Rhincodon typus isolate 14 chromosome 15, 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\nCM038812.1.\nAssembly name: sRhiTyp1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/03. The\noriginal whole-genome shotgun project has the accession\nJAHMAH000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Supernova v. 2.1.1; P_RNA_scaffolder v.\n commit 7941e0f; Tigmint v. 1.1.2; ARKS v.\n 1.1.0; 3D-DNA v. 180922\nAssembly Name :: sRhiTyp1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 46.7x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Rhincodon typus Annotation Release\n 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC326033 homolog, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized protein LOC326033 homolog, transcript variant X2
uncharacterized protein LOC326033 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
aldo-keto reductase family 1 member B1 isoform X1
aldo-keto reductase family 1 member B1 isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
vacuolar protein sorting-associated protein 4A
U3 small nucleolar RNA-associated protein 4 homolog
CTF8, chromosome transmission fidelity factor 8 homolog (S. cerevisiae)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
chromosome transmission fidelity protein 8 homolog
transport and golgi organization 6 homolog (Drosophila)
transport and Golgi organization protein 6 homolog
cadherin 15, type 1, M-cadherin (myotubule)
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
zinc finger CCCH domain-containing protein 18-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
malonate--CoA ligase ACSF3, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
malonate--CoA ligase ACSF3, mitochondrial-like, transcript variant X3
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 14 samples with support for all annotated introns
malonate--CoA ligase ACSF3, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
malonate--CoA ligase ACSF3, mitochondrial-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 6 samples with support for all annotated introns
malonate--CoA ligase ACSF3, mitochondrial-like
malonate--CoA ligase ACSF3, mitochondrial
zinc finger CCCH-type containing 18, transcript variant X1
zinc finger CCCH-type containing 18, transcript variant X2
zinc finger CCCH domain-containing protein 18 isoform X1
zinc finger CCCH domain-containing protein 18 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein KIAA0513, transcript variant X6
uncharacterized protein KIAA0513, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized protein KIAA0513, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein KIAA0513 isoform X4
uncharacterized protein KIAA0513 isoform X1
uncharacterized LOC125484932, transcript variant X1
uncharacterized LOC125484932, transcript variant X2
uncharacterized LOC125484932, transcript variant X3
uncharacterized protein LOC125484932 isoform X2
uncharacterized protein LOC125484932 isoform X1
uncharacterized protein LOC125484932 isoform X3
uncharacterized protein KIAA0513, transcript variant X4
uncharacterized protein KIAA0513, transcript variant X3
uncharacterized protein KIAA0513, transcript variant X5
Fanconi anemia core complex-associated protein 24 isoform X2
Fanconi anemia core complex-associated protein 24 isoform X3
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
low density lipoprotein receptor-related protein 3, transcript variant X1
low density lipoprotein receptor-related protein 3, transcript variant X2
low-density lipoprotein receptor-related protein 3 isoform X1
low-density lipoprotein receptor-related protein 3 isoform X2
large neutral amino acids transporter small subunit 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 47 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: large neutral amino acids transporter small subunit 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 long SRA reads, 20 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: 3 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
BTB/POZ domain-containing protein KCTD15, 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 7 samples with support for all annotated introns
BTB/POZ domain-containing protein KCTD15, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
BTB/POZ domain-containing protein KCTD15
transcription initiation factor TFIID subunit 4-like
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
LSM14A mRNA processing body assembly factor, transcript variant X5
LSM14A mRNA processing body assembly factor, transcript variant X2
LSM14A mRNA processing body assembly factor, transcript variant X3
LSM14A mRNA processing body assembly factor, transcript variant X4
LSM14A mRNA processing body assembly factor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 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 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: UDP-glucuronosyltransferase 2A2-like
ubiquitin-like modifier activating enzyme 2
Wilms tumor protein 1-interacting protein homolog, transcript variant X1
Wilms tumor protein 1-interacting protein homolog isoform X1
Wilms tumor protein 1-interacting protein homolog, transcript variant X2
Wilms tumor protein 1-interacting protein homolog isoform X2
granule associated Rac and RHOG effector 1, transcript variant X1
granule associated Rac and RHOG effector 1, transcript variant X3
granule associated Rac and RHOG effector 1, transcript variant X4
granule associated Rac and RHOG effector 1, transcript variant X5
granule associated Rac and RHOG effector 1, transcript variant X2
granule associated Rac and RHOG effector protein 1 isoform X1
granule associated Rac and RHOG effector protein 1 isoform X2
granule associated Rac and RHOG effector protein 1 isoform X3
granule associated Rac and RHOG effector protein 1 isoform X4
granule associated Rac and RHOG effector 1, transcript variant X6
granule associated Rac and RHOG effector protein 1 isoform X5
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: carboxylesterase 5A-like
fatty acyl-CoA hydrolase precursor, medium chain-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 57% coverage of the annotated genomic feature by RNAseq alignments
cytosolic iron-sulfur assembly component 2B
Ras-related associated with diabetes, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 20 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Ras-related associated with diabetes, transcript variant X2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
NEDD8-activating enzyme E1 regulatory subunit
telomere repeats-binding bouquet formation protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 41% coverage of the annotated genomic feature by RNAseq alignments
cytoplasmic dynein 1 light intermediate chain 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
NEDD8-activating enzyme E1 regulatory subunit-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CKLF-like MARVEL transmembrane domain containing 4
CKLF-like MARVEL transmembrane domain-containing protein 4
CKLF-like MARVEL transmembrane domain containing 3
CKLF-like MARVEL transmembrane domain-containing protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized protein si:ch211-189a15.5
brain expressed, associated with NEDD4, 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transfer RNA valine (anticodon CAC); 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: 99 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
ADAM metallopeptidase with thrombospondin type 1 motif, 18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
A disintegrin and metalloproteinase with thrombospondin motifs 18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nudix (nucleoside diphosphate linked moiety X)-type motif 7, transcript variant X5
peroxisomal coenzyme A diphosphatase NUDT7 isoform X5
nudix (nucleoside diphosphate linked moiety X)-type motif 7, transcript variant X3
nudix (nucleoside diphosphate linked moiety X)-type motif 7, transcript variant X1
nudix (nucleoside diphosphate linked moiety X)-type motif 7, transcript variant X2
peroxisomal coenzyme A diphosphatase NUDT7 isoform X3
peroxisomal coenzyme A diphosphatase NUDT7 isoform X1
nudix (nucleoside diphosphate linked moiety X)-type motif 7, transcript variant X4
peroxisomal coenzyme A diphosphatase NUDT7 isoform X2
peroxisomal coenzyme A diphosphatase NUDT7 isoform X4
synaptic vesicle membrane protein VAT-1 homolog-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein si:dkey-234i14.6
v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog a (paralog a), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog a (paralog a), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog a (paralog a), transcript variant X3
v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog a (paralog a), transcript variant X5
v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog a (paralog a), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
chromodomain Y-like protein 2, transcript variant X3
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 1 sample with support for all annotated introns
chromodomain Y-like protein 2, transcript variant X1
chromodomain Y-like protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
chromodomain Y-like protein 2, transcript variant X2
chromodomain Y-like protein 2 isoform X1
chromodomain Y-like protein 2 isoform X2
chromodomain Y-like protein 2 isoform X3
chromodomain Y-like protein 2 isoform X4
chromodomain Y-like protein 2, transcript variant X5
chromodomain Y-like protein 2 isoform X5
CBY1-interacting BAR domain-containing protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CBY1-interacting BAR domain-containing protein 2-like, transcript variant X3
CBY1-interacting BAR domain-containing protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CBY1-interacting BAR domain-containing protein 2-like isoform X1
CBY1-interacting BAR domain-containing protein 2-like isoform X3
CBY1-interacting BAR domain-containing protein 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 1 regulatory subunit 3E
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C16orf46, transcript variant X1
uncharacterized protein C16orf46, transcript variant X2
uncharacterized protein C16orf46, transcript variant X4
uncharacterized protein C16orf46, transcript variant X3
M-phase specific PLK1 interacting protein
M-phase-specific PLK1-interacting protein
COX assembly mitochondrial protein 2 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DNA replication complex GINS protein PSF2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
dual specificity protein phosphatase 22-A
interferon regulatory factor 8, transcript variant X2
interferon regulatory factor 8, transcript variant X1
interferon regulatory factor 8, transcript variant X4
interferon regulatory factor 8, transcript variant X3
interferon regulatory factor 8 isoform X1
interferon regulatory factor 8 isoform X4
interferon regulatory factor 8 isoform X2
interferon regulatory factor 8 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins
methenyltetrahydrofolate synthetase domain containing, transcript variant X4
methenyltetrahydrofolate synthetase domain containing, transcript variant X5
methenyltetrahydrofolate synthetase domain containing, transcript variant X1
methenyltetrahydrofolate synthetase domain containing, transcript variant X6
methenyltetrahydrofolate synthetase domain containing, transcript variant X2
methenyltetrahydrofolate synthetase domain containing, transcript variant X3
methenyltetrahydrofolate synthase domain-containing protein isoform X1
methenyltetrahydrofolate synthase domain-containing protein isoform X4
methenyltetrahydrofolate synthase domain-containing protein isoform X2
methenyltetrahydrofolate synthase domain-containing protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger DHHC-type palmitoyltransferase 7
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: 21 long SRA reads, 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: palmitoyltransferase ZDHHC7
hepatocyte nuclear factor 4-beta-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
hepatocyte nuclear factor 4-beta-like, transcript variant X1
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, including 2 samples with support for all annotated introns
hepatocyte nuclear factor 4-beta-like isoform X2
hepatocyte nuclear factor 4-beta-like isoform X1
cysteine-rich secretory protein LCCL domain containing 2
cysteine-rich secretory protein LCCL domain-containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
coactosin-like F-actin binding protein 1
calcium-transporting ATPase type 2C member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium-transporting ATPase type 2C member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
WAP four-disulfide core domain 1, 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 3 samples with support for all annotated introns
WAP four-disulfide core domain 1, transcript variant X1
WAP four-disulfide core domain protein 1
potassium voltage-gated channel, subfamily G, member 4a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
potassium voltage-gated channel subfamily G member 4a
solute carrier family 66 member 2, transcript variant X1
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
solute carrier family 66 member 2, transcript variant X2
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
malonyl-CoA decarboxylase, mitochondrial
hydroxysteroid (17-beta) dehydrogenase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X3
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X2
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X1
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X5
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X7
short-chain dehydrogenase/reductase family 42E member 1 isoform X1
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X6
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X4
short-chain dehydrogenase/reductase family 42E member 1 isoform X2
short-chain dehydrogenase/reductase family 42E member 1 isoform X3
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 14 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
glycine cleavage system H protein, mitochondrial
polycystic kidney disease protein 1-like 2
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: 2 Proteins, and 60% 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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: beta,beta-carotene 15,15'-dioxygenase
charged multivesicular body protein 1A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 148 long SRA reads, 35 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
charged multivesicular body protein 1A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 112 long SRA reads, 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
charged multivesicular body protein 1a isoform X1
charged multivesicular body protein 1a isoform X2
cyclin-dependent kinase 10, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 long SRA reads, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
cyclin-dependent kinase 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 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
cyclin-dependent kinase 10, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
spermatogenesis associated 2-like, transcript variant X1
spermatogenesis associated 2-like, transcript variant X2
spermatogenesis associated 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57% coverage of the annotated genomic feature by RNAseq alignments
VPS9 domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
VPS9 domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
VPS9 domain containing 1, transcript variant 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 4 samples with support for all annotated introns
VPS9 domain-containing protein 1 isoform X1
VPS9 domain-containing protein 1 isoform X2
VPS9 domain-containing protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC560780 homolog
uncharacterized protein si:dkey-238o13.4
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
zinc finger homeobox 3b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger homeobox 3b, transcript variant X2
polyamine-modulated factor 1-binding protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 63% coverage of the annotated genomic feature by RNAseq alignments
pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16-like
uncharacterized LOC125484976, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125484976, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125484976, 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 3 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, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane emp24 domain-containing protein 6
26S proteasome non-ATPase regulatory subunit 7
DEAH (Asp-Glu-Ala-His) box polypeptide 38
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16
WW domain containing E3 ubiquitin protein ligase 2, transcript variant X1
NEDD4-like E3 ubiquitin-protein ligase WWP2
WW domain containing E3 ubiquitin protein ligase 2, transcript variant X2
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 11 samples with support for all annotated introns
nuclear factor of activated T-cells 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 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 5-like, transcript variant X1
nuclear factor of activated T-cells 5-like
telomeric repeat-binding factor 2, transcript variant X2
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 7 samples with support for all annotated introns
telomeric repeat-binding factor 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
telomeric repeat-binding factor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
telomeric repeat-binding factor 2 isoform X2
telomeric repeat-binding factor 2 isoform X3
telomeric repeat-binding factor 2 isoform X1
telomeric repeat-binding factor 2, transcript variant X4
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 7 samples with support for all annotated introns
telomeric repeat-binding factor 2 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
lysine--tRNA ligase-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
lysine--tRNA ligase-like, transcript variant X1
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 11 samples with support for all annotated introns
lysine--tRNA ligase-like, 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 7 samples with support for all annotated introns
lysine--tRNA ligase-like, transcript variant X4
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 11 samples with support for all annotated introns
adenosine deaminase tRNA specific 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
adenosine deaminase tRNA specific 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
adenosine deaminase tRNA specific 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
adenosine deaminase tRNA specific 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 long SRA reads, 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
adenosine deaminase tRNA specific 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tRNA-specific adenosine deaminase 1 isoform X1
tRNA-specific adenosine deaminase 1 isoform X2
tRNA-specific adenosine deaminase 1 isoform X3
tRNA-specific adenosine deaminase 1 isoform X4
tRNA-specific adenosine deaminase 1 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
carbohydrate sulfotransferase 6, transcript variant X1
carbohydrate sulfotransferase 6, transcript variant X2
carbohydrate sulfotransferase 6, transcript variant X3
IST1 factor associated with ESCRT-III, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 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
IST1 factor associated with ESCRT-III, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
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 16 samples with support for all annotated introns
dihydroorotate dehydrogenase (quinone), mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: olfactory receptor 4K15-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
component of oligomeric golgi complex 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
component of oligomeric golgi complex 8, transcript variant X1
conserved oligomeric Golgi complex subunit 8 isoform X1
conserved oligomeric Golgi complex subunit 8 isoform X2
NIN1 (RPN12) binding protein 1 homolog, transcript variant X2
NIN1 (RPN12) binding protein 1 homolog, transcript variant X1
NIN1 (RPN12) binding protein 1 homolog, transcript variant X3
zinc finger protein 821-like, transcript variant X2
zinc finger protein 821-like, transcript variant X1
zinc finger protein 821-like, transcript variant X3
zinc finger protein 821-like, transcript variant X4
zinc finger protein 821-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
chromatin licensing and DNA replication factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
piezo-type mechanosensitive ion channel component 1, transcript variant X1
piezo-type mechanosensitive ion channel component 1, transcript variant X3
piezo-type mechanosensitive ion channel component 1, transcript variant X2
piezo-type mechanosensitive ion channel component 1 isoform X1
piezo-type mechanosensitive ion channel component 1 isoform X3
piezo-type mechanosensitive ion channel component 1 isoform X2
cytosolic thiouridylase subunit 2 homolog (S. pombe), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
cytosolic thiouridylase subunit 2 homolog (S. pombe), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
cytoplasmic tRNA 2-thiolation protein 2 isoform X1
cytoplasmic tRNA 2-thiolation protein 2 isoform X2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 11 Proteins, and 99% 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: 88% coverage of the annotated genomic feature by RNAseq alignments
5-hydroxyisourate hydrolase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
5-hydroxyisourate hydrolase-like, transcript variant X1
5-hydroxyisourate hydrolase-like isoform X1
5-hydroxyisourate hydrolase-like isoform X2
5-hydroxyisourate hydrolase-like, transcript variant X3
5-hydroxyisourate hydrolase-like isoform X3
dysbindin domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dysbindin domain containing 1, transcript variant X2
dysbindin domain-containing protein 1 isoform X1
dysbindin domain-containing protein 1 isoform X2
AFG3-like protein 2, transcript variant X1
AFG3-like protein 2, transcript variant X2
AFG3-like protein 2, transcript variant X3
differentially expressed in FDCP 8 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
differentially expressed in FDCP 8 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 long SRA reads, 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
differentially expressed in FDCP 8 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
differentially expressed in FDCP 8 homolog isoform X1
differentially expressed in FDCP 8 homolog isoform X2
differentially expressed in FDCP 8 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
differentially expressed in FDCP 8 homolog isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 5 Proteins, and 98% 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: 113 Proteins
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
solute carrier family 22 member 31, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 22 member 31, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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
putative solute carrier family 22 member 31 isoform X2
putative solute carrier family 22 member 31 isoform X1
ankyrin repeat domain 11, transcript variant X2
ankyrin repeat domain 11, transcript variant X1
ankyrin repeat domain-containing protein 11 isoform X2
ankyrin repeat domain-containing protein 11 isoform X1
ankyrin repeat domain 11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ankyrin repeat domain-containing protein 11 isoform X3
SPG7 matrix AAA peptidase subunit, paraplegin, transcript variant X2
SPG7 matrix AAA peptidase subunit, paraplegin, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74 Proteins, and 98% 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: 5 long SRA reads, 26 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
FA complementation group A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
FA complementation group A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
FA complementation group A, transcript variant X1
FA complementation group A, transcript variant X5
Fanconi anemia group A protein isoform X3
Fanconi anemia group A protein isoform X2
Fanconi anemia group A protein isoform X1
Fanconi anemia group A protein isoform X5
FA complementation group A, transcript variant X4
Fanconi anemia group A protein isoform X4
spire-type actin nucleation factor 2, transcript variant X1
spire-type actin nucleation factor 2, transcript variant X2
transcription factor 25 (basic helix-loop-helix)
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 20 samples with support for all annotated introns
thyrotropin-releasing hormone receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
thyrotropin-releasing hormone receptor-like isoform X2
thyrotropin-releasing hormone receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
thyrotropin-releasing hormone receptor-like isoform X1
zinc finger protein, FOG family member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein, FOG family member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 15 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: 50 long SRA reads, 18 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
large neutral amino acids transporter small subunit 1
carbonic anhydrase 5B, mitochondrial-like, transcript variant X1
carbonic anhydrase 5B, mitochondrial-like, transcript variant X3
carbonic anhydrase 5B, mitochondrial-like, transcript variant X2
carbonic anhydrase 5B, mitochondrial-like, transcript variant X5
carbonic anhydrase 5B, mitochondrial-like, transcript variant X4
carbonic anhydrase 5B, mitochondrial-like isoform X1
carbonic anhydrase 5B, mitochondrial-like isoform X3
carbonic anhydrase 5B, mitochondrial-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments
kelch domain containing 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99 long SRA reads, 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
kelch domain-containing protein 4 isoform X1
kelch domain containing 4, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
kelch domain containing 4, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
kelch domain containing 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
kelch domain containing 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
kelch domain containing 4, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
kelch domain-containing protein 4 isoform X2
kelch domain containing 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kelch domain containing 4, transcript variant X5
kelch domain-containing protein 4 isoform X3
kelch domain-containing protein 4 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
flavin-containing monooxygenase FMO GS-OX5-like, transcript variant X2
flavin-containing monooxygenase FMO GS-OX5-like, transcript variant X1
flavin-containing monooxygenase FMO GS-OX5-like, transcript variant X3
flavin-containing monooxygenase FMO GS-OX5-like, transcript variant X4
flavin-containing monooxygenase FMO GS-OX-like 1 isoform X2
flavin-containing monooxygenase FMO GS-OX5-like isoform X3
flavin-containing monooxygenase FMO GS-OX-like 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger CCHC domain-containing protein 14
adaptor related protein complex 1 subunit gamma 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 99% 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: 3 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
MARVEL domain-containing protein 3-like, 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 4 samples with support for all annotated introns
MARVEL domain-containing protein 3-like, transcript variant X5
MARVEL domain-containing protein 3-like, transcript variant X1
MARVEL domain-containing protein 3-like, transcript variant X3
MARVEL domain-containing protein 3-like, transcript variant X6
MARVEL domain-containing protein 3-like, transcript variant X2
MARVEL domain-containing protein 3-like, transcript variant X4
MARVEL domain-containing protein 3-like isoform X2
MARVEL domain-containing protein 3-like isoform X1
PH domain leucine-rich repeat-containing protein phosphatase 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
PH domain leucine-rich repeat-containing protein phosphatase 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PH domain leucine-rich repeat-containing protein phosphatase 2-like, transcript variant X2
PH domain leucine-rich repeat-containing protein phosphatase 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
PH domain leucine-rich repeat-containing protein phosphatase 2-like isoform X1
PH domain leucine-rich repeat-containing protein phosphatase 2-like isoform X2
PH domain leucine-rich repeat-containing protein phosphatase 2-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 7 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC100073327 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
tudor domain containing 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tudor domain containing 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tudor domain containing 12, transcript variant X5
tudor domain containing 12, transcript variant X4
tudor domain containing 12, transcript variant X3
putative ATP-dependent RNA helicase TDRD12 isoform X2
putative ATP-dependent RNA helicase TDRD12 isoform X4
putative ATP-dependent RNA helicase TDRD12 isoform X1
putative ATP-dependent RNA helicase TDRD12 isoform X3
tudor domain containing 12, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
putative ATP-dependent RNA helicase TDRD12 isoform X5
tudor domain containing 12, transcript variant X7
putative ATP-dependent RNA helicase TDRD12 isoform X6
ankyrin repeat domain 27 (VPS9 domain), transcript variant X2
regulator of G protein signaling 9 binding protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
regulator of G-protein signaling 9-binding protein
ankyrin repeat domain 27 (VPS9 domain), transcript variant X4
ankyrin repeat domain 27 (VPS9 domain), transcript variant X3
ankyrin repeat domain 27 (VPS9 domain), transcript variant X1
ankyrin repeat domain-containing protein 27 isoform X1
ankyrin repeat domain-containing protein 27 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125485029, transcript variant X2
uncharacterized LOC125485029, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC125485029 isoform X2
uncharacterized protein LOC125485029 isoform X1
dipeptidase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dipeptidase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
teashirt zinc finger homeobox 3b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
teashirt zinc finger homeobox 3b, transcript variant X1
teashirt zinc finger homeobox 3b, transcript variant X2
teashirt zinc finger homeobox 3b, transcript variant X5
teashirt zinc finger homeobox 3b, transcript variant X4
zinc finger protein 536, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 536, transcript variant X2
zinc finger protein 536, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 536, transcript variant X1
zinc finger protein 536, transcript variant X3
zinc finger protein 536, transcript variant X5
zinc finger protein 536, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 127 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
unconventional prefoldin RPB5 interactor 1
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 3 samples with support for all annotated introns
uncharacterized protein LOC555795 homolog, transcript variant X1
uncharacterized protein LOC555795 homolog, transcript variant X2
uncharacterized protein si:ch211-260e23.9
protein C19orf12 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
protein C19orf12 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein C19orf12 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pleckstrin homology domain containing, family F (with FYVE domain) member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
pleckstrin homology domain-containing family F member 1
NLR family CARD domain-containing protein 3-like, transcript variant X3
NLR family CARD domain-containing protein 3-like, transcript variant X4
NLR family CARD domain-containing protein 3-like, transcript variant X2
NLR family CARD domain-containing protein 3-like, transcript variant X1
NLR family CARD domain-containing protein 3-like isoform X1
NLR family CARD domain-containing protein 3-like isoform X2
NLR family CARD domain-containing protein 3-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NLR family CARD domain-containing protein 3-like, transcript variant X5
nucleotide-binding oligomerization domain-containing protein 1-like isoform X3
POP4 homolog, ribonuclease P/MRP subunit, transcript variant X2
POP4 homolog, ribonuclease P/MRP subunit, transcript variant X1
ribonuclease P protein subunit p29 isoform X2
ribonuclease P protein subunit p29 isoform X1
V-set and transmembrane domain containing 2B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
V-set and transmembrane domain-containing protein 2B
cytochrome b-c1 complex subunit Rieske, mitochondrial
uncharacterized LOC125485065, transcript variant X3
uncharacterized LOC125485065, transcript variant X2
uncharacterized LOC125485065, transcript variant X1
vacuolar protein sorting-associated protein 35
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
chromosome 15 C16orf87 homolog, transcript variant X2
chromosome 15 C16orf87 homolog, transcript variant X1
UPF0547 protein C16orf87 homolog isoform X2
UPF0547 protein C16orf87 homolog isoform X1
uncharacterized LOC125485057, 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 4 samples with support for all annotated introns
uncharacterized LOC125485057, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125485057, transcript variant X2
uncharacterized LOC125485057, transcript variant X3
glutamic pyruvate transaminase (alanine aminotransferase) 2
DnaJ heat shock protein family (Hsp40) member A2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
integrin alpha FG-GAP repeat containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 76% coverage of the annotated genomic feature by RNAseq alignments
phosphorylase b kinase regulatory subunit beta
ATP-binding cassette, sub-family C (CFTR/MRP), member 12
ATP-binding cassette sub-family C member 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC492735 homolog, transcript variant X1
uncharacterized protein LOC492735 homolog, transcript variant X2
zinc finger protein 423, transcript variant X2
zinc finger protein 423, transcript variant X5
zinc finger protein 423, transcript variant X4
zinc finger protein 423, transcript variant X3
zinc finger protein 423, transcript variant X1
zinc finger protein 423, transcript variant X6
zinc finger protein 423, transcript variant X9
zinc finger protein 423, transcript variant X8
zinc finger protein 423, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear receptor coactivator 5-like, transcript variant X7
nuclear receptor coactivator 5-like, transcript variant X4
nuclear receptor coactivator 5-like, transcript variant X6
nuclear receptor coactivator 5-like, transcript variant X1
nuclear receptor coactivator 5-like, transcript variant X2
nuclear receptor coactivator 5-like, transcript variant X5
nuclear receptor coactivator 5-like, transcript variant X3
nuclear receptor coactivator 5-like isoform X2
nuclear receptor coactivator 5-like isoform X1
nuclear receptor coactivator 5-like isoform X4
nuclear receptor coactivator 5-like isoform X3
CTD nuclear envelope phosphatase 1 regulatory subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 long SRA reads, 23 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
nuclear envelope phosphatase-regulatory subunit 1
HEAT repeat containing 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 6 samples with support for all annotated introns
HEAT repeat containing 3, transcript variant X1
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 10 samples with support for all annotated introns
HEAT repeat containing 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
HEAT repeat containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
HEAT repeat-containing protein 3 isoform X1
HEAT repeat-containing protein 3 isoform X2
HEAT repeat-containing protein 3 isoform X3
HEAT repeat-containing protein 3 isoform X4
terminal nucleotidyltransferase 4B, transcript variant X1
terminal nucleotidyltransferase 4B, transcript variant X2
terminal nucleotidyltransferase 4B isoform X1
terminal nucleotidyltransferase 4B isoform X2
adenylate cyclase 7, transcript variant X2
adenylate cyclase 7, transcript variant X1
adenylate cyclase 7, transcript variant X5
adenylate cyclase 7, transcript variant X3
adenylate cyclase 7, transcript variant X4
adenylate cyclase 7, transcript variant X6
NKD inhibitor of WNT signaling pathway 1
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 9 samples with support for all annotated introns
nucleotide-binding oligomerization domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
nucleotide-binding oligomerization domain containing 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
nucleotide-binding oligomerization domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
nucleotide-binding oligomerization domain containing 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
nucleotide-binding oligomerization domain containing 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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
nucleotide-binding oligomerization domain containing 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nucleotide-binding oligomerization domain containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nucleotide-binding oligomerization domain-containing protein 2 isoform X1
nucleotide-binding oligomerization domain-containing protein 2 isoform X2
nucleotide-binding oligomerization domain-containing protein 2 isoform X3
nucleotide-binding oligomerization domain-containing protein 2 isoform X4
cylindromatosis (turban tumor syndrome), a
ubiquitin carboxyl-terminal hydrolase CYLD
ubiquitin carboxyl-terminal hydrolase CYLD-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TOX high mobility group box family member 3, transcript variant X2
TOX high mobility group box family member 3, transcript variant X1
TOX high mobility group box family member 3 isoform X1
TOX high mobility group box family member 3 isoform X2
TOX high mobility group box family member 3, 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 7 samples with support for all annotated introns
TOX high mobility group box family member 3 isoform X3
chromodomain helicase DNA binding protein 9, transcript variant X1
chromodomain helicase DNA binding protein 9, transcript variant X3
chromodomain helicase DNA binding protein 9, transcript variant X2
chromodomain helicase DNA binding protein 9, transcript variant X4
chromodomain-helicase-DNA-binding protein 9 isoform X1
chromodomain-helicase-DNA-binding protein 9 isoform X3
chromodomain-helicase-DNA-binding protein 9 isoform X2
chromodomain-helicase-DNA-binding protein 9 isoform X4
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
chromodomain helicase DNA binding protein 9, transcript variant X5
chromodomain-helicase-DNA-binding protein 9 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
akt interacting protein, transcript variant X2
akt interacting protein, transcript variant X6
akt interacting protein, transcript variant X1
akt interacting protein, transcript variant X8
akt interacting protein, transcript variant X7
akt interacting protein, transcript variant X4
akt interacting protein, transcript variant X5
akt interacting protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
FTO alpha-ketoglutarate dependent dioxygenase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
alpha-ketoglutarate-dependent dioxygenase FTO
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
iroquois-class homeodomain protein IRX-3a
uncharacterized LOC125484927, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125484927, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC125484927, transcript variant X2
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 6 samples with support for all annotated introns
iroquois-class homeodomain protein IRX-5a
uncharacterized LOC125484928, transcript variant X1
uncharacterized LOC125484928, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
iroquois-class homeodomain protein IRX-6a
uncharacterized LOC125485059, transcript variant X2
uncharacterized LOC125485059, transcript variant X3
uncharacterized LOC125485059, transcript variant X1
lysophosphatidylcholine acyltransferase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 long SRA reads, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
lysophosphatidylcholine acyltransferase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 long SRA reads, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
lysophosphatidylcholine acyltransferase 2 isoform X1
lysophosphatidylcholine acyltransferase 2 isoform X2
solute carrier family 6 member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 124 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
sodium-dependent noradrenaline transporter isoform X1
solute carrier family 6 member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 6 member 2, transcript variant X3
sodium-dependent noradrenaline transporter isoform X2
uncharacterized LOC109930060, transcript variant X2
uncharacterized LOC109930060, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box polypeptide 28
probable ATP-dependent RNA helicase DDX28
dihydrouridine synthase 2, transcript variant X1
dihydrouridine synthase 2, transcript variant X5
dihydrouridine synthase 2, transcript variant X2
dihydrouridine synthase 2, transcript variant X3
dihydrouridine synthase 2, transcript variant X4
tRNA-dihydrouridine(20) synthase [NAD(P)+]-like isoform X1
tRNA-dihydrouridine(20) synthase [NAD(P)+]-like isoform X5
tRNA-dihydrouridine(20) synthase [NAD(P)+]-like isoform X2
tRNA-dihydrouridine(20) synthase [NAD(P)+]-like isoform X3
tRNA-dihydrouridine(20) synthase [NAD(P)+]-like isoform X4
dihydrouridine synthase 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
tRNA-dihydrouridine(20) synthase [NAD(P)+]-like isoform X6
nuclear factor of activated T cells 3a, transcript variant X1
nuclear factor of activated T cells 3a, transcript variant X2
nuclear factor of activated T-cells, cytoplasmic 3 isoform X1
nuclear factor of activated T-cells, cytoplasmic 3 isoform X2
epithelial splicing regulatory protein 2, transcript variant X3
epithelial splicing regulatory protein 2, transcript variant X1
epithelial splicing regulatory protein 2, transcript variant X2
epithelial splicing regulatory protein 2 isoform X1
epithelial splicing regulatory protein 2 isoform X2
uncharacterized LOC125484990, transcript variant X3
uncharacterized LOC125484990, transcript variant X1
uncharacterized LOC125484990, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 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: 3 long SRA reads, 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
BCAR1 scaffold protein, Cas family member, transcript variant X2
BCAR1 scaffold protein, Cas family member, transcript variant X1
breast cancer anti-estrogen resistance protein 1 isoform X2
breast cancer anti-estrogen resistance protein 1 isoform X1
craniofacial development protein 1, transcript variant X7
craniofacial development protein 1, transcript variant X2
craniofacial development protein 1, transcript variant X1
craniofacial development protein 1, transcript variant X9
craniofacial development protein 1, transcript variant X4
craniofacial development protein 1, transcript variant X3
craniofacial development protein 1 isoform X8
craniofacial development protein 1 isoform X4
craniofacial development protein 1 isoform X2
craniofacial development protein 1 isoform X3
craniofacial development protein 1 isoform X6
craniofacial development protein 1 isoform X1
craniofacial development protein 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
craniofacial development protein 1, transcript variant X5
craniofacial development protein 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
craniofacial development protein 1 isoform X7
craniofacial development protein 1 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 long SRA reads, 7 Proteins, and 99% 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: 11 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
VRK serine/threonine kinase 3, transcript variant X1
VRK serine/threonine kinase 3, transcript variant X2
VRK serine/threonine kinase 3, transcript variant X3
inactive serine/threonine-protein kinase VRK3
rho family-interacting cell polarization regulator 2-like, transcript variant X2
rho family-interacting cell polarization regulator 2-like, transcript variant X1
rho family-interacting cell polarization regulator 2-like, transcript variant X3
rho family-interacting cell polarization regulator 2-like isoform X1
rho family-interacting cell polarization regulator 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 56% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
rho family-interacting cell polarization regulator 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51% coverage of the annotated genomic feature by RNAseq alignments
CCCTC-binding factor (zinc finger protein), transcript variant X1
CCCTC-binding factor (zinc finger protein), transcript variant X3
CCCTC-binding factor (zinc finger protein), transcript variant X2
rho family-interacting cell polarization regulator 1
capping protein regulator and myosin 1 linker 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 1 Protein, and 68% coverage of the annotated genomic feature by RNAseq alignments
capping protein, Arp2/3 and myosin-I linker protein 2
uncharacterized LOC109927018, transcript variant X1
uncharacterized LOC109927018, transcript variant X2
uncharacterized protein LOC109927018 isoform X1
uncharacterized protein LOC109927018 isoform X2
partitioning defective 6 homolog alpha-like
glucose-fructose oxidoreductase domain-containing protein 2, transcript variant X2
glucose-fructose oxidoreductase domain-containing protein 2, transcript variant X1
glucose-fructose oxidoreductase domain-containing protein 2 isoform X2
glucose-fructose oxidoreductase domain-containing protein 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 long SRA reads, 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, NMDA 2A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
translin-associated factor X interacting protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
translin-associated factor X-interacting protein 1
centromere protein T, transcript variant X3
centromere protein T, transcript variant X4
centromere protein T, transcript variant X1
centromere protein T, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 long SRA reads, 9 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
nuclear transport factor 2, transcript variant X1
nuclear transport factor 2, transcript variant X2
nuclear transport factor 2, transcript variant X4
nuclear transport factor 2, transcript variant X3
enhancer of mRNA decapping 4, transcript variant X3
enhancer of mRNA decapping 4, transcript variant X1
enhancer of mRNA decapping 4, transcript variant X2
enhancer of mRNA-decapping protein 4 isoform X1
enhancer of mRNA-decapping protein 4 isoform X2
enhancer of mRNA-decapping protein 4 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein serine kinase H1, transcript variant X1
protein serine kinase H1, transcript variant X2
serine/threonine-protein kinase H1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chymotrypsinogen A-like, transcript variant X1
chymotrypsinogen A-like, transcript variant X2
agouti related neuropeptide, transcript variant X2
agouti related neuropeptide, transcript variant X3
agouti related neuropeptide, transcript variant X1
11-beta-hydroxysteroid dehydrogenase type 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
11-beta-hydroxysteroid dehydrogenase type 2-like, transcript variant 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 6 samples with support for all annotated introns
11-beta-hydroxysteroid dehydrogenase type 2-like isoform X2
11-beta-hydroxysteroid dehydrogenase type 2-like isoform X1
zinc finger DHHC-type containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger DHHC-type containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger DHHC-type containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger DHHC-type containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
11-beta-hydroxysteroid dehydrogenase type 2-like
tubulin polymerization-promoting protein family member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 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
BTB/POZ domain-containing protein KCTD19-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: BTB/POZ domain-containing protein KCTD19-like
pleckstrin homology domain containing, family G (with RhoGef domain) member 4, transcript variant X2
pleckstrin homology domain containing, family G (with RhoGef domain) member 4, transcript variant X1
uncharacterized protein plekhg4 isoform X2
uncharacterized protein plekhg4 isoform X1
sodium/hydrogen exchanger 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
sodium/hydrogen exchanger 5-like isoform X2
sodium/hydrogen exchanger 5-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
sodium/hydrogen exchanger 5-like isoform X1
formin homology 2 domain containing 1, transcript variant X2
formin homology 2 domain containing 1, transcript variant X1
FH1/FH2 domain-containing protein 1 isoform X2
FH1/FH2 domain-containing protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 long SRA reads, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
protein-glutamine gamma-glutamyltransferase 2
transmembrane protein with metallophosphoesterase domain
transfer RNA leucine (anticodon CAG); 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: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
ADP-ribosylation factor-like 2 binding protein
ADP-ribosylation factor-like protein 2-binding protein
ring finger and SPRY domain containing 1, transcript variant X1
RING finger and SPRY domain-containing protein 1 isoform X1
ring finger and SPRY domain containing 1, transcript variant X2
RING finger and SPRY domain-containing protein 1 isoform X2
proteasome activator subunit 3 interacting protein 1, transcript variant X1
proteasome activator subunit 3 interacting protein 1, transcript variant X2
proteasome activator subunit 3 interacting protein 1, transcript variant X3
proteasome activator subunit 3 interacting protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cholesteryl ester transfer protein, plasma
homocysteine-inducible, endoplasmic reticulum stress-inducible, ubiquitin-like domain member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
homocysteine-inducible, endoplasmic reticulum stress-inducible, ubiquitin-like domain member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
homocysteine-responsive endoplasmic reticulum-resident ubiquitin-like domain member 1 protein
metallothionein-like, transcript variant X1
metallothionein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized protein LOC125485000 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 long SRA reads, 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
anoctamin-10-like, transcript variant X2
anoctamin-10-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
phosphatidylcholine-sterol acyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Golgi-associated kinase 1A-like, transcript variant X2
Golgi-associated kinase 1A-like, transcript variant X1
Golgi-associated kinase 1A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
probable D-lactate dehydrogenase, mitochondrial
pancreatic secretory granule membrane major glycoprotein GP2-like
receptor-interacting serine/threonine-protein kinase 2-like, transcript variant X1
receptor-interacting serine/threonine-protein kinase 2-like, transcript variant X2
receptor-interacting serine/threonine-protein kinase 2-like isoform X1
receptor-interacting serine/threonine-protein kinase 2-like isoform X2
adhesion G-protein coupled receptor G1-like
tyrosine-protein phosphatase non-receptor type substrate 1-like
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
membrane-bound transcription factor peptidase, site 1, transcript variant X2
membrane-bound transcription factor peptidase, site 1, transcript variant X1
membrane-bound transcription factor site-1 protease isoform X2
membrane-bound transcription factor site-1 protease isoform X1
heat shock transcription factor 4, transcript variant X1
heat shock transcription factor 4, transcript variant X3
heat shock transcription factor 4, transcript variant X2
tnfrsf1a-associated via death domain, transcript variant X3
tnfrsf1a-associated via death domain, transcript variant X1
tnfrsf1a-associated via death domain, transcript variant X2
tumor necrosis factor receptor type 1-associated DEATH domain protein isoform X1
tumor necrosis factor receptor type 1-associated DEATH domain protein isoform X2
guanine nucleotide-binding protein G(o) subunit alpha, transcript variant X2
guanine nucleotide-binding protein G(o) subunit alpha, transcript variant X3
guanine nucleotide-binding protein G(o) subunit alpha, transcript variant X4
guanine nucleotide-binding protein G(o) subunit alpha, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
guanine nucleotide-binding protein G(o) subunit alpha isoform X2
guanine nucleotide-binding protein G(o) subunit alpha isoform X3
guanine nucleotide-binding protein G(o) subunit alpha isoform X4
guanine nucleotide-binding protein G(o) subunit alpha isoform X1
core-binding factor subunit beta, transcript variant X2
core-binding factor subunit beta, transcript variant X1
core-binding factor subunit beta isoform X1
core-binding factor subunit beta isoform X2
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
WD repeat domain 59, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
WD repeat domain 59, transcript variant X2
WD repeat domain 59, transcript variant X1
mixed lineage kinase domain-like protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mixed lineage kinase domain-like protein, transcript variant X6
mixed lineage kinase domain-like protein, transcript variant X1
mixed lineage kinase domain-like protein, transcript variant X3
mixed lineage kinase domain-like protein isoform X1
mixed lineage kinase domain-like protein, transcript variant X4
mixed lineage kinase domain-like protein, transcript variant X2
mixed lineage kinase domain-like protein isoform X2
ring finger and WD repeat domain 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 long SRA reads, 10 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ring finger and WD repeat domain 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 long SRA reads, 10 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments
golgi glycoprotein 1a, transcript variant X1
golgi glycoprotein 1a, transcript variant X2
pyruvate dehydrogenase phosphatase regulatory subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
pyruvate dehydrogenase phosphatase regulatory subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial isoform X1
pyruvate dehydrogenase phosphatase regulatory subunit, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
pyruvate dehydrogenase phosphatase regulatory subunit, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial isoform X2
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial isoform X3
DEAD (Asp-Glu-Ala-Asp) box polypeptide 23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
probable ATP-dependent RNA helicase DDX23
gastrula zinc finger protein XlCGF17.1-like
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 19 samples with support for all annotated introns
solute carrier family 7 member 6 opposite strand
probable RNA polymerase II nuclear localization protein SLC7A6OS
Y+L amino acid transporter 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
Y+L amino acid transporter 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Y+L amino acid transporter 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclic nucleotide gated channel subunit beta 1
LOW QUALITY PROTEIN: cyclic nucleotide-gated cation channel beta-3
kinesin family member C3, transcript variant X1
kinesin family member C3, transcript variant X5
kinesin family member C3, transcript variant X3
kinesin family member C3, transcript variant X4
kinesin family member C3, transcript variant X2
katanin p80 (WD repeat containing) subunit B 1, transcript variant X4
katanin p80 (WD repeat containing) subunit B 1, transcript variant X2
katanin p80 (WD repeat containing) subunit B 1, transcript variant X1
katanin p80 WD40 repeat-containing subunit B1 isoform X2
katanin p80 WD40 repeat-containing subunit B1 isoform X1
katanin p80 WD40 repeat-containing subunit B1 isoform X4
katanin p80 (WD repeat containing) subunit B 1, transcript variant X3
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 3 samples with support for all annotated introns
katanin p80 WD40 repeat-containing subunit B1 isoform X3
testis, prostate and placenta-expressed protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125485006, transcript variant X1
uncharacterized LOC125485006, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
coiled-coil domain-containing protein 113
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 14 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
DNA replication complex GINS protein PSF3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 51% coverage of the annotated genomic feature by RNAseq alignments
casein kinase 2, alpha prime polypeptide b
NDRG family member 4, transcript variant X2
NDRG family member 4, transcript variant X4
NDRG family member 4, transcript variant X3
NDRG family member 4, transcript variant X5
NDRG family member 4, transcript variant X1
NDRG family member 4, transcript variant X6
Bardet-Biedl syndrome 2, transcript variant X3
Bardet-Biedl syndrome 2, transcript variant X1
Bardet-Biedl syndrome 2, transcript variant X4
Bardet-Biedl syndrome 2 protein homolog isoform X3
Bardet-Biedl syndrome 2 protein homolog isoform X1
Bardet-Biedl syndrome 2 protein homolog isoform X4
Bardet-Biedl syndrome 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Bardet-Biedl syndrome 2 protein homolog isoform X2
cleavage and polyadenylation specificity factor subunit 5
2-oxoglutarate and iron-dependent oxygenase domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
natural cytotoxicity triggering receptor 3 ligand 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like, transcript variant X5
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like, transcript variant X2
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like, transcript variant X4
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like isoform X1
endonuclease/exonuclease/phosphatase family domain-containing protein 1-like isoform X2
uncharacterized protein KIAA0895-like, transcript variant X2
uncharacterized protein KIAA0895-like, transcript variant X1
uncharacterized protein KIAA0895-like isoform X1
uncharacterized protein KIAA0895-like, transcript variant X3
uncharacterized protein KIAA0895-like isoform X2
uncharacterized LOC109913014, transcript variant X1
uncharacterized LOC109913014, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
exocyst complex component 3-like protein
transmembrane protein 208, transcript variant X1
transmembrane protein 208, transcript variant X2
tripartite motif containing 71, E3 ubiquitin protein ligase
leucine rich repeat containing 29, transcript variant X1
leucine rich repeat containing 29, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine rich repeat containing 29, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 15 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
vac14 homolog (S. cerevisiae), transcript variant X1
vac14 homolog (S. cerevisiae), transcript variant X2
splicing factor 3B subunit 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
splicing factor 3B subunit 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
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
ST3 beta-galactoside alpha-2,3-sialyltransferase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 45 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ST3 beta-galactoside alpha-2,3-sialyltransferase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 44 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ST3 beta-galactoside alpha-2,3-sialyltransferase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 2 isoform X1
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 2 isoform X2
alanyl-tRNA synthetase 1, transcript variant X1
alanine--tRNA ligase, cytoplasmic isoform X1
alanyl-tRNA synthetase 1, transcript variant X2
alanine--tRNA ligase, cytoplasmic isoform X2
SET domain containing 6, protein lysine methyltransferase, transcript variant X2
SET domain containing 6, protein lysine methyltransferase, transcript variant X1
SET domain containing 6, protein lysine methyltransferase, transcript variant X3
N-lysine methyltransferase setd6 isoform X1
N-lysine methyltransferase setd6 isoform X2
CCR4-NOT transcription complex, subunit 1, transcript variant X6
CCR4-NOT transcription complex, subunit 1, transcript variant X3
CCR4-NOT transcription complex, subunit 1, transcript variant X5
CCR4-NOT transcription complex, subunit 1, transcript variant X2
CCR4-NOT transcription complex, subunit 1, transcript variant X1
CCR4-NOT transcription complex, subunit 1, transcript variant X4
CCR4-NOT transcription complex subunit 1 isoform X6
CCR4-NOT transcription complex subunit 1 isoform X3
CCR4-NOT transcription complex subunit 1 isoform X5
CCR4-NOT transcription complex subunit 1 isoform X2
CCR4-NOT transcription complex subunit 1 isoform X1
CCR4-NOT transcription complex subunit 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
lysosomal protective protein-like, transcript variant X2
lysosomal protective protein-like, transcript variant X1
lysosomal protective protein-like isoform X1
lysosomal protective protein-like isoform X2
putative sodium-coupled neutral amino acid transporter 7
aspartate aminotransferase, mitochondrial
purine nucleoside phosphorylase 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
purine nucleoside phosphorylase 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
purine nucleoside phosphorylase 6 isoform X1
purine nucleoside phosphorylase 6 isoform X2
cap methyltransferase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cap methyltransferase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
cap methyltransferase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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
cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 2 isoform X1
cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 2 isoform X2
HYDIN axonemal central pair apparatus protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
N-terminal EF-hand calcium binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
N-terminal EF-hand calcium binding protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
N-terminal EF-hand calcium-binding protein 2 isoform X1
N-terminal EF-hand calcium-binding protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
putative sodium-coupled neutral amino acid transporter 8a
oxidative stress-induced growth inhibitor 1-like, transcript variant X1
oxidative stress-induced growth inhibitor 1-like, transcript variant X2
oxidative stress-induced growth inhibitor 1-like, transcript variant X3
oxidative stress-induced growth inhibitor 1-like isoform X1
oxidative stress-induced growth inhibitor 1-like isoform X2
oxidative stress-induced growth inhibitor 1-like isoform X3
H-2 class II histocompatibility antigen, E-Q beta chain-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: 35 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 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: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LOW QUALITY PROTEIN: C-C motif chemokine 3-like
cytokine induced apoptosis inhibitor 1, transcript variant X3
cytokine induced apoptosis inhibitor 1, transcript variant X4
cytokine induced apoptosis inhibitor 1, transcript variant X1
cytokine induced apoptosis inhibitor 1, transcript variant X2
cytokine induced apoptosis inhibitor 1, transcript variant X5
coenzyme Q9 homolog (S. cerevisiae), transcript variant X2
coenzyme Q9 homolog (S. cerevisiae), transcript variant X1
ubiquinone biosynthesis protein COQ9, mitochondrial isoform X1
ubiquinone biosynthesis protein COQ9, mitochondrial isoform X2
RNA polymerase II subunit C, transcript variant X1
RNA polymerase II subunit C, transcript variant X2
DNA-directed RNA polymerase II subunit RPB3 isoform X1
DNA-directed RNA polymerase II subunit RPB3 isoform X2
docking protein 4, transcript variant X3
docking protein 4, transcript variant X2
docking protein 4, transcript variant X4
docking protein 4, transcript variant X1
coiled-coil domain containing 102A, transcript variant X4
coiled-coil domain containing 102A, transcript variant X5
coiled-coil domain containing 102A, transcript variant X1
coiled-coil domain containing 102A, transcript variant X2
coiled-coil domain containing 102A, transcript variant X3
coiled-coil domain-containing protein 102A isoform X2
coiled-coil domain-containing protein 102A isoform X1
coiled-coil domain-containing protein 102A isoform X3
coiled-coil domain containing 102A, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
coiled-coil domain-containing protein 102A isoform X4
uncharacterized LOC125485042, transcript variant X1
uncharacterized LOC125485042, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns