Rhincodon typus isolate 14 chromosome 19, 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\nCM038816.1.\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.
gastrula zinc finger protein XlCGF49.1-like
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 long SRA reads, 31 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
short transient receptor potential channel 4-associated protein
myosin heavy chain, cardiac muscle isoform-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 148 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 20 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
oxidative stress induced growth inhibitor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125485429, transcript variant X1
uncharacterized LOC125485429, transcript variant X2
eukaryotic translation initiation factor 6
uncharacterized LOC109936311, transcript variant X1
uncharacterized LOC109936311, transcript variant X2
uncharacterized protein LOC109936311 isoform X1
uncharacterized protein LOC109936311 isoform X2
oxidative stress induced growth inhibitor 1, transcript variant X1
oxidative stress induced growth inhibitor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
oxidative stress induced growth inhibitor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 68% coverage of the annotated genomic feature by RNAseq alignments
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 2-like, transcript variant X1
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 2-like, transcript variant X2
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 2-like
cytochrome c1, heme protein, mitochondrial
ERGIC and golgi 3, transcript variant X1
ERGIC and golgi 3, transcript variant X2
ERGIC and golgi 3, transcript variant X3
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 12 samples with support for all annotated introns
endoplasmic reticulum-Golgi intermediate compartment protein 3 isoform X1
endoplasmic reticulum-Golgi intermediate compartment protein 3 isoform X2
endoplasmic reticulum-Golgi intermediate compartment protein 3 isoform X3
reactive oxygen species modulator 1, transcript variant X1
reactive oxygen species modulator 1, transcript variant X2
reactive oxygen species modulator 1 isoform X1
reactive oxygen species modulator 1 isoform X2
myelocytomatosis oncogene homolog, transcript variant X3
myelocytomatosis oncogene homolog, transcript variant X2
myelocytomatosis oncogene homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
retinoblastoma-like 1 (p107), transcript variant X1
retinoblastoma-like 1 (p107), transcript variant X3
retinoblastoma-like protein 1 isoform X1
retinoblastoma-like protein 1 isoform X3
retinoblastoma-like 1 (p107), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
retinoblastoma-like protein 1 isoform X2
chromodomain helicase DNA binding protein 6, transcript variant X3
chromodomain helicase DNA binding protein 6, transcript variant X4
chromodomain helicase DNA binding protein 6, transcript variant X2
chromodomain helicase DNA binding protein 6, transcript variant X1
chromodomain-helicase-DNA-binding protein 6 isoform X3
chromodomain-helicase-DNA-binding protein 6 isoform X4
chromodomain-helicase-DNA-binding protein 6 isoform X2
chromodomain-helicase-DNA-binding protein 6 isoform X1
Ral GTPase activating protein non-catalytic subunit beta, transcript variant X2
Ral GTPase activating protein non-catalytic subunit beta, transcript variant X10
Ral GTPase activating protein non-catalytic subunit beta, transcript variant X9
Ral GTPase activating protein non-catalytic subunit beta, transcript variant X11
Ral GTPase activating protein non-catalytic subunit beta, transcript variant X8
Ral GTPase activating protein non-catalytic subunit beta, transcript variant X7
Ral GTPase activating protein non-catalytic subunit beta, transcript variant X5
Ral GTPase activating protein non-catalytic subunit beta, transcript variant X6
Ral GTPase activating protein non-catalytic subunit beta, transcript variant X3
Ral GTPase activating protein non-catalytic subunit beta, transcript variant X4
Ral GTPase activating protein non-catalytic subunit beta, transcript variant X1
Ral GTPase activating protein non-catalytic subunit beta, transcript variant X12
ral GTPase-activating protein subunit beta isoform X9
ral GTPase-activating protein subunit beta isoform X8
ral GTPase-activating protein subunit beta isoform X10
ral GTPase-activating protein subunit beta isoform X7
ral GTPase-activating protein subunit beta isoform X6
ral GTPase-activating protein subunit beta isoform X4
ral GTPase-activating protein subunit beta isoform X5
ral GTPase-activating protein subunit beta isoform X2
ral GTPase-activating protein subunit beta isoform X3
ral GTPase-activating protein subunit beta isoform X1
ral GTPase-activating protein subunit beta isoform X11
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
TOX high mobility group box family member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
RNA binding motif protein 12, transcript variant X3
RNA binding motif protein 12, transcript variant X2
RNA binding motif protein 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
elongation factor 1-alpha 2, transcript variant X1
elongation factor 1-alpha 2, transcript variant X2
potassium voltage-gated channel subfamily KQT member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
neuronal acetylcholine receptor subunit alpha-4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
neuronal acetylcholine receptor subunit alpha-4-like isoform X2
neuronal acetylcholine receptor subunit alpha-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
neuronal acetylcholine receptor subunit alpha-4-like isoform X1
potassium channel subfamily K member 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins
regulating synaptic membrane exocytosis protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 77% 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 long SRA read, 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
14-3-3 protein beta/alpha-1-like, transcript variant X1
14-3-3 protein beta/alpha-1-like, transcript variant X2
14-3-3 protein beta/alpha-1-like, transcript variant X3
14-3-3 protein beta/alpha-1-like, transcript variant X4
embryonic polyadenylate-binding protein A-like
translocase of outer mitochondrial membrane 34
mitochondrial import receptor subunit TOM34
opioid growth factor receptor-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
death-inducer obliterator 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
death-inducer obliterator 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
death-inducer obliterator 1-like isoform X1
death-inducer obliterator 1-like isoform X2
protein O-glucosyltransferase 1, transcript variant X2
protein O-glucosyltransferase 1, transcript variant X1
protein O-glucosyltransferase 1 isoform X2
protein O-glucosyltransferase 1 isoform X1
translocase of inner mitochondrial membrane domain containing 1
complex I assembly factor TIMMDC1, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
double-strand-break repair protein rad21 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
peptidyl-prolyl cis-trans isomerase FKBP1A-like, transcript variant X1
peptidyl-prolyl cis-trans isomerase FKBP1A-like, transcript variant X2
peptidyl-prolyl cis-trans isomerase FKBP1A-like isoform X1
peptidyl-prolyl cis-trans isomerase FKBP1A-like isoform X2
agouti signaling protein 1, transcript variant X1
agouti signaling protein 1, transcript variant X2
agouti signaling protein 1, transcript variant X3
eukaryotic translation initiation factor 2, subunit 2 beta
eukaryotic translation initiation factor 2 subunit 2
RALY heterogeneous nuclear ribonucleoprotein, transcript variant X2
RALY heterogeneous nuclear ribonucleoprotein, transcript variant X3
RALY heterogeneous nuclear ribonucleoprotein, transcript variant X4
RALY heterogeneous nuclear ribonucleoprotein, transcript variant X1
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1-like, transcript variant X1
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1-like, transcript variant X3
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1-like, transcript variant X2
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1-like, transcript variant X4
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1-like, transcript variant X6
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1-like, transcript variant X5
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1-like isoform X3
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1-like isoform X2
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1-like isoform X1
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1-like isoform X4
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1-like isoform X5
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1-like isoform X6
family with sequence similarity 83 member C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
recombination signal binding protein for immunoglobulin kappa J region-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
recombining binding protein suppressor of hairless-like protein
potassium voltage-gated channel subfamily S member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine kinase 3 (STE20 homolog, yeast), transcript variant X8
serine/threonine kinase 3 (STE20 homolog, yeast), transcript variant X9
serine/threonine kinase 3 (STE20 homolog, yeast), transcript variant X7
serine/threonine kinase 3 (STE20 homolog, yeast), transcript variant X5
serine/threonine kinase 3 (STE20 homolog, yeast), transcript variant X3
serine/threonine kinase 3 (STE20 homolog, yeast), transcript variant X6
serine/threonine kinase 3 (STE20 homolog, yeast), transcript variant X2
serine/threonine kinase 3 (STE20 homolog, yeast), transcript variant X4
serine/threonine kinase 3 (STE20 homolog, yeast), transcript variant X1
serine/threonine-protein kinase 3/4 isoform X2
serine/threonine-protein kinase 3/4 isoform X3
serine/threonine-protein kinase 3/4 isoform X1
uncharacterized LOC125485422, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125485422, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
chromosome 19 C20orf96 homolog, transcript variant X2
chromosome 19 C20orf96 homolog, transcript variant X1
chromosome 19 C20orf96 homolog, transcript variant X3
uncharacterized protein C20orf96 homolog isoform X2
uncharacterized protein C20orf96 homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 469 long SRA reads, 32 Proteins, and 98% 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: 36 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: 8 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: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RanBP-type and C3HC4-type zinc finger containing 1
ranBP-type and C3HC4-type zinc finger-containing protein 1
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
casein kinase II subunit alpha, transcript variant X7
casein kinase II subunit alpha, transcript variant X6
casein kinase II subunit alpha, transcript variant X5
casein kinase II subunit alpha, transcript variant X1
casein kinase II subunit alpha, transcript variant X2
casein kinase II subunit alpha, transcript variant X4
casein kinase II subunit alpha, transcript variant X3
casein kinase II subunit alpha isoform X2
casein kinase II subunit alpha isoform X1
transcriptional repressor scratch 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins
solute carrier family 52, riboflavin transporter, member 3-A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 52, riboflavin transporter, member 3-A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
solute carrier family 52, riboflavin transporter, member 3-A-like
deoxynucleoside triphosphate triphosphohydrolase SAMHD1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 24 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: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
E3 ubiquitin-protein ligase Itchy homolog
dynein light chain roadblock-type 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 15 Proteins, and 58% 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 1 sample 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, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
histocompatibility (minor) 13, transcript variant X2
histocompatibility (minor) 13, transcript variant X1
minor histocompatibility antigen H13 isoform X2
minor histocompatibility antigen H13 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 52% coverage of the annotated genomic feature by RNAseq alignments
PHD finger protein 20-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
PHD finger protein 20-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 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
PHD finger protein 20-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PHD finger protein 20-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
ER degradation-enhancing alpha-mannosidase-like protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 74% coverage of the annotated genomic feature by RNAseq alignments
microtubule-associated proteins 1A/1B light chain 3A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ER degradation enhancer, mannosidase alpha-like 2
phosphatidylinositol glycan anchor biosynthesis, class U
phosphatidylinositol glycan anchor biosynthesis class U protein
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 3 samples with support for all annotated introns
tumor protein p53-inducible nuclear protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 long SRA reads, 17 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tumor protein p53-inducible nuclear protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 long SRA reads, 17 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tumor protein p53-inducible nuclear protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 long SRA reads, 17 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tumor protein p53-inducible nuclear protein 1, transcript variant X1
