Rhincodon typus isolate 14 chromosome 16, 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\nCM038813.1.\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.
sodium- and chloride-dependent creatine transporter 1-like
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 37 Proteins, and 93% 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: 27 Proteins
serine/threonine-protein kinase pim-3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine/threonine-protein kinase pim-3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
serine/threonine-protein kinase pim-3-like
uncharacterized LOC125485102, transcript variant X4
uncharacterized LOC125485102, transcript variant X1
uncharacterized LOC125485102, transcript variant X3
uncharacterized LOC125485102, transcript variant X2
glutaminyl-tRNA synthetase 1, transcript variant X1
glutaminyl-tRNA synthetase 1, transcript variant X2
transcriptional regulator QRICH1-like, transcript variant X2
transcriptional regulator QRICH1-like, transcript variant X1
transcriptional regulator QRICH1-like isoform X1
transcriptional regulator QRICH1-like isoform X2
inosine-5'-monophosphate dehydrogenase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 long SRA reads, 41 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
neural Wiskott-Aldrich syndrome protein-like
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 4-like, transcript variant X3
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 4-like isoform X3
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 4-like, transcript variant X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 4-like, transcript variant X2
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 4-like isoform X1
6-phosphofructo-2-kinase/fructose-2, 6-bisphosphatase 4-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
musculoskeletal embryonic nuclear protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
STIM activating enhance, 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
STIM activating enhance, transcript variant X1
store-operated calcium entry regulator STIMATE
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 19-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 92% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
cytosolic 10-formyltetrahydrofolate dehydrogenase-like
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA phenylalanine (anticodon AAA); 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: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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
cilia- and flagella-associated protein 100-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil-helix-coiled-coil-helix domain containing 4a
mitochondrial intermembrane space import and assembly protein 40
transmembrane protein 43, transcript variant X1
transmembrane protein 43, transcript variant X2
transmembrane protein 43, transcript variant X3
DNA repair protein complementing XP-C cells-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LSM3 homolog, U6 small nuclear RNA and mRNA degradation associated
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
sodium- and chloride-dependent taurine transporter-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 long SRA reads, 96 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 71-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
coiled-coil domain-containing protein 71-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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
coiled-coil domain-containing protein 71-like, transcript variant X1
coiled-coil domain-containing protein 71-like, transcript variant X4
coiled-coil domain-containing protein 71-like
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform-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 4 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 96% 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: 21 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
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 9 samples with support for all annotated introns
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 1
GATA-binding factor 2-like, transcript variant X1
GATA-binding factor 2-like, transcript variant X2
GATA-binding factor 2-like, transcript variant X3
endothelial transcription factor GATA-2-like isoform X2
eukaryotic elongation factor, selenocysteine-tRNA-specific, transcript variant X1
eukaryotic elongation factor, selenocysteine-tRNA-specific, transcript variant X2
selenocysteine-specific elongation factor isoform X1
selenocysteine-specific elongation factor isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 118 long SRA reads, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
protein transport protein Sec61 subunit alpha-like 1
kelch repeat and BTB (POZ) domain containing 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
kelch repeat and BTB domain-containing protein 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 22% coverage of the annotated genomic feature by RNAseq alignments
monoglyceride lipase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 28 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
monoglyceride lipase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and BTB (POZ) domain containing 1, transcript variant X4
ankyrin repeat and BTB (POZ) domain containing 1, transcript variant X2
ankyrin repeat and BTB (POZ) domain containing 1, transcript variant X5
ankyrin repeat and BTB (POZ) domain containing 1, transcript variant X3
ankyrin repeat and BTB (POZ) domain containing 1, transcript variant X1
ankyrin repeat and BTB/POZ domain-containing protein 1
podocalyxin-like 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
podocalyxin-like 2, transcript variant X1
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
minichromosome maintenance complex component 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transmembrane protein, adipocyte asscociated 1, transcript variant X2
transmembrane protein, adipocyte asscociated 1, transcript variant X4
transmembrane protein, adipocyte asscociated 1, transcript variant X3
transmembrane protein, adipocyte asscociated 1, transcript variant X1
transmembrane protein adipocyte-associated 1 homolog
MICOS complex subunit mic25a-like, transcript variant X1
MICOS complex subunit mic25a-like, transcript variant X2
MICOS complex subunit mic25a-like isoform X1
MICOS complex subunit mic25a-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 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: 75% 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.
5-hydroxymethylcytosine binding, ES cell specific, transcript variant X2
5-hydroxymethylcytosine binding, ES cell specific, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DALR anticodon binding domain containing 3, transcript variant X1
DALR anticodon binding domain containing 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
DALR anticodon binding domain containing 3, 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 3 samples with support for all annotated introns
DALR anticodon-binding domain-containing protein 3 isoform X1
DALR anticodon-binding domain-containing protein 3 isoform X3
DALR anticodon-binding domain-containing protein 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
secreted frizzled-related protein 5-like
protein kinase, cAMP-dependent, regulatory, type II, alpha A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 long SRA reads, 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
mitochondrial carnitine/acylcarnitine carrier protein
rab GDP dissociation inhibitor beta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
cytokine-inducible SH2-containing protein
HemK methyltransferase family member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
HemK methyltransferase family member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
MTRF1L release factor glutamine methyltransferase isoform X2
MTRF1L release factor glutamine methyltransferase isoform X1
uncharacterized protein C3orf18, transcript variant X1
uncharacterized protein C3orf18, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3bl
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 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: 68 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ETS domain-containing protein Elk-1-like
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
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
ubiquitin carboxyl-terminal hydrolase 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin specific peptidase 4 (proto-oncogene), transcript variant X1
ubiquitin specific peptidase 4 (proto-oncogene), 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 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 15 Proteins, 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: 7 long SRA reads, 15 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: 4 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glycerate kinase, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 15 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: 4 long SRA reads, 15 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 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glycerate kinase, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
T-cell leukemia translocation-altered gene protein homolog
transforming protein RhoA, transcript variant X2
transforming protein RhoA, transcript variant X5
transforming protein RhoA, transcript variant X6
transforming protein RhoA, transcript variant X4
transforming protein RhoA, transcript variant X3
transforming protein RhoA, transcript variant X1
protein phosphatase 1M, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein phosphatase 1M, 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 2 samples with support for all annotated introns
ubiquitin-like modifier activating enzyme 1
ubiquitin-like modifier-activating enzyme 1
TRAF-interacting protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
TRAF-interacting protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
TRAF-interacting protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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
E3 ubiquitin-protein ligase TRAIP isoform X2
E3 ubiquitin-protein ligase TRAIP isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
caM kinase-like vesicle-associated protein
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
macrophage stimulating 1 receptor b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
macrophage stimulating 1 receptor b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
macrophage stimulating 1 receptor b, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
polyribonucleotide nucleotidyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments
MON1 secretory trafficking family member A, transcript variant X1
MON1 secretory trafficking family member A, transcript variant X3
MON1 secretory trafficking family member A, transcript variant X2
vacuolar fusion protein MON1 homolog A isoform X1
vacuolar fusion protein MON1 homolog A isoform X2
RNA-binding protein 5-like, transcript variant X2
RNA-binding protein 5-like, transcript variant X3
RNA-binding protein 5-like, transcript variant X1
RNA binding motif protein 5, transcript variant X4
RNA binding motif protein 5, transcript variant X5
RNA binding motif protein 5, transcript variant X2
RNA binding motif protein 5, transcript variant X1
RNA binding motif protein 5, transcript variant X3
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3Fb, transcript variant X1
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3Fb, transcript variant X3
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3Fb, transcript variant X2
guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 162 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein G(t) subunit alpha-1
guanine nucleotide-binding protein G(i) subunit alpha-2
spindle apparatus coiled-coil protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
spindle apparatus coiled-coil 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 5 samples with support for all annotated introns
spindle apparatus coiled-coil protein 1, transcript variant X3
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 4 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 1 sample with support for all annotated introns
sodium-coupled neutral amino acid transporter 3
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 3 samples with support for all annotated introns
interferon-related developmental regulator 2, transcript variant X2
interferon-related developmental regulator 2, transcript variant X1
interferon-related developmental regulator 2 isoform X2
interferon-related developmental regulator 2 isoform X1
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, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 4 Proteins, 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 11% 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: hyaluronidase-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cadherin, EGF LAG seven-pass G-type receptor 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
cadherin EGF LAG seven-pass G-type receptor 3
deoxyribonuclease gamma-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments
deoxyribonuclease gamma-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
translation machinery associated 7 homolog
translation machinery-associated protein 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
myotubularin related protein 14, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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
myotubularin related protein 14, transcript variant X12
myotubularin related protein 14, transcript variant X9
myotubularin related protein 14, transcript variant X8
myotubularin related protein 14, transcript variant X11
myotubularin related protein 14, transcript variant X10
myotubularin related protein 14, transcript variant X7
myotubularin related protein 14, transcript variant X5
myotubularin related protein 14, transcript variant X3
myotubularin related protein 14, transcript variant X2
myotubularin related protein 14, transcript variant X4
myotubularin related protein 14, transcript variant X1
myotubularin-related protein 14 isoform X4
myotubularin-related protein 14 isoform X2
myotubularin-related protein 14 isoform X3
myotubularin-related protein 14 isoform X1
myotubularin related protein 14, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
myotubularin-related protein 14 isoform X5
LHFPL tetraspan subfamily member 4a, transcript variant X2
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
LHFPL tetraspan subfamily member 4a, transcript variant X1
LHFPL tetraspan subfamily member 4 protein isoform X2
LHFPL tetraspan subfamily member 3 protein isoform X1
histone-lysine N-methyltransferase SETD5-like, transcript variant X2
histone-lysine N-methyltransferase SETD5-like, transcript variant X1
histone-lysine N-methyltransferase SETD5-like isoform X2
histone-lysine N-methyltransferase SETD5-like isoform X1
UBA_like_SF and PTH2 domain-containing protein, transcript variant X2
UBA_like_SF and PTH2 domain-containing protein, transcript variant X1
UBA_like_SF and PTH2 domain-containing protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
histone-lysine N-methyltransferase SETD5
ankyrin repeat and SOCS box protein 13-like
mitogen-activated protein kinase 14B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain containing 51, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
coiled-coil domain containing 51, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
coiled-coil domain containing 51, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 long SRA reads, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
coiled-coil domain containing 51, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
coiled-coil domain containing 51, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 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
bromodomain and PHD finger containing, 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
bromodomain and PHD finger containing, 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
8-oxoguanine DNA glycosylase, transcript variant X1
8-oxoguanine DNA glycosylase, transcript variant X2
elongation factor 1-alpha, somatic form-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC109927078, transcript variant X2
uncharacterized LOC109927078, transcript variant X1
uncharacterized protein LOC109927078 isoform X1
uncharacterized protein LOC109927078 isoform X2
uncharacterized LOC109927078, transcript variant X3
uncharacterized protein LOC109927078 isoform X3
protein disulfide isomerase Creld1, transcript variant X2
protein disulfide isomerase Creld1, transcript variant X1
protein disulfide isomerase CRELD1 isoform X2
protein disulfide isomerase Creld1 isoform X1
interleukin-17 receptor C, transcript variant X2
interleukin-17 receptor C, transcript variant X1
interleukin-17 receptor C, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 62% coverage of the annotated genomic feature by RNAseq alignments
cell death inducing DFFA like effector c, transcript variant X2
cell death inducing DFFA like effector c, transcript variant X1
cell death inducing DFFA like effector c, transcript variant X3
mitochondrial mRNA pseudouridine synthase Rpusd3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
actin related protein 2/3 complex, subunit 4, transcript variant X1
actin-related protein 2/3 complex subunit 4 isoform X1
actin related protein 2/3 complex, subunit 4, 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 17 samples with support for all annotated introns
actin-related protein 2/3 complex subunit 4 isoform X2
transcriptional adaptor 3 (NGG1 homolog, yeast)-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 17 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
calcium/calmodulin-dependent protein kinase type 1D-like
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
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
uncharacterized LOC125485174, transcript variant X2
uncharacterized LOC125485174, transcript variant X1
kelch domain-containing protein 8B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
kelch domain-containing protein 8B isoform X1
kelch domain-containing protein 8B, 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 1 sample with support for all annotated introns
kelch domain-containing protein 8B isoform X2
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 13 samples with support for all annotated introns
inter-alpha-trypsin inhibitor heavy chain H3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 99% 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: 50 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: 44 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase Nek4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 88% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide binding protein-like 3 (nucleolar), transcript variant X1
guanine nucleotide binding protein-like 3 (nucleolar), transcript variant X2
guanine nucleotide-binding protein-like 3 isoform X1
guanine nucleotide-binding protein-like 3 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00569
glycosyltransferase 8 domain containing 1, transcript variant X4
glycosyltransferase 8 domain containing 1, transcript variant X6
glycosyltransferase 8 domain containing 1, transcript variant X3
glycosyltransferase 8 domain containing 1, transcript variant X7
glycosyltransferase 8 domain containing 1, transcript variant X5
glycosyltransferase 8 domain containing 1, transcript variant X2
glycosyltransferase 8 domain containing 1, transcript variant X1
glycosyltransferase 8 domain-containing protein 1 isoform X6
glycosyltransferase 8 domain-containing protein 1 isoform X5
glycosyltransferase 8 domain-containing protein 1 isoform X3
glycosyltransferase 8 domain-containing protein 1 isoform X4
glycosyltransferase 8 domain-containing protein 1 isoform X2
glycosyltransferase 8 domain-containing protein 1 isoform X1
5'-nucleotidase domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 47% 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, 4 Proteins, 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: 7 long SRA reads, 4 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: 5 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
troponin C, slow skeletal and cardiac muscles
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
ATR interacting protein, transcript variant X1
ATR interacting protein, transcript variant X4
ATR interacting protein, transcript variant X3
ATR interacting protein, transcript variant X2
ATR interacting protein, transcript variant X5
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 6 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 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC492503 homolog
inositol 1,3,4,5,6-pentakisphosphate 2-kinase, 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 6 samples with support for all annotated introns
inositol 1,3,4,5,6-pentakisphosphate 2-kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 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
inositol-pentakisphosphate 2-kinase isoform X1
inositol-pentakisphosphate 2-kinase isoform X2
centromere protein P, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
centromere protein P, transcript variant X1
extracellular matrix protein 2, female organ and adipocyte specific
asporin (LRR class 1), 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
asporin (LRR class 1), transcript variant X2
asporin (LRR class 1), transcript variant X1
asporin (LRR class 1), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
nucleolar protein 8-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
nucleolar protein 8-like, transcript variant X3
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 6 samples with support for all annotated introns
nucleolar protein 8-like, 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 19 samples with support for all annotated introns
nucleolar protein 8-like, transcript variant X4
nucleolar protein 8-like, transcript variant X6
nucleolar protein 8-like, transcript variant X5
ATPase plasma membrane Ca2+ transporting 2, transcript variant X3
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
ATPase plasma membrane Ca2+ transporting 2, transcript variant X2
ATPase plasma membrane Ca2+ transporting 2, transcript variant X4
ATPase plasma membrane Ca2+ transporting 2, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATPase plasma membrane Ca2+ transporting 2, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ATPase plasma membrane Ca2+ transporting 2, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATPase plasma membrane Ca2+ transporting 2, transcript variant X15
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
ATPase plasma membrane Ca2+ transporting 2, transcript variant X11
ATPase plasma membrane Ca2+ transporting 2, transcript variant X6
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 2 samples with support for all annotated introns
ATPase plasma membrane Ca2+ transporting 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ATPase plasma membrane Ca2+ transporting 2, transcript variant X1
ATPase plasma membrane Ca2+ transporting 2, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ATPase plasma membrane Ca2+ transporting 2, transcript variant X16
ATPase plasma membrane Ca2+ transporting 2, transcript variant X5
ATPase plasma membrane Ca2+ transporting 2, transcript variant X8
ATPase plasma membrane Ca2+ transporting 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATPase plasma membrane Ca2+ transporting 2, transcript variant X12
plasma membrane calcium-transporting ATPase 2 isoform X1
plasma membrane calcium-transporting ATPase 2 isoform X3
plasma membrane calcium-transporting ATPase 2 isoform X2
plasma membrane calcium-transporting ATPase 2 isoform X4
plasma membrane calcium-transporting ATPase 2 isoform X5
plasma membrane calcium-transporting ATPase 2 isoform X6
plasma membrane calcium-transporting ATPase 2 isoform X11
plasma membrane calcium-transporting ATPase 2 isoform X9
plasma membrane calcium-transporting ATPase 2 isoform X13
plasma membrane calcium-transporting ATPase 2 isoform X7
plasma membrane calcium-transporting ATPase 2 isoform X10
plasma membrane calcium-transporting ATPase 2 isoform X14
plasma membrane calcium-transporting ATPase 2 isoform X12
plasma membrane calcium-transporting ATPase 2 isoform X8
POC1 centriolar protein homolog A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
POC1 centriolar protein homolog A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
POC1 centriolar protein homolog A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
POC1 centriolar protein homolog A-like isoform X1
POC1 centriolar protein homolog A-like isoform X2
POC1 centriolar protein homolog A-like isoform X3
uncharacterized LOC125485114, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125485114, transcript variant X1
dual specificity protein phosphatase 7-like
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, including 2 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00056
shisa family member 10, tandem duplicate 1, transcript variant X1
shisa family member 10, tandem duplicate 1, transcript variant X2
5-aminolevulinate synthase, non-specific, mitochondrial-like
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
solute carrier family 6 member 11b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 6 member 11b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sodium- and chloride-dependent GABA transporter 3 isoform X1
sodium- and chloride-dependent GABA transporter 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 112 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
sodium- and chloride-dependent GABA transporter 1b
ATG7 autophagy related 7 homolog (S. cerevisiae)
ubiquitin-like modifier-activating enzyme ATG7
TAM41 mitochondrial translocator assembly and maintenance homolog, transcript variant X1
TAM41 mitochondrial translocator assembly and maintenance homolog, transcript variant X3
phosphatidate cytidylyltransferase, mitochondrial isoform X1
phosphatidate cytidylyltransferase, mitochondrial isoform X2
TAM41 mitochondrial translocator assembly and maintenance homolog, 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 10 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 92% coverage of the annotated genomic feature by RNAseq alignments
TIMP metallopeptidase inhibitor 4, tandem duplicate 2
peroxisome proliferator-activated receptor gamma, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 224 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
peroxisome proliferator-activated receptor gamma, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 224 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
peroxisome proliferator-activated receptor gamma
TSEN2 tRNA splicing endonuclease subunit, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
TSEN2 tRNA splicing endonuclease subunit, transcript variant X1
TSEN2 tRNA splicing endonuclease subunit, transcript variant X2
tRNA-splicing endonuclease subunit Sen2 isoform X1
tRNA-splicing endonuclease subunit Sen2 isoform X2
TSEN2 tRNA splicing endonuclease subunit, transcript variant X4
tRNA-splicing endonuclease subunit Sen2 isoform X3
MKRN2 opposite strand protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
MKRN2 opposite strand protein, 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
MKRN2 opposite strand protein isoform X1
MKRN2 opposite strand protein isoform X2
makorin, ring finger protein, 2, transcript variant X1
makorin, ring finger protein, 2, transcript variant X2
E3 ubiquitin-protein ligase makorin-2 isoform X1
E3 ubiquitin-protein ligase makorin-2 isoform X2
Raf-1 proto-oncogene, serine/threonine kinase b, transcript variant X2
Raf-1 proto-oncogene, serine/threonine kinase b, transcript variant X3
Raf-1 proto-oncogene, serine/threonine kinase b, transcript variant X1
Raf-1 proto-oncogene, serine/threonine kinase b, transcript variant X4
RAF proto-oncogene serine/threonine-protein kinase
uncharacterized LOC125485108, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC125485108, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125485108, transcript variant X2
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 7 samples with support for all annotated introns
uncharacterized LOC125485108, 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 2 samples with support for all annotated introns
CCHC-type zinc finger, nucleic acid binding protein b, transcript variant X2
CCHC-type zinc finger, nucleic acid binding protein b, transcript variant X6
CCHC-type zinc finger, nucleic acid binding protein b, transcript variant X1
CCHC-type zinc finger, nucleic acid binding protein b, transcript variant X5
CCHC-type zinc finger, nucleic acid binding protein b, transcript variant X3
CCHC-type zinc finger, nucleic acid binding protein b, transcript variant X8
CCHC-type zinc finger, nucleic acid binding protein b, transcript variant X7
CCHC-type zinc finger, nucleic acid binding protein b, transcript variant X4
CCHC-type zinc finger, nucleic acid binding protein b isoform X2
CCHC-type zinc finger, nucleic acid binding protein b isoform X1
uncharacterized LOC125485110, transcript variant X2
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 3 samples with support for all annotated introns
uncharacterized LOC125485110, 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 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC402927 homolog
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 4 samples with support for all annotated introns
haloacid dehalogenase-like hydrolase domain-containing 5
glycoprotein IX (platelet), transcript variant X9
glycoprotein IX (platelet), transcript variant X7
glycoprotein IX (platelet), transcript variant X5
glycoprotein IX (platelet), transcript variant X2
glycoprotein IX (platelet), transcript variant X8
glycoprotein IX (platelet), transcript variant X4
glycoprotein IX (platelet), transcript variant X3
glycoprotein IX (platelet), transcript variant X1
glycoprotein IX (platelet), transcript variant X6
glycoprotein IX (platelet), transcript variant X10
EF-hand and coiled-coil domain containing 1
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 3 samples with support for all annotated introns
EF-hand and coiled-coil domain-containing protein 1
cilia and flagella associated protein 92 (putative)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 11 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
complex I assembly factor ACAD9, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 25% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
IQ motif and SEC7 domain-containing protein 1-like, transcript variant X8
IQ motif and SEC7 domain-containing protein 1-like, transcript variant X1
IQ motif and SEC7 domain-containing protein 1-like, transcript variant X2
IQ motif and SEC7 domain-containing protein 1-like, transcript variant X7
IQ motif and SEC7 domain-containing protein 1-like, transcript variant X3
IQ motif and SEC7 domain-containing protein 1-like, transcript variant X5
IQ motif and SEC7 domain-containing protein 1-like, transcript variant X4
IQ motif and SEC7 domain-containing protein 1-like, transcript variant X6
IQ motif and SEC7 domain-containing protein 1-like isoform X2
IQ motif and SEC7 domain-containing protein 1-like isoform X1
IQ motif and SEC7 domain-containing protein 1-like isoform X7
IQ motif and SEC7 domain-containing protein 1-like isoform X3
IQ motif and SEC7 domain-containing protein 1-like isoform X5
IQ motif and SEC7 domain-containing protein 1-like isoform X4
IQ motif and SEC7 domain-containing protein 1-like isoform X6
IQ motif and SEC7 domain-containing protein 1-like isoform X8
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
wingless-type MMTV integration site family, member 7Aa
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
F-box and WD repeat domain containing 12, 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 1 sample with support for all annotated introns
F-box and WD repeat domain containing 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
F-box and WD repeat domain containing 12, transcript variant X4
F-box/WD repeat-containing protein 12 isoform X1
F-box/WD repeat-containing protein 12 isoform X3
F-box and WD repeat domain containing 12, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
F-box/WD repeat-containing protein 12 isoform X2
protein tyrosine phosphatase domain containing 1b, transcript variant X4
protein tyrosine phosphatase domain containing 1b, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein tyrosine phosphatase domain containing 1b, transcript variant X2
protein tyrosine phosphatase domain containing 1b, transcript variant X3
protein tyrosine phosphatase domain containing 1b, transcript variant X1
protein tyrosine phosphatase domain-containing protein 1 isoform X1
protein tyrosine phosphatase domain-containing protein 1 isoform X2
protein tyrosine phosphatase domain containing 1b, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein tyrosine phosphatase domain-containing protein 1 isoform X3
PHD finger protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 140 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
lysine-specific demethylase phf2 isoform X1
PHD finger protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
lysine-specific demethylase phf2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 long SRA reads, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
constitutive coactivator of PPAR-gamma-like protein 1 homolog, transcript variant X3
constitutive coactivator of PPAR-gamma-like protein 1 homolog, transcript variant X2
constitutive coactivator of PPAR-gamma-like protein 1 homolog, transcript variant X1
constitutive coactivator of PPAR-gamma-like protein 1 homolog isoform X3
constitutive coactivator of PPAR-gamma-like protein 1 homolog isoform X2
constitutive coactivator of PPAR-gamma-like protein 1 homolog isoform X1
serine/threonine-protein kinase WNK2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase WNK2-like, 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 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine-protein kinase WNK2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein kinase WNK2-like isoform X2
serine/threonine-protein kinase WNK2-like isoform X1
caspase recruitment domain family, member 19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
faciogenital dysplasia, transcript variant X1
faciogenital dysplasia, transcript variant X2
faciogenital dysplasia, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins
protein bicaudal D homolog 2, transcript variant X2
protein bicaudal D homolog 2, transcript variant X1
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 8 samples with support for all annotated introns
calcium channel, voltage-dependent, L type, alpha 1D subunit, a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109936563, transcript variant X1
uncharacterized LOC109936563, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
calcium channel, voltage-dependent, alpha 2/delta subunit 3a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent calcium channel subunit alpha-2/delta-3
leucine-rich repeat and transmembrane domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
wingless-type MMTV integration site family, member 5a, transcript variant X4
wingless-type MMTV integration site family, member 5a, transcript variant X3
wingless-type MMTV integration site family, member 5a, transcript variant X2
wingless-type MMTV integration site family, member 5a, transcript variant X1
wingless-type MMTV integration site family, member 5a, transcript variant X5
uncharacterized LOC125485123, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125485123, transcript variant X2
coiled-coil domain containing 66, transcript variant X1
coiled-coil domain containing 66, transcript variant X4
coiled-coil domain containing 66, transcript variant X6
coiled-coil domain containing 66, transcript variant X3
coiled-coil domain containing 66, transcript variant X5
coiled-coil domain containing 66, transcript variant X2
coiled-coil domain-containing protein 66 isoform X3
coiled-coil domain-containing protein 66 isoform X5
coiled-coil domain-containing protein 66 isoform X1
coiled-coil domain-containing protein 66 isoform X4
coiled-coil domain-containing protein 66 isoform X6
coiled-coil domain-containing protein 66 isoform X2
transcription activation suppressor a, transcript variant X2
transcription activation suppressor a, transcript variant X1
transcription activation suppressor a, transcript variant X4
transcription activation suppressor a, transcript variant X3
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 9 samples with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 35 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 35 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 34 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Rho guanine nucleotide exchange factor (GEF) 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 34 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor (GEF) 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 35 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
rho guanine nucleotide exchange factor 3 isoform X1
rho guanine nucleotide exchange factor 3 isoform X2
rho guanine nucleotide exchange factor 3 isoform X3
rho guanine nucleotide exchange factor 3 isoform X5
rho guanine nucleotide exchange factor 3 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1, transcript variant X1
DCC-interacting protein 13-alpha isoform X1
adaptor protein, phosphotyrosine interaction, PH domain and leucine zipper containing 1, transcript variant X2
DCC-interacting protein 13-alpha isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
ATPase H+ transporting accessory protein 1 like a
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
DENN/MADD domain containing 6Aa, transcript variant X1
DENN/MADD domain containing 6Aa isoform X1
DENN/MADD domain containing 6Aa, 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 7 samples with support for all annotated introns
DENN/MADD domain containing 6Aa isoform X2
sarcolemma associated protein a, transcript variant X2
sarcolemma associated protein a isoform X2
sarcolemma associated protein a, transcript variant X1
sarcolemma associated protein a isoform X1
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, including 2 samples with support for all annotated introns
deoxyribonuclease gamma, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
deoxyribonuclease gamma, transcript variant X2
abhydrolase domain containing 6, acylglycerol lipase a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
hydroxyacyl-thioester dehydratase type 2, mitochondrial
PX domain containing serine/threonine kinase
PX domain-containing protein kinase-like protein
pyruvate dehydrogenase E1 subunit beta, transcript variant X2
pyruvate dehydrogenase E1 subunit beta, transcript variant X1
pyruvate dehydrogenase E1 component subunit beta, mitochondrial isoform X1
pyruvate dehydrogenase E1 component subunit beta, mitochondrial isoform X2
potassium channel tetramerization domain containing 6a, transcript variant X1
BTB/POZ domain-containing protein KCTD6a isoform X1
potassium channel tetramerization domain containing 6a, transcript variant X4
potassium channel tetramerization domain containing 6a, transcript variant X2
potassium channel tetramerization domain containing 6a, transcript variant X3
BTB/POZ domain-containing protein KCTD6a isoform X2
BTB/POZ domain-containing protein KCTD6a isoform X3
BTB/POZ domain-containing protein KCTD6a isoform X4
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 long SRA reads, 13 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: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: peroxisomal acyl-coenzyme A oxidase 2
protein FAM107B-like, transcript variant X1
protein FAM107B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein FAM107B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
protein FAM107B-like, transcript variant X4
protein FAM3A-like, 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 9 samples with support for all annotated introns
protein FAM3A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
CFAP20 domain containing, transcript variant X2
uncharacterized protein C3orf67 homolog isoform X2
CFAP20 domain containing, 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 1 sample with support for all annotated introns
CFAP20 domain containing, transcript variant X1
CFAP20 domain containing, transcript variant X4
uncharacterized protein C3orf67 homolog isoform X1
uncharacterized protein C3orf67 homolog isoform X3
uncharacterized protein C3orf67 homolog isoform 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 19 samples with support for all annotated introns
fragile histidine triad diadenosine triphosphatase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
receptor-type tyrosine-protein phosphatase gamma-like
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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
Ca2+-dependent activator protein for secretion a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Ca2+-dependent activator protein for secretion a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Ca2+-dependent activator protein for secretion a, transcript variant X2
calcium-dependent secretion activator 1 isoform X1
calcium-dependent secretion activator 1 isoform X3
calcium-dependent secretion activator 1 isoform X2
nicotinamide phosphoribosyltransferase 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nicotinamide phosphoribosyltransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
cadherin-related family member 3-like, transcript variant X1
cadherin-related family member 3-like, transcript variant X2
cadherin-related family member 3-like isoform X1
cadherin-related family member 3-like isoform X2
putative uncharacterized protein C3orf49
THO complex subunit 7 homolog isoform X1
THO complex subunit 7 homolog isoform X2
26S proteasome non-ATPase regulatory subunit 6
prickle homolog 2b, transcript variant X5
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
prickle homolog 2b, transcript variant X6
prickle homolog 2b, transcript variant X4
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
prickle homolog 2b, transcript variant X3
prickle homolog 2b, transcript variant X8
prickle homolog 2b, transcript variant X9
prickle homolog 2b, transcript variant X7
prickle homolog 2b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
prickle homolog 2b, transcript variant X2
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 4 samples with support for all annotated introns
prickle homolog 2b, transcript variant X10
prickle homolog 2b, transcript variant X11
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 2 samples with support for all annotated introns
prickle homolog 2b, transcript variant X12
prickle homolog 2b, transcript variant X13
ADAM metallopeptidase with thrombospondin type 1 motif, 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ADAM metallopeptidase with thrombospondin type 1 motif, 9, transcript variant X3
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
ADAM metallopeptidase with thrombospondin type 1 motif, 9, transcript variant X1
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
A disintegrin and metalloproteinase with thrombospondin motifs 9 isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 9 isoform X3
A disintegrin and metalloproteinase with thrombospondin motifs 9 isoform X1
uncharacterized LOC125485097, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC125485097, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
membrane associated guanylate kinase, WW and PDZ domain containing 1b, transcript variant X3
membrane associated guanylate kinase, WW and PDZ domain containing 1b, transcript variant X2
membrane associated guanylate kinase, WW and PDZ domain containing 1b, transcript variant X1
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1b isoform X3
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1b isoform X2
membrane-associated guanylate kinase, WW and PDZ domain-containing protein 1b isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 8 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
S-adenosylmethionine mitochondrial carrier protein
leucine-rich repeats and immunoglobulin-like domains 1
leucine-rich repeats and immunoglobulin-like domains protein 1
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 6 samples with support for all annotated introns
kelch repeat and BTB (POZ) domain containing 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 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
kelch repeat and BTB domain-containing protein 8 isoform X2
kelch repeat and BTB (POZ) domain containing 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 long SRA reads, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
kelch repeat and BTB domain-containing protein 8 isoform X1
kelch repeat and BTB (POZ) domain containing 8, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 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
kelch repeat and BTB domain-containing protein 8 isoform X3
succinate-CoA ligase GDP-forming subunit beta
succinyl-CoA ligase [GDP-forming] subunit beta, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 74% 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: chemokine-like protein TAFA-1
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
EGF domain-specific O-linked N-acetylglucosamine (GlcNAc) transferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 long SRA reads, 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
EGF domain-specific O-linked N-acetylglucosamine transferase
ubiquitin-like modifier activating enzyme 3, transcript variant X1
ubiquitin-like modifier activating enzyme 3, transcript variant X2
ubiquitin-like modifier activating enzyme 3, transcript variant X3
NEDD8-activating enzyme E1 catalytic subunit isoform X2
NEDD8-activating enzyme E1 catalytic subunit isoform X1
NEDD8-activating enzyme E1 catalytic subunit isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 93% 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, 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
melanocyte inducing transcription factor b, transcript variant X1
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 2 samples with support for all annotated introns
melanocyte inducing transcription factor b isoform X1
