Rhincodon typus isolate 14 chromosome 21, 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\nCM038818.1.\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.
NADH dehydrogenase [ubiquinone] iron-sulfur protein 8, mitochondrial
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
VPS35 endosomal protein sorting factor like
VPS35 endosomal protein-sorting factor-like
uncharacterized LOC109921786, transcript variant X3
uncharacterized LOC109921786, transcript variant X2
uncharacterized LOC109921786, transcript variant X1
centriolar coiled-coil protein of 110 kDa, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
centriolar coiled-coil protein of 110 kDa, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
centriolar coiled-coil protein of 110 kDa, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
centriolar coiled-coil protein of 110 kDa, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
centriolar coiled-coil protein of 110 kDa, transcript variant X9
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 6 samples with support for all annotated introns
centriolar coiled-coil protein of 110 kDa, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
centriolar coiled-coil protein of 110 kDa, transcript variant X2
centriolar coiled-coil protein of 110 kDa, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
centriolar coiled-coil protein of 110 kDa, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
centriolar coiled-coil protein of 110 kDa isoform X3
centriolar coiled-coil protein of 110 kDa isoform X2
centriolar coiled-coil protein of 110 kDa isoform X1
centriolar coiled-coil protein of 110 kDa, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
centriolar coiled-coil protein of 110 kDa isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycerophosphodiester phosphodiesterase 1, transcript variant X1
glycerophosphodiester phosphodiesterase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
glycerophosphodiester phosphodiesterase 1 isoform X1
glycerophosphodiester phosphodiesterase 1 isoform X2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon UAC); 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: 2 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
5-demethoxyubiquinone hydroxylase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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
inositol 1,4,5-trisphosphate receptor-interacting protein-like 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
SMG1 nonsense mediated mRNA decay associated PI3K related kinase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins
ADP-ribosylation factor-like 6 interacting protein 1
ADP-ribosylation factor-like protein 6-interacting protein 1
uncharacterized LOC109934750, transcript variant X1
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
uncharacterized LOC109934750, transcript variant X4
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 2 samples with support for all annotated introns
uncharacterized LOC109934750, transcript variant X3
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
uncharacterized LOC109934750, transcript variant X2
uncharacterized protein LOC109934750 isoform X2
uncharacterized protein LOC109934750 isoform X1
ribosomal protein S15a, transcript variant X3
ribosomal protein S15a, transcript variant X2
ribosomal protein S15a, transcript variant X1
ATP-binding cassette, sub-family C (CFTR/MRP), member 1
multidrug resistance-associated protein 1
nudE neurodevelopment protein 1, transcript variant X1
nudE neurodevelopment protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
nuclear distribution protein nudE homolog 1 isoform X1
nudE neurodevelopment protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
nuclear distribution protein nudE homolog 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
meiosis regulator and mRNA stability factor 1, transcript variant X1
meiosis regulator and mRNA stability factor 1, transcript variant X3
meiosis regulator and mRNA stability factor 1, transcript variant X5
meiosis regulator and mRNA stability factor 1, transcript variant X2
meiosis regulator and mRNA stability factor 1, transcript variant X4
meiosis regulator and mRNA stability factor 1 isoform X1
meiosis regulator and mRNA stability factor 1 isoform X2
meiosis regulator and mRNA stability factor 1 isoform X3
meiosis regulator and mRNA stability factor 1 isoform X4
meiosis regulator and mRNA stability factor 1 isoform X5
MPV17 mitochondrial membrane protein like, transcript variant X1
MPV17 mitochondrial membrane protein like, transcript variant X2
bMERB domain-containing protein 1 isoform X1
bMERB domain-containing protein 1 isoform X2
pyridoxal-dependent decarboxylase domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
pyridoxal-dependent decarboxylase domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X1
pyridoxal-dependent decarboxylase domain-containing protein 1 isoform X2
N-terminal asparagine amidase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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
protein N-terminal asparagine amidohydrolase isoform X2
N-terminal asparagine amidase, transcript variant X1
protein N-terminal asparagine amidohydrolase isoform X1
RRN3 homolog, RNA polymerase I transcription factor
RNA polymerase I-specific transcription initiation factor RRN3
ribosomal L1 domain-containing protein 1
eukaryotic peptide chain release factor GTP-binding subunit ERF3A
tumor necrosis factor receptor superfamily member 17-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
calcineurin-like phosphoesterase domain containing 1, transcript variant X1
calcineurin-like phosphoesterase domain containing 1, transcript variant X3
calcineurin-like phosphoesterase domain containing 1, transcript variant X2
serine/threonine-protein phosphatase CPPED1 isoform X1
serine/threonine-protein phosphatase CPPED1 isoform X2
serine/threonine-protein phosphatase CPPED1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
excision repair cross-complementation group 4, transcript variant X1
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 11 samples with support for all annotated introns
excision repair cross-complementation group 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
excision repair cross-complementation group 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
myocardin related transcription factor Ba, transcript variant X2
myocardin related transcription factor Ba, transcript variant X1
myocardin related transcription factor Ba, transcript variant X3
myocardin related transcription factor Ba, transcript variant X4
myocardin-related transcription factor B isoform X1
myocardin-related transcription factor B isoform X2
myocardin-related transcription factor B isoform X3
myocardin related transcription factor Ba, transcript variant X5
myocardin-related transcription factor B isoform X4
defective in cullin neddylation 1 domain containing 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
LYR motif containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
LYR motif containing 1, transcript variant X8
LYR motif containing 1, transcript variant X5
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
LYR motif containing 1, transcript variant X6
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 8 samples with support for all annotated introns
LYR motif containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
LYR motif containing 1, transcript variant X4
LYR motif containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LYR motif containing 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LYR motif containing protein 1 isoform X3
LYR motif containing protein 1 isoform X1
LYR motif containing protein 1 isoform X4
LYR motif containing protein 1 isoform X2
lipid droplet assembly factor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
lipid droplet assembly factor 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 long SRA reads, 5 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
lipid droplet assembly factor 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 long SRA reads, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
lipid droplet assembly factor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
lipid droplet assembly factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
lipid droplet assembly factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
lipid droplet assembly factor 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
lipid droplet assembly factor 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 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
melanin-concentrating hormone receptor 1-like
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: 30 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: melanin-concentrating hormone receptor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
cilia and flagella associated protein 70
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cilia- and flagella-associated protein 70
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: H/ACA ribonucleoprotein complex subunit 2-like protein
tudor domain-containing protein 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tudor domain-containing protein 5-like, transcript variant X4
tudor domain-containing protein 5-like, transcript variant X2
tudor domain-containing protein 5-like, transcript variant X3
tudor domain-containing protein 5-like isoform X1
tudor domain-containing protein 5-like isoform X2
Jupiter microtubule associated homolog 2
major facilitator superfamily domain containing 1-like, transcript variant X2
major facilitator superfamily domain containing 1-like, transcript variant X1
major facilitator superfamily domain-containing protein 1 isoform X1
major facilitator superfamily domain-containing protein 1 isoform X2
mitogen-activated protein kinase 8 interacting protein 3
C-Jun-amino-terminal kinase-interacting protein 3
NME/NM23 nucleoside diphosphate kinase 3, transcript variant X1
NME/NM23 nucleoside diphosphate kinase 3, transcript variant X2
nucleoside diphosphate kinase 3 isoform X1
nucleoside diphosphate kinase 3 isoform X2
rhomboid, veinlet-like 1 (Drosophila), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
rhomboid, veinlet-like 1 (Drosophila), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC541336 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized protein LOC541336 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC541336 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC541336 homolog, transcript variant X3
uncharacterized protein LOC541336 homolog, transcript variant X5
STIP1 homology and U-Box containing protein 1, transcript variant X2
STIP1 homology and U-Box containing protein 1, transcript variant X1
E3 ubiquitin-protein ligase CHIP isoform X1
E3 ubiquitin-protein ligase CHIP isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
F-box and leucine-rich repeat protein 16, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
F-box and leucine-rich repeat protein 16, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
cramped chromatin regulator homolog 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cramped chromatin regulator homolog 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
WD repeat domain 24, transcript variant X4
WD repeat domain 24, transcript variant X3
WD repeat domain 24, transcript variant X2
WD repeat domain 24, transcript variant X5
WD repeat domain 24, transcript variant X6
WD repeat domain 24, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
small integral membrane protein 22, transcript variant X2
small integral membrane protein 22, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 long SRA reads, 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
glyoxylate reductase 1 homolog (Arabidopsis), 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
glyoxylate reductase 1 homolog (Arabidopsis), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
glyoxylate reductase 1 homolog (Arabidopsis), 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 16 samples with support for all annotated introns
putative oxidoreductase GLYR1 isoform X2
putative oxidoreductase GLYR1 isoform X1
putative oxidoreductase GLYR1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
recQ-mediated genome instability protein 2
Dexi homolog (mouse), transcript variant X2
Dexi homolog (mouse), transcript variant X1
Dexi homolog (mouse), transcript variant X3
Dexi homolog (mouse), transcript variant X4
Dexi homolog (mouse), transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Golgi apparatus membrane protein TVP23 homolog A, transcript variant X7
Golgi apparatus membrane protein TVP23 homolog A, transcript variant X1
Golgi apparatus membrane protein TVP23 homolog A, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Golgi apparatus membrane protein TVP23 homolog A, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Golgi apparatus membrane protein TVP23 homolog A, transcript variant X3
Golgi apparatus membrane protein TVP23 homolog A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Golgi apparatus membrane protein TVP23 homolog A, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Golgi apparatus membrane protein TVP23 homolog A, transcript variant X2
Golgi apparatus membrane protein TVP23 homolog A isoform X5
Golgi apparatus membrane protein TVP23 homolog A isoform X1
Golgi apparatus membrane protein TVP23 homolog A isoform X6
Golgi apparatus membrane protein TVP23 homolog A isoform X3
Golgi apparatus membrane protein TVP23 homolog A isoform X2
Golgi apparatus membrane protein TVP23 homolog A isoform X4
nucleotide binding protein 1 (MinD homolog, E. coli)
cytosolic Fe-S cluster assembly factor nubp1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
epithelial membrane protein 2, transcript variant X2
epithelial membrane protein 2, transcript variant X1
activating transcription factor 7-interacting protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
activating transcription factor 7-interacting protein 2-like, transcript variant X2
activating transcription factor 7-interacting protein 2-like, transcript variant X4
activating transcription factor 7-interacting protein 2-like isoform X2
activating transcription factor 7-interacting protein 2-like isoform X1
activating transcription factor 7-interacting protein 2-like, transcript variant X5
activating transcription factor 7-interacting protein 2-like, transcript variant X3
activating transcription factor 7-interacting protein 2-like, transcript variant X6
activating transcription factor 7-interacting protein 2-like isoform X3
glutamate receptor, ionotropic, N-methyl D-aspartate 2A, a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
thioredoxin domain-containing protein 11
ubiquitin specific peptidase 7 (herpes virus-associated), transcript variant X2
ubiquitin specific peptidase 7 (herpes virus-associated), transcript variant X1
ubiquitin carboxyl-terminal hydrolase 7 isoform X2
ubiquitin carboxyl-terminal hydrolase 7 isoform X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
zinc finger CCCH-type containing 7A, transcript variant X3
zinc finger CCCH-type containing 7A, transcript variant X4
zinc finger CCCH-type containing 7A, transcript variant X1
zinc finger CCCH-type containing 7A, transcript variant X2
zinc finger CCCH-type containing 7A, transcript variant X5
zinc finger CCCH domain-containing protein 7A isoform X2
zinc finger CCCH domain-containing protein 7A isoform X3
zinc finger CCCH domain-containing protein 7A isoform X1
nuclear apoptosis-inducing factor 1-like
probable crossover junction endonuclease EME2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SPRY domain-containing SOCS box protein 3, transcript variant X6
SPRY domain-containing SOCS box protein 3, transcript variant X4
SPRY domain-containing SOCS box protein 3, transcript variant X1
SPRY domain-containing SOCS box protein 3, transcript variant X7
SPRY domain-containing SOCS box protein 3, transcript variant X5
SPRY domain-containing SOCS box protein 3, transcript variant X2
SPRY domain-containing SOCS box protein 3, transcript variant X3
SPRY domain-containing SOCS box protein 3 isoform X1
SPRY domain-containing SOCS box protein 3 isoform X2
SPRY domain-containing SOCS box protein 3 isoform X3
nucleotide binding protein 2 (MinD homolog, E. coli), transcript variant X5
nucleotide binding protein 2 (MinD homolog, E. coli), transcript variant X1
nucleotide binding protein 2 (MinD homolog, E. coli), transcript variant X4
cytosolic Fe-S cluster assembly factor nubp2 isoform X1
nucleotide binding protein 2 (MinD homolog, E. coli), transcript variant X2
nucleotide binding protein 2 (MinD homolog, E. coli), transcript variant X3
cytosolic Fe-S cluster assembly factor nubp2 isoform X2
cytosolic Fe-S cluster assembly factor nubp2 isoform X3
nucleotide binding protein 2 (MinD homolog, E. coli), transcript variant X6
cytosolic Fe-S cluster assembly factor nubp2 isoform X4
insulin-like growth factor-binding protein complex acid labile subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 78-like
adenine nucleotide translocase lysine methyltransferase, transcript variant X3
adenine nucleotide translocase lysine methyltransferase, transcript variant X5
adenine nucleotide translocase lysine methyltransferase, transcript variant X2
adenine nucleotide translocase lysine methyltransferase, transcript variant X4
adenine nucleotide translocase lysine methyltransferase, transcript variant X1
adenine nucleotide translocase lysine N-methyltransferase isoform X2
adenine nucleotide translocase lysine N-methyltransferase isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol transfer protein cytoplasmic 1a
cytoplasmic phosphatidylinositol transfer protein 1
myeloid-associated differentiation marker homolog
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
general transcription factor 3C polypeptide 1, transcript variant X2
general transcription factor 3C polypeptide 1, transcript variant X1
general transcription factor 3C polypeptide 1, transcript variant X4
general transcription factor 3C polypeptide 1, transcript variant X3
general transcription factor 3C polypeptide 1 isoform X2
general transcription factor 3C polypeptide 1 isoform X1
general transcription factor 3C polypeptide 1 isoform X3
general transcription factor 3C polypeptide 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins
THUMP domain containing 1, transcript variant X2
THUMP domain containing 1, transcript variant X1
THUMP domain-containing protein 1 isoform X1
THUMP domain-containing protein 1 isoform X2
acyl-CoA synthetase medium chain family member 3, transcript variant X1
acyl-CoA synthetase medium chain family member 3, transcript variant X5
acyl-CoA synthetase medium chain family member 3, transcript variant X3
acyl-CoA synthetase medium chain family member 3, transcript variant X4
acyl-CoA synthetase medium chain family member 3, transcript variant X2
acyl-CoA synthetase medium chain family member 3, transcript variant X6
acyl-CoA synthetase medium chain family member 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
acyl-CoA synthetase medium chain family member 3, transcript variant X7
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 4 samples with support for all annotated introns
acyl-CoA synthetase medium chain family member 3, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
acyl-coenzyme A synthetase ACSM3, mitochondrial isoform X1
acyl-coenzyme A synthetase ACSM3, mitochondrial isoform X5
acyl-coenzyme A synthetase ACSM3, mitochondrial isoform X3
acyl-coenzyme A synthetase ACSM3, mitochondrial isoform X4
acyl-coenzyme A synthetase ACSM3, mitochondrial isoform X2
acyl-coenzyme A synthetase ACSM3, mitochondrial isoform X6
acyl-coenzyme A synthetase ACSM3, mitochondrial isoform X7
acyl-coenzyme A synthetase ACSM3, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RNA exonuclease 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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
RNA exonuclease 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
RNA exonuclease 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RNA exonuclease 5-like, 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acyl-coenzyme A synthetase ACSM3, mitochondrial-like, transcript variant X2
acyl-coenzyme A synthetase ACSM3, mitochondrial-like, transcript variant X1
poly(A)-specific ribonuclease (deadenylation nuclease)
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
voltage-dependent T-type calcium channel subunit alpha-1H-like
B9 protein domain 1, transcript variant X2
B9 protein domain 1, transcript variant X1
B9 domain-containing protein 1 isoform X2
B9 domain-containing protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transmembrane protein 94-like
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X6
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X2
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X3
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X10
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X11
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X8
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X9
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X5
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X7
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X1
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X7
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X5
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X3
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X1
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X8
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X4
phosphoribosyl pyrophosphate synthase-associated protein 2, transcript variant X4
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X6
phosphoribosyl pyrophosphate synthase-associated protein 2 isoform X2
CASK interacting protein 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 1 sample with support for all annotated introns
CASK interacting protein 1, transcript variant X2
TNF receptor-associated factor 7, transcript variant X3
TNF receptor-associated factor 7, transcript variant X1
TNF receptor-associated factor 7, transcript variant X2
TNF receptor-associated factor 7, transcript variant X4
E3 ubiquitin-protein ligase TRAF7 isoform X2
E3 ubiquitin-protein ligase TRAF7 isoform X1
E3 ubiquitin-protein ligase TRAF7 isoform X3
uncharacterized LOC109914469, transcript variant X2
uncharacterized LOC109914469, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00271
ras-related protein Rab-26, transcript variant X1
ras-related protein Rab-26, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 20 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
nth-like DNA glycosylase 1, transcript variant X1
nth-like DNA glycosylase 1, transcript variant X2
endonuclease III-like protein 1 isoform X2
endonuclease III-like protein 1 isoform X1
Na(+)/H(+) exchange regulatory cofactor NHE-RF2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 239 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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
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: cytochrome P450 2K6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
cytochrome c oxidase assembly protein COX19
arf-GAP with dual PH domain-containing protein 1, transcript variant X1
arf-GAP with dual PH domain-containing protein 1, transcript variant X2
arf-GAP with dual PH domain-containing protein 1 isoform X1
arf-GAP with dual PH domain-containing protein 1 isoform X2
arf-GAP with dual PH domain-containing protein 1, transcript variant X4
arf-GAP with dual PH domain-containing protein 1, transcript variant X5
arf-GAP with dual PH domain-containing protein 1, transcript variant X3
arf-GAP with dual PH domain-containing protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein kinase, cAMP-dependent, regulatory, type I, beta, transcript variant X1
protein kinase, cAMP-dependent, regulatory, type I, beta, transcript variant X2
cAMP-dependent protein kinase type I-beta regulatory subunit isoform X1
protein kinase, cAMP-dependent, regulatory, type I, beta, transcript variant X3
protein kinase, cAMP-dependent, regulatory, type I, beta, transcript variant X4
protein kinase, cAMP-dependent, regulatory, type I, beta, transcript variant X5
protein kinase, cAMP-dependent, regulatory, type I, beta, transcript variant X6
protein kinase, cAMP-dependent, regulatory, type I, beta, transcript variant X7
protein kinase, cAMP-dependent, regulatory, type I, beta, transcript variant X8
cAMP-dependent protein kinase type I-beta regulatory subunit isoform X2
cAMP-dependent protein kinase type I-beta regulatory subunit isoform X3
cAMP-dependent protein kinase type I-beta regulatory subunit isoform X4
platelet-derived growth factor subunit A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 long SRA reads, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
platelet-derived growth factor subunit A, transcript variant X1
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 15 samples with support for all annotated introns
platelet-derived growth factor subunit A isoform X2
platelet-derived growth factor subunit A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
extracellular serine/threonine protein kinase FAM20C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
transformation/transcription domain-associated protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
tectonin beta-propeller repeat containing 1a, transcript variant X1
tectonin beta-propeller repeat containing 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tectonin beta-propeller repeat-containing protein 1 isoform X1
tectonin beta-propeller repeat-containing protein 1 isoform X2
lemur tyrosine kinase 2, transcript variant X1
lemur tyrosine kinase 2, transcript variant X2
lemur tyrosine kinase 2, transcript variant X4
serine/threonine-protein kinase LMTK2 isoform X1
serine/threonine-protein kinase LMTK2 isoform X2
serine/threonine-protein kinase LMTK2 isoform X4
lemur tyrosine kinase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine-protein kinase LMTK2 isoform X3
parvalbumin alpha-like, transcript variant X1
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 2 samples with support for all annotated introns
parvalbumin alpha-like, transcript variant X2
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 3 samples with support for all annotated introns
parvalbumin alpha-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
parvalbumin, thymic CPV3-like, transcript variant X2
parvalbumin, thymic CPV3-like, transcript variant X1
CCZ1 homolog, vacuolar protein trafficking and biogenesis associated, transcript variant X2
CCZ1 homolog, vacuolar protein trafficking and biogenesis associated, transcript variant X4
CCZ1 homolog, vacuolar protein trafficking and biogenesis associated, transcript variant X1
CCZ1 homolog, vacuolar protein trafficking and biogenesis associated, transcript variant X3
vacuolar fusion protein CCZ1 homolog isoform X1
vacuolar fusion protein CCZ1 homolog isoform X3
CCZ1 homolog, vacuolar protein trafficking and biogenesis associated, transcript variant X5
vacuolar fusion protein CCZ1 homolog isoform X2
vacuolar fusion protein CCZ1 homolog isoform X4
LOW QUALITY PROTEIN: radial spoke head 10 homolog B
PMS1 homolog 2, mismatch repair system component
eukaryotic translation initiation factor 2-alpha kinase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain-containing protein 61
ubiquitin specific peptidase 42, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 42 isoform X1
ubiquitin specific peptidase 42, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 42 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
small integral membrane protein 10-like protein 2A, transcript variant X3
small integral membrane protein 10-like protein 2A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
small integral membrane protein 10-like protein 2A, transcript variant X1
small integral membrane protein 10-like protein 2A, transcript variant X4
small integral membrane protein 10-like protein 2A
ras-related C3 botulinum toxin substrate 1
diacylglycerol lipase, beta, transcript variant X1
diacylglycerol lipase, beta, transcript variant X2
diacylglycerol lipase, beta, transcript variant X3
diacylglycerol lipase, beta, transcript variant X4
KDEL endoplasmic reticulum protein retention receptor 2b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
immunoglobulin superfamily member 6, transcript variant X1
immunoglobulin superfamily member 6, transcript variant X2
immunoglobulin superfamily member 6 isoform X2
immunoglobulin superfamily member 6 isoform X1
immunoglobulin superfamily member 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
immunoglobulin superfamily member 6 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
complement C1q tumor necrosis factor-related protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
complement C1q tumor necrosis factor-related protein 1-like, transcript variant X2
complement C1q tumor necrosis factor-related protein 1-like, transcript variant X3
complement C1q tumor necrosis factor-related protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins
lipase maturation factor 1, transcript variant X1
lipase maturation factor 1, transcript variant X2
uncharacterized LOC125485642, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125485642, transcript variant X1
mitogen-activated protein kinase kinase 6, transcript variant X1
mitogen-activated protein kinase kinase 6, transcript variant X2
dual specificity mitogen-activated protein kinase kinase 6 isoform X2
dual specificity mitogen-activated protein kinase kinase 6 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
ATP-sensitive inward rectifier potassium channel 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 142 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
serine hydroxymethyltransferase, cytosolic-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
zinc finger, AN1-type domain 2A, transcript variant X4
zinc finger, AN1-type domain 2A, transcript variant X2
zinc finger, AN1-type domain 2A, transcript variant X1
zinc finger, AN1-type domain 2A, transcript variant X3
AN1-type zinc finger protein 2A isoform X1
AN1-type zinc finger protein 2A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
integrator complex subunit 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
integrator complex subunit 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ADP-ribose pyrophosphatase, mitochondrial-like
alpha glucosidase 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
alpha glucosidase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
alpha glucosidase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
alpha glucosidase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
methyltransferase 4, N6-adenosine, transcript variant X10
methyltransferase 4, N6-adenosine, transcript variant X5
methyltransferase 4, N6-adenosine, transcript variant X2
methyltransferase 4, N6-adenosine, transcript variant X3
methyltransferase 4, N6-adenosine, transcript variant X4
methyltransferase 4, N6-adenosine, transcript variant X6
methyltransferase 4, N6-adenosine, transcript variant X1
methyltransferase 4, N6-adenosine, transcript variant X9
methyltransferase 4, N6-adenosine, transcript variant X7
methyltransferase 4, N6-adenosine, transcript variant X13
methyltransferase 4, N6-adenosine, transcript variant X8
v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog K
methyltransferase 4, N6-adenosine, transcript variant X12
methyltransferase 4, N6-adenosine, transcript variant X14
methyltransferase 4, N6-adenosine, transcript variant X11
N(6)-adenine-specific methyltransferase METTL4
transmembrane protein 184a, 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 2 samples with support for all annotated introns
transmembrane protein 184a, transcript variant X1
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 4 samples with support for all annotated introns
proteasome (prosome, macropain) assembly chaperone 3, transcript variant X1
proteasome (prosome, macropain) assembly chaperone 3, transcript variant X7
proteasome (prosome, macropain) assembly chaperone 3, transcript variant X2
proteasome (prosome, macropain) assembly chaperone 3, transcript variant X5
proteasome (prosome, macropain) assembly chaperone 3, transcript variant X3
proteasome (prosome, macropain) assembly chaperone 3, transcript variant X4
proteasome (prosome, macropain) assembly chaperone 3, transcript variant X6
proteasome (prosome, macropain) assembly chaperone 3, transcript variant X8
proteasome (prosome, macropain) assembly chaperone 3, transcript variant X9
extracellular leucine-rich repeat and fibronectin type III domain containing 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
mitotic spindle assembly checkpoint protein MAD1-like, 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
mitotic spindle assembly checkpoint protein MAD1-like isoform X3
mitotic spindle assembly checkpoint protein MAD1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 59% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitotic spindle assembly checkpoint protein MAD1-like isoform X1
mitotic spindle assembly checkpoint protein MAD1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitotic spindle assembly checkpoint protein MAD1-like, 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 1 sample with support for all annotated introns
mitotic spindle assembly checkpoint protein MAD1-like isoform X4
mitotic spindle assembly checkpoint protein MAD1-like isoform X2
nudix (nucleoside diphosphate linked moiety X)-type motif 1
oxidized purine nucleoside triphosphate hydrolase
IQ motif containing E, transcript variant X6
IQ motif containing E, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
IQ motif containing E, transcript variant X1
IQ motif containing E, transcript variant X2
IQ motif containing E, transcript variant X4
IQ motif containing E, transcript variant X3
IQ domain-containing protein E isoform X5
IQ domain-containing protein E isoform X4
IQ domain-containing protein E isoform X1
IQ domain-containing protein E isoform X2
IQ domain-containing protein E isoform X3
IQ domain-containing protein E isoform X6
retinoic acid-induced protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
retinoic acid-induced protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
retinoic acid-induced protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
retinoic acid-induced protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
retinoic acid-induced protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
retinoic acid-induced protein 1, transcript variant X6
retinoic acid-induced protein 1, transcript variant X7
sterol regulatory element binding transcription factor 1, transcript variant X1
sterol regulatory element binding transcription factor 1, transcript variant X2
sterol regulatory element-binding protein 1 isoform X1
sterol regulatory element-binding protein 1 isoform X2
target of myb1 like 2 membrane trafficking protein, transcript variant X8
target of myb1 like 2 membrane trafficking protein, transcript variant X3
target of myb1 like 2 membrane trafficking protein, transcript variant X7
target of myb1 like 2 membrane trafficking protein, transcript variant X4
target of myb1 like 2 membrane trafficking protein, transcript variant X5
target of myb1 like 2 membrane trafficking protein, transcript variant X2
target of myb1 like 2 membrane trafficking protein, transcript variant X1
target of myb1 like 2 membrane trafficking protein, transcript variant X9
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
target of myb1 like 2 membrane trafficking protein, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynein regulatory complex subunit 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynein regulatory complex subunit 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynein regulatory complex subunit 3, transcript variant X3
dynein regulatory complex subunit 3, transcript variant X4
dynein regulatory complex subunit 3 isoform X1
dynein regulatory complex subunit 3 isoform X2
dynein regulatory complex subunit 3 isoform X3
ATP synthase mitochondrial F1 complex assembly factor 2
ubiquitin carboxyl-terminal hydrolase 22
tumor necrosis factor receptor superfamily member 13B, transcript variant X3
tumor necrosis factor receptor superfamily member 13B, transcript variant X1
tumor necrosis factor receptor superfamily member 13B, transcript variant X2
tumor necrosis factor receptor superfamily member 13B
myosin phosphatase Rho-interacting protein, transcript variant X6
myosin phosphatase Rho-interacting protein, transcript variant X1
myosin phosphatase Rho-interacting protein, transcript variant X7
myosin phosphatase Rho-interacting protein, transcript variant X3
myosin phosphatase Rho-interacting protein, transcript variant X2
myosin phosphatase Rho-interacting protein, transcript variant X4
myosin phosphatase Rho-interacting protein, transcript variant X8
myosin phosphatase Rho-interacting protein isoform X6
myosin phosphatase Rho-interacting protein isoform X7
myosin phosphatase Rho-interacting protein isoform X8
myosin phosphatase Rho-interacting protein, transcript variant X5
phospholipase D family, member 6, transcript variant X2
phospholipase D family, member 6, transcript variant X1
MTOR associated protein, LST8 homolog (S. cerevisiae), transcript variant X1
MTOR associated protein, LST8 homolog (S. cerevisiae), transcript variant X2
MTOR associated protein, LST8 homolog (S. cerevisiae), transcript variant X3
MTOR associated protein, LST8 homolog (S. cerevisiae), transcript variant X4
target of rapamycin complex subunit lst8
E4F transcription factor 1, transcript variant X1
E4F transcription factor 1, transcript variant X2
E4F transcription factor 1, transcript variant X3
zinc finger DHHC-type palmitoyltransferase 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 4, transcript variant X4
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 2 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 94% 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: sodium/myo-inositol cotransporter 2
sodium/myo-inositol cotransporter 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 24% coverage of the annotated genomic feature by RNAseq alignments
rho GTPase-activating protein 17-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 13 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
rho GTPase-activating protein 17-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 16 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
rho GTPase-activating protein 17-like isoform X2
rho GTPase-activating protein 17-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 long SRA reads, 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments
probable helicase with zinc finger domain
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments
calcium channel, voltage-dependent, gamma subunit 3a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
voltage-dependent calcium channel gamma-3 subunit
E3 ubiquitin-protein ligase RBBP6-like, transcript variant X1
E3 ubiquitin-protein ligase RBBP6-like, transcript variant X2
E3 ubiquitin-protein ligase RBBP6-like, transcript variant X3
E3 ubiquitin-protein ligase RBBP6-like isoform X3
E3 ubiquitin-protein ligase RBBP6-like isoform X2
E3 ubiquitin-protein ligase RBBP6-like isoform X1
E3 ubiquitin-protein ligase RBBP6-like, transcript variant X4
E3 ubiquitin-protein ligase RBBP6-like isoform 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 10 samples with support for all annotated introns
trinucleotide repeat containing adaptor 6A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
trinucleotide repeat-containing gene 6A protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
endoplasmic reticulum to nucleus signaling 2, transcript variant X3
endoplasmic reticulum to nucleus signaling 2, transcript variant X2
endoplasmic reticulum to nucleus signaling 2, transcript variant X1
serine/threonine-protein kinase/endoribonuclease IRE1 isoform X2
serine/threonine-protein kinase/endoribonuclease IRE1 isoform X1
serine/threonine-protein kinase/endoribonuclease IRE1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 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
LOW QUALITY PROTEIN: ubiquitin domain-containing protein UBFD1
UNC93-like protein MFSD11, transcript variant X2
UNC93-like protein MFSD11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamyl-tRNA synthetase 2, mitochondrial, transcript variant X1
glutamyl-tRNA synthetase 2, mitochondrial, transcript variant X2
probable glutamate--tRNA ligase, mitochondrial isoform X1
probable glutamate--tRNA ligase, mitochondrial isoform X2
ADP-ribosylation factor-binding protein GGA3-like, transcript variant X1
ADP-ribosylation factor-binding protein GGA3-like, transcript variant X3
ADP-ribosylation factor-binding protein GGA3-like, transcript variant X2
ADP-ribosylation factor-binding protein GGA3-like, transcript variant X4
ADP-ribosylation factor-binding protein GGA1-like isoform X1
ADP-ribosylation factor-binding protein GGA3-like isoform X3
ADP-ribosylation factor-binding protein GGA1-like isoform X2
ADP-ribosylation factor-binding protein GGA1-like isoform X4
conserved oligomeric Golgi complex subunit 7
amiloride-sensitive sodium channel subunit beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sodium channel epithelial 1 subunit gamma, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium channel epithelial 1 subunit gamma, transcript variant X2
amiloride-sensitive sodium channel subunit gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 31
heparan sulfate (glucosamine) 3-O-sulfotransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 2
heparan sulfate glucosamine 3-O-sulfotransferase 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
lysine (K)-specific demethylase 8, transcript variant X1
lysine (K)-specific demethylase 8, transcript variant X6
lysine (K)-specific demethylase 8, transcript variant X2
lysine (K)-specific demethylase 8, transcript variant X3
lysine (K)-specific demethylase 8, transcript variant X4
lysine (K)-specific demethylase 8, transcript variant X5
lysine-specific demethylase 8 isoform X1
lysine-specific demethylase 8 isoform X2
NSE1 homolog, SMC5-SMC6 complex component, transcript variant X5
NSE1 homolog, SMC5-SMC6 complex component, transcript variant X2
NSE1 homolog, SMC5-SMC6 complex component, transcript variant X3
NSE1 homolog, SMC5-SMC6 complex component, transcript variant X1
NSE1 homolog, SMC5-SMC6 complex component, transcript variant X4
non-structural maintenance of chromosomes element 1 homolog isoform X3
non-structural maintenance of chromosomes element 1 homolog isoform X1
non-structural maintenance of chromosomes element 1 homolog isoform X4
non-structural maintenance of chromosomes element 1 homolog isoform X2
interleukin-4 receptor subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 87% 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 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
3-phosphoinositide-dependent protein kinase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
BTB/POZ domain-containing protein KCTD5-like
SUMO-conjugating enzyme UBC9-A-like, transcript variant X2
SUMO-conjugating enzyme UBC9-A-like, transcript variant X3
SUMO-conjugating enzyme UBC9-A-like, transcript variant X1
SUMO-conjugating enzyme UBC9-A-like isoform X3
SUMO-conjugating enzyme UBC9-B-like isoform X1
SUMO-conjugating enzyme UBC9-A-like isoform X2
unk like zinc finger, transcript variant X1
unk like zinc finger, transcript variant X2
putative E3 ubiquitin-protein ligase UNKL isoform X2
putative E3 ubiquitin-protein ligase UNKL isoform X1
unk like zinc finger, transcript variant X3
putative E3 ubiquitin-protein ligase UNKL isoform X3
unk like zinc finger, transcript variant X4
putative E3 ubiquitin-protein ligase UNKL isoform X4
N-acetylglucosamine-1-phosphate transferase subunit gamma, transcript variant X3
N-acetylglucosamine-1-phosphate transferase subunit gamma, transcript variant X5
N-acetylglucosamine-1-phosphate transferase subunit gamma, transcript variant X1
N-acetylglucosamine-1-phosphate transferase subunit gamma, transcript variant X4
N-acetylglucosamine-1-phosphate transferase subunit gamma, transcript variant X2
N-acetylglucosamine-1-phosphotransferase subunit gamma isoform X4
N-acetylglucosamine-1-phosphotransferase subunit gamma isoform X3
N-acetylglucosamine-1-phosphotransferase subunit gamma isoform X5
N-acetylglucosamine-1-phosphotransferase subunit gamma isoform X2
N-acetylglucosamine-1-phosphotransferase subunit gamma isoform X1
LLGL scribble cell polarity complex component 1, transcript variant X2
LLGL scribble cell polarity complex component 1, transcript variant X1
lethal(2) giant larvae protein homolog 1 isoform X1
lethal(2) giant larvae protein homolog 1 isoform X2
FLII actin remodeling protein, transcript variant X2
FLII actin remodeling protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 58% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glucose-induced degradation protein 4 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RNA binding fox-1 homolog 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RNA binding fox-1 homolog 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RNA binding protein fox-1 homolog 1 isoform X1
RNA binding protein fox-1 homolog 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 41 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transmembrane protein 114, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 54% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 114, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
methyltransferase 22, Kin17 lysine, transcript variant X1
methyltransferase 22, Kin17 lysine, transcript variant X5
methyltransferase 22, Kin17 lysine, transcript variant X2
methyltransferase 22, Kin17 lysine, transcript variant X4
methyltransferase 22, Kin17 lysine, transcript variant X3
methyltransferase-like protein 22 isoform X1
methyltransferase-like protein 22 isoform X2
4-aminobutyrate aminotransferase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
calcium regulated heat stable protein 1, transcript variant X1
calcium regulated heat stable protein 1, transcript variant X3
calcium regulated heat stable protein 1, transcript variant X2
calcium regulated heat stable protein 1, transcript variant X4
N-acetyltransferase 15 (GCN5-related, putative), transcript variant X1
N-acetyltransferase 15 (GCN5-related, putative), transcript variant X4
N-acetyltransferase 15 (GCN5-related, putative), transcript variant X2
N-acetyltransferase 15 (GCN5-related, putative), transcript variant X3
integrator complex subunit 15, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 long SRA reads, 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
integrator complex subunit 15, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
integrator complex subunit 15, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
integrator complex subunit 15 isoform X1
integrator complex subunit 15 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: deoxyribonuclease-1
enoyl-CoA delta isomerase 1, mitochondrial
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 16 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain-containing protein 154-like, transcript variant X1
coiled-coil domain-containing protein 154-like, transcript variant X2
coiled-coil domain-containing protein 154-like, transcript variant X3
coiled-coil domain-containing protein 154-like isoform X1
coiled-coil domain-containing protein 154-like isoform X2
coiled-coil domain-containing protein 154-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
post-glycosylphosphatidylinositol attachment to proteins 6, transcript variant X1
post-GPI attachment to proteins factor 6 isoform X1
post-glycosylphosphatidylinositol attachment to proteins 6, transcript variant X2
post-glycosylphosphatidylinositol attachment to proteins 6, transcript variant X3
post-GPI attachment to proteins factor 6 isoform X2
post-GPI attachment to proteins factor 6 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Rho GDP dissociation inhibitor (GDI) gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 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: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X2
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X1
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X3
ankyrin repeat and fibronectin type-III domain-containing protein 1-like isoform X1
ankyrin repeat and fibronectin type-III domain-containing protein 1-like isoform X2
uncharacterized LOC109924040, transcript variant X1
uncharacterized LOC109924040, transcript variant X2
uncharacterized LOC109924040, transcript variant X5
uncharacterized LOC109924040, transcript variant X4
uncharacterized protein LOC109924040 isoform X1
uncharacterized LOC109924040, transcript variant X3
uncharacterized LOC109924040, transcript variant X6
uncharacterized protein LOC109924040 isoform X2
uncharacterized protein LOC109924040 isoform X3
ATP-binding cassette, sub-family A (ABC1), member 3b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00548
ankyrin repeat and sterile alpha motif domain containing 3
ankyrin repeat and SAM domain-containing protein 3
dynein axonemal assembly factor 8, transcript variant X2
dynein axonemal assembly factor 8, transcript variant X1
dynein axonemal assembly factor 8, transcript variant X3
dynein axonemal assembly factor 8 isoform X2
dynein axonemal assembly factor 8 isoform X1
dynein axonemal assembly factor 8 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
NLR family CARD domain-containing protein 3
tubulin epsilon and delta complex protein 1
chromosome 21 C8orf33 homolog, transcript variant X2
chromosome 21 C8orf33 homolog, transcript variant X1
MAPK regulated corepressor interacting protein 2, transcript variant X1
MAPK regulated corepressor interacting protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
MAPK regulated corepressor interacting protein 2 isoform X1
MAPK regulated corepressor interacting protein 2 isoform X2
clusterin associated protein 1, transcript variant X1
clusterin associated protein 1, transcript variant X2
clusterin-associated protein 1 homolog isoform X1
clusterin-associated protein 1 homolog isoform X2
RAB11 family interacting protein 3 (class II), transcript variant X3
RAB11 family interacting protein 3 (class II), transcript variant X2
RAB11 family interacting protein 3 (class II), transcript variant X1
rab11 family-interacting protein 3 isoform X2
rab11 family-interacting protein 3 isoform X1
2,4-dienoyl CoA reductase 2, peroxisomal, transcript variant X1
2,4-dienoyl CoA reductase 2, peroxisomal, transcript variant X4
2,4-dienoyl CoA reductase 2, peroxisomal, transcript variant X3
2,4-dienoyl CoA reductase 2, peroxisomal, transcript variant X2
2,4-dienoyl CoA reductase 2, peroxisomal, transcript variant X5
peroxisomal 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing] isoform X1
peroxisomal 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing] isoform X4
peroxisomal 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing] isoform X3
peroxisomal 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing] isoform X2
peroxisomal 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing] isoform X5
intraflagellar transport 140 homolog (Chlamydomonas)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
intraflagellar transport protein 140 homolog
transmembrane protein 204, transcript variant X1
transmembrane protein 204, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109932336, transcript variant X2
uncharacterized LOC109932336, transcript variant X1
uncharacterized protein LOC109932336 isoform X2
uncharacterized protein LOC109932336 isoform X1
NME/NM23 nucleoside diphosphate kinase 4, transcript variant X1
NME/NM23 nucleoside diphosphate kinase 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
nucleoside diphosphate kinase, mitochondrial isoform X1
nucleoside diphosphate kinase, mitochondrial isoform X2
NME/NM23 nucleoside diphosphate kinase 4, transcript variant X3
nucleoside diphosphate kinase, mitochondrial isoform X3
NME/NM23 nucleoside diphosphate kinase 4, transcript variant X4
nucleoside diphosphate kinase, mitochondrial isoform X4
RNA-binding protein with serine-rich domain 1, transcript variant X1
RNA-binding protein with serine-rich domain 1, transcript variant X2
RNA-binding protein with serine-rich domain 1 isoform X1
RNA-binding protein with serine-rich domain 1 isoform X2
TEL2, telomere maintenance 2, homolog (S. cerevisiae), transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
TEL2, telomere maintenance 2, homolog (S. cerevisiae), transcript variant X4
TEL2, telomere maintenance 2, homolog (S. cerevisiae), transcript variant X1
TEL2, telomere maintenance 2, homolog (S. cerevisiae), transcript variant X3
TEL2, telomere maintenance 2, homolog (S. cerevisiae), transcript variant X2
telomere length regulation protein TEL2 homolog
SEC14-like protein 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SEC14-like protein 5, transcript variant X2
dnaJ homolog subfamily A member 3, mitochondrial, transcript variant X2
dnaJ homolog subfamily A member 3, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
dnaJ homolog subfamily A member 3, mitochondrial isoform X2
dnaJ homolog subfamily A member 3, mitochondrial isoform 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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
heat shock protein 75 kDa, mitochondrial
heat shock protein 75 kDa, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
transcription factor AP-4 (activating enhancer binding protein 4), transcript variant X1
transcription factor AP-4 (activating enhancer binding protein 4), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
presequence translocase associated motor 16
mitochondrial import inner membrane translocase subunit tim16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 6 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: 1 long SRA read, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: N-acetylglucosamine-6-phosphate deacetylase
SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae)
structure-specific endonuclease subunit SLX4
serine/threonine-protein kinase 19, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 long SRA reads, 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
serine/threonine-protein kinase 19, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 long SRA reads, 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
serine/threonine-protein kinase 19, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 long SRA reads, 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein kinase 19, transcript variant X1
serine/threonine-protein kinase 19, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine-protein kinase 19, transcript variant X2
serine/threonine-protein kinase 19, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 long SRA reads, 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
serine/threonine-protein kinase 19 isoform X1
serine/threonine-protein kinase 19 isoform X2
serine/threonine-protein kinase 19 isoform X3
decapping exoribonuclease, transcript variant X2
decapping exoribonuclease, transcript variant X3
decapping exoribonuclease, transcript variant X1
peroxisomal membrane protein PMP34, transcript variant X1
peroxisomal membrane protein PMP34, transcript variant X2
peroxisomal membrane protein PMP34 isoform X1
peroxisomal membrane protein PMP34 isoform X2
ankyrin repeat and sterile alpha motif domain containing 4B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and SAM domain-containing protein 4B
kelch-like protein 20, transcript variant X1
kelch-like protein 20, transcript variant X4
kelch-like protein 20, transcript variant X2
kelch-like protein 20, transcript variant X3
SNU13 homolog, small nuclear ribonucleoprotein a (U4/U6.U5)
cytochrome b-c1 complex subunit 2, mitochondrial
PDZ domain-containing protein 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
PDZ domain-containing protein 9, transcript variant X1
PDZ domain-containing protein 9 isoform X2
PDZ domain-containing protein 9 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C16orf52 homolog B
von Willebrand factor A domain containing 3A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
von Willebrand factor A domain containing 3A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
von Willebrand factor A domain-containing protein 3A
short chain dehydrogenase/reductase family 42E, member 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: 5 Proteins, and 7% 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 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: putative short-chain dehydrogenase/reductase family 42E member 2
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
eukaryotic elongation factor 2 kinase, transcript variant X1
eukaryotic elongation factor 2 kinase, transcript variant X9
eukaryotic elongation factor 2 kinase, transcript variant X7
eukaryotic elongation factor 2 kinase, transcript variant X3
eukaryotic elongation factor 2 kinase, transcript variant X2
eukaryotic elongation factor 2 kinase, transcript variant X5
eukaryotic elongation factor 2 kinase, transcript variant X4
eukaryotic elongation factor 2 kinase, transcript variant X6
eukaryotic elongation factor 2 kinase, transcript variant X8
eukaryotic elongation factor 2 kinase isoform X1
eukaryotic elongation factor 2 kinase isoform X3
eukaryotic elongation factor 2 kinase isoform X2
polymerase (RNA) III (DNA directed) polypeptide E, transcript variant X6
polymerase (RNA) III (DNA directed) polypeptide E, transcript variant X3
polymerase (RNA) III (DNA directed) polypeptide E, transcript variant X1
polymerase (RNA) III (DNA directed) polypeptide E, transcript variant X2
polymerase (RNA) III (DNA directed) polypeptide E, transcript variant X4
polymerase (RNA) III (DNA directed) polypeptide E, transcript variant X5
DNA-directed RNA polymerase III subunit RPC5 isoform X1
DNA-directed RNA polymerase III subunit RPC5 isoform X2
DNA-directed RNA polymerase III subunit RPC5 isoform X4
DNA-directed RNA polymerase III subunit RPC5 isoform X5
DNA-directed RNA polymerase III subunit RPC5 isoform X3
DNA-directed RNA polymerase III subunit RPC5 isoform X6
cerebellar degeneration-related protein 2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
cerebellar degeneration-related protein 2
uncharacterized protein C7orf50, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein C7orf50, transcript variant X2
uncharacterized protein C7orf50 homolog isoform X1
uncharacterized protein C7orf50 homolog isoform X2
uncharacterized protein C7orf50, transcript variant X3
uncharacterized protein C7orf50 homolog isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Smith-Magenis syndrome chromosome region, candidate 8a, transcript variant X1
guanine nucleotide exchange protein smcr8a isoform X1
Smith-Magenis syndrome chromosome region, candidate 8a, transcript variant X2
guanine nucleotide exchange protein smcr8a isoform X2
dehydrogenase/reductase (SDR family) member 7B
dehydrogenase/reductase SDR family member 7B
guanine nucleotide binding protein (G protein) alpha 12a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
guanine nucleotide binding protein (G protein) alpha 12a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
guanine nucleotide-binding protein subunit alpha-12a isoform X1
guanine nucleotide-binding protein subunit alpha-12a isoform X2
guanine nucleotide binding protein (G protein) alpha 12a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
guanine nucleotide-binding protein subunit alpha-12a isoform X3
caspase recruitment domain family, member 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
caspase recruitment domain-containing protein 11
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 15 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
LOW QUALITY PROTEIN: cytochrome P450 3A21-like
cytochrome P450 3A19, transcript variant X2
cytochrome P450 3A19, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
adaptor related protein complex 5 subunit zeta 1, transcript variant X1
adaptor related protein complex 5 subunit zeta 1, transcript variant X2
adaptor related protein complex 5 subunit zeta 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
ras-associating and dilute domain-containing protein
monocyte to macrophage differentiation-associated 2a
monocyte to macrophage differentiation factor 2a
WD repeat domain, phosphoinositide interacting 2, transcript variant X1
WD repeat domain phosphoinositide-interacting protein 2 isoform X1
WD repeat domain, phosphoinositide interacting 2, transcript variant X2
WD repeat domain phosphoinositide-interacting protein 2 isoform X2
actin-related protein 2/3 complex subunit 1B-like
actin related protein 2/3 complex, subunit 1A
actin-related protein 2/3 complex subunit 1A-B
uncharacterized LOC125485651, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125485651, transcript variant X3
uncharacterized LOC125485651, transcript variant X4
uncharacterized LOC125485651, transcript variant X1
uncharacterized LOC125485651, transcript variant X2
uncharacterized LOC109913067, transcript variant X1
uncharacterized LOC109913067, transcript variant X2
uncharacterized protein LOC109913067 isoform X2
uncharacterized protein LOC109913067 isoform X1
mesothelin-like protein, transcript variant X1
mesothelin-like protein, transcript variant X2
mesothelin-like protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins
probable ATP-dependent RNA helicase DDX4
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: 13 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: probable ATP-dependent RNA helicase DDX4
importin subunit alpha-5-like, transcript variant X2
importin subunit alpha-5-like, transcript variant X3
importin subunit alpha-5-like, transcript variant X1
importin subunit alpha-5-like, transcript variant X4
importin subunit alpha-5-like isoform X2
importin subunit alpha-5-like isoform X1
importin subunit alpha-5-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 162 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
F-box and leucine-rich repeat protein 18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 long SRA reads, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
trinucleotide repeat-containing gene 18 protein
uncharacterized LOC109933606, transcript variant X4
uncharacterized LOC109933606, transcript variant X3
uncharacterized LOC109933606, transcript variant X2
uncharacterized LOC109933606, transcript variant X6
uncharacterized LOC109933606, transcript variant X5
uncharacterized LOC109933606, transcript variant X7
uncharacterized LOC109933606, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66% coverage of the annotated genomic feature by RNAseq alignments
equilibrative nucleoside transporter 4-like
cleavage and polyadenylation specific factor 4, transcript variant X2
cleavage and polyadenylation specific factor 4, transcript variant X1
cleavage and polyadenylation specificity factor subunit 4 isoform X2
cleavage and polyadenylation specificity factor subunit 4 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC503706 homolog, transcript variant X5
uncharacterized protein LOC503706 homolog, transcript variant X1
uncharacterized protein LOC503706 homolog, transcript variant X4
uncharacterized protein LOC503706 homolog, transcript variant X7
uncharacterized protein LOC503706 homolog, transcript variant X2
uncharacterized protein LOC503706 homolog, transcript variant X3
uncharacterized protein LOC503706 homolog, transcript variant X6
uncharacterized protein zgc:112980 isoform X1
uncharacterized protein zgc:112980 isoform X2
uncharacterized protein zgc:112980 isoform X3
uncharacterized protein zgc:112980 isoform X4
guanine nucleotide binding protein (G protein), gamma 13b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
guanine nucleotide binding protein (G protein), gamma 13b, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
guanine nucleotide binding protein (G protein), gamma 13b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
guanine nucleotide binding protein (G protein), gamma 13b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-13b
CTF18, chromosome transmission fidelity factor 18 homolog (S. cerevisiae), transcript variant X1
chromosome transmission fidelity protein 18 homolog isoform X1
CTF18, chromosome transmission fidelity factor 18 homolog (S. cerevisiae), transcript variant X2
chromosome transmission fidelity protein 18 homolog isoform X2
RNA pseudouridine synthase domain containing 1, transcript variant X2
RNA pseudouridine synthase domain containing 1, transcript variant X1
RNA pseudouridine synthase domain containing 1, transcript variant X3
RNA pseudouridylate synthase domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 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: 43 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear prelamin A recognition factor-like, transcript variant X1
cytosolic Fe-S cluster assembly factor narfl isoform X1
nuclear prelamin A recognition factor-like, transcript variant X2
cytosolic Fe-S cluster assembly factor narfl isoform X2
hydroxyacylglutathione hydrolase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 335 long SRA reads, 30 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
hydroxyacylglutathione hydrolase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 296 long SRA reads, 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
hydroxyacylglutathione hydrolase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 296 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
hydroxyacylglutathione hydrolase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 297 long SRA reads, 20 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
hydroxyacylglutathione hydrolase, mitochondrial isoform X1
hydroxyacylglutathione hydrolase, mitochondrial isoform X2
fumarylacetoacetate hydrolase domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
meiosis-specific with OB domain-containing protein
heparan sulfate glucosamine 3-O-sulfotransferase 3A1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
peptide methionine sulfoxide reductase MsrB
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase subunit B10
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 10
COORDINATES: nucleotide motif:Rfam:12.0:RF01225
ring finger protein 151, transcript variant X1
ring finger protein 151, transcript variant X2
transducin beta like 3, transcript variant X1
transducin beta-like protein 3 isoform X1
transducin beta like 3, transcript variant X2
transducin beta-like protein 3 isoform X2
growth factor, augmenter of liver regeneration (ERV1 homolog, S. cerevisiae)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ectonucleotide pyrophosphatase/phosphodiesterase family member 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
eukaryotic elongation factor 2 lysine methyltransferase, transcript variant X1
eukaryotic elongation factor 2 lysine methyltransferase, transcript variant X2
protein-lysine N-methyltransferase EEF2KMT isoform X1
protein-lysine N-methyltransferase EEF2KMT isoform X2
ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase
chitobiosyldiphosphodolichol beta-mannosyltransferase
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized si:ch211-76l23.4, transcript variant X1
uncharacterized si:ch211-76l23.4, transcript variant X2
uncharacterized protein si:ch211-76l23.4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
germ cell-specific gene 1-like protein isoform X1
germ cell-specific gene 1-like protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
putative RNA-binding protein Luc7-like 1
cytochrome c oxidase subunit 6B1, transcript variant X2
cytochrome c oxidase subunit 6B1, transcript variant X1
cytochrome c oxidase subunit 6B1, transcript variant X3
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125485661, transcript variant X2
uncharacterized LOC125485661, transcript variant X1
rhomboid 5 homolog 1a (Drosophila), transcript variant X3
rhomboid 5 homolog 1a (Drosophila), transcript variant X1
rhomboid 5 homolog 1a (Drosophila), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 62 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase MGRN1-like, transcript variant X3
E3 ubiquitin-protein ligase MGRN1-like, transcript variant X2
E3 ubiquitin-protein ligase MGRN1-like, transcript variant X1
E3 ubiquitin-protein ligase MGRN1-like isoform X2
E3 ubiquitin-protein ligase MGRN1-like isoform X1
uncharacterized protein C16orf96 homolog
cell death-inducing p53 target 1, transcript variant X1
cell death-inducing p53 target 1, transcript variant X3
cell death-inducing p53 target 1, transcript variant X2
cell death-inducing p53 target 1, transcript variant X4
cell death-inducing p53-target protein 1
U11/U12 small nuclear ribonucleoprotein 25 kDa protein
lipopolysaccharide-induced TNF factor, transcript variant X1
lipopolysaccharide-induced TNF factor, transcript variant X2
lipopolysaccharide-induced tumor necrosis factor-alpha factor homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q-like
tripartite motif-containing protein 2-like
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 2 samples with support for all annotated introns
meteorin, glial cell differentiation regulator, 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
meteorin, glial cell differentiation regulator, transcript variant X2
28S ribosomal protein S34, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
dexamethasone-induced Ras-related protein 1
mediator of RNA polymerase II transcription subunit 9
uncharacterized LOC125485671, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC125485671, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
carbohydrate (chondroitin 4) sulfotransferase 12a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 long SRA reads, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
carbohydrate (chondroitin 4) sulfotransferase 12a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 long SRA reads, 31 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
carbohydrate (chondroitin 4) sulfotransferase 12a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 31 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase, transcript variant X2
LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase, transcript variant X1
beta-1,3-N-acetylglucosaminyltransferase lunatic fringe isoform X2
beta-1,3-N-acetylglucosaminyltransferase lunatic fringe isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
tweety family member 3a, transcript variant X4
tweety family member 3a, transcript variant X2
tweety family member 3a, transcript variant X3
tweety family member 3a, transcript variant X1
tweety family member 3a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
eukaryotic translation initiation factor 3, subunit Ba
BRCA1-associated ATM activator 1, transcript variant X3
BRCA1-associated ATM activator 1, transcript variant X4
BRCA1-associated ATM activator 1, transcript variant X6
BRCA1-associated ATM activator 1, transcript variant X2
BRCA1-associated ATM activator 1, transcript variant X1
BRCA1-associated ATM activator 1, transcript variant X5
BRCA1-associated ATM activator 1 isoform X1
BRCA1-associated ATM activator 1 isoform X2
zinc finger protein 598, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 110 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
zinc finger protein 598, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
28S ribosomal protein S25, mitochondrial