Rhincodon typus isolate 14 chromosome 37, sRhiTyp1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Rhincodontidae; Rhincodon.
REFSEQ INFORMATION: The reference sequence is identical to\nCM038834.1.\nAssembly name: sRhiTyp1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/03. The\noriginal whole-genome shotgun project has the accession\nJAHMAH000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Supernova v. 2.1.1; P_RNA_scaffolder v.\n commit 7941e0f; Tigmint v. 1.1.2; ARKS v.\n 1.1.0; 3D-DNA v. 180922\nAssembly Name :: sRhiTyp1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 46.7x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Rhincodon typus Annotation Release\n 101\nAnnotation Version :: 101\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##
Derived by automated computational analysis using gene prediction method: Gnomon.
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
NACHT, LRR and PYD domains-containing protein 3-like isoform X1
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
NLR family CARD domain-containing protein 3-like isoform X2
gastrula zinc finger protein XlCGF71.1-like, transcript variant X1
gastrula zinc finger protein XlCGF71.1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gastrula zinc finger protein XlCGF71.1-like
small G protein signaling modulator 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
small G protein signaling modulator 3, transcript variant X2
small G protein signaling modulator 3, transcript variant X1
small G protein signaling modulator 3, transcript variant X3
small G protein signaling modulator 3, transcript variant X4
small G protein signaling modulator 3 isoform X1
small G protein signaling modulator 3 isoform X3
small G protein signaling modulator 3 isoform X2
small G protein signaling modulator 3, transcript variant X6
small G protein signaling modulator 3 isoform X4
ATP-sensitive inward rectifier potassium channel 12-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 Proteins
ATP-sensitive inward rectifier potassium channel 12-like isoform X2
ATP-sensitive inward rectifier potassium channel 12-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 133 Proteins
ATP-sensitive inward rectifier potassium channel 12-like isoform X1
probable ATP-dependent RNA helicase DDX17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
meiotic recombination protein DMC1/LIM15 homolog
SUN domain-containing protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
SUN domain-containing protein 2, 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 2 samples with support for all annotated introns
SUN domain-containing protein 2 isoform X2
SUN domain-containing protein 2 isoform X1
platelet-derived growth factor subunit B-like
extracellular serine/threonine protein kinase FAM20C-like
chibby homolog 1 (Drosophila), transcript variant X1
chibby homolog 1 (Drosophila), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TGF-beta activated kinase 1/MAP3K7 binding protein 1, transcript variant X1
TGF-beta activated kinase 1/MAP3K7 binding protein 1, transcript variant X4
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase isoform X1
TGF-beta-activated kinase 1 and MAP3K7-binding protein 1 isoform X4
TGF-beta activated kinase 1/MAP3K7 binding protein 1, transcript variant X2
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase isoform X2
TGF-beta activated kinase 1/MAP3K7 binding protein 1, transcript variant X5
TGF-beta activated kinase 1/MAP3K7 binding protein 1, transcript variant X3
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase isoform X3
TGF-beta activated kinase 1/MAP3K7 binding protein 1, transcript variant X6
beta-1,4-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase isoform X5
ribosomal RNA-processing protein 7 homolog A
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00007
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 89% 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: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein interacting with prkca 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein interacting with prkca 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein interacting with prkca 1, transcript variant X1
translocase of outer mitochondrial membrane 22 homolog (yeast)
mitochondrial import receptor subunit TOM22 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
polymerase (DNA-directed), delta interacting protein 3
transcription factor 20, transcript variant X2
transcription factor 20, transcript variant X1
uncharacterized LOC125487157, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125487157, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC125487157, transcript variant X3
uncharacterized LOC125487157, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized protein LOC125487157 isoform X1
uncharacterized protein LOC125487157 isoform X2
uncharacterized protein LOC125487157 isoform X3
uncharacterized protein LOC125487157 isoform X4
coagulation factor VIII associated, transcript variant X1
coagulation factor VIII associated, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
40-kDa huntingtin-associated protein isoform X1
40-kDa huntingtin-associated protein isoform X2
family with sequence similarity 234 member B, transcript variant X2
family with sequence similarity 234 member B, transcript variant X1
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X3
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X1
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 59, transcript variant X4
probable ATP-dependent RNA helicase DDX59
LUC7-like (S. cerevisiae), transcript variant X4
LUC7-like (S. cerevisiae), transcript variant X1
LUC7-like (S. cerevisiae), transcript variant X3
putative RNA-binding protein Luc7-like 1 isoform X1
putative RNA-binding protein Luc7-like 1 isoform X3
LUC7-like (S. cerevisiae), transcript variant X5
LUC7-like (S. cerevisiae), transcript variant X6
LUC7-like (S. cerevisiae), transcript variant X2
putative RNA-binding protein Luc7-like 1 isoform X4
putative RNA-binding protein Luc7-like 1 isoform X2
serine hydrolase like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine hydrolase-like protein isoform X2
serine hydrolase like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine hydrolase like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine hydrolase like, transcript variant X6
serine hydrolase like, transcript variant X7
serine hydrolase like, transcript variant X5
serine hydrolase like, transcript variant X3
serine hydrolase-like protein isoform X1
serine hydrolase-like protein isoform X6
serine hydrolase-like protein isoform X3
serine hydrolase-like protein isoform X5
serine hydrolase-like protein isoform X7
serine hydrolase-like protein isoform X4
single-pass membrane protein with aspartate-rich tail 1b
NADH:ubiquinone oxidoreductase subunit A6
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 6
DNA replication licensing factor mcm5-A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
FAD-dependent oxidoreductase domain-containing protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
FAD-dependent oxidoreductase domain-containing protein 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
FAD-dependent oxidoreductase domain-containing protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
FAD-dependent oxidoreductase domain-containing protein 2-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
FAD-dependent oxidoreductase domain-containing protein 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
FAD-dependent oxidoreductase domain-containing protein 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
FAD-dependent oxidoreductase domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
small nucleolar RNA SNORA62/SNORA6 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00091
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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 6 samples with support for all annotated introns
tetratricopeptide repeat domain 26, transcript variant X2
tetratricopeptide repeat domain 26, transcript variant X1
intraflagellar transport protein 56 isoform X1
intraflagellar transport protein 56 isoform X2
tetratricopeptide repeat domain 26, 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 1 sample with support for all annotated introns
intraflagellar transport protein 56 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon CCU); 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 134, transcript variant X1
coiled-coil domain-containing protein 134 isoform X1
coiled-coil domain-containing protein 134, transcript variant X2
coiled-coil domain-containing protein 134, transcript variant X3
coiled-coil domain-containing protein 134 isoform X2
sterol regulatory element binding transcription factor 2, transcript variant X1
sterol regulatory element binding transcription factor 2, transcript variant X2
sterol regulatory element binding transcription factor 2, transcript variant X3
sterol regulatory element-binding protein 2 isoform X1
sterol regulatory element-binding protein 2 isoform X2
sterol regulatory element-binding protein 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 9 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
TRIO and F-actin binding protein b, transcript variant X1
TRIO and F-actin binding protein b, transcript variant X2
TRIO and F-actin binding protein b isoform X2
TRIO and F-actin binding protein b isoform X1
2-amino-3-ketobutyrate coenzyme A ligase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, 2 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: 28 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and fibronectin type-III domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
transcription factor AP-4-like, transcript variant X1
transcription factor AP-4-like isoform X1
transcription factor AP-4-like, transcript variant X2
transcription factor AP-4-like isoform X2
X-prolyl aminopeptidase 3, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 11 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
L3MBTL histone methyl-lysine binding protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
lethal(3)malignant brain tumor-like protein 2 isoform X3
L3MBTL histone methyl-lysine binding protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
L3MBTL histone methyl-lysine binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
lethal(3)malignant brain tumor-like protein 2 isoform X2
lethal(3)malignant brain tumor-like protein 2 isoform X1
L3MBTL histone methyl-lysine binding protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
lethal(3)malignant brain tumor-like protein 2 isoform X4
L3MBTL histone methyl-lysine binding protein 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
lethal(3)malignant brain tumor-like protein 2 isoform X5
