Rhincodon typus isolate 14 chromosome 27, 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\nCM038824.1.\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.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 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: 11 long SRA reads, 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
coiled-coil domain-containing protein 28B
histone-binding protein RBBP4, transcript variant X2
histone-binding protein RBBP4, transcript variant X4
histone-binding protein RBBP4, transcript variant X5
histone-binding protein RBBP4 isoform X2
histone-binding protein RBBP4 isoform X4
histone-binding protein RBBP4 isoform X5
histone-binding protein RBBP4, transcript variant X3
histone-binding protein RBBP4, transcript variant X1
histone-binding protein RBBP4 isoform X3
histone-binding protein RBBP4 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
uncharacterized protein KIAA1522 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor alpha-induced protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
testis-specific serine/threonine-protein kinase 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
proto-oncogene tyrosine-protein kinase LCK-like
family with sequence similarity 167 member B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
myotubularin-related protein 9-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
myotubularin-related protein 9-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
myotubularin-related protein 9-like isoform X1
myotubularin-related protein 9-like isoform X2
transmembrane protein 234, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane protein 234, transcript variant X1
transmembrane protein 234, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
eukaryotic translation initiation factor 3, subunit I
eukaryotic translation initiation factor 3 subunit I
doublecortin domain containing 2B, transcript variant X2
doublecortin domain containing 2B, transcript variant X3
doublecortin domain containing 2B, 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 1 sample with support for all annotated introns
doublecortin domain-containing protein 2B isoform X2
doublecortin domain-containing protein 2B isoform X3
doublecortin domain-containing protein 2B 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
IQ motif containing C, 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
IQ motif containing C, transcript variant X3
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 13 samples with support for all annotated introns
IQ domain-containing protein C isoform X3
IQ domain-containing protein C isoform X1
IQ motif containing C, transcript variant X2
IQ motif containing C, transcript variant X4
IQ domain-containing protein C isoform X4
IQ domain-containing protein C isoform X2
zinc finger and BTB domain containing 8 opposite strand
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon CUG); 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: 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: 6 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
fatty acid binding protein 10a, liver basic
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 4 samples with support for all annotated introns
fatty acid-binding protein 10-A, liver basic
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 106 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
interleukin-22 receptor subunit alpha-1-like, transcript variant X2
interleukin-22 receptor subunit alpha-1-like, transcript variant X1
interleukin-22 receptor subunit alpha-1-like isoform X1
uncharacterized protein LOC109910735 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
digestive cysteine proteinase 2-like, transcript variant X2
digestive cysteine proteinase 2-like, transcript variant X1
digestive cysteine proteinase 2-like isoform X2
digestive cysteine proteinase 2-like isoform X1
counting factor associated protein D-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
proto-oncogene tyrosine-protein kinase Yrk
probable G-protein coupled receptor 139, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
probable G-protein coupled receptor 139, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
probable G-protein coupled receptor 139, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
probable G-protein coupled receptor 139, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
probable G-protein coupled receptor 139, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
probable G-protein coupled receptor 139, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
probable G-protein coupled receptor 139, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments
probable G-protein coupled receptor 139, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, 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 139 isoform X2
probable G-protein coupled receptor 139 isoform X1
probable G-protein coupled receptor 139, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
AT hook, DNA binding motif, containing 1
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
AT-hook DNA-binding motif-containing protein 1
uncharacterized LOC125486304, 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 4 samples with support for all annotated introns
uncharacterized LOC125486304, transcript variant X1
S-adenosylmethionine decarboxylase proenzyme 2-like, transcript variant X3
S-adenosylmethionine decarboxylase proenzyme 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
S-adenosylmethionine decarboxylase proenzyme 2-like, transcript variant X1
S-adenosylmethionine decarboxylase proenzyme 2-like isoform X1
S-adenosylmethionine decarboxylase proenzyme 2-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
S-adenosylmethionine decarboxylase proenzyme 2-like isoform X2
wiskott-Aldrich syndrome protein family member 2
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 2 samples with support for all annotated introns
CD164 sialomucin-like 2, transcript variant X3
CD164 sialomucin-like 2, transcript variant X4
CD164 sialomucin-like 2, transcript variant X1
CD164 sialomucin-like 2, transcript variant X2
CD164 sialomucin-like 2 protein isoform X3
CD164 sialomucin-like 2 protein isoform X4
mediator of RNA polymerase II transcription, subunit 18 homolog (yeast)
mediator of RNA polymerase II transcription subunit 18
polycomb protein SCMH1-like, transcript variant X3
polycomb protein SCMH1-like, transcript variant X9
polycomb protein SCMH1-like, transcript variant X6
polycomb protein SCMH1-like, transcript variant X2
polycomb protein SCMH1-like, transcript variant X5
polycomb protein SCMH1-like, transcript variant X4
polycomb protein SCMH1-like, transcript variant X8
polycomb protein SCMH1-like, transcript variant X1
polycomb protein SCMH1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Cbp/p300-interacting transactivator, with Glu/Asp-rich carboxy-terminal domain, 4b
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
TAF12 RNA polymerase II, TATA box binding protein (TBP)-associated factor
transcription initiation factor TFIID subunit 12
discoidin, CUB and LCCL domain-containing protein 1, transcript variant X2
discoidin, CUB and LCCL domain-containing protein 1, transcript variant X1
discoidin, CUB and LCCL domain-containing protein 1 isoform X2
discoidin, CUB and LCCL domain-containing protein 1 isoform X1
discoidin, CUB and LCCL domain-containing protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
discoidin, CUB and LCCL domain-containing protein 1 isoform X3
transcription cofactor vestigial-like protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transcription cofactor vestigial-like protein 2 isoform X2
transcription cofactor vestigial-like protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcription cofactor vestigial-like protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcription cofactor vestigial-like protein 2, transcript variant X3
transcription cofactor vestigial-like protein 2 isoform X1
transcription cofactor vestigial-like protein 2 isoform X3
transcription cofactor vestigial-like protein 2 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 62 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC109921460, transcript variant X2
uncharacterized LOC109921460, transcript variant X1
uncharacterized protein LOC109921460 isoform X2
uncharacterized protein LOC109921460 isoform X1
uncharacterized LOC109921460, transcript variant X3
uncharacterized protein LOC109921460 isoform X3
sodium/potassium-transporting ATPase subunit beta-1-interacting protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
rho-related GTP-binding protein RhoB-like, transcript variant X1
rho-related GTP-binding protein RhoB-like, transcript variant X2
rho-related GTP-binding protein RhoB-like isoform X1
rho-related GTP-binding protein RhoB-like 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
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.
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00188
COORDINATES: nucleotide motif:Rfam:12.0:RF00598
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 55% 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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 1, regulatory subunit 8a, transcript variant X2
protein phosphatase 1, regulatory subunit 8a, transcript variant X1
protein phosphatase 1, regulatory subunit 8a isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00553
protein phosphatase 1, regulatory subunit 8a isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
tRNA selenocysteine 1-associated protein 1, transcript variant X1
tRNA selenocysteine 1-associated protein 1, transcript variant X2
tRNA selenocysteine 1-associated protein 1, transcript variant X3
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 16 samples with support for all annotated introns
tRNA selenocysteine 1-associated protein 1 isoform X1
tRNA selenocysteine 1-associated protein 1 isoform X2
tRNA selenocysteine 1-associated protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 long SRA reads, 49 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized LOC125486234, transcript variant X2
uncharacterized LOC125486234, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane protein 200A-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 7 samples with support for all annotated introns
transmembrane protein 200A-like, 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 5 samples with support for all annotated introns
transmembrane protein 200A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
transmembrane protein 200A-like, 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 2 samples with support for all annotated introns
serine/arginine-rich splicing factor 4-like, transcript variant X1
serine/arginine-rich splicing factor 4-like, transcript variant X2
serine/arginine-rich splicing factor 4-like isoform X1
serine/arginine-rich splicing factor 4-like isoform X2
transmembrane protein 244-like, transcript variant X1
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 9 samples with support for all annotated introns
transmembrane protein 244-like, transcript variant X2
transmembrane protein 244-like isoform X1
transmembrane protein 244-like isoform X2
mitochondrial trans-2-enoyl-CoA reductase, transcript variant X3
mitochondrial trans-2-enoyl-CoA reductase, transcript variant X1
enoyl-[acyl-carrier-protein] reductase, mitochondrial isoform X3
enoyl-[acyl-carrier-protein] reductase, mitochondrial isoform X1
mitochondrial trans-2-enoyl-CoA reductase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
enoyl-[acyl-carrier-protein] reductase, mitochondrial isoform X2
receptor-type tyrosine-protein phosphatase U-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 25% 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 long SRA reads, 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
acid sphingomyelinase-like phosphodiesterase 3b, transcript variant X1
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
acid sphingomyelinase-like phosphodiesterase 3b isoform X2
acid sphingomyelinase-like phosphodiesterase 3b isoform X1
replication protein A 32 kDa subunit-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 20 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, 16 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine/threonine-protein kinase Sgk1-like, transcript variant X2
serine/threonine-protein kinase Sgk1-like, transcript variant X1
serine/threonine-protein kinase Sgk1-like isoform X2
serine/threonine-protein kinase Sgk1-like isoform X1
nuclear receptor coactivator 7, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear receptor coactivator 7, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear receptor coactivator 7, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
nuclear receptor coactivator 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear receptor coactivator 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nuclear receptor coactivator 7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear receptor coactivator 7, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nuclear receptor coactivator 7, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
nuclear receptor coactivator 7, transcript variant X2
nuclear receptor coactivator 7, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
nuclear receptor coactivator 7, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear receptor coactivator 7, transcript variant X6
nuclear receptor coactivator 7 isoform X1
nuclear receptor coactivator 7 isoform X2
nuclear receptor coactivator 7 isoform X4
nuclear receptor coactivator 7 isoform X3
zinc finger protein 593, transcript variant X3
zinc finger protein 593, transcript variant X1
zinc finger protein 593, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
dynein light chain Tctex-type 1, transcript variant X2
dynein light chain Tctex-type 1, transcript variant X1
dynein light chain Tctex-type 1 isoform X2
dynein light chain Tctex-type 1 isoform X1
zinc metallopeptidase, STE24 homolog, transcript variant X1
zinc metallopeptidase, STE24 homolog, transcript variant X4
zinc metallopeptidase, STE24 homolog, transcript variant X3
zinc metallopeptidase, STE24 homolog, transcript variant X2
CAAX prenyl protease 1 homolog isoform X1
CAAX prenyl protease 1 homolog isoform X2
transmembrane protein 30B, transcript variant X3
transmembrane protein 30B, transcript variant X1
transmembrane protein 30B, transcript variant X2
cell cycle control protein 50B isoform X2
cell cycle control protein 50B isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
5-hydroxytryptamine (serotonin) receptor 1D, G protein-coupled
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
heterogeneous nuclear ribonucleoprotein R
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00147
small nucleolar RNA Z195/SNORD33/SNORD32 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00133
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ATP synthase inhibitory factor subunit 1
DnaJ (Hsp40) homolog, subfamily C, member 8
platelet-activating factor receptor, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
platelet-activating factor receptor, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
platelet-activating factor receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
platelet-activating factor receptor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
platelet-activating factor receptor, transcript variant X2
platelet-activating factor receptor, transcript variant X4
uncharacterized LOC125486283, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125486283, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
QKI, KH domain containing, RNA binding a, transcript variant X9
QKI, KH domain containing, RNA binding a, transcript variant X5
QKI, KH domain containing, RNA binding a, transcript variant X3
QKI, KH domain containing, RNA binding a, transcript variant X4
QKI, KH domain containing, RNA binding a, transcript variant X1
QKI, KH domain containing, RNA binding a, transcript variant X2
QKI, KH domain containing, RNA binding a, transcript variant X7
QKI, KH domain containing, RNA binding a, transcript variant X6
QKI, KH domain containing, RNA binding a, transcript variant X10
QKI, KH domain containing, RNA binding a, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
U5 small nuclear ribonucleoprotein 40 kDa protein
major facilitator superfamily domain containing 2ab
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
sodium-dependent lysophosphatidylcholine symporter 1-B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
CD276 antigen-like, transcript variant X1
CD276 antigen-like, transcript variant X3
CD276 antigen-like, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00431
peptidylprolyl isomerase E (cyclophilin E)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
protein disulfide isomerase family A, member 6
mannosyl-oligosaccharide 1,2-alpha-mannosidase IA-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 29 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
synaptotagmin-like protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
synaptotagmin-like protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
WD and tetratricopeptide repeats protein 1-like
V-type proton ATPase subunit d 2-like, transcript variant X1
V-type proton ATPase subunit d 2-like, transcript variant X2
V-type proton ATPase subunit d 2-like isoform X1
V-type proton ATPase subunit d 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
keratinocyte differentiation factor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
keratinocyte differentiation factor 1, 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 4 samples with support for all annotated introns
keratinocyte differentiation factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
keratinocyte differentiation factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
keratinocyte differentiation factor 1 isoform X1
keratinocyte differentiation factor 1 isoform X2
WD and tetratricopeptide repeats protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
dehydrodolichyl diphosphate synthase complex subunit DHDDS
GPN-loop GTPase 2, transcript variant X1
GPN-loop GTPase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
nuclear receptor subfamily 0, group B, member 2a
nuclear receptor subfamily 0 group B member 2
AT-rich interactive domain-containing protein 1A, transcript variant X1
AT-rich interactive domain-containing protein 1A, transcript variant X2
AT-rich interactive domain-containing protein 1A, transcript variant X3
AT-rich interactive domain-containing protein 1A, transcript variant X4
AT-rich interactive domain-containing protein 1A isoform X1
AT-rich interactive domain-containing protein 1A isoform X2
AT-rich interactive domain-containing protein 1A isoform X3
AT-rich interactive domain-containing protein 1A isoform X4
phosphatidylinositol glycan anchor biosynthesis, class V, transcript variant X1
phosphatidylinositol glycan anchor biosynthesis, class V, transcript variant X2
phosphatidylinositol glycan anchor biosynthesis, class V, transcript variant X3
palmitoyltransferase ZDHHC18-A isoform X1
palmitoyltransferase ZDHHC18-A isoform X2
zinc finger DHHC-type palmitoyltransferase 18a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 18a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 18a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 18a, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 26 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 18a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
palmitoyltransferase ZDHHC18a isoform X1
palmitoyltransferase ZDHHC18a isoform X2
palmitoyltransferase ZDHHC18a isoform X3
palmitoyltransferase ZDHHC18a isoform X4
uncharacterized protein C1orf232, transcript variant X1
uncharacterized protein C1orf232, 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 13 samples with support for all annotated introns
cation channel sperm-associated protein 4, transcript variant X3
cation channel sperm-associated protein 4, transcript variant X2
cation channel sperm-associated protein 4, transcript variant X5
cation channel sperm-associated protein 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cation channel sperm-associated protein 4, transcript variant X1
cation channel sperm-associated protein 4 isoform X3
cation channel sperm-associated protein 4 isoform X2
cation channel sperm-associated protein 4 isoform X5
cation channel sperm-associated protein 4 isoform X4
cation channel sperm-associated protein 4 isoform X1
connector enhancer of kinase suppressor of Ras 1, transcript variant X2
connector enhancer of kinase suppressor of Ras 1, transcript variant X1
connector enhancer of kinase suppressor of ras 1 isoform X2
connector enhancer of kinase suppressor of ras 1 isoform X1
ribosomal protein S6 kinase 2 alpha-like, transcript variant X1
ribosomal protein S6 kinase 2 alpha-like, transcript variant X2
ribosomal protein S6 kinase 2 alpha-like isoform X1
ribosomal protein S6 kinase 2 alpha-like isoform X2
ribosomal protein S6 kinase 2 alpha-like, transcript variant X6
ribosomal protein S6 kinase 2 alpha-like, transcript variant X3
ribosomal protein S6 kinase 2 alpha-like isoform X3
ribosomal protein S6 kinase 2 alpha-like, transcript variant X4
ribosomal protein S6 kinase 2 alpha-like, transcript variant X5
ribosomal protein S6 kinase 2 alpha-like isoform X4
centrosomal protein 85, transcript variant X3
centrosomal protein 85, transcript variant X2
centrosomal protein 85, transcript variant X1
centrosomal protein 85, transcript variant X4
centrosomal protein of 85 kDa isoform X1
centrosomal protein of 85 kDa isoform X2
SH3 domain-binding glutamic acid-rich-like protein 3
taste receptor type 1 member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
taste receptor type 1 member 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 25 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins
beta/gamma crystallin domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
YTH N(6)-methyladenosine RNA binding protein 2
glucocorticoid modulatory element-binding protein 1, transcript variant X1
glucocorticoid modulatory element-binding protein 1, transcript variant X2
glucocorticoid modulatory element-binding protein 1 isoform X1
glucocorticoid modulatory element-binding protein 1 isoform X2
dnaJ homolog subfamily C member 5-like, transcript variant X3
dnaJ homolog subfamily C member 5-like, transcript variant X4
dnaJ homolog subfamily C member 5-like, transcript variant X1
dnaJ homolog subfamily C member 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Mediator of RNA polymerase II transcription subunit 30-like, transcript variant X1
Mediator of RNA polymerase II transcription subunit 30-like, transcript variant X2
mediator of RNA polymerase II transcription subunit 30-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
platelet-activating factor acetylhydrolase 2, cytoplasmic, transcript variant X2
platelet-activating factor acetylhydrolase 2, cytoplasmic, transcript variant X1
platelet-activating factor acetylhydrolase 2, cytoplasmic, transcript variant X12
platelet-activating factor acetylhydrolase 2, cytoplasmic, transcript variant X4
platelet-activating factor acetylhydrolase 2, cytoplasmic, transcript variant X6
platelet-activating factor acetylhydrolase 2, cytoplasmic, transcript variant X10
platelet-activating factor acetylhydrolase 2, cytoplasmic, transcript variant X5
platelet-activating factor acetylhydrolase 2, cytoplasmic, transcript variant X8
platelet-activating factor acetylhydrolase 2, cytoplasmic, transcript variant X3
platelet-activating factor acetylhydrolase 2, cytoplasmic, transcript variant X11
platelet-activating factor acetylhydrolase 2, cytoplasmic, transcript variant X9
platelet-activating factor acetylhydrolase 2, cytoplasmic, transcript variant X7
platelet-activating factor acetylhydrolase 2, cytoplasmic isoform X1
platelet-activating factor acetylhydrolase 2, cytoplasmic isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
progestin and adipoQ receptor family member VII, b, transcript variant X1
progestin and adipoQ receptor family member VII, b, transcript variant X2
uncharacterized LOC125486307, transcript variant X9
uncharacterized LOC125486307, transcript variant X6
uncharacterized LOC125486307, transcript variant X2
uncharacterized LOC125486307, transcript variant X1
uncharacterized LOC125486307, transcript variant X5
uncharacterized LOC125486307, transcript variant X8
uncharacterized LOC125486307, transcript variant X7
uncharacterized LOC125486307, transcript variant X3
uncharacterized protein LOC125486307 isoform X1
uncharacterized LOC125486307, transcript variant X4
uncharacterized protein LOC125486307 isoform X2
uncharacterized protein LOC125486307 isoform X3
serine/threonine-protein kinase PDIK1L-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
E2F transcription factor 2, transcript variant X1
E2F transcription factor 2, 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
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2-like, transcript variant X2
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2-like, transcript variant X1
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2-like isoform X1
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 2-like isoform 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 11 samples with support for all annotated introns
transcription elongation factor A (SII), 3, transcript variant X3
transcription elongation factor A (SII), 3, transcript variant X1
transcription elongation factor A (SII), 3, transcript variant X4
transcription elongation factor A (SII), 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transcription elongation factor A (SII), 3, transcript variant X5
transcription elongation factor A (SII), 3, transcript variant X6
transcription elongation factor A protein 3 isoform X1
transcription elongation factor A protein 3 isoform X2
regulator of G-protein signaling 17-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
regulator of G-protein signaling 17-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, 36 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
regulator of G-protein signaling 17-like isoform X2
regulator of G-protein signaling 17-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins
regulator of chromosome condensation 1, transcript variant X2
regulator of chromosome condensation 1, transcript variant X1
regulator of chromosome condensation 1, transcript variant X3
regulator of chromosome condensation 1, transcript variant X6
regulator of chromosome condensation 1, transcript variant X5
regulator of chromosome condensation 1, transcript variant X4
regulator of chromosome condensation 1, transcript variant X7
regulator of chromosome condensation isoform X2
regulator of chromosome condensation isoform X1
regulator of chromosome condensation isoform X3
regulator of chromosome condensation isoform X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00045
phosphatase and actin regulator 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphatase and actin regulator 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
phosphatase and actin regulator 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
phosphatase and actin regulator 4, transcript variant X1
phosphatase and actin regulator 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phosphatase and actin regulator 4 isoform X4
phosphatase and actin regulator 4 isoform X5
phosphatase and actin regulator 4 isoform X3
phosphatase and actin regulator 4 isoform X1
phosphatase and actin regulator 4 isoform 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 10 samples with support for all annotated introns
transcription factor HIVEP3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcription factor HIVEP3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transcription factor HIVEP3, transcript variant X5
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
transcription factor HIVEP3, 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 8 samples with support for all annotated introns
transcription factor HIVEP3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transcription factor HIVEP3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription factor HIVEP3, transcript variant X7
fatty acid-binding protein, brain-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
fatty acid-binding protein, brain-like isoform X3
fatty acid-binding protein, brain-like, 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 2 samples with support for all annotated introns
fatty acid-binding protein, brain-like isoform X2
fatty acid-binding protein, brain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
fatty acid-binding protein, brain-like isoform X1
amine sulfotransferase-like, transcript variant X1
amine sulfotransferase-like, transcript variant X4
amine sulfotransferase-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 5 samples with support for all annotated introns
amine sulfotransferase-like, transcript variant X2
trafficking protein particle complex subunit 3, transcript variant X5
trafficking protein particle complex subunit 3, transcript variant X1
trafficking protein particle complex subunit 3, transcript variant X2
trafficking protein particle complex subunit 3, transcript variant X3
trafficking protein particle complex subunit 3, transcript variant X4
trafficking protein particle complex subunit 3 isoform X1
trafficking protein particle complex subunit 3 isoform X3
trafficking protein particle complex subunit 3 isoform X2
fibronectin type III domain-containing protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
S100P-binding protein-like, transcript variant X2
S100P-binding protein-like, transcript variant X5
S100P-binding protein-like, transcript variant X3
S100P-binding protein-like, transcript variant X1
S100P-binding protein-like, transcript variant X4
uncharacterized protein LOC125486289 isoform X1
low density lipoprotein receptor adaptor protein 1b, transcript variant X1
low density lipoprotein receptor adaptor protein 1b, transcript variant X2
low density lipoprotein receptor adapter protein 1b isoform X1
low density lipoprotein receptor adapter protein 1b isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, 2 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
runt-related transcription factor 3-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
chloride intracellular channel protein 4-like
non-compact myelin associated protein, transcript variant X2
non-compact myelin associated protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
noncompact myelin-associated protein isoform X1
noncompact myelin-associated protein isoform X2
serine/arginine repetitive matrix 1, transcript variant X1
serine/arginine repetitive matrix 1, transcript variant X3
serine/arginine repetitive matrix 1, transcript variant X2
serine/arginine repetitive matrix 1, transcript variant X4
serine/arginine repetitive matrix 1, transcript variant X5
serine/arginine repetitive matrix protein 1 isoform X1
serine/arginine repetitive matrix protein 1 isoform X3
serine/arginine repetitive matrix protein 1 isoform X2
serine/arginine repetitive matrix protein 1 isoform X4
serine/arginine repetitive matrix protein 1 isoform X5
serine/arginine repetitive matrix 1, transcript variant X6
serine/arginine repetitive matrix 1, transcript variant X7
serine/arginine repetitive matrix 1, transcript variant X8
serine/arginine repetitive matrix protein 1 isoform X6
serine/arginine repetitive matrix protein 1 isoform X7
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 15 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 94% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
hippocalcin-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 77 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
hippocalcin-like protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
hippocalcin-like protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
hippocalcin-like protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
ribonucleoside-diphosphate reductase subunit M2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
UPF0500 protein C1orf216 homolog, transcript variant X1
UPF0500 protein C1orf216 homolog, transcript variant X2
UPF0500 protein C1orf216 homolog, transcript variant X3
UPF0500 protein C1orf216 homolog isoform X1
UPF0500 protein C1orf216 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
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
protein argonaute-1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein argonaute-1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein argonaute-1, transcript variant X3
uncharacterized LOC125486225, transcript variant X2
uncharacterized LOC125486225, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125486225, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125486225, transcript variant X5
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 1 sample with support for all annotated introns
uncharacterized LOC125486225, transcript variant X1
argonaute RISC component 4, transcript variant X2
argonaute RISC component 4, transcript variant X1
argonaute RISC catalytic component 3b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
argonaute RISC catalytic component 3b, transcript variant X2
argonaute RISC catalytic component 3b, transcript variant X4
argonaute RISC catalytic component 3b, transcript variant X1
tektin 2 (testicular), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
tektin 2 (testicular), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RNA-binding protein 38-like, transcript variant X2
RNA-binding protein 38-like, transcript variant X3
RNA-binding protein 38-like, transcript variant X1
RNA-binding protein 38-like, transcript variant X5
RNA-binding protein 38-like, transcript variant X4
CAP, adenylate cyclase-associated protein 1 (yeast), transcript variant X1
CAP, adenylate cyclase-associated protein 1 (yeast), transcript variant X2
CAP, adenylate cyclase-associated protein 1 (yeast), transcript variant X4
CAP, adenylate cyclase-associated protein 1 (yeast), transcript variant X3
CAP, adenylate cyclase-associated protein 1 (yeast), transcript variant X5
palmitoyl-protein thioesterase 1 (ceroid-lipofuscinosis, neuronal 1, infantile), transcript variant X1
palmitoyl-protein thioesterase 1 (ceroid-lipofuscinosis, neuronal 1, infantile), transcript variant X3
palmitoyl-protein thioesterase 1 (ceroid-lipofuscinosis, neuronal 1, infantile), transcript variant X2
palmitoyl-protein thioesterase 1 (ceroid-lipofuscinosis, neuronal 1, infantile), transcript variant X4
palmitoyl-protein thioesterase 1 isoform X1
palmitoyl-protein thioesterase 1 isoform X3
palmitoyl-protein thioesterase 1 isoform X2
palmitoyl-protein thioesterase 1 isoform X4
PITH (C-terminal proteasome-interacting domain of thioredoxin-like) domain containing 1
hydroxymethylglutaryl-CoA lyase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 73% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
elongation factor 1-alpha 1-like, transcript variant X1
elongation factor 1-alpha 1-like, transcript variant X2
ribosomal protein L11, transcript variant X2
ribosomal protein L11, transcript variant X1
microtubule-actin cross-linking factor 1, isoforms 1/2/3/4/5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NADH:ubiquinone oxidoreductase subunit S5, transcript variant X1
NADH:ubiquinone oxidoreductase subunit S5, transcript variant X2
NADH:ubiquinone oxidoreductase subunit S5, transcript variant X3
NADH dehydrogenase [ubiquinone] iron-sulfur protein 5
microtubule actin crosslinking factor 1a
microtubule-actin cross-linking factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
hydroxymethylglutaryl-CoA lyase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
hairy/enhancer-of-split related with YRPW motif protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 8B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 8B, transcript variant X1
zinc finger and BTB domain-containing protein 8B, transcript variant X2
zinc finger and BTB domain-containing protein 8B, transcript variant X4
zinc finger and BTB domain-containing protein 8B, transcript variant X5
zinc finger and BTB domain-containing protein 8B
uncharacterized LOC125486282, transcript variant X1
uncharacterized LOC125486282, transcript variant X2
zinc finger and BTB domain-containing protein 8A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 8A-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 8A-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger and BTB domain-containing protein 8A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 8A-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 8A-like, transcript variant X3
zinc finger and BTB domain-containing protein 8A-like isoform X1
zinc finger and BTB domain-containing protein 8A-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
rhomboid, veinlet-like 2 (Drosophila), transcript variant X2
rhomboid, veinlet-like 2 (Drosophila), transcript variant X1
rhomboid, veinlet-like 2 (Drosophila), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 81% 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, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
POU domain, class 3, transcription factor 1
UTP11 small subunit processome component
probable U3 small nucleolar RNA-associated protein 11
four and a half LIM domains 3a, transcript variant X1
four and a half LIM domains 3a, transcript variant X2
four and a half LIM domains 3a, transcript variant X3
uncharacterized LOC125486242, transcript variant X1
uncharacterized LOC125486242, transcript variant X2
interferon alpha-inducible protein 6-like, transcript variant X2
interferon alpha-inducible protein 6-like, transcript variant X1
interferon alpha-inducible protein 6-like, transcript variant X3
interferon alpha-inducible protein 6-like
interferon alpha-inducible protein 27-like protein 2A
interferon alpha-inducible protein 27, mitochondrial-like, transcript variant X1
interferon alpha-inducible protein 27, mitochondrial-like, transcript variant X2
interferon alpha-inducible protein 27-like protein 2A isoform X1
interferon alpha-inducible protein 27, mitochondrial-like isoform X2
interferon alpha-inducible protein 27-like protein 2, transcript variant X1
interferon alpha-inducible protein 27-like protein 2, transcript variant X2
interferon alpha-inducible protein 27-like protein 2 isoform X1
interferon alpha-inducible protein 27-like protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
platelet-activating factor receptor-like, transcript variant X2
platelet-activating factor receptor-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 3 samples with support for all annotated introns
platelet-activating factor receptor-like
splicing factor, proline- and glutamine-rich-like, transcript variant X2
splicing factor, proline- and glutamine-rich-like, transcript variant X1
splicing factor, proline- and glutamine-rich-like isoform X2
splicing factor, proline- and glutamine-rich-like isoform X1
uncharacterized LOC125486293, transcript variant X2
uncharacterized LOC125486293, transcript variant X1
uncharacterized protein LOC125486293 isoform X1
uncharacterized protein LOC125486293 isoform X2
zinc finger MYM-type protein 4-like, transcript variant X1
zinc finger MYM-type protein 4-like, transcript variant X3
zinc finger MYM-type protein 4-like, transcript variant X2
zinc finger MYM-type protein 4-like, transcript variant X4
zinc finger MYM-type protein 4-like isoform X1
zinc finger MYM-type protein 4-like isoform X3
zinc finger MYM-type protein 4-like isoform X2
zinc finger MYM-type protein 4-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 108 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
gap junction beta-3 protein-like, transcript variant X1
gap junction beta-3 protein-like, transcript variant X3
gap junction beta-3 protein-like, transcript variant X2
gap junction beta-4 protein-like, transcript variant X1
gap junction beta-4 protein-like, transcript variant X2
gap junction beta-4 protein-like isoform X1
gap junction beta-4 protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
CUB and sushi domain-containing protein 1
transfer RNA lysine (anticodon UUU); 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: 50 long SRA reads, 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide binding protein-like 2 (nucleolar), transcript variant X2
guanine nucleotide binding protein-like 2 (nucleolar), transcript variant X1
nucleolar GTP-binding protein 2 isoform X1
nucleolar GTP-binding protein 2 isoform X2
dynein, axonemal, light intermediate chain 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 17 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
axonemal dynein light intermediate polypeptide 1
MYST/Esa1-associated factor 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
MYST/Esa1-associated factor 6, transcript variant X1
chromatin modification-related protein MEAF6 isoform X1
chromatin modification-related protein MEAF6 isoform X2
CAP-Gly domain-containing linker protein 4, transcript variant X2
CAP-Gly domain-containing linker protein 4, transcript variant X1
uncharacterized protein LOC109935746 isoform X2
CAP-Gly domain-containing linker protein 4 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
glutamate ionotropic receptor kainate type subunit 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, kainate 3
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
c19h1orf109 homolog (H. sapiens), transcript variant X2
c19h1orf109 homolog (H. sapiens), transcript variant X1
uncharacterized protein C1orf109 homolog
cell division cycle associated 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
cell division cycle associated 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 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: 16 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
glycoprotein endo-alpha-1,2-mannosidase-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
yrdC N(6)-threonylcarbamoyltransferase domain containing
yrdC domain-containing protein, mitochondrial
metal regulatory transcription factor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, and 58% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
inositol polyphosphate-5-phosphatase B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
inositol polyphosphate-5-phosphatase B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
type II inositol 1,4,5-trisphosphate 5-phosphatase isoform X1
type II inositol 1,4,5-trisphosphate 5-phosphatase isoform X2
protein eva-1 homolog B-like, 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 9 samples with support for all annotated introns
protein eva-1 homolog B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein eva-1 homolog B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 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: 1 long SRA read, 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: CD2-associated protein-like
thyroid hormone receptor-associated protein 3, transcript variant X5
thyroid hormone receptor-associated protein 3, transcript variant X2
thyroid hormone receptor-associated protein 3, transcript variant X4
thyroid hormone receptor-associated protein 3, transcript variant X1
thyroid hormone receptor-associated protein 3, transcript variant X3
thyroid hormone receptor-associated protein 3 isoform X5
thyroid hormone receptor-associated protein 3 isoform X2
thyroid hormone receptor-associated protein 3 isoform X4
thyroid hormone receptor-associated protein 3 isoform X1
thyroid hormone receptor-associated protein 3 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
mitogen-activated protein kinase kinase kinase 5-like
organic solute carrier partner 1b, transcript variant X1
organic solute carrier partner 1b, transcript variant X2
organic solute carrier partner 1b, transcript variant X3
U7 snRNA-associated Sm-like protein LSm10, transcript variant X2
U7 snRNA-associated Sm-like protein LSm10, transcript variant X4
U7 snRNA-associated Sm-like protein LSm10, transcript variant X1
U7 snRNA-associated Sm-like protein LSm10, transcript variant X3
U7 snRNA-associated Sm-like protein LSm10
protein tyrosine phosphatase type IVA 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
protein tyrosine phosphatase type IVA 2, transcript variant X1
protein tyrosine phosphatase type IVA 2, transcript variant X3
protein tyrosine phosphatase type IVA 2, transcript variant X2
protein tyrosine phosphatase type IVA 2 isoform X1
protein tyrosine phosphatase type IVA 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 62% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125486309, transcript variant X2
uncharacterized LOC125486309, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% coverage of the annotated genomic feature by RNAseq alignments
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 3 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: 92% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
regulating synaptic membrane exocytosis protein 3
nuclear transcription factor Y, gamma, transcript variant X2
nuclear transcription factor Y, gamma, transcript variant X1
nuclear transcription factor Y, gamma, transcript variant X5
nuclear transcription factor Y, gamma, transcript variant X6
nuclear transcription factor Y, gamma, transcript variant X7
nuclear transcription factor Y, gamma, transcript variant X3
nuclear transcription factor Y, gamma, transcript variant X4
nuclear transcription factor Y subunit gamma isoform X1
nuclear transcription factor Y subunit gamma isoform X2
nuclear transcription factor Y subunit gamma isoform X3
nuclear transcription factor Y subunit gamma isoform X4
potassium voltage-gated channel subfamily KQT member 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
tubulointerstitial nephritis antigen-like 1, transcript variant X2
tubulointerstitial nephritis antigen-like 1, transcript variant X1
tubulointerstitial nephritis antigen-like isoform X1
tubulointerstitial nephritis antigen-like isoform X2
mitochondrial ribosomal protein S15, transcript variant X1
mitochondrial ribosomal protein S15, transcript variant X3
mitochondrial ribosomal protein S15, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
28S ribosomal protein S15, mitochondrial isoform X1
28S ribosomal protein S15, mitochondrial isoform X3
28S ribosomal protein S15, mitochondrial isoform X2
uncharacterized LOC125486277, transcript variant X3
uncharacterized LOC125486277, transcript variant X1
uncharacterized LOC125486277, transcript variant X2
KH domain-containing, RNA-binding, signal transduction-associated protein 1-like, transcript variant X2
KH domain-containing, RNA-binding, signal transduction-associated protein 1-like, transcript variant X4
KH domain-containing, RNA-binding, signal transduction-associated protein 1-like, transcript variant X3
KH domain-containing, RNA-binding, signal transduction-associated protein 1-like, transcript variant X1
KH domain-containing, RNA-binding, signal transduction-associated protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily S member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins
NIPA like domain containing 3, transcript variant X4
NIPA like domain containing 3, transcript variant X1
NIPA like domain containing 3, transcript variant X2
NIPA like domain containing 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 23 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
granulocyte colony-stimulating factor receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments