIM-type containing 7, transcript variant X1
zinc finger, SWIM-type containing 7, transcript variant X2
zinc finger SWIM domain-containing protein 7 isoform X2
zinc finger SWIM domain-containing protein 7 isoform X1
sperm antigen with calponin homology and coiled-coil domains 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
sperm antigen with calponin homology and coiled-coil domains 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
sperm antigen with calponin homology and coiled-coil domains 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
sperm antigen with calponin homology and coiled-coil domains 1, 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 33 samples with support for all annotated introns
sperm antigen with calponin homology and coiled-coil domains 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
sperm antigen with calponin homology and coiled-coil domains 1, transcript variant X6
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 36 samples with support for all annotated introns
sperm antigen with calponin homology and coiled-coil domains 1, transcript variant X7
translocase of inner mitochondrial membrane 22 homolog (yeast)
mitochondrial import inner membrane translocase subunit Tim22
active breakpoint cluster region-related protein
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
clathrin, heavy chain a (Hc), transcript variant X1
clathrin, heavy chain a (Hc), transcript variant X2
peptidyl-tRNA hydrolase 2, mitochondrial
vacuole membrane protein 1-like, transcript variant X5
vacuole membrane protein 1-like, transcript variant X6
vacuole membrane protein 1-like, transcript variant X1
vacuole membrane protein 1-like, transcript variant X4
vacuole membrane protein 1-like, transcript variant X8
vacuole membrane protein 1-like, transcript variant X7
vacuole membrane protein 1-like, transcript variant X2
vacuole membrane protein 1-like, transcript variant X3
vacuole membrane protein 1-like isoform X2
vacuole membrane protein 1-like isoform X1
ribosomal protein S6 kinase b, polypeptide 1a
mediator of RNA polymerase II transcription subunit 13-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 8 bases in 6 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 8 bases in 6 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: integrator complex subunit 2
activator of transcription and developmental regulator AUTS2 a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
autism susceptibility gene 2 protein homolog
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.