Rhincodon typus isolate 14 chromosome 25, 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\nCM038822.1.\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.
striatin interacting protein 1, transcript variant X8
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 8 samples with support for all annotated introns
striatin interacting protein 1, transcript variant X6
COORDINATES: polyA evidence [ECO:0006239]
striatin interacting protein 1, transcript variant X3
striatin interacting protein 1, transcript variant X1
striatin interacting protein 1, transcript variant X2
striatin interacting protein 1, transcript variant X4
striatin interacting protein 1, transcript variant X5
striatin interacting protein 1, transcript variant X7
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 14 samples with support for all annotated introns
striatin-interacting protein 1 homolog isoform X1
striatin-interacting protein 1 homolog isoform X2
potassium voltage-gated channel subfamily C member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
late endosomal/lysosomal adaptor, MAPK and MTOR activator 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
myoD family inhibitor domain-containing protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myoD family inhibitor domain-containing protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
myoD family inhibitor domain-containing protein-like
transcription factor EB, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcription factor EB, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
SLIT-ROBO Rho GTPase activating protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SLIT-ROBO Rho GTPase activating protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SLIT-ROBO Rho GTPase-activating protein 2 isoform X1
SLIT-ROBO Rho GTPase-activating protein 2 isoform X2
serine/threonine-protein kinase TBK1-like, transcript variant X1
serine/threonine-protein kinase TBK1-like, transcript variant X2
serine/threonine-protein kinase TBK1-like isoform X2
serine/threonine-protein kinase TBK1-like isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ataxin-7-like protein 1
probable transmembrane reductase CYB561D1, transcript variant X1
probable transmembrane reductase CYB561D1 isoform X1
probable transmembrane reductase CYB561D1, transcript variant X3
probable transmembrane reductase CYB561D1, transcript variant X2
probable transmembrane reductase CYB561D1 isoform X2
probable transmembrane reductase CYB561D1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
tyrosine-protein phosphatase non-receptor type 22-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 19 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
membrane associated guanylate kinase, WW and PDZ domain containing 3a, transcript variant X3
membrane associated guanylate kinase, WW and PDZ domain containing 3a, transcript variant X2
membrane associated guanylate kinase, WW and PDZ domain containing 3a, transcript variant X1
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3a isoform X3
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3a isoform X2
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3a isoform X1
membrane associated guanylate kinase, WW and PDZ domain containing 3a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3a isoform X5
membrane associated guanylate kinase, WW and PDZ domain containing 3a, transcript variant X4
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 7 samples with support for all annotated introns
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 3a isoform X4
leucine-rich repeats and immunoglobulin-like domains 2, transcript variant X1
leucine-rich repeats and immunoglobulin-like domains 2, transcript variant X2
leucine-rich repeats and immunoglobulin-like domains protein 2 isoform X2
leucine-rich repeats and immunoglobulin-like domains protein 2 isoform X1
monocarboxylate transporter 1-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 2 samples with support for all annotated introns
monocarboxylate transporter 1-like, transcript variant X1
monocarboxylate transporter 1-like, transcript variant X2
monocarboxylate transporter 1-like, transcript variant X3
monocarboxylate transporter 1-like, transcript variant X7
monocarboxylate transporter 1-like, transcript variant X5
monocarboxylate transporter 1-like, transcript variant X6
monocarboxylate transporter 1-like, transcript variant X9
monocarboxylate transporter 1-like, transcript variant X8
TAFA chemokine like family member 3b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
TAFA chemokine like family member 3b, 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 2 samples with support for all annotated introns
TAFA chemokine like family member 3b, transcript variant X2
chemokine-like protein TAFA-2 isoform X1
chemokine-like protein TAFA-2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 long SRA reads, 5 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
capping actin protein of muscle Z-line subunit alpha 1b, transcript variant X1
capping actin protein of muscle Z-line subunit alpha 1b, transcript variant X2
F-actin-capping protein subunit alpha-1b isoform X1
F-actin-capping protein subunit alpha-1b isoform X2
suppressor of tumorigenicity 7 protein homolog
wingless-type MMTV integration site family, member 2Bb
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
DEAD (Asp-Glu-Ala-Asp) box polypeptide 20
probable ATP-dependent RNA helicase DDX20
potassium voltage-gated channel, Shal-related subfamily, member 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel, Shal-related subfamily, member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel, Shal-related subfamily, member 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily D member 3 isoform X3
potassium voltage-gated channel subfamily D member 3 isoform X2
potassium voltage-gated channel subfamily D member 3 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
ETS domain-containing protein Elk-4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
major facilitator superfamily domain containing 4Aa
major facilitator superfamily domain-containing protein 4A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
lamina-associated polypeptide 2, isoforms beta/delta/epsilon/gamma-like, transcript variant X3
lamina-associated polypeptide 2, isoforms beta/delta/epsilon/gamma-like, transcript variant X4
lamina-associated polypeptide 2, isoforms beta/delta/epsilon/gamma-like, transcript variant X1
lamina-associated polypeptide 2, isoforms beta/delta/epsilon/gamma-like, transcript variant X2
lamina-associated polypeptide 2, isoforms beta/gamma-like isoform X4
lamina-associated polypeptide 2, isoforms beta/gamma-like isoform X3
lamina-associated polypeptide 2, isoforms beta/delta/epsilon/gamma-like isoform X2
lamina-associated polypeptide 2, isoforms beta/delta/epsilon/gamma-like isoform X1
kelch domain containing 8A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kelch domain containing 8A, transcript variant X1
kelch domain containing 8A, transcript variant X5
kelch domain containing 8A, transcript variant X3
kelch domain containing 8A, transcript variant X6
kelch domain containing 8A, transcript variant X4
kelch domain-containing protein 8A isoform X1
kelch domain-containing protein 8A isoform X4
kelch domain-containing protein 8A isoform X2
kelch domain-containing protein 8A isoform X5
kelch domain-containing protein 8A isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 13 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
transmembrane and coiled-coil domain family 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, 31 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane and coiled-coil domain family 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transmembrane and coiled-coil domain family 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane and coiled-coil domain family 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane and coiled-coil domain family 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 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
transmembrane and coiled-coil domains protein 2 isoform X2
transmembrane and coiled-coil domains protein 2 isoform X1
transmembrane and coiled-coil domains protein 2 isoform X3
transmembrane and coiled-coil domains protein 2 isoform X4
transmembrane and coiled-coil domains protein 2 isoform X5
dual serine/threonine and tyrosine protein kinase
retinoblastoma binding protein 5, transcript variant X3
retinoblastoma-binding protein 5 isoform X2
retinoblastoma binding protein 5, transcript variant X1
retinoblastoma binding protein 5, transcript variant X2
retinoblastoma-binding protein 5 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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: 27 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat neuronal protein 2-like
nuclear transcription factor Y subunit alpha, transcript variant X4
nuclear transcription factor Y subunit alpha, transcript variant X5
nuclear transcription factor Y subunit alpha, transcript variant X6
nuclear transcription factor Y subunit alpha, transcript variant X1
nuclear transcription factor Y subunit alpha, transcript variant X2
nuclear transcription factor Y subunit alpha, transcript variant X3
nuclear transcription factor Y subunit alpha isoform X1
nuclear transcription factor Y subunit alpha isoform X3
nuclear transcription factor Y subunit alpha isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
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
epidermal growth factor receptor kinase substrate 8-like protein 3b isoform X2
epidermal growth factor receptor kinase substrate 8-like protein 3b isoform X1
phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 beta
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit beta
protein phosphatase 1 regulatory subunit 15B
pleckstrin homology domain-containing family A member 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
SRY-box transcription factor 13, transcript variant X2
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 1 sample with support for all annotated introns
SRY-box transcription factor 13, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SRY-box transcription factor 13, transcript variant X4
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 3 samples with support for all annotated introns
SRY-box transcription factor 13, transcript variant X1
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 2 samples with support for all annotated introns
small nuclear ribonucleoprotein polypeptide E
zinc finger CCCH-type containing 11A, transcript variant X3
zinc finger CCCH-type containing 11A, transcript variant X2
zinc finger CCCH-type containing 11A, transcript variant X1
zinc finger CCCH-type containing 11A, transcript variant X6
zinc finger CCCH-type containing 11A, transcript variant X4
zinc finger CCCH-type containing 11A, transcript variant X5
zinc finger CCCH domain-containing protein 11A isoform X4
zinc finger CCCH domain-containing protein 11A isoform X2
zinc finger CCCH domain-containing protein 11A isoform X3
zinc finger CCCH domain-containing protein 11A isoform X1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC109922628, transcript variant X1
uncharacterized LOC109922628, transcript variant X3
uncharacterized LOC109922628, transcript variant X2
uncharacterized protein LOC109922628 isoform X1
uncharacterized protein LOC109922628 isoform X3
uncharacterized protein LOC109922628 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
EF-hand and coiled-coil domain-containing protein 1-like
guanine nucleotide-binding protein G(t) subunit alpha-2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 143 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
guanine nucleotide-binding protein G(i) subunit alpha-3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 93% 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: 36 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
CMRF35-like molecule 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CMRF35-like molecule 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
S-adenosylhomocysteine hydrolase-like protein 1, transcript variant X1
S-adenosylhomocysteine hydrolase-like protein 1, transcript variant X2
S-adenosylhomocysteine hydrolase-like protein 1 isoform X1