Ran GTPase activating protein 1b, transcript variant X1
Ran GTPase activating protein 1b, transcript variant X2
zinc finger CCCH-type containing 7Bb, transcript variant X2
zinc finger CCCH-type containing 7Bb, transcript variant X1
zinc finger CCCH domain-containing protein 7B
TEF transcription factor, PAR bZIP family member a
PHD finger-like domain-containing protein 5A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
polymerase (RNA) III (DNA directed) polypeptide H, transcript variant X1
polymerase (RNA) III (DNA directed) polypeptide H, transcript variant X2
DNA-directed RNA polymerase III subunit RPC8 isoform X1
DNA-directed RNA polymerase III subunit RPC8 isoform X2
cold shock domain containing C2, RNA binding a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cold shock domain containing C2, RNA binding a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cold shock domain-containing protein C2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: phosphomannomutase 1-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 3 samples with support for all annotated introns
myocardin-related transcription factor A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
cytochrome b-c1 complex subunit 2, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
X-ray repair complementing defective repair in Chinese hamster cells 6
X-ray repair cross-complementing protein 6
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% 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: 20 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
proliferation associated nuclear element
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
tumor necrosis factor ligand superfamily member 13B-like
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 LOC109928638, transcript variant X3
uncharacterized LOC109928638, transcript variant X2
uncharacterized LOC109928638, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125487162, transcript variant X1
uncharacterized LOC125487162, transcript variant X2
peripheral myelin protein 22-like, transcript variant X6
peripheral myelin protein 22-like, transcript variant X1
peripheral myelin protein 22-like, transcript variant X2
peripheral myelin protein 22-like, transcript variant X7
peripheral myelin protein 22-like, transcript variant X4
peripheral myelin protein 22-like, transcript variant X3
peripheral myelin protein 22-like, transcript variant X5
transfer RNA opal suppressor (anticodon UCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
glutamate receptor ionotropic, NMDA 2B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
activating transcription factor 7-interacting protein 1-like, transcript variant X2
activating transcription factor 7-interacting protein 1-like isoform X2
activating transcription factor 7-interacting protein 1-like, transcript variant X1
activating transcription factor 7-interacting protein 1-like isoform X1
ankyrin repeat domain-containing protein 54
cyclic AMP-dependent transcription factor ATF-4
MIEF1 upstream open reading frame 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
eukaryotic translation initiation factor 3 subunit L-like
ribosomal protein S19 binding protein 1, transcript variant X1
ribosomal protein S19 binding protein 1, transcript variant X2
ribosomal protein S19 binding protein 1 isoform X2
ribosomal protein S19 binding protein 1 isoform X1
uncharacterized LOC125487192, transcript variant X4
uncharacterized LOC125487192, transcript variant X2
uncharacterized LOC125487192, transcript variant X1
uncharacterized LOC125487192, transcript variant X3
SUMO-conjugating enzyme UBC9, transcript variant X2
SUMO-conjugating enzyme UBC9, transcript variant X1
testis-expressed protein 33, transcript variant X1
testis-expressed protein 33, transcript variant X2
testis-expressed protein 33, transcript variant X4
testis-expressed protein 33, transcript variant X5
testis-expressed protein 33, transcript variant X3
BTB/POZ domain-containing protein KCTD5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
cytokine receptor common subunit beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
beta-1,3-N-acetylglucosaminyltransferase lunatic fringe-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
caspase recruitment domain-containing protein 11-like
guanine nucleotide-binding protein subunit alpha-12-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
guanine nucleotide-binding protein subunit alpha-12-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein subunit alpha-12-like, 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 1 sample with support for all annotated introns
guanine nucleotide-binding protein subunit alpha-12-like isoform X3
guanine nucleotide-binding protein subunit alpha-12-like isoform X2
guanine nucleotide-binding protein subunit alpha-12-like isoform X1
cytochrome P450 2J2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cytochrome P450 2J2-like, transcript variant X1
cytochrome P450 2J2-like, transcript variant X2
cytochrome P450 2J2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytochrome P450 2J2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 29
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00563
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments
transcription factor MafK-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 37 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
transcription factor MafK-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 38 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
phospholipase A2, group VI (cytosolic, calcium-independent), transcript variant X1
phospholipase A2, group VI (cytosolic, calcium-independent), transcript variant X4
phospholipase A2, group VI (cytosolic, calcium-independent), transcript variant X2
phospholipase A2, group VI (cytosolic, calcium-independent), transcript variant X3
85/88 kDa calcium-independent phospholipase A2 isoform X1
85/88 kDa calcium-independent phospholipase A2 isoform X2
BAR/IMD domain containing adaptor protein 2 like 2b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00096
ras-related C3 botulinum toxin substrate 1
ras-related C3 botulinum toxin substrate 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 228 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
golgi-associated, gamma adaptin ear containing, ARF binding protein 1, transcript variant X1
ADP-ribosylation factor-binding protein GGA1 isoform X1
golgi-associated, gamma adaptin ear containing, ARF binding protein 1, transcript variant X2
ADP-ribosylation factor-binding protein GGA1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
ferritin, heavy subunit-like, transcript variant X2
ferritin, heavy subunit-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase 6 regulatory subunit 3
histone-lysine N-methyltransferase KMT5C-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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine-protein kinase BRSK2-like
MOB kinase activator 2-like, transcript variant X2
MOB kinase activator 2-like, transcript variant X1
dual specificity protein phosphatase 8-like
cyclin-dependent kinase inhibitor 1B-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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
transient receptor potential cation channel, subfamily M, member 4a, 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
transient receptor potential cation channel, subfamily M, member 4a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transient receptor potential cation channel subfamily M member 4a isoform X1
transient receptor potential cation channel subfamily M member 4a isoform X2
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
ras-related and estrogen-regulated growth inhibitor-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 11 samples with support for all annotated introns
ras-related and estrogen-regulated growth inhibitor-like isoform X1
ras-related and estrogen-regulated growth inhibitor-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
ras-related and estrogen-regulated growth inhibitor-like isoform X2
transportin-3-like, transcript variant X2
transportin-3-like, transcript variant X1
transportin-3-like, transcript variant X3
transportin-3-like, 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 3 samples with support for all annotated introns
transportin-3-like, transcript variant X4
carnitine O-palmitoyltransferase 1, liver isoform, transcript variant X1
carnitine O-palmitoyltransferase 1, liver isoform, transcript variant X3
carnitine O-palmitoyltransferase 1, liver isoform, transcript variant X6
carnitine O-palmitoyltransferase 1, liver isoform, transcript variant X2
carnitine O-palmitoyltransferase 1, liver isoform, transcript variant X4
carnitine O-palmitoyltransferase 1, liver isoform, transcript variant X5
carnitine O-palmitoyltransferase 1, liver isoform isoform X2
carnitine O-palmitoyltransferase 1, liver isoform isoform X1
uncharacterized LOC125487147, transcript variant X2
uncharacterized LOC125487147, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC125487160, transcript variant X2
uncharacterized LOC125487160, transcript variant X1
tumor protein p53-inducible protein 11-like, transcript variant X2
tumor protein p53-inducible protein 11-like, transcript variant X1
tumor protein p53-inducible protein 11-like
paired box protein Pax-6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
paired box protein Pax-6-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 2 samples with support for all annotated introns
paired box protein Pax-6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
paired box protein Pax-6-like isoform X2
paired box protein Pax-6-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
reticulocalbin 3, EF-hand calcium binding domain, transcript variant X2
reticulocalbin 3, EF-hand calcium binding domain, transcript variant X1
reticulocalbin 3, EF-hand calcium binding domain, transcript variant X4
reticulocalbin 3, EF-hand calcium binding domain, transcript variant X3
nitric oxide synthase interacting protein, transcript variant X2
nitric oxide synthase interacting protein, transcript variant X1
nitric oxide synthase-interacting protein
proline rich Gla (G-carboxyglutamic acid) 2, transcript variant X5
proline rich Gla (G-carboxyglutamic acid) 2, transcript variant X6
proline rich Gla (G-carboxyglutamic acid) 2, transcript variant X4
proline rich Gla (G-carboxyglutamic acid) 2, transcript variant X3
proline rich Gla (G-carboxyglutamic acid) 2, transcript variant X2
proline rich Gla (G-carboxyglutamic acid) 2, transcript variant X1
transmembrane gamma-carboxyglutamic acid protein 2 isoform X1
transmembrane gamma-carboxyglutamic acid protein 2 isoform X2
proline-rich protein 12, transcript variant X1
proline-rich protein 12, transcript variant X2