melanocyte inducing transcription factor b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
melanocyte inducing transcription factor b isoform X2
myoD family inhibitor domain-containing protein-like
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
forkhead box protein P1-like, transcript variant X2
forkhead box protein P1-like, transcript variant X9
forkhead box protein P1-like, transcript variant X13
forkhead box protein P1-like, transcript variant X1
forkhead box protein P1-like, transcript variant X3
forkhead box protein P1-like, transcript variant X5
forkhead box protein P1-like, transcript variant X4
forkhead box protein P1-like, transcript variant X6
forkhead box protein P1-like, transcript variant X8
forkhead box protein P1-like, transcript variant X7
forkhead box protein P1-like, transcript variant X11
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
forkhead box protein P1-like, transcript variant X12
forkhead box protein P1-like, transcript variant X10
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 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
eukaryotic translation initiation factor 4E family member 3
eukaryotic translation initiation factor 4E type 3
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 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
serine/threonine-protein phosphatase 4 regulatory subunit 2, transcript variant X1
serine/threonine-protein phosphatase 4 regulatory subunit 2, transcript variant X6
serine/threonine-protein phosphatase 4 regulatory subunit 2, transcript variant X5
serine/threonine-protein phosphatase 4 regulatory subunit 2 isoform X1
serine/threonine-protein phosphatase 4 regulatory subunit 2 isoform X4
serine/threonine-protein phosphatase 4 regulatory subunit 2 isoform X3
serine/threonine-protein phosphatase 4 regulatory subunit 2, transcript variant X2
serine/threonine-protein phosphatase 4 regulatory subunit 2, transcript variant X3
serine/threonine-protein phosphatase 4 regulatory subunit 2, transcript variant X4
serine/threonine-protein phosphatase 4 regulatory subunit 2 isoform X2
E3 ubiquitin-protein ligase PDZRN3-like, transcript variant X2
E3 ubiquitin-protein ligase PDZRN3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase PDZRN3-like, transcript variant X3
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
E3 ubiquitin-protein ligase PDZRN3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E3 ubiquitin-protein ligase PDZRN3-like isoform X1
E3 ubiquitin-protein ligase PDZRN3-like isoform X2
E3 ubiquitin-protein ligase PDZRN3-like 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 1 sample with support for all annotated introns
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: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
neural cell adhesion molecule L1-like protein
tRNA nucleotidyl transferase, CCA-adding, 1, transcript variant X1
tRNA nucleotidyl transferase, CCA-adding, 1, transcript variant X2
CCA tRNA nucleotidyltransferase 1, mitochondrial isoform X1
CCA tRNA nucleotidyltransferase 1, mitochondrial isoform X2
leucine rich repeat neuronal 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
leucine rich repeat neuronal 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein NEDD1-like, transcript variant X5
protein NEDD1-like, transcript variant X2
protein NEDD1-like, transcript variant X6
protein NEDD1-like, transcript variant X4
protein NEDD1-like, transcript variant X3
protein NEDD1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dual specificity tyrosine-phosphorylation-regulated kinase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins
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: 14 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
acylaminoacyl-peptide hydrolase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acylamino-acid-releasing enzyme isoform X3
acylaminoacyl-peptide hydrolase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acylamino-acid-releasing enzyme isoform X5
acylaminoacyl-peptide hydrolase, transcript variant X2
acylaminoacyl-peptide hydrolase, transcript variant X4
acylaminoacyl-peptide hydrolase, transcript variant X1
acylamino-acid-releasing enzyme isoform X2
acylamino-acid-releasing enzyme isoform X1
acylamino-acid-releasing enzyme isoform X4
acylamino-acid-releasing enzyme-like, 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 3 samples with support for all annotated introns
acylamino-acid-releasing enzyme-like, transcript variant X5
acylamino-acid-releasing enzyme-like, transcript variant X8
acylamino-acid-releasing enzyme-like, transcript variant X10
acylamino-acid-releasing enzyme-like, transcript variant X11
acylamino-acid-releasing enzyme-like, 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acylamino-acid-releasing enzyme-like, transcript variant X4
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
acylamino-acid-releasing enzyme-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acylamino-acid-releasing enzyme-like, transcript variant X2
acylamino-acid-releasing enzyme-like, transcript variant X9
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 3 samples with support for all annotated introns
acylamino-acid-releasing enzyme-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
acylamino-acid-releasing enzyme-like isoform X5
acylamino-acid-releasing enzyme-like isoform X7
acylamino-acid-releasing enzyme-like isoform X4
acylamino-acid-releasing enzyme-like isoform X10
acylamino-acid-releasing enzyme-like isoform X9
acylamino-acid-releasing enzyme-like isoform X1
acylamino-acid-releasing enzyme-like isoform X3
acylamino-acid-releasing enzyme-like isoform X2
acylamino-acid-releasing enzyme-like isoform X8
acylamino-acid-releasing enzyme-like isoform X6
F-actin-capping protein subunit alpha-2-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 39 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
intraflagellar transport 122 homolog (Chlamydomonas), transcript variant X1
intraflagellar transport protein 122 homolog isoform X1
intraflagellar transport 122 homolog (Chlamydomonas), transcript variant X2
intraflagellar transport protein 122 homolog isoform X2
methyl-CpG binding domain protein 4, transcript variant X1
methyl-CpG binding domain protein 4, transcript variant X5
methyl-CpG binding domain protein 4, transcript variant X2
methyl-CpG binding domain protein 4, transcript variant X4
methyl-CpG binding domain protein 4, transcript variant X3
calcium channel, voltage-dependent, alpha 2/delta subunit 2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent calcium channel subunit alpha-2/delta-2a
inositol hexakisphosphate kinase 1, transcript variant X1
inositol hexakisphosphate kinase 1 isoform X1
inositol hexakisphosphate kinase 1, transcript variant X2
inositol hexakisphosphate kinase 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
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
GDP-mannose pyrophosphorylase B, transcript variant X2
GDP-mannose pyrophosphorylase B, transcript variant X3
GDP-mannose pyrophosphorylase B, transcript variant X1
mannose-1-phosphate guanyltransferase beta isoform X2
mannose-1-phosphate guanyltransferase beta isoform X1
mannose-1-phosphate guanyltransferase beta isoform X3
abhydrolase domain containing 14B, transcript variant X2
abhydrolase domain containing 14B, transcript variant X3
abhydrolase domain containing 14B, transcript variant X1
telomeric repeat binding factor 2, interacting protein, transcript variant X2
telomeric repeat binding factor 2, interacting protein, transcript variant X1
telomeric repeat-binding factor 2-interacting protein 1
E3 SUMO-protein ligase ZBED1-like, transcript variant X6
E3 SUMO-protein ligase ZBED1-like, transcript variant X5
E3 SUMO-protein ligase ZBED1-like, transcript variant X2
E3 SUMO-protein ligase ZBED1-like, transcript variant X3
E3 SUMO-protein ligase ZBED1-like, transcript variant X1
E3 SUMO-protein ligase ZBED1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
ribosomal RNA processing 9, U3 small nucleolar RNA binding protein
U3 small nucleolar RNA-interacting protein 2
transfer RNA cysteine (anticodon ACA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
poly (ADP-ribose) polymerase family, member 3
protein mono-ADP-ribosyltransferase PARP3
cadherin-related family member 4-like, transcript variant X8
cadherin-related family member 4-like, transcript variant X3
cadherin-related family member 4-like, transcript variant X9
cadherin-related family member 4-like, transcript variant X2
cadherin-related family member 4-like, transcript variant X7
cadherin-related family member 4-like, transcript variant X5
cadherin-related family member 4-like, transcript variant X1
cadherin-related family member 4-like, transcript variant X6
cadherin-related family member 4-like, transcript variant X4
cadherin-related family member 4-like, transcript variant X10
cadherin-related family member 4-like isoform X8
cadherin-related family member 4-like isoform X3
cadherin-related family member 4-like isoform X2
cadherin-related family member 4-like isoform X1
cadherin-related family member 4-like isoform X10
cadherin-related family member 4-like isoform X9
cadherin-related family member 4-like isoform X7
cadherin-related family member 4-like isoform X5
cadherin-related family member 4-like isoform X6
cadherin-related family member 4-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
mesencephalic astrocyte-derived neurotrophic factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
NPR2 like, GATOR1 complex subunit, transcript variant X1
NPR2 like, GATOR1 complex subunit, transcript variant X2
NPR2 like, GATOR1 complex subunit, transcript variant X3
NPR2 like, GATOR1 complex subunit, transcript variant X4
NPR2 like, GATOR1 complex subunit, transcript variant X5
poly(rC) binding protein 4, transcript variant X2
poly(rC) binding protein 4, transcript variant X1
poly(rC) binding protein 4, transcript variant X3
uncharacterized LOC125485137, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125485137, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
MAP kinase-activated protein kinase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
aminomethyltransferase, mitochondrial-like
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
von Hippel-Lindau disease tumor suppressor-like
THUMP domain containing 3, transcript variant X2
THUMP domain containing 3, transcript variant X3
THUMP domain containing 3, transcript variant X1
THUMP domain-containing protein 3 isoform X2
THUMP domain-containing protein 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 long SRA reads, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
SLIT-ROBO Rho GTPase activating protein 3, 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 6 samples with support for all annotated introns
SLIT-ROBO Rho GTPase-activating protein 3 isoform X1
SLIT-ROBO Rho GTPase activating protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
SLIT-ROBO Rho GTPase-activating protein 3 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: pro-thyrotropin-releasing hormone
glutamate receptor interacting protein 2b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor-interacting protein 2
SEC13 homolog, nuclear pore and COPII coat complex component
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 long SRA reads, 21 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
interleukin-1 receptor-associated kinase-like 2, transcript variant X3
interleukin-1 receptor-associated kinase-like 2, transcript variant X2
interleukin-1 receptor-associated kinase-like 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
interleukin-1 receptor-associated kinase-like 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cullin-associated NEDD8-dissociated protein 1-like, transcript variant X1
cullin-associated NEDD8-dissociated protein 1-like isoform X1
cullin-associated NEDD8-dissociated protein 1-like, transcript variant X2
cullin-associated NEDD8-dissociated protein 1-like 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: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: putative deoxyribonuclease TATDN2
protein SSUH2 homolog, transcript variant X3
protein SSUH2 homolog, transcript variant X7
protein SSUH2 homolog, transcript variant X1
protein SSUH2 homolog, transcript variant X6
protein SSUH2 homolog, transcript variant X5
protein SSUH2 homolog, transcript variant X4
protein SSUH2 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RAD18 E3 ubiquitin protein ligase, transcript variant X4
E3 ubiquitin-protein ligase RAD18 isoform X4
RAD18 E3 ubiquitin protein ligase, transcript variant X1
RAD18 E3 ubiquitin protein ligase, transcript variant X8
E3 ubiquitin-protein ligase RAD18 isoform X1
E3 ubiquitin-protein ligase RAD18 isoform X8
RAD18 E3 ubiquitin protein ligase, transcript variant X2
E3 ubiquitin-protein ligase RAD18 isoform X2
RAD18 E3 ubiquitin protein ligase, transcript variant X3
E3 ubiquitin-protein ligase RAD18 isoform X3
RAD18 E3 ubiquitin protein ligase, transcript variant X5
E3 ubiquitin-protein ligase RAD18 isoform X5
RAD18 E3 ubiquitin protein ligase, transcript variant X6
E3 ubiquitin-protein ligase RAD18 isoform X6
RAD18 E3 ubiquitin protein ligase, transcript variant X7
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 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase RAD18 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125485126, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 long SRA reads, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125485126, transcript variant X1
tumor suppressor 2, mitochondrial calcium regulator
Ras association domain family member 1, transcript variant X2
Ras association domain family member 1, transcript variant X1
Ras association domain family member 1, transcript variant X3
ras association domain-containing protein 1 isoform X2
ras association domain-containing protein 1 isoform X1
ras association domain-containing protein 1 isoform X3
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 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger MYND domain-containing protein 10
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3H, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3H, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3H isoform X1
sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3H isoform X2
SET domain and mariner transposase fusion gene
histone-lysine N-methyltransferase SETMAR
formylglycine-generating enzyme-like, transcript variant X2
formylglycine-generating enzyme-like isoform X2
formylglycine-generating enzyme-like, transcript variant X1
formylglycine-generating enzyme-like isoform X1
formylglycine-generating enzyme-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 7 samples with support for all annotated introns
formylglycine-generating enzyme-like isoform X3
inositol 1,4,5-trisphosphate receptor, type 1b, transcript variant X2
inositol 1,4,5-trisphosphate receptor, type 1b, transcript variant X1
inositol 1,4,5-trisphosphate receptor, type 1b, transcript variant X4
inositol 1,4,5-trisphosphate receptor, type 1b, transcript variant X3
inositol 1,4,5-trisphosphate receptor type 1 isoform X1
inositol 1,4,5-trisphosphate receptor type 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
basic helix-loop-helix family, member e40
class E basic helix-loop-helix protein 40
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1012 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 64 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ribosomal protein L32, transcript variant X2
ribosomal protein L32, transcript variant X1
ribosomal protein L32, transcript variant X4
ribosomal protein L32, transcript variant X3
abhydrolase domain containing 14A, transcript variant X2
abhydrolase domain containing 14A, transcript variant X1
transmembrane and coiled-coil domains protein 1-like
FYVE, RhoGEF and PH domain-containing protein 5-like
nuclear receptor subfamily 2, group C, member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor subfamily 2 group C member 2
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