S-adenosylhomocysteine hydrolase-like protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 47 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: 2 long SRA reads, 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Krueppel-like factor 15, transcript variant X1
Krueppel-like factor 15, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins
solute carrier family 45 member 3, transcript variant X1
solute carrier family 45 member 3, transcript variant X2
solute carrier family 45 member 3, transcript variant X3
peptidase M20 domain containing 1, tandem duplicate 1
N-fatty-acyl-amino acid synthase/hydrolase PM20D1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor receptor substrate 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fibroblast growth factor receptor substrate 2-like, transcript variant X2
fibroblast growth factor receptor substrate 2-like, transcript variant X3
fibroblast growth factor receptor substrate 2-like, transcript variant X1
fibroblast growth factor receptor substrate 2-like, transcript variant X4
fibroblast growth factor receptor substrate 2-like, transcript variant X6
fibroblast growth factor receptor substrate 2-like isoform X1
fibroblast growth factor receptor substrate 2-like isoform X2
fibroblast growth factor receptor substrate 2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 29 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
fibroblast growth factor receptor substrate 2-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments
mediator complex subunit 20, transcript variant X2
mediator complex subunit 20, transcript variant X1
mediator of RNA polymerase II transcription subunit 20 isoform X1
mediator of RNA polymerase II transcription subunit 20 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 49
TAF8 RNA polymerase II, TATA box binding protein (TBP)-associated factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transcription initiation factor TFIID subunit 8
MDM4 regulator of p53, transcript variant X2
MDM4 regulator of p53, transcript variant X1
plasma membrane calcium-transporting ATPase 1-like
proline/arginine-rich end leucine-rich repeat protein, transcript variant X1
proline/arginine-rich end leucine-rich repeat protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
acidic mammalian chitinase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 129 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acidic mammalian chitinase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 111 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acidic mammalian chitinase-like isoform X1
acidic mammalian chitinase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: acidic mammalian chitinase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 107 Proteins
acidic mammalian chitinase-like, transcript variant X3
acidic mammalian chitinase-like, transcript variant X6
acidic mammalian chitinase-like, transcript variant X9
acidic mammalian chitinase-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 115 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
acidic mammalian chitinase-like, transcript variant X5
acidic mammalian chitinase-like, transcript variant X4
acidic mammalian chitinase-like isoform X5
acidic mammalian chitinase-like isoform X4
acidic mammalian chitinase-like, transcript variant X7
acidic mammalian chitinase-like isoform X3
cleavage and polyadenylation specificity factor subunit 6-like, transcript variant X3
cleavage and polyadenylation specificity factor subunit 6-like, transcript variant X2
cleavage and polyadenylation specificity factor subunit 6-like, transcript variant X1
cleavage and polyadenylation specificity factor subunit 6-like isoform X1
cleavage and polyadenylation specificity factor subunit 6-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 1 sample with support for all annotated introns
uncharacterized LOC125486084, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125486084, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125486084, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125486084, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125486084, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 98% 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Ras association domain family member 5, transcript variant X1
ras association domain-containing protein 5 isoform X1
Ras association domain family member 5, transcript variant X2
ras association domain-containing protein 5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 75% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 2D
dual specificity tyrosine-phosphorylation-regulated kinase 2-like, transcript variant X1
dual specificity tyrosine-phosphorylation-regulated kinase 2-like, transcript variant X2
dual specificity tyrosine-phosphorylation-regulated kinase 2-like isoform X2
dual specificity tyrosine-phosphorylation-regulated kinase 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125486093, transcript variant X2
uncharacterized LOC125486093, transcript variant X1
interferon regulatory factor 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
interferon regulatory factor 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
interferon regulatory factor 6 isoform X1
interferon regulatory factor 6 isoform X2
venom prothrombin activator pseutarin-C catalytic subunit-like
chromosome 25 C1orf74 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 126 long SRA reads, 11 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
chromosome 25 C1orf74 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 158 long SRA reads, 11 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
chromosome 25 C1orf74 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 136 long SRA reads, 11 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TRAF3-interacting JNK-activating modulator, transcript variant X2
TRAF3-interacting JNK-activating modulator, transcript variant X1
TRAF3-interacting JNK-activating modulator, transcript variant X6
TRAF3-interacting JNK-activating modulator isoform X1
TRAF3-interacting JNK-activating modulator, transcript variant X5
TRAF3-interacting JNK-activating modulator, transcript variant X3
TRAF3-interacting JNK-activating modulator isoform X3
TRAF3-interacting JNK-activating modulator, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
TRAF3-interacting JNK-activating modulator isoform X2
laminin subunit beta 3, transcript variant X1
laminin subunit beta 3, transcript variant X2
laminin subunit beta 3, transcript variant X3
calcium/calmodulin-dependent protein kinase IGb, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium/calmodulin-dependent protein kinase IGb, transcript variant X4
calcium/calmodulin-dependent protein kinase IGb, transcript variant X3
calcium/calmodulin-dependent protein kinase IGb, transcript variant X1
calcium/calmodulin-dependent protein kinase type 1D
specifically androgen-regulated gene protein, transcript variant X2
specifically androgen-regulated gene protein, transcript variant X1
specifically androgen-regulated gene protein, transcript variant X3
specifically androgen-regulated gene protein isoform X1
specifically androgen-regulated gene protein isoform X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 44 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 72 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 2 isoform X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 2 isoform X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 2, transcript variant X5
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, including 2 samples with support for all annotated introns
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 2, transcript variant X6
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, including 5 samples with support for all annotated introns
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 2, transcript variant X3
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, including 8 samples with support for all annotated introns
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 2, transcript variant X4
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, including 4 samples with support for all annotated introns
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 2 isoform X3
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 2 isoform X4
zona pellucida sperm-binding protein 3 receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, and 90% coverage of the annotated genomic feature by RNAseq alignments
complement decay-accelerating factor-like, transcript variant X3
complement decay-accelerating factor-like, transcript variant X1
complement decay-accelerating factor-like, transcript variant X2
complement decay-accelerating factor-like isoform X1
complement decay-accelerating factor-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
CUB and sushi domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-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
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 20 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, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125486061, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125486061, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
uncharacterized LOC125486060, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125486060, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
C4b-binding protein-like, transcript variant X6
C4b-binding protein-like, transcript variant X4
C4b-binding protein-like, transcript variant X3
C4b-binding protein-like, transcript variant X5
C4b-binding protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
C4b-binding protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
C4b-binding protein-like, transcript variant X8
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 11 samples with support for all annotated introns
C4b-binding protein-like, transcript variant X7
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 14 samples with support for all annotated introns
uncharacterized protein LOC109936675 isoform X4
C4b-binding protein beta chain-like isoform X1
C4b-binding protein beta chain-like isoform X2
uncharacterized protein LOC109936675 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125486048, transcript variant X2
uncharacterized LOC125486048, transcript variant X1
transmembrane and death domain protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane and death domain protein 1-like isoform X1
transmembrane and death domain protein 1-like, transcript variant X2
transmembrane and death domain protein 1-like isoform X2
olfactory receptor class A-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
ADP-ribose glycohydrolase OARD1, transcript variant X2
ADP-ribose glycohydrolase OARD1, transcript variant X1
apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins
translocator protein, transcript variant X1
translocator protein, transcript variant X2
bcl-2 homologous antagonist/killer, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
bcl-2 homologous antagonist/killer, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
bcl-2 homologous antagonist/killer, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
bcl-2 homologous antagonist/killer, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
bcl-2 homologous antagonist/killer, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
bcl-2 homologous antagonist/killer, transcript variant X5
bcl-2 homologous antagonist/killer, transcript variant X4
bcl-2 homologous antagonist/killer, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
bcl-2 homologous antagonist/killer, transcript variant X8
bcl-2 homologous antagonist/killer isoform X1
bcl-2 homologous antagonist/killer isoform X2
bcl-2 homologous antagonist/killer isoform X3
polyglutamylase complex subunit TTLL1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
protein kinase C and casein kinase substrate in neurons 1b, transcript variant X3
protein kinase C and casein kinase substrate in neurons 1b, transcript variant X2
protein kinase C and casein kinase substrate in neurons 1b, transcript variant X1
protein kinase C and casein kinase substrate in neurons 1b, transcript variant X5
protein kinase C and casein kinase substrate in neurons 1b, transcript variant X4
protein kinase C and casein kinase substrate in neurons protein 1 isoform X1
protein kinase C and casein kinase substrate in neurons protein 1 isoform X2
SAM pointed domain-containing Ets transcription factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SAM pointed domain-containing Ets transcription factor, transcript variant X1
SAM pointed domain-containing Ets transcription factor isoform X2
SAM pointed domain-containing Ets transcription factor isoform X1
inflammation and lipid regulator with UBA-like and NBR1-like domains
UHRF1 binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
UHRF1 binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ankyrin repeat and SAM domain-containing protein 1A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
transcription initiation factor TFIID subunit 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
ankyrin repeat and SAM domain-containing protein 1A-like, 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, including 1 sample with support for all annotated introns
ankyrin repeat and SAM domain-containing protein 1A-like, transcript variant X3
ankyrin repeat and SAM domain-containing protein 1A-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ankyrin repeat and SAM domain-containing protein 1A-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ankyrin repeat and SAM domain-containing protein 1A-like, transcript variant X5
ankyrin repeat and SAM domain-containing protein 1A-like isoform X3
ankyrin repeat and SAM domain-containing protein 1A-like isoform X5
ankyrin repeat and SAM domain-containing protein 1A-like isoform X1
ankyrin repeat and SAM domain-containing protein 1A-like isoform X4
ankyrin repeat and SAM domain-containing protein 1A-like isoform X6
ankyrin repeat and SAM domain-containing protein 1A-like, transcript variant X2
ankyrin repeat and SAM domain-containing protein 1A-like isoform X2
ankyrin repeat and SAM domain-containing protein 1A-like, transcript variant X7
ankyrin repeat and SAM domain-containing protein 1A-like, transcript variant X8
ankyrin repeat and SAM domain-containing protein 1A-like isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
signal peptide, CUB domain, EGF-like 3, transcript variant X1
signal peptide, CUB domain, EGF-like 3, transcript variant X4
signal peptide, CUB domain, EGF-like 3, transcript variant X2
signal peptide, CUB domain, EGF-like 3, transcript variant X3
signal peptide, CUB and EGF-like domain-containing protein 3 isoform X1
signal peptide, CUB and EGF-like domain-containing protein 3 isoform X2
signal peptide, CUB domain, EGF-like 3, transcript variant X5
signal peptide, CUB and EGF-like domain-containing protein 3 isoform X3
zinc finger protein 76-like, transcript variant X1
zinc finger protein 76-like, transcript variant X2
DEF6 guanine nucleotide exchange factor a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 long SRA reads, 30 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
DEF6 guanine nucleotide exchange factor a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
differentially expressed in FDCP 6 homolog isoform X1
differentially expressed in FDCP 6 homolog isoform X2
peroxisome proliferator-activated receptor delta b
probable E3 ubiquitin-protein ligase makorin-1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
complement C1q tumor necrosis factor-related protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 long SRA reads, 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
liprin-alpha-2-like, transcript variant X2
liprin-alpha-2-like, transcript variant X1
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: 98 Proteins, and 81% 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: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 12B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuron navigator 1-like, transcript variant X3
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
neuron navigator 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neuron navigator 1-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 2 samples with support for all annotated introns
pleckstrin homology-like domain family A member 3
troponin I, slow skeletal muscle, transcript variant X1
troponin I, slow skeletal muscle, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
immunoglobulin-like and fibronectin type III domain-containing protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: immunoglobulin-like and fibronectin type III domain-containing protein 1
protein tyrosine phosphatase receptor type R
receptor-type tyrosine-protein phosphatase R
leucine-rich repeat-containing G-protein coupled receptor 6, transcript variant X1
leucine-rich repeat-containing G-protein coupled receptor 6, transcript variant X2
leucine-rich repeat-containing G-protein coupled receptor 6 isoform X1
leucine-rich repeat-containing G-protein coupled receptor 6 isoform X2
ubiquitin-conjugating enzyme E2T (putative), transcript variant X4
ubiquitin-conjugating enzyme E2T (putative), transcript variant X5
ubiquitin-conjugating enzyme E2T (putative), transcript variant X1
ubiquitin-conjugating enzyme E2T (putative), transcript variant X2
ubiquitin-conjugating enzyme E2T (putative), transcript variant X3
ubiquitin-conjugating enzyme E2T (putative), transcript variant X6
ubiquitin-conjugating enzyme E2T (putative), transcript variant X7
ubiquitin-conjugating enzyme E2T (putative), transcript variant X8
ubiquitin-conjugating enzyme E2 T isoform X1
ubiquitin-conjugating enzyme E2 T isoform X3
ubiquitin-conjugating enzyme E2 T isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
ubiquinol-cytochrome-c reductase complex assembly factor 2
inositol 1,4,5-trisphosphate receptor, type 3, transcript variant X2
inositol 1,4,5-trisphosphate receptor, type 3, transcript variant X1
inositol 1,4,5-trisphosphate receptor, type 3, transcript variant X3
inositol 1,4,5-trisphosphate receptor type 3 isoform X2
inositol 1,4,5-trisphosphate receptor type 3 isoform X1
inositol 1,4,5-trisphosphate receptor type 3 isoform X3
gametogenetin-binding protein 1-like, transcript variant X6
gametogenetin-binding protein 1-like, transcript variant X5
gametogenetin-binding protein 1-like isoform X4
gametogenetin-binding protein 1-like, transcript variant X2
gametogenetin-binding protein 1-like, transcript variant X3
gametogenetin-binding protein 1-like isoform X2
gametogenetin-binding protein 1-like, transcript variant X1
gametogenetin-binding protein 1-like, transcript variant X4
gametogenetin-binding protein 1-like isoform X1
gametogenetin-binding protein 1-like isoform X3
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 9 samples with support for all annotated introns
small integral membrane protein 29, transcript variant X2
small integral membrane protein 29, transcript variant X1
high mobility group AT-hook 1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
high mobility group AT-hook 1a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
high mobility group AT-hook 1a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
high mobility group AT-hook 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
high mobility group AT-hook 1a isoform X3
high mobility group AT-hook 1a isoform X1
high mobility group AT-hook 1a, 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 3 samples with support for all annotated introns
high mobility group AT-hook 1a isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
bombesin receptor-activated protein C6orf89 homolog, transcript variant X2
bombesin receptor-activated protein C6orf89 homolog, transcript variant X1
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 6 samples with support for all annotated introns
bombesin receptor-activated protein C6orf89 homolog, transcript variant X3
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 5 samples with support for all annotated introns
uncharacterized protein LOC109930748 isoform X1
bombesin receptor-activated protein C6orf89 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
translocase of inner mitochondrial membrane 17 homolog A (yeast), transcript variant X1
mitochondrial import inner membrane translocase subunit Tim17-A isoform X1
translocase of inner mitochondrial membrane 17 homolog A (yeast), transcript variant X2
mitochondrial import inner membrane translocase subunit Tim17-A isoform X2
arginyl aminopeptidase (aminopeptidase B)
innate immunity activator protein-like, transcript variant X3
innate immunity activator protein-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
innate immunity activator protein-like, transcript variant X4
innate immunity activator protein-like, transcript variant X10
innate immunity activator protein-like, transcript variant X9
innate immunity activator protein-like, transcript variant X7
innate immunity activator protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
innate immunity activator protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
innate immunity activator protein-like, transcript variant X5
innate immunity activator protein-like, transcript variant X8
innate immunity activator protein-like isoform X2
innate immunity activator protein-like isoform X1
innate immunity activator protein-like isoform X3
innate immunity activator protein-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
mitogen-activated protein kinase 13-like
bromodomain and PHD finger containing, 3b, transcript variant X3
bromodomain and PHD finger containing, 3b, transcript variant X1
bromodomain and PHD finger containing, 3b, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
bromodomain and PHD finger containing, 3b, transcript variant X4
bromodomain and PHD finger containing, 3b, transcript variant X2
bromodomain and PHD finger-containing protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
chemokine-like protein TAFA-5, 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 1 sample with support for all annotated introns
chemokine-like protein TAFA-5 isoform X3
chemokine-like protein TAFA-5, transcript variant X2
chemokine-like protein TAFA-5 isoform X2
chemokine-like protein TAFA-5, 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
chemokine-like protein TAFA-5 isoform X1
TBC1 domain family, member 22B, 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 1 sample with support for all annotated introns
TBC1 domain family member 22B isoform X3
TBC1 domain family, member 22B, transcript variant X2
TBC1 domain family, member 22B, transcript variant X1
TBC1 domain family member 22B isoform X2
TBC1 domain family member 22B isoform X1
TBC1 domain family, member 22B, transcript variant X4
TBC1 domain family member 22B isoform X4
Pim-1 proto-oncogene, serine/threonine kinase
uncharacterized LOC125486055, transcript variant X1
uncharacterized LOC125486055, transcript variant X3
uncharacterized LOC125486055, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
peptidylprolyl isomerase (cyclophilin)-like 1
peptidyl-prolyl cis-trans isomerase-like 1
proline/serine-rich coiled-coil protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
proline/serine-rich coiled-coil protein 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
proline/serine-rich coiled-coil protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
proline/serine-rich coiled-coil protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
proline/serine-rich coiled-coil protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
proline/serine-rich coiled-coil protein 1-like isoform X1
proline/serine-rich coiled-coil protein 1-like isoform X3
proline/serine-rich coiled-coil protein 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC109913837 isoform X2
cadherin EGF LAG seven-pass G-type receptor 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
endosome-lysosome associated apoptosis and autophagy regulator 1, transcript variant X1
endosome-lysosome associated apoptosis and autophagy regulator 1, transcript variant X2
endosome/lysosome-associated apoptosis and autophagy regulator 1 isoform X1
endosome/lysosome-associated apoptosis and autophagy regulator 1 isoform X2
cilia and flagella associated protein 276
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ETS-related transcription factor Elf-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 62% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DNA cross-link repair 1B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
DNA cross-link repair 1B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC109915657, transcript variant X1
uncharacterized LOC109915657, transcript variant X2
adaptor related protein complex 4 subunit beta 1, transcript variant X2
adaptor related protein complex 4 subunit beta 1, transcript variant X1
homeodomain-interacting protein kinase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
homeodomain-interacting protein kinase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
homeodomain-interacting protein kinase 1-like isoform X2
homeodomain-interacting protein kinase 1-like isoform X1
methylmalonyl-CoA epimerase, mitochondrial
synaptotagmin-6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
synaptotagmin-6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
BCAS2 pre-mRNA processing factor, transcript variant X2
BCAS2 pre-mRNA processing factor, transcript variant X1
pre-mRNA-splicing factor SPF27 isoform X2
pre-mRNA-splicing factor SPF27 isoform X1
ras association domain-containing protein 8-like, transcript variant X1
ras association domain-containing protein 8-like, transcript variant X3
ras association domain-containing protein 8-like, transcript variant X2
ras association domain-containing protein 8-like isoform X1
ras association domain-containing protein 8-like isoform X3
ras association domain-containing protein 8-like isoform X2
adenosine monophosphate deaminase 1 (isoform M)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
NRAS proto-oncogene, GTPase, transcript variant X2
NRAS proto-oncogene, GTPase, transcript variant X1
NRAS proto-oncogene, GTPase, transcript variant X3
inositol 1,4,5-triphosphate receptor associated 1-like, transcript variant X3
inositol 1,4,5-triphosphate receptor associated 1-like, transcript variant X2
inositol 1,4,5-triphosphate receptor associated 1-like, transcript variant X1
inositol 1,4,5-triphosphate receptor associated 1-like isoform X3
inositol 1,4,5-triphosphate receptor associated 1-like isoform X2
inositol 1,4,5-triphosphate receptor associated 1-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
sphingomyelin phosphodiesterase 2b, transcript variant X2
sphingomyelin phosphodiesterase 2b, transcript variant X1
sphingomyelin phosphodiesterase 2 isoform X2
sphingomyelin phosphodiesterase 2 isoform X1
transcriptional enhancer factor TEF-5-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 3 samples with support for all annotated introns
transcriptional enhancer factor TEF-5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transcriptional enhancer factor TEF-5-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 4 samples with support for all annotated introns
transcriptional enhancer factor TEF-5-like isoform X2
transcriptional enhancer factor TEF-5-like isoform X3
transcriptional enhancer factor TEF-5-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
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
peptidyl-prolyl cis-trans isomerase FKBP5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 9, transcript variant X1
transmembrane protein 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
DENN domain-containing protein 2C-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DENN domain-containing protein 2C-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
DENN domain-containing protein 2C-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
DENN domain-containing protein 2C-like, transcript variant X2
DENN domain-containing protein 2C-like, transcript variant X1
DENN domain-containing protein 2C-like, transcript variant X3
DENN domain-containing protein 2C-like isoform X1
DENN domain-containing protein 2C-like isoform X3
DENN domain-containing protein 2C-like isoform X2
DENN domain-containing protein 2C-like isoform X4
AT-rich interactive domain-containing protein 2-like, transcript variant X1
AT-rich interactive domain-containing protein 2-like, transcript variant X2
AT-rich interactive domain-containing protein 2-like isoform X1
AT-rich interactive domain-containing protein 2-like isoform X2
cold shock domain containing E1, RNA-binding, transcript variant X9
cold shock domain containing E1, RNA-binding, transcript variant X4
cold shock domain containing E1, RNA-binding, transcript variant X7
cold shock domain containing E1, RNA-binding, transcript variant X13
cold shock domain containing E1, RNA-binding, transcript variant X12
cold shock domain containing E1, RNA-binding, transcript variant X15
cold shock domain containing E1, RNA-binding, transcript variant X10
cold shock domain containing E1, RNA-binding, transcript variant X6
cold shock domain containing E1, RNA-binding, transcript variant X14
cold shock domain containing E1, RNA-binding, transcript variant X5
cold shock domain containing E1, RNA-binding, transcript variant X11
cold shock domain containing E1, RNA-binding, transcript variant X2
cold shock domain containing E1, RNA-binding, transcript variant X3
cold shock domain containing E1, RNA-binding, transcript variant X1
cold shock domain containing E1, RNA-binding, transcript variant X8
cold shock domain-containing protein E1 isoform X12
cold shock domain-containing protein E1 isoform X7
cold shock domain-containing protein E1 isoform X5
cold shock domain-containing protein E1 isoform X9
cold shock domain-containing protein E1 isoform X4
cold shock domain-containing protein E1 isoform X2
cold shock domain-containing protein E1 isoform X3
cold shock domain-containing protein E1 isoform X1
cold shock domain-containing protein E1 isoform X11
cold shock domain-containing protein E1 isoform X10
cold shock domain-containing protein E1 isoform X13
cold shock domain-containing protein E1 isoform X8
cold shock domain-containing protein E1 isoform X6
sialomucin core protein 24-like, transcript variant X3
sialomucin core protein 24-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sialomucin core protein 24-like, transcript variant X1
sialomucin core protein 24-like isoform X1
sialomucin core protein 24-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 7 samples with support for all annotated introns
sialomucin core protein 24-like isoform X2
sodium-coupled monocarboxylate transporter 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium-coupled monocarboxylate transporter 1-like, transcript variant X1
sodium-coupled monocarboxylate transporter 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
sodium-coupled monocarboxylate transporter 1-like isoform X3
sodium-coupled monocarboxylate transporter 1-like isoform X2
sodium-coupled monocarboxylate transporter 1-like isoform X1
sodium-coupled monocarboxylate transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC109913730, transcript variant X4
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 2 samples with support for all annotated introns
uncharacterized LOC109913730, transcript variant X3
uncharacterized LOC109913730, transcript variant X2
uncharacterized LOC109913730, transcript variant X1
uncharacterized protein LOC109913730 isoform X4
uncharacterized protein LOC109913730 isoform X3
uncharacterized protein LOC109913730 isoform X2
uncharacterized protein LOC109913730 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% 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: 76% coverage of the annotated genomic feature by RNAseq alignments
kelch-like family member 12, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
kelch-like family member 12, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
kelch-like family member 12, transcript variant X2
kelch-like family member 12, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kelch-like family member 12, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
kelch-like family member 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
kelch-like family member 12, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
39S ribosomal protein L16, mitochondrial
uncharacterized protein LOC100005854 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
ETS variant transcription factor 7, transcript variant X2
ETS variant transcription factor 7, transcript variant X1
ETS variant transcription factor 7, transcript variant X3
mitochondrial glutamate carrier 1-like, transcript variant X1
mitochondrial glutamate carrier 1-like, transcript variant X2
mitochondrial glutamate carrier 1-like isoform X1
mitochondrial glutamate carrier 1-like isoform X2
serine/threonine-protein kinase 38, transcript variant X2
serine/threonine-protein kinase 38, transcript variant X3
serine/threonine-protein kinase 38, transcript variant X1
serine/threonine-protein kinase 38 isoform X1
serine/threonine-protein kinase 38 isoform X2
BTB/POZ domain-containing protein KCTD20-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
serine/arginine-rich splicing factor 3, transcript variant X2
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 17 samples with support for all annotated introns
serine/arginine-rich splicing factor 3, transcript variant X1
cyclin-dependent kinase inhibitor 1-like
EF-hand calcium-binding domain-containing protein 4B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments
EF-hand calcium-binding domain-containing protein 4B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
EF-hand calcium-binding domain-containing protein 4B-like isoform X1
EF-hand calcium-binding domain-containing protein 4B-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
ankyrin repeat and BTB/POZ domain-containing protein BTBD11-like
cryptochrome-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 131 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cryptochrome-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 130 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 13, transcript variant X2
26S proteasome non-ATPase regulatory subunit 13, transcript variant X1
26S proteasome non-ATPase regulatory subunit 13 isoform X1
26S proteasome non-ATPase regulatory subunit 13 isoform X2
ligand dependent nuclear receptor interacting factor 1, transcript variant X1
ligand dependent nuclear receptor interacting factor 1, transcript variant X4
ligand dependent nuclear receptor interacting factor 1, transcript variant X3
ligand dependent nuclear receptor interacting factor 1, transcript variant X2
uncharacterized LOC109919292, transcript variant X2
uncharacterized LOC109919292, transcript variant X3
uncharacterized LOC109919292, transcript variant X5
uncharacterized LOC109919292, transcript variant X4
uncharacterized LOC109919292, transcript variant X1
uncharacterized LOC109919292, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
DNA-damage regulated autophagy modulator 2b, transcript variant X2
DNA-damage regulated autophagy modulator 2b, transcript variant X1
DNA-damage regulated autophagy modulator 2b, transcript variant X3
DNA damage-regulated autophagy modulator protein 2b isoform X2
DNA damage-regulated autophagy modulator protein 2b isoform X1
DNA damage-regulated autophagy modulator protein 2b isoform X3
choline/ethanolaminephosphotransferase 1
voltage-dependent L-type calcium channel subunit alpha-1S-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
lysine (K)-specific demethylase 5Ba, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
lysine (K)-specific demethylase 5Ba, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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
lysine-specific demethylase 5B isoform X1
lysine-specific demethylase 5B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 13 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: 5 long SRA reads, 13 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: 1 long SRA read, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
potassium voltage-gated channel subfamily A member 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 138 Proteins
potassium voltage-gated channel subfamily A member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 142 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gastrula zinc finger protein XlCGF26.1-like, transcript variant X1
gastrula zinc finger protein XlCGF26.1-like, transcript variant X5
gastrula zinc finger protein XlCGF26.1-like, transcript variant X3
gastrula zinc finger protein XlCGF26.1-like, transcript variant X2
gastrula zinc finger protein XlCGF26.1-like, transcript variant X4
gastrula zinc finger protein XlCGF26.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
phospholipid phosphatase-related protein type 2a