Rhincodon typus isolate 14 chromosome 33, 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\nCM038830.1.\nAssembly name: sRhiTyp1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/03. The\noriginal whole-genome shotgun project has the accession\nJAHMAH000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Supernova v. 2.1.1; P_RNA_scaffolder v.\n commit 7941e0f; Tigmint v. 1.1.2; ARKS v.\n 1.1.0; 3D-DNA v. 180922\nAssembly Name :: sRhiTyp1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 46.7x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Rhincodon typus Annotation Release\n 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
unc-93 homolog B1, TLR signaling regulator, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
unc-93 homolog B1, TLR signaling regulator, transcript variant X2
SPG21 abhydrolase domain containing, maspardin
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ankyrin repeat and death domain containing 1A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ankyrin repeat and death domain containing 1A, transcript variant X2
ankyrin repeat and death domain containing 1A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 9 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and death domain-containing protein 1A isoform X3
ankyrin repeat and death domain-containing protein 1A isoform X2
ankyrin repeat and death domain-containing protein 1A isoform X1
calcium-binding mitochondrial carrier protein SCaMC-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
pleckstrin homology domain-containing family O member 1-like
small nuclear ribonucleoprotein polypeptide A'
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 126 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
leucine-rich repeat kinase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine-rich repeat kinase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine-rich repeat serine/threonine-protein kinase 1 isoform X2
leucine-rich repeat serine/threonine-protein kinase 1 isoform X1
leucine-rich repeat kinase 1, transcript variant X3
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 1 sample with support for all annotated introns
leucine-rich repeat serine/threonine-protein kinase 1 isoform X3
leucine-rich repeat kinase 1, transcript variant X4
leucine-rich repeat serine/threonine-protein kinase 1 isoform X4
aldehyde dehydrogenase 1 family, member A3, 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
aldehyde dehydrogenase 1 family, member A3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
aldehyde dehydrogenase family 1 member A3 isoform X2
aldehyde dehydrogenase family 1 member A3 isoform X1
ankyrin repeat and SOCS box containing 7, transcript variant X1
ankyrin repeat and SOCS box containing 7, transcript variant X3
ankyrin repeat and SOCS box containing 7, transcript variant X2
ankyrin repeat and SOCS box protein 7 isoform X1
ankyrin repeat and SOCS box protein 7 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, 8 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: 20 long SRA reads, 8 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: 32 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
ADAM metallopeptidase with thrombospondin type 1 motif, 17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
A disintegrin and metalloproteinase with thrombospondin motifs 17
membrane integral NOTCH2 associated receptor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
major intrinsically disordered Notch2-binding receptor 1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
complement C1q tumor necrosis factor-related protein 3-like
5,10-methenyltetrahydrofolate synthetase (5-formyltetrahydrofolate cyclo-ligase)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger, AN1-type domain 6, transcript variant X1
zinc finger, AN1-type domain 6, transcript variant X6
zinc finger, AN1-type domain 6, transcript variant X5
zinc finger, AN1-type domain 6, transcript variant X9
zinc finger, AN1-type domain 6, transcript variant X2
zinc finger, AN1-type domain 6, transcript variant X7
zinc finger, AN1-type domain 6, transcript variant X3
zinc finger, AN1-type domain 6, transcript variant X4
zinc finger, AN1-type domain 6, transcript variant X8
AN1-type zinc finger protein 6 isoform X1
AN1-type zinc finger protein 6 isoform X3
AN1-type zinc finger protein 6 isoform X2
AN1-type zinc finger protein 6 isoform X4
fumarylacetoacetate hydrolase (fumarylacetoacetase)
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
aryl-hydrocarbon receptor nuclear translocator 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
aryl hydrocarbon receptor nuclear translocator 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
alpha/beta hydrolase domain-containing protein 17C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
cell migration inducing hyaluronidase 1, transcript variant X2
cell migration inducing hyaluronidase 1, transcript variant X1
cell migration-inducing and hyaluronan-binding protein
cilia and flagella associated protein 161, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
cilia- and flagella-associated protein 161 isoform X1
cilia and flagella associated protein 161, 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 8 samples with support for all annotated introns
cilia- and flagella-associated protein 161 isoform X2
StAR-related lipid transfer (START) domain containing 5
steroidogenic acute regulatory protein, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
elongation factor like GTPase 1, transcript variant X1
elongation factor like GTPase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC791214 homolog, transcript variant X2
uncharacterized protein LOC791214 homolog, transcript variant X3
uncharacterized protein LOC791214 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 179 long SRA reads, 28 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
hepatoma-derived growth factor-related protein 3 isoform X5
hepatoma-derived growth factor-related protein 3 isoform X8
hepatoma-derived growth factor-related protein 3 isoform X2
hepatoma-derived growth factor-related protein 3 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
hepatoma-derived growth factor-related protein 3 isoform X3
hepatoma-derived growth factor-related protein 3 isoform X7
hepatoma-derived growth factor-related protein 3 isoform X1
hepatoma-derived growth factor-related protein 3 isoform X4
hepatoma-derived growth factor-related protein 3 isoform X9
transmembrane 6 superfamily member 1, transcript variant X1
transmembrane 6 superfamily member 1 isoform X1
transmembrane 6 superfamily member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane 6 superfamily member 1 isoform X2
isocitrate dehydrogenase (NADP(+)) 2, transcript variant X1
isocitrate dehydrogenase (NADP(+)) 2, transcript variant X2
isocitrate dehydrogenase [NADP], mitochondrial isoform X1
isocitrate dehydrogenase [NADP], mitochondrial isoform X2
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ba, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ba, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ba, transcript variant X1
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ba, transcript variant X4
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ba, transcript variant X5
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ba, transcript variant X3
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ba isoform X1
sema domain, immunoglobulin domain (Ig), transmembrane domain (TM) and short cytoplasmic domain, (semaphorin) 4Ba isoform X2
ras and EF-hand domain-containing protein, transcript variant X3
ras and EF-hand domain-containing protein, transcript variant X2
ras and EF-hand domain-containing protein, transcript variant X1
ras and EF-hand domain-containing protein isoform X1
ras and EF-hand domain-containing protein isoform X3
ras and EF-hand domain-containing protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
RNA polymerase II elongation factor ELL, transcript variant X1
RNA polymerase II elongation factor ELL, transcript variant X3
RNA polymerase II elongation factor ELL, transcript variant X2
RNA polymerase II elongation factor ELL, transcript variant X4
RNA polymerase II elongation factor ELL, transcript variant X6
RNA polymerase II elongation factor ELL, transcript variant X5
RNA polymerase II elongation factor ELL, transcript variant X8
RNA polymerase II elongation factor ELL, transcript variant X7
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
RNA polymerase II elongation factor ELL isoform X1
RNA polymerase II elongation factor ELL isoform X3
RNA polymerase II elongation factor ELL isoform X2
RNA polymerase II elongation factor ELL isoform X4
RNA polymerase II elongation factor ELL isoform X6
RNA polymerase II elongation factor ELL isoform X5
RNA polymerase II elongation factor ELL isoform X8
RNA polymerase II elongation factor ELL isoform X7
multiple C2 and transmembrane domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 95% 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: multiple C2 and transmembrane domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins
uncharacterized LOC125486785, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125486785, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
COUP transcription factor 2, transcript variant X3
COUP transcription factor 2, transcript variant X2
COUP transcription factor 2, transcript variant X1
uncharacterized LOC125486794, transcript variant X1
uncharacterized LOC125486794, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 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 5 samples with support for all annotated introns
LysM, putative peptidoglycan-binding, domain containing 4
lysM and putative peptidoglycan-binding domain-containing protein 4
myocyte enhancer factor 2aa, transcript variant X1
myocyte enhancer factor 2aa, transcript variant X2
myocyte enhancer factor 2aa, transcript variant X3
uncharacterized LOC125486804, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC125486804, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
leucine-rich repeat-containing protein 28
cation channel sperm-associated protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
protein disulfide isomerase family A, member 3
protein unc-13 homolog C-like, transcript variant X4
protein unc-13 homolog C-like, transcript variant X3
protein unc-13 homolog B-like isoform X3
protein unc-13 homolog B-like isoform X4
protein unc-13 homolog C-like, transcript variant X2
protein unc-13 homolog C-like, transcript variant X1
protein unc-13 homolog C-like isoform X2
protein unc-13 homolog C-like isoform X1
probable ribosome biogenesis protein RLP24
RAB27A, member RAS oncogene family, transcript variant X3
RAB27A, member RAS oncogene family, transcript variant X1
RAB27A, member RAS oncogene family, transcript variant X5
RAB27A, member RAS oncogene family, transcript variant X2
RAB27A, member RAS oncogene family, transcript variant X7
RAB27A, member RAS oncogene family, transcript variant X6
RAB27A, member RAS oncogene family, transcript variant X4
RAB27A, member RAS oncogene family, transcript variant X8
uncharacterized LOC109919909, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC109919909, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
cell cycle progression 1, transcript variant X2
cell cycle progression 1, transcript variant X9
cell cycle progression 1, transcript variant X8
cell cycle progression 1, transcript variant X5
cell cycle progression 1, transcript variant X3
cell cycle progression 1, transcript variant X7
cell cycle progression 1, transcript variant X6
cell cycle progression 1, transcript variant X4
cell cycle progression 1, transcript variant X1
cell cycle progression protein 1 isoform X1
cell cycle progression protein 1 isoform X5
cell cycle progression protein 1 isoform X3
cell cycle progression protein 1 isoform X7
cell cycle progression protein 1 isoform X2
cell cycle progression protein 1 isoform X6
cell cycle progression protein 1 isoform X4
cell cycle progression protein 1 isoform X8
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 30 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
DNA-binding protein RFX7-like, transcript variant X2
DNA-binding protein RFX7-like, transcript variant X1
DNA-binding protein RFX7-like isoform X2
DNA-binding protein RFX7-like isoform X1
testis expressed 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 14 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
testis expressed 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
testis expressed 9, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
testis expressed 9, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
testis expressed 9, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
testis expressed 9, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 97% 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, 10 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
meiosis-specific nuclear structural protein 1
zinc finger protein 280D-like, transcript variant X3
zinc finger protein 280D-like, transcript variant X6
zinc finger protein 280D-like, transcript variant X5
zinc finger protein 280D-like, transcript variant X4
zinc finger protein 280D-like, transcript variant X1
zinc finger protein 280D-like, transcript variant X2
zinc finger protein 280D-like isoform X2
zinc finger protein 280D-like isoform X5
zinc finger protein 280D-like isoform X4
zinc finger protein 280D-like isoform X3
zinc finger protein 280D-like isoform X1
transcription factor 12-like, transcript variant X1
transcription factor 12-like, transcript variant X2
transcription factor 12-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 12 samples with support for all annotated introns
transcription factor 12, transcript variant X1
transcription factor 12, transcript variant X2
transcription factor 12, transcript variant X5
transcription factor 12, transcript variant X4
transcription factor 12, transcript variant X3
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
aldehyde dehydrogenase 1 family, member A2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
aldehyde dehydrogenase 1 family, member A2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
disintegrin and metalloproteinase domain-containing protein 10
ubiquitin carboxyl-terminal hydrolase MINDY-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase MINDY-2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 111, transcript variant X3
ring finger protein 111, transcript variant X2
ring finger protein 111, transcript variant X1
E3 ubiquitin-protein ligase Arkadia isoform X1
E3 ubiquitin-protein ligase Arkadia isoform 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 3 samples with support for all annotated introns
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
selenocysteine insertion sequence-binding protein 2-like
regulator of G-protein signaling 7-binding protein-like
SHC (Src homology 2 domain containing) transforming protein 1, transcript variant X1
SHC (Src homology 2 domain containing) transforming protein 1, transcript variant X2
SHC (Src homology 2 domain containing) transforming protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
protein FAM227B-like, transcript variant X2
protein FAM227B-like, transcript variant X1
protein FAM227B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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
DTW domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DTW domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DTW domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DTW domain containing 1, transcript variant X1
DTW domain containing 1, transcript variant X5
tRNA-uridine aminocarboxypropyltransferase 1
NAD(P) transhydrogenase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 214 member A, transcript variant X2
family with sequence similarity 214 member A, transcript variant X1
family with sequence similarity 214 member A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 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 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: 3 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 beta-5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 21 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
guanine nucleotide-binding protein subunit beta-5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
guanine nucleotide-binding protein subunit beta-5 isoform X1
guanine nucleotide-binding protein subunit beta-5 isoform X2
mitogen-activated protein kinase 6, transcript variant X3
mitogen-activated protein kinase 6, transcript variant X1
mitogen-activated protein kinase 6, transcript variant X2
LEO1 homolog, Paf1/RNA polymerase II complex component
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125486807, transcript variant X2
uncharacterized LOC125486807, transcript variant X1
LysM, putative peptidoglycan-binding, domain containing 2, transcript variant X2
LysM, putative peptidoglycan-binding, domain containing 2, transcript variant X3
LysM, putative peptidoglycan-binding, domain containing 2, transcript variant X1
LysM, putative peptidoglycan-binding, domain containing 2, transcript variant X4
lysM and putative peptidoglycan-binding domain-containing protein 2
adaptor related protein complex 4 subunit epsilon 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 long SRA reads, 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor, alpha-induced protein 8-like 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tumor necrosis factor, alpha-induced protein 8-like 3, transcript variant X4
tumor necrosis factor, alpha-induced protein 8-like 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tumor necrosis factor, alpha-induced protein 8-like 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
tumor necrosis factor, alpha-induced protein 8-like 3, 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 2 samples with support for all annotated introns
tumor necrosis factor, alpha-induced protein 8-like 3, transcript variant X6
tumor necrosis factor alpha-induced protein 8-like protein 3 isoform X2
tumor necrosis factor alpha-induced protein 8-like protein 3 isoform X1
tumor necrosis factor alpha-induced protein 8-like protein 3 isoform 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 5 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 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D, like, transcript variant X2
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D, like, transcript variant X1
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D, like, transcript variant X4
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D, like, transcript variant X3
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D, like, transcript variant X5
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D, like isoform X1
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D, like isoform X3
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D, like isoform X2
sema domain, transmembrane domain (TM), and cytoplasmic domain, (semaphorin) 6D, like isoform X4
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
caseinolytic mitochondrial matrix peptidase chaperone subunit Xa
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
ATP-dependent Clp protease ATP-binding subunit clpX-like, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 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: 1 long SRA read, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
kelch repeat and BTB domain containing 13a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
kelch repeat and BTB domain-containing protein 13
solute carrier family 51 subunit beta, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
solute carrier family 51 subunit beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
solute carrier family 51 subunit beta, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 51 subunit beta, transcript variant X4
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 6 samples with support for all annotated introns
solute carrier family 51 subunit beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
solute carrier family 51 subunit beta isoform X2
solute carrier family 51 subunit beta isoform X1
dipeptidyl peptidase 8, transcript variant X1
dipeptidyl peptidase 8, transcript variant X2
dipeptidyl peptidase 8, transcript variant X3
immunoglobulin superfamily, DCC subclass, member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
immunoglobulin superfamily DCC subclass member 4
immunoglobulin superfamily DCC subclass member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 19% coverage of the annotated genomic feature by RNAseq alignments
poly (ADP-ribose) polymerase family, member 16
protein mono-ADP-ribosyltransferase PARP16
gonadotropin-releasing hormone II receptor-like, transcript variant X1
gonadotropin-releasing hormone II receptor-like, transcript variant X2
gonadotropin-releasing hormone II receptor-like isoform X1
gonadotropin-releasing hormone II receptor-like isoform X2
neurotrophic tyrosine kinase, receptor, type 3a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L46, mitochondrial
28S ribosomal protein S11, mitochondrial
DET1 partner of COP1 E3 ubiquitin ligase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
DET1 partner of COP1 E3 ubiquitin ligase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 long SRA reads, 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
kinesin family member 7, transcript variant X2
kinesin family member 7, transcript variant X1
kinesin family member 7, transcript variant X4
kinesin family member 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 113 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 Proteins
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
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: UDP-glucuronosyltransferase 2A1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
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: 74 Proteins, and 80% 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 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
polymerase (DNA directed), gamma, transcript variant X2
polymerase (DNA directed), gamma, transcript variant X1
transfer RNA arginine (anticodon UCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC109930375, transcript variant X3
uncharacterized LOC109930375, transcript variant X2
uncharacterized LOC109930375, transcript variant X1
ammonium transporter Rh type C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 119 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ammonium transporter Rh type C, transcript variant X2
TopBP1-interacting, checkpoint, and replication regulator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
abhydrolase domain containing 2, acylglycerol lipase, transcript variant X1
abhydrolase domain containing 2, acylglycerol lipase, transcript variant X2
EGF-like repeat and discoidin I-like domain-containing protein 3, 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 13 samples with support for all annotated introns
EGF-like repeat and discoidin I-like domain-containing protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
EGF-like repeat and discoidin I-like domain-containing protein 3 isoform X1
EGF-like repeat and discoidin I-like domain-containing protein 3 isoform X2
hyaluronan and proteoglycan link protein 3-like, transcript variant X1
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 5 samples with support for all annotated introns
hyaluronan and proteoglycan link protein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
hyaluronan and proteoglycan link protein 3-like isoform X1
hyaluronan and proteoglycan link protein 3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
gonadotropin-releasing hormone II receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins
WD repeat domain 93, transcript variant X2
WD repeat domain 93, transcript variant X3
WD repeat domain 93, transcript variant X1
WD repeat-containing protein 93 isoform X2
WD repeat-containing protein 93 isoform X1
WD repeat domain 93, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
WD repeat-containing protein 93 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 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, 11 Proteins, and 99% 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: 1 long SRA read, 24 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
chromodomain helicase DNA binding protein 2, transcript variant X2
chromodomain helicase DNA binding protein 2, transcript variant X1
chromodomain helicase DNA binding protein 2, transcript variant X3
chromodomain-helicase-DNA-binding protein 2 isoform X2
chromodomain-helicase-DNA-binding protein 2 isoform X1
chromodomain-helicase-DNA-binding protein 2 isoform X3
CTS telomere maintenance complex component 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
CTS telomere maintenance complex component 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
CTS telomere maintenance complex component 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
CTS telomere maintenance complex component 1, transcript variant X4
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 11 samples with support for all annotated introns
family with sequence similarity 174 member B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
family with sequence similarity 174 member B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins
solute carrier organic anion transporter family member 3A1a, transcript variant X2
solute carrier organic anion transporter family member 3A1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier organic anion transporter family member 3A1 isoform X2
solute carrier organic anion transporter family member 3A1 isoform X1
solute carrier organic anion transporter family member 3A1a, transcript variant X3
solute carrier organic anion transporter family member 3A1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, 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: 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
kelch-like protein 25, transcript variant X3
kelch-like protein 25, transcript variant X1
kelch-like protein 25, transcript variant X2
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
apoptosis-enhancing nuclease-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
apoptosis-enhancing nuclease-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
apoptosis-enhancing nuclease-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
apoptosis-enhancing nuclease-like isoform X1
apoptosis-enhancing nuclease-like isoform X2
interferon-stimulated gene 20 kDa protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
membrane progestin receptor gamma-B, transcript variant X2
membrane progestin receptor gamma-B, transcript variant X1
membrane progestin receptor gamma-B, transcript variant X4
membrane progestin receptor gamma-B, transcript variant X3
membrane progestin receptor gamma-B, transcript variant X5
membrane progestin receptor gamma-B isoform X3
membrane progestin receptor gamma-B isoform X4
membrane progestin receptor gamma-B isoform X1
membrane progestin receptor gamma-B isoform X2
NADPH oxidase, EF-hand calcium binding domain 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
acidic leucine-rich nuclear phosphoprotein 32 family member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 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: 4 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
CLN6 transmembrane ER protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ceroid-lipofuscinosis neuronal protein 6 homolog isoform X1
CLN6 transmembrane ER protein, transcript variant X2
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
ceroid-lipofuscinosis neuronal protein 6 homolog isoform X2
SKI family transcriptional corepressor 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
SKI family transcriptional corepressor 1 homolog-B
mitogen-activated protein kinase kinase 5, transcript variant X1
mitogen-activated protein kinase kinase 5, transcript variant X7
mitogen-activated protein kinase kinase 5, transcript variant X3
mitogen-activated protein kinase kinase 5, transcript variant X2
dual specificity mitogen-activated protein kinase kinase 5 isoform X6
dual specificity mitogen-activated protein kinase kinase 5 isoform X3
dual specificity mitogen-activated protein kinase kinase 5 isoform X2
dual specificity mitogen-activated protein kinase kinase 5 isoform X1
mitogen-activated protein kinase kinase 5, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
mitogen-activated protein kinase kinase 5, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
mitogen-activated protein kinase kinase 5, transcript variant X5
dual specificity mitogen-activated protein kinase kinase 5 isoform X4
dual specificity mitogen-activated protein kinase kinase 5 isoform X5
chromosome 33 C15orf61 homolog, transcript variant X1
chromosome 33 C15orf61 homolog, transcript variant X3
chromosome 33 C15orf61 homolog, transcript variant X2
uncharacterized protein C15orf61 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
alpha and gamma adaptin binding protein, transcript variant X4
alpha and gamma adaptin binding protein, transcript variant X1
alpha and gamma adaptin binding protein, transcript variant X2
alpha and gamma adaptin binding protein, transcript variant X3
alpha- and gamma-adaptin-binding protein p34 isoform X1
alpha- and gamma-adaptin-binding protein p34 isoform X2
alpha- and gamma-adaptin-binding protein p34 isoform X3
alpha- and gamma-adaptin-binding protein p34 isoform X4
mothers against decapentaplegic homolog 3b
mothers against decapentaplegic homolog 6b
kinesin family member 23, transcript variant X1
kinesin family member 23, transcript variant X2
kinesin family member 23, transcript variant X3
TLE family member 3, transcriptional corepressor a, transcript variant X16
TLE family member 3, transcriptional corepressor a, transcript variant X15
TLE family member 3, transcriptional corepressor a, transcript variant X17
TLE family member 3, transcriptional corepressor a, transcript variant X14
TLE family member 3, transcriptional corepressor a, transcript variant X11
TLE family member 3, transcriptional corepressor a, transcript variant X10
TLE family member 3, transcriptional corepressor a, transcript variant X9
TLE family member 3, transcriptional corepressor a, transcript variant X7
TLE family member 3, transcriptional corepressor a, transcript variant X18
TLE family member 3, transcriptional corepressor a, transcript variant X8
TLE family member 3, transcriptional corepressor a, transcript variant X12
TLE family member 3, transcriptional corepressor a, transcript variant X6
TLE family member 3, transcriptional corepressor a, transcript variant X4
TLE family member 3, transcriptional corepressor a, transcript variant X3
TLE family member 3, transcriptional corepressor a, transcript variant X2
TLE family member 3, transcriptional corepressor a, transcript variant X13
TLE family member 3, transcriptional corepressor a, transcript variant X5
TLE family member 3, transcriptional corepressor a, transcript variant X1
transducin-like enhancer protein 3-A isoform X16
transducin-like enhancer protein 3-A isoform X15
transducin-like enhancer protein 3-A isoform X17
transducin-like enhancer protein 3-A isoform X14
transducin-like enhancer protein 3-A isoform X11
transducin-like enhancer protein 3-A isoform X10
transducin-like enhancer protein 3-A isoform X9
transducin-like enhancer protein 3-A isoform X7
transducin-like enhancer protein 3-A isoform X18
transducin-like enhancer protein 3-A isoform X8
transducin-like enhancer protein 3-A isoform X12
transducin-like enhancer protein 3-A isoform X6
transducin-like enhancer protein 3-A isoform X4
transducin-like enhancer protein 3-A isoform X3
transducin-like enhancer protein 3-A isoform X2
transducin-like enhancer protein 3-A isoform X13
transducin-like enhancer protein 3-A isoform X5
transducin-like enhancer protein 3-A isoform X1
uveal autoantigen with coiled-coil domains and ankyrin repeats a
uveal autoantigen with coiled-coil domains and ankyrin repeats
mortality factor 4 like 1, transcript variant X3
mortality factor 4 like 1, transcript variant X1
mortality factor 4 like 1, transcript variant X2
mortality factor 4-like protein 1 isoform X1
mortality factor 4-like protein 1 isoform X2
transfer RNA lysine (anticodon CUU); 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: 31 Proteins
A disintegrin and metalloproteinase with thrombospondin motifs 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 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: 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 65% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
cytosolic iron-sulfur assembly component 2A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 long SRA reads, 13 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
SPG11 vesicle trafficking associated, spatacsin
eukaryotic translation initiation factor 3, subunit Ja
eukaryotic translation initiation factor 3 subunit J-A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 52% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC125486790, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125486790, transcript variant X3
uncharacterized LOC125486790, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
FERM domain-containing protein 5, transcript variant X1
FERM domain-containing protein 5, transcript variant X2
FERM domain-containing protein 5 isoform X1
FERM domain-containing protein 5 isoform X2
FERM domain-containing protein 5, transcript variant X3
FERM domain-containing protein 5 isoform X3
BLM RecQ like helicase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, 19 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
BLM RecQ like helicase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
BLM RecQ like helicase, transcript variant X2
Ras protein specific guanine nucleotide releasing factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
ras-specific guanine nucleotide-releasing factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
ankyrin repeat domain-containing protein 34C
uncharacterized protein LOC407663 homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 24 Proteins, and 84% 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: retinol dehydrogenase 13
small nuclear RNA activating complex, polypeptide 5, transcript variant X1
small nuclear RNA activating complex, polypeptide 5, transcript variant X2
snRNA-activating protein complex subunit 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
zwilch kinetochore protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
zwilch kinetochore protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00138
COORDINATES: nucleotide motif:Rfam:12.0:RF00093
mitogen-activated protein kinase kinase 1
dual specificity mitogen-activated protein kinase kinase 1
timeless interacting protein, transcript variant X1
timeless interacting protein, transcript variant X5
timeless interacting protein, transcript variant X2
timeless interacting protein, transcript variant X4
timeless interacting protein, transcript variant X3
DIS3 like exosome 3'-5' exoribonuclease, transcript variant X2
DIS3 like exosome 3'-5' exoribonuclease, transcript variant X1
DIS3 like exosome 3'-5' exoribonuclease, transcript variant X4
DIS3 like exosome 3'-5' exoribonuclease, transcript variant X3
DIS3 like exosome 3'-5' exoribonuclease, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
multiple epidermal growth factor-like domains protein 11
DENN/MADD domain containing 4A, transcript variant X1
DENN/MADD domain containing 4A, transcript variant X3
DENN/MADD domain containing 4A, transcript variant X2
DENN/MADD domain containing 4A, transcript variant X4
DENN/MADD domain containing 4A, transcript variant X8
DENN/MADD domain containing 4A, transcript variant X5
DENN/MADD domain containing 4A, transcript variant X7
DENN/MADD domain containing 4A, transcript variant X6
DENN/MADD domain containing 4A, transcript variant X9
C-myc promoter-binding protein isoform X1
C-myc promoter-binding protein isoform X3
C-myc promoter-binding protein isoform X4
C-myc promoter-binding protein isoform X8
C-myc promoter-binding protein isoform X2
C-myc promoter-binding protein isoform X5
C-myc promoter-binding protein isoform X7
C-myc promoter-binding protein isoform X6
C-myc promoter-binding protein isoform X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
integrator complex subunit 14, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 long SRA reads, 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
integrator complex subunit 14, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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
integrator complex subunit 14, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
integrator complex subunit 14, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
integrator complex subunit 14, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 long SRA reads, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
integrator complex subunit 14, transcript variant X9
integrator complex subunit 14, transcript variant X8
integrator complex subunit 14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
integrator complex subunit 14, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
integrator complex subunit 14 isoform X3
integrator complex subunit 14 isoform X1
integrator complex subunit 14 isoform X2
integrator complex subunit 14 isoform X5
integrator complex subunit 14 isoform X4
3-hydroxyacyl-CoA dehydratase 3, transcript variant X1
3-hydroxyacyl-CoA dehydratase 3, transcript variant X2
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase isoform X1
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase isoform X2
WASP homolog-associated protein with actin, membranes and microtubules
homer scaffold protein 2, transcript variant X3
homer scaffold protein 2, transcript variant X4
homer scaffold protein 2, transcript variant X2
homer scaffold protein 2, transcript variant X1
RNA guanine-N7 methyltransferase activating subunit-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
RNA guanine-N7 methyltransferase activating subunit-like, transcript variant X1
RNA guanine-N7 methyltransferase activating subunit-like isoform X2
RNA guanine-N7 methyltransferase activating subunit-like isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: UPF0235 protein C15orf40 homolog
BTB/POZ domain-containing protein 1, transcript variant X2
BTB/POZ domain-containing protein 1, transcript variant X1
BTB/POZ domain-containing protein 1 isoform X2
BTB/POZ domain-containing protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8A
high affinity cAMP-specific and IBMX-insensitive 3',5'-cyclic phosphodiesterase 8B-like
glycine amidinotransferase (L-arginine:glycine amidinotransferase)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glycine amidinotransferase, mitochondrial
very long-chain acyl-CoA synthetase, transcript variant X3
very long-chain acyl-CoA synthetase isoform X3
very long-chain acyl-CoA synthetase, transcript variant X4
very long-chain acyl-CoA synthetase isoform X4
very long-chain acyl-CoA synthetase, transcript variant X2
very long-chain acyl-CoA synthetase, transcript variant X1
very long-chain acyl-CoA synthetase isoform X1
very long-chain acyl-CoA synthetase isoform X2
histidine decarboxylase, transcript variant X1
histidine decarboxylase, transcript variant X2
GA binding protein transcription factor subunit beta 1, transcript variant X9
GA binding protein transcription factor subunit beta 1, transcript variant X3
GA binding protein transcription factor subunit beta 1, transcript variant X4
GA binding protein transcription factor subunit beta 1, transcript variant X1
GA binding protein transcription factor subunit beta 1, transcript variant X2
GA-binding protein subunit beta-1 isoform X6
GA-binding protein subunit beta-1 isoform X3
GA-binding protein subunit beta-1 isoform X2
GA-binding protein subunit beta-1 isoform X1
GA binding protein transcription factor subunit beta 1, transcript variant X8
GA binding protein transcription factor subunit beta 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
GA-binding protein subunit beta-1 isoform X5
GA binding protein transcription factor subunit beta 1, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 4 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
GA binding protein transcription factor subunit beta 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
GA binding protein transcription factor subunit beta 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
GA-binding protein subunit beta-1 isoform X7
GA-binding protein subunit beta-1 isoform X4
ubiquitin specific peptidase 8, transcript variant X1
ubiquitin specific peptidase 8, transcript variant X2
ubiquitin specific peptidase 8, transcript variant X3
putative ubiquitin carboxyl-terminal hydrolase 50, transcript variant X4
putative ubiquitin carboxyl-terminal hydrolase 50, transcript variant X1
putative ubiquitin carboxyl-terminal hydrolase 50, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 8-like isoform X4
putative ubiquitin carboxyl-terminal hydrolase 50 isoform X1
putative ubiquitin carboxyl-terminal hydrolase 50 isoform X2
putative ubiquitin carboxyl-terminal hydrolase 50, transcript variant X3
putative ubiquitin carboxyl-terminal hydrolase 50 isoform X3
transient receptor potential cation channel, subfamily M, member 7
transient receptor potential cation channel subfamily M member 7
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 11 samples with support for all annotated introns
signal peptide peptidase-like 2A, transcript variant X4
signal peptide peptidase-like 2A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
signal peptide peptidase-like 2A, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
signal peptide peptidase-like 2A, transcript variant X1
signal peptide peptidase-like 2A, transcript variant X3
signal peptide peptidase-like 2A, transcript variant X5
signal peptide peptidase-like 2A, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
signal peptide peptidase-like 2A isoform X3
signal peptide peptidase-like 2A isoform X5
signal peptide peptidase-like 2A isoform X1
signal peptide peptidase-like 2A isoform X4
signal peptide peptidase-like 2A isoform X2
signal peptide peptidase-like 2A isoform X6
sulfide:quinone oxidoreductase, mitochondrial
biogenesis of lysosomal organelles complex-1, subunit 6, pallidin
biogenesis of lysosome-related organelles complex 1 subunit 6
actin related protein 2/3 complex inhibitor, transcript variant X2
actin related protein 2/3 complex inhibitor, transcript variant X3
actin related protein 2/3 complex inhibitor, 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 7 samples with support for all annotated introns
spermatogenesis-associated protein 5-like protein 1
mitochondrial methionyl-tRNA formyltransferase, transcript variant X1
mitochondrial methionyl-tRNA formyltransferase, transcript variant X6
mitochondrial methionyl-tRNA formyltransferase, transcript variant X4
mitochondrial methionyl-tRNA formyltransferase, transcript variant X3
mitochondrial methionyl-tRNA formyltransferase, transcript variant X5
mitochondrial methionyl-tRNA formyltransferase, transcript variant X2
mitochondrial methionyl-tRNA formyltransferase, transcript variant X7
methionyl-tRNA formyltransferase, mitochondrial isoform X4
methionyl-tRNA formyltransferase, mitochondrial isoform X1
methionyl-tRNA formyltransferase, mitochondrial isoform X3
methionyl-tRNA formyltransferase, mitochondrial isoform X5
methionyl-tRNA formyltransferase, mitochondrial isoform X2
methionyl-tRNA formyltransferase, mitochondrial isoform X6
methionyl-tRNA formyltransferase, mitochondrial isoform X7
cartilage intermediate layer protein, nucleotide pyrophosphohydrolase
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 5 samples with support for all annotated introns