tumor protein p53-inducible nuclear protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 long SRA reads, 12 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tumor protein p53-inducible nuclear protein 1, 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 2 samples with support for all annotated introns
tumor protein p53-inducible nuclear protein 2 isoform X1
tumor protein p53-inducible nuclear protein 2 isoform X2
tumor protein p53-inducible nuclear protein 1 isoform X3
nuclear receptor coactivator 6, transcript variant X7
nuclear receptor coactivator 6, transcript variant X1
nuclear receptor coactivator 6, transcript variant X10
nuclear receptor coactivator 6, transcript variant X8
nuclear receptor coactivator 6, transcript variant X9
nuclear receptor coactivator 6, transcript variant X4
nuclear receptor coactivator 6, transcript variant X5
nuclear receptor coactivator 6, transcript variant X2
nuclear receptor coactivator 6, transcript variant X3
nuclear receptor coactivator 6 isoform X8
nuclear receptor coactivator 6 isoform X6
nuclear receptor coactivator 6 isoform X7
nuclear receptor coactivator 6 isoform X5
nuclear receptor coactivator 6 isoform X2
nuclear receptor coactivator 6 isoform X3
nuclear receptor coactivator 6 isoform X1
nuclear receptor coactivator 6, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
nuclear receptor coactivator 6, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
nuclear receptor coactivator 6, transcript variant X6
nuclear receptor coactivator 6 isoform X10
nuclear receptor coactivator 6 isoform X9
nuclear receptor coactivator 6 isoform X4
glutathione hydrolase 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutathione hydrolase 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase CYLD-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase CYLD-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase CYLD-like, transcript variant X7
ubiquitin carboxyl-terminal hydrolase CYLD-like, transcript variant X5
ubiquitin carboxyl-terminal hydrolase CYLD-like isoform X1
ubiquitin carboxyl-terminal hydrolase CYLD-like isoform X2
ubiquitin carboxyl-terminal hydrolase CYLD-like isoform X5
ubiquitin carboxyl-terminal hydrolase CYLD-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase CYLD-like, transcript variant X6
ubiquitin carboxyl-terminal hydrolase CYLD-like, transcript variant X4
ubiquitin carboxyl-terminal hydrolase CYLD-like isoform X3
ubiquitin carboxyl-terminal hydrolase CYLD-like isoform X4
ubiquitin carboxyl-terminal hydrolase CYLD-like, transcript variant X8
ubiquitin carboxyl-terminal hydrolase CYLD-like isoform X6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein RAB5IF
TP53 regulating kinase, transcript variant X2
TP53 regulating kinase, transcript variant X1
osteoclast stimulatory transmembrane protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 70% 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: 23 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 13 member 3-like, transcript variant X2
solute carrier family 13 member 3-like, transcript variant X1
solute carrier family 13 member 3-like isoform X2
solute carrier family 13 member 3-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 11 Proteins, and 98% 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: 2 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 1, regulatory subunit 16B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein phosphatase 1 regulatory inhibitor subunit 16B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
probable ATP-dependent RNA helicase DHX35
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
zinc fingers and homeoboxes protein 3, transcript variant X2
zinc fingers and homeoboxes protein 3, transcript variant X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-1
DNA topoisomerase 1, transcript variant X1
DNA topoisomerase 1, transcript variant X2
DNA topoisomerase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00568
transcription factor MafB, transcript variant X2
transcription factor MafB, transcript variant X3
transcription factor MafB, transcript variant X1
transcription factor MafB, 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
uncharacterized LOC125485481, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125485481, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125485443, transcript variant X2
uncharacterized LOC125485443, transcript variant X3
uncharacterized LOC125485443, transcript variant X1
translocating chain-associated membrane protein 1-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
eyes absent homolog 1-like, transcript variant X7
eyes absent homolog 1-like, transcript variant X2
eyes absent homolog 1-like, transcript variant X5
eyes absent homolog 1-like, transcript variant X3
eyes absent homolog 1-like, transcript variant X4
eyes absent homolog 1-like, transcript variant X8
eyes absent homolog 1-like, transcript variant X1
eyes absent homolog 1-like, transcript variant X6
solute carrier family 2, facilitated glucose transporter member 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
serum/glucocorticoid regulated kinase 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serum/glucocorticoid regulated kinase 2a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein kinase Sgk2 isoform X1
serine/threonine-protein kinase Sgk2 isoform X2
intraflagellar transport protein 52 homolog
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 19 samples with support for all annotated introns
intraflagellar transport 52 homolog (Chlamydomonas), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 15 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
intraflagellar transport 52 homolog (Chlamydomonas), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
intraflagellar transport protein 52 homolog isoform X1
intraflagellar transport protein 52 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription initiation factor TFIID subunit 4-like
protein LSM14 homolog B, transcript variant X3
protein LSM14 homolog B, transcript variant X1
protein LSM14 homolog B, transcript variant X2
protein LSM14 homolog B, transcript variant X4
protein LSM14 homolog B, transcript variant X5
protein LSM14 homolog B, transcript variant X6
protein LSM14 homolog B, transcript variant X7
SS18L1 subunit of BAF chromatin remodeling complex
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial ribosome-associated GTPase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: histamine H3 receptor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 97% coverage of the annotated genomic feature by RNAseq alignments
oxysterol-binding protein-related protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% 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 long SRA read, 20 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
ribosomal protein S21, transcript variant X1
ribosomal protein S21, transcript variant X2
ribosomal protein S21, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 184 long SRA reads, 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
retinoblastoma binding protein 8-like, transcript variant X4
retinoblastoma binding protein 8-like, transcript variant X1
retinoblastoma binding protein 8-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
uncharacterized protein rbbp8l isoform X1
RBBP8 N-terminal-like protein isoform X3
retinoblastoma binding protein 8-like, transcript variant X3
RBBP8 N-terminal-like protein isoform X2
uncharacterized LOC125485521, transcript variant X1
uncharacterized LOC125485521, transcript variant X2
GATA binding protein 5, transcript variant X4
GATA binding protein 5, transcript variant X7
GATA binding protein 5, transcript variant X3
GATA binding protein 5, transcript variant X2
GATA binding protein 5, transcript variant X8
GATA binding protein 5, transcript variant X1
GATA binding protein 5, transcript variant X5
GATA binding protein 5, transcript variant X6
solute carrier organic anion transporter family, member 4A1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
solute carrier organic anion transporter family, member 4A1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
solute carrier organic anion transporter family, member 4A1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier organic anion transporter family, member 4A1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier organic anion transporter family member 4A1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
proto-oncogene tyrosine-protein kinase Src, transcript variant X1
proto-oncogene tyrosine-protein kinase Src, transcript variant X2
proto-oncogene tyrosine-protein kinase Src
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 11 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 2 isoform X1
uncharacterized LOC125485475, transcript variant X1
uncharacterized LOC125485475, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 33 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
myosin regulatory light polypeptide 9, transcript variant X2
myosin regulatory light polypeptide 9, transcript variant X1
homeobox protein TGIF2-like, transcript variant X1
homeobox protein TGIF2-like, transcript variant X2
disks large-associated protein 4-like, transcript variant X2
disks large-associated protein 4-like, transcript variant X1
disks large-associated protein 4-like, transcript variant X4
disks large-associated protein 4-like, transcript variant X5
disks large-associated protein 4-like, transcript variant X3
disks large-associated protein 4-like isoform X2
disks large-associated protein 4-like isoform X1
disks large-associated protein 4-like isoform X3
disks large-associated protein 4-like isoform X4
AAR2 splicing factor, transcript variant X3
AAR2 splicing factor, transcript variant X2
AAR2 splicing factor, transcript variant X4
AAR2 splicing factor, transcript variant X1
AAR2 splicing factor, transcript variant X5
band 4.1-like protein 1, transcript variant X6
band 4.1-like protein 1, transcript variant X4
band 4.1-like protein 1, transcript variant X2
band 4.1-like protein 1, transcript variant X1
band 4.1-like protein 1, transcript variant X7
band 4.1-like protein 1, transcript variant X3
band 4.1-like protein 1, transcript variant X5
serine/arginine-rich splicing factor 6, transcript variant X1
serine/arginine-rich splicing factor 6, transcript variant X2
serine/arginine-rich splicing factor 6 isoform X1
serine/arginine-rich splicing factor 6 isoform X2
L3MBTL histone methyl-lysine binding protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
lethal(3)malignant brain tumor-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
vesicular inhibitory amino acid transporter
protein tyrosine phosphatase receptor type T
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
receptor-type tyrosine-protein phosphatase T
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
acyl-CoA synthetase short chain family member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
acyl-CoA synthetase short chain family member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
acetyl-coenzyme A synthetase, cytoplasmic isoform X2
acetyl-coenzyme A synthetase, cytoplasmic isoform X1
microtubule-associated protein RP/EB family member 1, transcript variant X7
microtubule-associated protein RP/EB family member 1, transcript variant X3
microtubule-associated protein RP/EB family member 1, transcript variant X1
microtubule-associated protein RP/EB family member 1, transcript variant X5
microtubule-associated protein RP/EB family member 1, transcript variant X4
microtubule-associated protein RP/EB family member 1, transcript variant X6
microtubule-associated protein RP/EB family member 1, transcript variant X2
microtubule-associated protein RP/EB family member 1 isoform X2
microtubule-associated protein RP/EB family member 1 isoform X1
microtubule-associated protein RP/EB family member 1 isoform X3
DNA (cytosine-5)-methyltransferase 3B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
COMM domain containing 7, transcript variant X1
COMM domain containing 7, transcript variant X2
COMM domain containing 7, transcript variant X4
COMM domain containing 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
COMM domain-containing protein 7 isoform X1
COMM domain-containing protein 7 isoform X3
COMM domain-containing protein 7 isoform X2
polycomb group protein ASXL1-like, transcript variant X1
polycomb group protein ASXL1-like, transcript variant X2
polycomb group protein ASXL1-like, transcript variant X3
polycomb group protein ASXL1-like isoform X1
polycomb group protein ASXL1-like isoform X2
polycomb group protein ASXL1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73% 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 long SRA read, and 68% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
kinesin family member 3B, transcript variant X2
kinesin family member 3B, transcript variant X1
zinc finger protein PLAG1-like, transcript variant X1
zinc finger protein PLAG1-like, transcript variant X2
zinc finger protein PLAG1-like, transcript variant X5
zinc finger protein PLAG1-like, transcript variant X3
zinc finger protein PLAG1-like, transcript variant X4
zinc finger protein PLAG1-like, transcript variant X8
zinc finger protein PLAG1-like, transcript variant X7
zinc finger protein PLAG1-like, transcript variant X6
zinc finger protein PLAG1-like, transcript variant X10
zinc finger protein PLAG1-like isoform X6
zinc finger protein PLAG1-like isoform X1
zinc finger protein PLAG1-like isoform X2
zinc finger protein PLAG1-like isoform X5
zinc finger protein PLAG1-like, transcript variant X11
zinc finger protein PLAG1-like isoform X3
zinc finger protein PLAG1-like isoform X4
zinc finger protein PLAG1-like, transcript variant X9
zinc finger protein PLAG1-like isoform X7
transmembrane 9 superfamily protein member 4, transcript variant X1
transmembrane 9 superfamily protein member 4, transcript variant X2
transmembrane 9 superfamily member 4 isoform X1
transmembrane 9 superfamily member 4 isoform X2
HCK proto-oncogene, Src family tyrosine kinase
CCM2 like scaffold protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
CCM2 like scaffold protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CCM2 like scaffold protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 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
cerebral cavernous malformations 2 protein-like isoform X1
cerebral cavernous malformations 2 protein-like isoform X2
cerebral cavernous malformations 2 protein-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription elongation factor A protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
regulator of G protein signaling 19, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 38 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulator of G protein signaling 19, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 34 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
regulator of G protein signaling 19, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
regulator of G protein signaling 19, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulator of G protein signaling 19, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulator of G-protein signaling 19 isoform X1
regulator of G-protein signaling 19 isoform X2
regulator of G-protein signaling 19 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC125485528, transcript variant X4
uncharacterized LOC125485528, transcript variant X1
uncharacterized LOC125485528, transcript variant X5
uncharacterized LOC125485528, transcript variant X2
uncharacterized LOC125485528, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: nociceptin receptor
neuropeptides B/W receptor type 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neuropeptides B/W receptor type 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuropeptides B/W receptor type 2-like, transcript variant X3
uncharacterized LOC125485479, transcript variant X2
uncharacterized LOC125485479, transcript variant X1
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
peroxidasin homolog, transcript variant X1
peroxidasin homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 16 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
protein-tyrosine kinase 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 65 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein-tyrosine kinase 6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein-tyrosine kinase 6-like isoform X2
protein-tyrosine kinase 6-like isoform X1
pancreatic progenitor cell differentiation and proliferation factor b
pancreatic progenitor cell differentiation and proliferation factor
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
hairy/enhancer-of-split related with YRPW motif protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
histone-lysine N-methyltransferase PRDM9, transcript variant X3
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 4 samples with support for all annotated introns
histone-lysine N-methyltransferase PRDM9, transcript variant X1
histone-lysine N-methyltransferase PRDM9, transcript variant X2
histone-lysine N-methyltransferase PRDM9 isoform X1
histone-lysine N-methyltransferase PRDM9 isoform X2
zinc finger protein 704-like, transcript variant X5
zinc finger protein 704-like, transcript variant X3
zinc finger protein 704-like, transcript variant X4
zinc finger protein 704-like, transcript variant X2
zinc finger protein 704-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC570575 homolog
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
phosphoprotein associated with glycosphingolipid-enriched microdomains 1
sodium/potassium-transporting ATPase subunit beta-1-interacting protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 long SRA reads, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC125485426, transcript variant X1
uncharacterized LOC125485426, transcript variant X2
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
YTH N(6)-methyladenosine RNA binding protein 1, transcript variant X4
YTH N(6)-methyladenosine RNA binding protein 1, transcript variant X1
YTH N(6)-methyladenosine RNA binding protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
YTH domain-containing family protein 1 isoform X2
YTH domain-containing family protein 1 isoform X1
YTH N(6)-methyladenosine RNA binding protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
YTH N(6)-methyladenosine RNA binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
basic helix-loop-helix family, member e23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
class E basic helix-loop-helix protein 23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glucose-induced degradation protein 8 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uridine-cytidine kinase-like 1, transcript variant X1
uridine-cytidine kinase-like 1, transcript variant X2
uridine-cytidine kinase-like 1 isoform X1
uridine-cytidine kinase-like 1 isoform X2
zinc finger protein 512B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
zinc finger protein 512B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 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
sterile alpha motif domain-containing protein 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
PRP6 pre-mRNA processing factor 6 homolog (S. cerevisiae)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ADP-ribosylation factor GTPase activating protein 1, transcript variant X2
ADP-ribosylation factor GTPase activating protein 1, transcript variant X1
ADP-ribosylation factor GTPase-activating protein 1 isoform X1
ADP-ribosylation factor GTPase-activating protein 1 isoform X2
DEP domain-containing mTOR-interacting protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
prostaglandin I2 (prostacyclin) synthase
potassium voltage-gated channel, Shab-related subfamily, member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily B member 1
transfer RNA serine (anticodon GGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
somatomedin-B and thrombospondin type-1 domain-containing protein
COORDINATES: nucleotide motif:Rfam:12.0:RF00581
staufen double-stranded RNA binding protein 1, transcript variant X6
staufen double-stranded RNA binding protein 1, transcript variant X4
staufen double-stranded RNA binding protein 1, transcript variant X3
staufen double-stranded RNA binding protein 1, transcript variant X5
staufen double-stranded RNA binding protein 1, transcript variant X2
staufen double-stranded RNA binding protein 1, transcript variant X1
double-stranded RNA-binding protein Staufen homolog 1 isoform X6
double-stranded RNA-binding protein Staufen homolog 1 isoform X4
double-stranded RNA-binding protein Staufen homolog 1 isoform X3
double-stranded RNA-binding protein Staufen homolog 1 isoform X5
double-stranded RNA-binding protein Staufen homolog 1 isoform X2
double-stranded RNA-binding protein Staufen homolog 1 isoform X1
CSE1 chromosome segregation 1-like (yeast), transcript variant X1
CSE1 chromosome segregation 1-like (yeast), transcript variant X2
brefeldin A-inhibited guanine nucleotide-exchange protein 2, transcript variant X2
brefeldin A-inhibited guanine nucleotide-exchange protein 2, transcript variant X1
brefeldin A-inhibited guanine nucleotide-exchange protein 2 isoform X2
brefeldin A-inhibited guanine nucleotide-exchange protein 2 isoform X1
brefeldin A-inhibited guanine nucleotide-exchange protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
brefeldin A-inhibited guanine nucleotide-exchange protein 1 isoform X3
phosphatidylinositol-3,4, 5-trisphosphate-dependent Rac exchange factor 1, transcript variant X1
phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 1 protein isoform X1
phosphatidylinositol-3,4, 5-trisphosphate-dependent Rac exchange factor 1, transcript variant X2
phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 1 protein isoform 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
sodium-dependent lysophosphatidylcholine symporter 1-A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
sodium-dependent lysophosphatidylcholine symporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein FAM110B-like, transcript variant X2
protein FAM110B-like, transcript variant X1
protein FAM110B-like, transcript variant X4
protein FAM110B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ganglioside induced differentiation associated protein 1-like 1
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
ganglioside-induced differentiation-associated protein 1-like 1
fat storage inducing transmembrane protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125485478, transcript variant X2
uncharacterized LOC125485478, transcript variant X1
hepatocyte nuclear factor 4, alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
hepatocyte nuclear factor 4, alpha, transcript variant X2
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
hepatocyte nuclear factor 4-alpha isoform X1
hepatocyte nuclear factor 4-alpha isoform X2
tocopherol (alpha) transfer protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 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
tocopherol (alpha) transfer protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, 12 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: 3 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
serine/arginine repetitive matrix protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
zinc finger, CCCH-type with G patch domain, transcript variant X1
zinc finger, CCCH-type with G patch domain, transcript variant X2
zinc finger CCCH-type with G patch domain-containing protein isoform X2
zinc finger CCCH-type with G patch domain-containing protein isoform X1
ADP-ribosylation factor related protein 1
ADP-ribosylation factor-related protein 1
tumor necrosis factor receptor superfamily member 6B
regulator of telomere elongation helicase 1, transcript variant X4
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 1 sample with support for all annotated introns
regulator of telomere elongation helicase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulator of telomere elongation helicase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulator of telomere elongation helicase 1 isoform X3
regulator of telomere elongation helicase 1 isoform X4
regulator of telomere elongation helicase 1 isoform X2
regulator of telomere elongation helicase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulator of telomere elongation helicase 1 isoform X1
regulator of telomere elongation helicase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
glucocorticoid modulatory element binding protein 2, transcript variant X1
glucocorticoid modulatory element binding protein 2, transcript variant X2
glucocorticoid modulatory element binding protein 2, transcript variant X3
glucocorticoid modulatory element-binding protein 2 isoform X1
glucocorticoid modulatory element-binding protein 2 isoform X2
helicase with zinc finger 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
helicase with zinc finger 2a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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
helicase with zinc finger domain 2 isoform X1
helicase with zinc finger domain 2 isoform X2
helicase with zinc finger 2a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
helicase with zinc finger domain 2 isoform X3
fibronectin type III domain-containing protein 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
beta-1,4-galactosyltransferase 5, transcript variant X3
beta-1,4-galactosyltransferase 5, transcript variant X5
beta-1,4-galactosyltransferase 5, transcript variant X2
beta-1,4-galactosyltransferase 5, transcript variant X1
beta-1,4-galactosyltransferase 5, transcript variant X4
beta-1,4-galactosyltransferase 5 isoform X3
beta-1,4-galactosyltransferase 5 isoform X2
beta-1,4-galactosyltransferase 5 isoform X1
beta-1,4-galactosyltransferase 5 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 16 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 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: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
ubiquitin-conjugating enzyme E2 variant 1
CCAAT/enhancer-binding protein beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
protein tyrosine phosphatase non-receptor type 1
tyrosine-protein phosphatase non-receptor type 1
partitioning defective 6 homolog beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 86% 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: 22 long SRA reads, 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
activity-dependent neuroprotector homeobox b, transcript variant X1
activity-dependent neuroprotector homeobox b, transcript variant X3
activity-dependent neuroprotector homeobox b, transcript variant X2
activity-dependent neuroprotector homeobox b, transcript variant X4
activity-dependent neuroprotector homeobox b isoform X1
activity-dependent neuroprotector homeobox b isoform X2
dolichyl-phosphate mannosyltransferase subunit 1, catalytic
dolichol-phosphate mannosyltransferase subunit 1
potassium voltage-gated channel, subfamily G, member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily G member 1
uncharacterized LOC125485523, transcript variant X3
uncharacterized LOC125485523, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125485523, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 72% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
nuclear factor of activated T cells 2a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear factor of activated T cells 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
nuclear factor of activated T-cells, cytoplasmic 2 isoform X2
nuclear factor of activated T-cells, cytoplasmic 2 isoform X1
probable phospholipid-transporting ATPase IIA
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
spalt-like transcription factor 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
spalt-like transcription factor 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
1,25-dihydroxyvitamin D(3) 24-hydroxylase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
brain enriched myelin associated protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
teashirt homolog 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
teashirt homolog 2, transcript variant X1
teashirt homolog 2, transcript variant X3
teashirt homolog 2, transcript variant X4
prefoldin subunit 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 long SRA reads, 15 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
prefoldin subunit 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 long SRA reads, 15 Proteins, and 88% 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: 29 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 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: 38 Proteins, and 64% 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% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 Proteins
family with sequence similarity 210 member B
aurora kinase C-like, transcript variant X1
aurora kinase C-like, transcript variant X2
aurora kinase C-like, transcript variant X3
aurora kinase C-like, 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
serine/threonine-protein kinase Aurora-2-like isoform X2
zinc finger, NFX1-type containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 long SRA reads, 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
zinc finger, NFX1-type containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 long SRA reads, 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NFX1-type zinc finger-containing protein 1 isoform X1
zinc finger, NFX1-type containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 long SRA reads, 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger, NFX1-type containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 long SRA reads, 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NFX1-type zinc finger-containing protein 1 isoform X2
cyclin D-type binding-protein 1, transcript variant X1
cyclin-D1-binding protein 1 homolog isoform X1
cyclin D-type binding-protein 1, transcript variant X2
cyclin D-type binding-protein 1, transcript variant X3
cyclin-D1-binding protein 1 homolog isoform X2
protein-glutamine gamma-glutamyltransferase 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein-glutamine gamma-glutamyltransferase 2-like, transcript variant X1
protein-glutamine gamma-glutamyltransferase 2-like, transcript variant X2
protein-glutamine gamma-glutamyltransferase 2-like, transcript variant X3
protein-glutamine gamma-glutamyltransferase 2-like, transcript variant X4
protein-glutamine gamma-glutamyltransferase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein-glutamine gamma-glutamyltransferase 2-like isoform X1
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 3 samples with support for all annotated introns
protein-glutamine gamma-glutamyltransferase 2-like isoform X2
regulation of nuclear pre-mRNA domain-containing protein 1B
V-set and transmembrane domain-containing protein 2-like protein
pleckstrin homology domain-containing family G member 4B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 34% coverage of the annotated genomic feature by RNAseq alignments
CDK5 regulatory subunit associated protein 1
CDK5 regulatory subunit-associated protein 1
bactericidal permeability-increasing protein-like, transcript variant X1
bactericidal permeability-increasing 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 13 samples with support for all annotated introns
bactericidal permeability-increasing protein-like isoform X1
bactericidal permeability-increasing protein-like isoform X2
iroquois-class homeodomain protein irx-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91 long SRA reads, 33 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125485446, transcript variant X1
uncharacterized LOC125485446, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: solute carrier family 12 member 5-like
nuclear receptor coactivator 5, transcript variant X2
nuclear receptor coactivator 5, transcript variant X4
nuclear receptor coactivator 5, transcript variant X1
nuclear receptor coactivator 5, transcript variant X3
nuclear receptor coactivator 5 isoform X2
nuclear receptor coactivator 5 isoform X1
nuclear receptor coactivator 5 isoform X3
nuclear receptor coactivator 5 isoform X4
uncharacterized LOC125485467, transcript variant X1
uncharacterized LOC125485467, transcript variant X2
uncharacterized LOC125485467, transcript variant X3
neuralized E3 ubiquitin protein ligase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 19% 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: 3 long SRA reads, 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
troponin C, skeletal muscle, transcript variant X1
troponin C, skeletal muscle, transcript variant X2
troponin C, skeletal muscle, transcript variant X3
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor receptor superfamily member 5-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 1 sample with support for all annotated introns
tumor necrosis factor receptor superfamily member 5-like isoform X2
tumor necrosis factor receptor superfamily member 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
tumor necrosis factor receptor superfamily member 5-like isoform X1
tumor necrosis factor receptor superfamily member 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tumor necrosis factor receptor superfamily member 5-like isoform X3
tumor necrosis factor receptor superfamily member 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
AP-1 complex subunit gamma-1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
AP-1 complex subunit gamma-1-like, transcript variant X1
AP-1 complex subunit gamma-1-like, transcript variant X2
AP-1 complex subunit gamma-1-like isoform X1
AP-1 complex subunit gamma-1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 15 Proteins, and 94% 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 83% coverage of the annotated genomic feature by RNAseq alignments
cleavage stimulation factor, 3' pre-RNA, subunit 1, transcript variant X2
cleavage stimulation factor, 3' pre-RNA, subunit 1, transcript variant X5
cleavage stimulation factor, 3' pre-RNA, subunit 1, transcript variant X3
cleavage stimulation factor, 3' pre-RNA, subunit 1, transcript variant X1
cleavage stimulation factor, 3' pre-RNA, subunit 1, transcript variant X4
acyl-coenzyme A diphosphatase NUDT19-like, transcript variant X3
acyl-coenzyme A diphosphatase NUDT19-like, transcript variant X2
acyl-coenzyme A diphosphatase NUDT19-like, transcript variant X1
acyl-coenzyme A diphosphatase NUDT19-like isoform X1
acyl-coenzyme A diphosphatase NUDT19-like isoform X2
acyl-coenzyme A diphosphatase NUDT19-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 65% 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: 544 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 27
probable ATP-dependent RNA helicase DDX27
small nuclear ribonucleoprotein polypeptides B and B1
small nuclear ribonucleoprotein-associated proteins B and B'
solute carrier family 35 member C2, transcript variant X1
solute carrier family 35 member C2, transcript variant X3
solute carrier family 35 member C2 isoform X1
solute carrier family 35 member C2 isoform X3
solute carrier family 35 member C2, transcript variant X2
solute carrier family 35 member C2 isoform X2
bactericidal permeability-increasing protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 long SRA reads, 20 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein G(s) subunit alpha, transcript variant X1
guanine nucleotide-binding protein G(s) subunit alpha, transcript variant X2
guanine nucleotide-binding protein G(s) subunit alpha, transcript variant X3
guanine nucleotide-binding protein G(s) subunit alpha isoform X1
guanine nucleotide-binding protein G(s) subunit alpha isoform X2
guanine nucleotide-binding protein G(s) subunit alpha isoform X3
negative elongation factor complex member C/D, transcript variant X3
negative elongation factor complex member C/D, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
negative elongation factor complex member C/D, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
negative elongation factor complex member C/D, transcript variant X1
negative elongation factor C/D isoform X1
negative elongation factor complex member C/D, transcript variant X5
negative elongation factor C/D isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
protein TMEPAI-like, transcript variant X3
protein TMEPAI-like, transcript variant X2
protein TMEPAI-like, transcript variant X1
protein TMEPAI-like, transcript variant X5
protein TMEPAI-like, transcript variant X4
tubulin tyrosine ligase-like family, member 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
WAP four-disulfide core domain 2, transcript variant X1
WAP four-disulfide core domain 2, transcript variant X2
WAP four-disulfide core domain protein 3 isoform X1
WAP four-disulfide core domain protein 3 isoform X2
regulator of G-protein signaling 9-binding protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
deoxynucleotidyltransferase terminal-interacting protein 1
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
phosphorylated CTD interacting factor 1, transcript variant X4
phosphorylated CTD interacting factor 1, transcript variant X1
phosphorylated CTD interacting factor 1, transcript variant X2
phosphorylated CTD interacting factor 1, transcript variant X3
mRNA (2'-O-methyladenosine-N(6)-)-methyltransferase isoform X3
mRNA (2'-O-methyladenosine-N(6)-)-methyltransferase isoform X1
mRNA (2'-O-methyladenosine-N(6)-)-methyltransferase isoform X2
phosphorylated CTD interacting factor 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphorylated CTD interacting factor 1, transcript variant X6
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 2 samples with support for all annotated introns
phosphorylated CTD interacting factor 1, transcript variant X5
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
mRNA (2'-O-methyladenosine-N(6)-)-methyltransferase isoform X4
phospholipid transfer protein, transcript variant X2
phospholipid transfer protein, transcript variant X1
phospholipid transfer protein, transcript variant X3
phospholipid transfer protein, transcript variant X4
phospholipid transfer protein, transcript variant X6
phospholipid transfer protein, transcript variant X5
phospholipid transfer protein isoform X1
phospholipid transfer protein isoform X2
cytochrome c oxidase subunit 4 isoform 1, mitochondrial-like, transcript variant X1
cytochrome c oxidase subunit 4 isoform 1, mitochondrial-like, transcript variant X2
cytochrome c oxidase subunit 4 isoform 1, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 75 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
targeting protein for Xklp2-A-like, transcript variant X1
targeting protein for Xklp2-A-like, transcript variant X2
targeting protein for Xklp2-A-like isoform X1
targeting protein for Xklp2-A-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
SPO11 initiator of meiotic double stranded breaks, transcript variant X2
SPO11 initiator of meiotic double stranded breaks, transcript variant X3
SPO11 initiator of meiotic double stranded breaks, transcript variant X1
SPO11 initiator of meiotic double stranded breaks, transcript variant X4
meiotic recombination protein SPO11 isoform X2
meiotic recombination protein SPO11 isoform X1
meiotic recombination protein SPO11 isoform X4
meiotic recombination protein SPO11 isoform X3
ribonucleic acid export 1, transcript variant X2
ribonucleic acid export 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62% coverage of the annotated genomic feature by RNAseq alignments
transcriptional repressor CTCF-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcriptional repressor CTCF-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphoenolpyruvate carboxykinase 1 (soluble)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 58 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
phosphoenolpyruvate carboxykinase, cytosolic [GTP]
ATP synthase subunit epsilon, mitochondrial
tubulin beta-4 chain-like, transcript variant X1
tubulin beta-4 chain-like, transcript variant X2
phosphatidylinositol glycan anchor biosynthesis, class T
uncharacterized LOC125485526, transcript variant X2
uncharacterized LOC125485526, transcript variant X4
uncharacterized LOC125485526, transcript variant X1
uncharacterized LOC125485526, transcript variant X3
piezo-type mechanosensitive ion channel component 2-like
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
piezo-type mechanosensitive ion channel component 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
VAMP (vesicle-associated membrane protein)-associated protein B and C
vesicle-associated membrane protein-associated protein B/C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 62% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein phosphatase 4 regulatory subunit 1-like
ankyrin repeat domain-containing protein 60
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
androgen dependent TFPI regulating protein 1, transcript variant X4
androgen dependent TFPI regulating protein 1, transcript variant X2
androgen dependent TFPI regulating protein 1 isoform X4
androgen dependent TFPI regulating protein 1 isoform X2
androgen dependent TFPI regulating protein 1, transcript variant X1
androgen dependent TFPI regulating protein 1 isoform X1
androgen dependent TFPI regulating protein 1, transcript variant X5
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
androgen dependent TFPI regulating protein 1 isoform X5
androgen dependent TFPI regulating protein 1, transcript variant X6
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 4 samples with support for all annotated introns
androgen dependent TFPI regulating protein 1 isoform X6
androgen dependent TFPI regulating protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
androgen dependent TFPI regulating protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 74% 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: 75% coverage of the annotated genomic feature by RNAseq alignments