proline-rich protein 12, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
proline-rich protein 12, transcript variant X4
mediator complex subunit 25, transcript variant X2
mediator complex subunit 25, transcript variant X1
mediator complex subunit 25, transcript variant X4
mediator complex subunit 25, transcript variant X3
mediator of RNA polymerase II transcription subunit 25 isoform X1
mediator of RNA polymerase II transcription subunit 25 isoform X3
mediator of RNA polymerase II transcription subunit 25 isoform X2
protein kinase C and casein kinase substrate in neurons protein 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein kinase C and casein kinase substrate in neurons protein 3, 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 8 samples with support for all annotated introns
protein kinase C and casein kinase substrate in neurons protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
protein kinase C and casein kinase substrate in neurons protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein kinase C and casein kinase substrate in neurons protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein kinase C and casein kinase substrate in neurons protein 3, transcript variant X5
protein kinase C and casein kinase substrate in neurons protein 3 isoform X1
protein kinase C and casein kinase substrate in neurons protein 1 isoform X2
polymerase (DNA directed), delta 1, catalytic subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
polymerase (DNA directed), delta 1, catalytic subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
polymerase (DNA directed), delta 1, catalytic subunit, transcript variant X3
transcription factor Spi-B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transcription factor Spi-B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transcription factor Spi-B-like isoform X1
transcription factor Spi-B-like isoform X2
myosin-binding protein C, fast-type-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 53 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
ER membrane protein complex subunit 10, 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 14 samples with support for all annotated introns
ER membrane protein complex subunit 10, transcript variant X1
ER membrane protein complex subunit 10, transcript variant X3
ER membrane protein complex subunit 10 isoform X1
ER membrane protein complex subunit 10 isoform X3
ER membrane protein complex subunit 10 isoform X2
ETS-related transcription factor Elf-5-like, transcript variant X2
ETS-related transcription factor Elf-5-like, transcript variant X3
ETS-related transcription factor Elf-5-like, transcript variant X1
ETS-related transcription factor Elf-5-like isoform X2
ETS translocation variant 4-like isoform X1
E3 SUMO-protein ligase ZBED1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E3 SUMO-protein ligase ZBED1-like, transcript variant X2
E3 SUMO-protein ligase ZBED1-like isoform X1
E3 SUMO-protein ligase ZBED1-like isoform X2
leucine rich repeat containing 4Ba, 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 2 samples with support for all annotated introns
leucine rich repeat containing 4Ba, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine-rich repeat-containing protein 4B isoform X2
leucine-rich repeat-containing protein 4B isoform X1
DNA ligase 1-like, transcript variant X2
DNA ligase 1-like, transcript variant X1
serine/arginine-rich splicing factor 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
putative uncharacterized protein C19orf81
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
SH3 and multiple ankyrin repeat domains 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
SH3 and multiple ankyrin repeat domains protein 1
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
epidermal growth factor receptor kinase substrate 8-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
excitatory amino acid transporter 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109924710, transcript variant X3
uncharacterized LOC109924710, transcript variant X2
uncharacterized LOC109924710, transcript variant X4
uncharacterized LOC109924710, transcript variant X1
uncharacterized protein LOC109924710 isoform X2
uncharacterized protein LOC109924710 isoform X1
aldehyde dehydrogenase 16 family, member A1
aldehyde dehydrogenase family 16 member A1
PIH1 domain containing 1, transcript variant X3
PIH1 domain containing 1, transcript variant X2
PIH1 domain containing 1, transcript variant X5
PIH1 domain containing 1, transcript variant X1
PIH1 domain containing 1, transcript variant X7
PIH1 domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
PIH1 domain containing 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 17% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 155 Proteins
U1 small nuclear ribonucleoprotein 70 kDa
uncharacterized LOC125487176, transcript variant X1
uncharacterized LOC125487176, transcript variant X2
protein phosphatase 1 regulatory subunit 12C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 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: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily A member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125487178, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 89% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125487178, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kinesin-like protein KIF18A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kinesin-like protein KIF18A, transcript variant X1
neurotrophin-4-like, 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 2 samples with support for all annotated introns
neurotrophin-4-like, transcript variant X3
neurotrophin-4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 44 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein lin-7 homolog B, 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 1 sample with support for all annotated introns
protein lin-7 homolog B, transcript variant X2
protein lin-7 homolog B, transcript variant X3
protein lin-7 homolog B, transcript variant X5
protein lin-7 homolog B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcription intermediary factor 1-beta-like
ferritin, middle subunit-like, transcript variant X2
ferritin, middle subunit-like, transcript variant X1
ferritin, middle subunit-like isoform X1
ferritin, heavy subunit-like, transcript variant X3
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
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: ferritin heavy chain B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 263 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
ferritin heavy chain A-like, transcript variant X2
ferritin heavy chain A-like, transcript variant X1
ferritin, middle subunit-like isoform X2
ferritin, heavy subunit-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ferritin, higher subunit-like isoform X1
ferritin, higher subunit-like isoform X3
ferritin, higher subunit-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 328 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 42 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ferritin, lower subunit-like, transcript variant X1
ferritin, lower subunit-like, transcript variant X2
multiple epidermal growth factor-like domains protein 6, transcript variant X2
multiple epidermal growth factor-like domains protein 6, 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
multiple epidermal growth factor-like domains protein 6, 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
multiple epidermal growth factor-like domains protein 6 isoform X2
uncharacterized protein LOC125487188 isoform X1
uncharacterized protein LOC125487188 isoform X3
receptor-type tyrosine-protein phosphatase H-like, transcript variant X4
receptor-type tyrosine-protein phosphatase H-like, transcript variant X5
receptor-type tyrosine-protein phosphatase H-like, transcript variant X6
receptor-type tyrosine-protein phosphatase H-like isoform X3
receptor-type tyrosine-protein phosphatase H-like isoform X4
receptor-type tyrosine-protein phosphatase H-like, transcript variant X2
receptor-type tyrosine-protein phosphatase H-like, transcript variant X1
receptor-type tyrosine-protein phosphatase H-like, transcript variant X7
receptor-type tyrosine-protein phosphatase H-like, transcript variant X3
receptor-type tyrosine-protein phosphatase H-like isoform X1
receptor-type tyrosine-protein phosphatase H-like isoform X6
receptor-type tyrosine-protein phosphatase H-like isoform X2
receptor-type tyrosine-protein phosphatase H-like isoform X5
AKT1 substrate 1 (proline-rich), transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 long SRA reads, 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
proline-rich AKT1 substrate 1 isoform X3
AKT1 substrate 1 (proline-rich), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
AKT1 substrate 1 (proline-rich), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
AKT1 substrate 1 (proline-rich), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
AKT1 substrate 1 (proline-rich), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
AKT1 substrate 1 (proline-rich), transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
proline-rich AKT1 substrate 1 isoform X1
proline-rich AKT1 substrate 1 isoform X2
TBC1 domain family, member 17, transcript variant X2
TBC1 domain family, member 17, transcript variant X4
TBC1 domain family, member 17, transcript variant X3
TBC1 domain family, member 17, transcript variant X1
TBC1 domain family, member 17, transcript variant X5
potassium voltage-gated channel subfamily C member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 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: 29 Proteins
fuzzy planar cell polarity protein, transcript variant X2
fuzzy planar cell polarity protein, transcript variant X1
adaptor related protein complex 2 subunit alpha 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
DNA-directed RNA polymerases I, II, and III subunit RPABC5
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 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: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SR-related CTD-associated factor 1, transcript variant X2
SR-related CTD-associated factor 1, transcript variant X4
SR-related CTD-associated factor 1, transcript variant X3
SR-related CTD-associated factor 1, transcript variant X1
serine/arginine repetitive matrix protein 2 isoform X2
serine/arginine repetitive matrix protein 2 isoform X1
serine/arginine repetitive matrix protein 2 isoform X3
ATP-sensitive inward rectifier potassium channel 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 117 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ras-related protein R-Ras2-like, transcript variant X1
ras-related protein R-Ras2-like, transcript variant X2
ras-related protein R-Ras2-like isoform X1
ras-related protein R-Ras2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
probable G-protein coupled receptor 146, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable G-protein coupled receptor 146, transcript variant 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 2 samples with support for all annotated introns
probable G-protein coupled receptor 146, transcript variant X3
ATP synthase subunit f, mitochondrial-like, transcript variant X2
ATP synthase subunit f, mitochondrial-like, transcript variant X1
ATP synthase subunit f, mitochondrial-like isoform X1
ATP synthase subunit f, mitochondrial-like isoform X2
lectin, galactoside-binding, soluble, 2b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins
arf-GAP with dual PH domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
calcium voltage-gated channel subunit alpha1 Ia
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent T-type calcium channel subunit alpha-1I
DNA-directed RNA polymerases I, II, and III subunit RPABC2
trinucleotide repeat-containing gene 6B protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent calcium channel gamma-2 subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
voltage-dependent calcium channel gamma-2 subunit-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
COORDINATES: nucleotide motif:Rfam:12.0:RF00593
synaptogyrin-1-like, transcript variant X1
synaptogyrin-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
eukaryotic translation initiation factor 3, subunit D, transcript variant X2
eukaryotic translation initiation factor 3, subunit D, transcript variant X1
eukaryotic translation initiation factor 3 subunit D
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
GTP-binding protein 1, transcript variant X2
GTP-binding protein 1, transcript variant X3
GTP-binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
intraflagellar transport 27 homolog (Chlamydomonas)
intraflagellar transport protein 27 homolog
matrix Gla protein, transcript variant X1
matrix Gla protein, 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 13 samples with support for all annotated introns
toll-like receptor 13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
toll-like receptor 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 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: 25 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
dynein axonemal light chain 4, transcript variant X1
dynein axonemal light chain 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
endoplasmic reticulum resident protein 27
E3 ubiquitin-protein ligase TRIM56-like, transcript variant X2
E3 ubiquitin-protein ligase TRIM56-like isoform X2
E3 ubiquitin-protein ligase TRIM56-like, transcript variant X1
E3 ubiquitin-protein ligase TRIM56-like isoform X1
G-protein coupled receptor family C group 5 member B-like, transcript variant X1
G-protein coupled receptor family C group 5 member B-like, transcript variant X2
G-protein coupled receptor family C group 5 member B-like
CCR4-NOT transcription complex subunit 3, transcript variant X6
CCR4-NOT transcription complex subunit 3, transcript variant X4
CCR4-NOT transcription complex subunit 3, transcript variant X2
CCR4-NOT transcription complex subunit 3, transcript variant X5
CCR4-NOT transcription complex subunit 3, transcript variant X3
CCR4-NOT transcription complex subunit 3, transcript variant X1
CCR4-NOT transcription complex subunit 3 isoform X6
CCR4-NOT transcription complex subunit 3 isoform X4
CCR4-NOT transcription complex subunit 3 isoform X2
CCR4-NOT transcription complex subunit 3 isoform X5
CCR4-NOT transcription complex subunit 3 isoform X3
CCR4-NOT transcription complex subunit 3 isoform X1
retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain containing 96, transcript variant X1
coiled-coil domain containing 96, transcript variant X5
coiled-coil domain containing 96, transcript variant X4
coiled-coil domain containing 96, transcript variant X2
coiled-coil domain containing 96, transcript variant X3
coiled-coil domain-containing protein 96 isoform X1
coiled-coil domain-containing protein 96 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
RNA binding protein fox-1 homolog 1-like, transcript variant X8
RNA binding protein fox-1 homolog 1-like, transcript variant X4
RNA binding protein fox-1 homolog 1-like, transcript variant X3
RNA binding protein fox-1 homolog 1-like isoform X4
RNA binding protein fox-1 homolog 1-like isoform X3
RNA binding protein fox-1 homolog 1-like isoform X7
RNA binding protein fox-1 homolog 1-like, transcript variant X5
RNA binding protein fox-1 homolog 1-like, transcript variant X2
RNA binding protein fox-1 homolog 1-like, transcript variant X1
RNA binding protein fox-1 homolog 1-like, transcript variant X7
RNA binding protein fox-1 homolog 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RNA binding protein fox-1 homolog 2-like isoform X2
RNA binding protein fox-1 homolog 2-like isoform X1
RNA binding protein fox-1 homolog 1-like isoform X6
RNA binding protein fox-1 homolog 1-like isoform X5
formation of mitochondrial complex V assembly factor 1 homolog, transcript variant X2
formation of mitochondrial complex V assembly factor 1 homolog, transcript variant X1
transfer RNA leucine (anticodon AAG); 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.
THAP domain containing 7, transcript variant X4
THAP domain containing 7, transcript variant X5
THAP domain containing 7, transcript variant X3
THAP domain containing 7, transcript variant X2
THAP domain containing 7, transcript variant X1
THAP domain-containing protein 7 isoform X2
THAP domain-containing protein 7 isoform X1
THAP domain-containing protein 7 isoform X3
zinc finger and BTB domain-containing protein 20-like, transcript variant X1
zinc finger and BTB domain-containing protein 20-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 10 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 20-like, transcript variant X4
zinc finger and BTB domain-containing protein 20-like, transcript variant X2
zinc finger and BTB domain-containing protein 20-like isoform X1
zinc finger and BTB domain-containing protein 20-like isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00211
trans-1,2-dihydrobenzene-1,2-diol dehydrogenase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 15B-like
nucleobindin-2-like, transcript variant X1
nucleobindin-2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109915577, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC109915577, transcript variant X1
uncharacterized protein LOC109915577 isoform X2
uncharacterized protein LOC109915577 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
branched-chain-amino-acid aminotransferase, cytosolic-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
branched-chain-amino-acid aminotransferase, cytosolic-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
branched-chain-amino-acid aminotransferase, cytosolic-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
branched-chain-amino-acid aminotransferase, cytosolic-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, 24 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
branched-chain-amino-acid aminotransferase, cytosolic-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
branched-chain-amino-acid aminotransferase, cytosolic-like isoform X1
branched-chain-amino-acid aminotransferase, cytosolic-like isoform X2
branched-chain-amino-acid aminotransferase, cytosolic-like isoform X4
branched-chain-amino-acid aminotransferase, cytosolic-like isoform X3
uncharacterized LOC109917402, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC109917402, transcript variant X1
uncharacterized protein LOC109917402 isoform X1
uncharacterized LOC109917402, transcript variant X2
uncharacterized protein LOC109917402 isoform X2
cytidine deaminase, transcript variant X2
cytidine deaminase, transcript variant X3
cytidine deaminase, transcript variant X1
leukocyte antigen CD37-like, transcript variant X2
leukocyte antigen CD37-like, transcript variant X1
leukocyte antigen CD37-like, transcript variant X5
leukocyte antigen CD37-like, transcript variant X4
leukocyte antigen CD37-like, transcript variant X6
leukocyte antigen CD37-like, transcript variant X3
leukocyte antigen CD37-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transcriptional enhancer factor TEF-1-like, transcript variant X6
transcriptional enhancer factor TEF-1-like, transcript variant X1
transcriptional enhancer factor TEF-1-like, transcript variant X3
transcriptional enhancer factor TEF-1-like, transcript variant X2
transcriptional enhancer factor TEF-1-like, transcript variant X5
transcriptional enhancer factor TEF-1-like, transcript variant X4
transcriptional enhancer factor TEF-1-like isoform X3
transcriptional enhancer factor TEF-1-like isoform X1
transcriptional enhancer factor TEF-1-like isoform X2
uncharacterized LOC109933250, transcript variant X2
uncharacterized LOC109933250, transcript variant X1
uncharacterized protein LOC109933250 isoform X1
uncharacterized protein LOC109933250 isoform X2
protein KASH5-like, transcript variant X2
protein KASH5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 112 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC125487171, transcript variant X1
uncharacterized protein LOC125487171 isoform X1
uncharacterized LOC125487171, transcript variant X2
uncharacterized protein LOC125487171 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
circularly permutated Ras protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns