Rhincodon typus isolate 14 chromosome 12, 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\nCM038809.1.\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.
hepatitis A virus cellular receptor 1 homolog, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
hepatitis A virus cellular receptor 1 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
hepatitis A virus cellular receptor 1 homolog
lateral signaling target protein 2 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lateral signaling target protein 2 homolog, transcript variant X2
lateral signaling target protein 2 homolog, 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 5 samples with support for all annotated introns
lateral signaling target protein 2 homolog isoform X1
lateral signaling target protein 2 homolog isoform X2
lateral signaling target protein 2 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lateral signaling target protein 2 homolog isoform X3
PRELI domain-containing protein 1, mitochondrial
RAB24, member RAS oncogene family, transcript variant X2
RAB24, member RAS oncogene family, transcript variant X1
histone-lysine N-methyltransferase NSD2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 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: 91% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor receptor 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fibroblast growth factor receptor 4-like, transcript variant X2
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
fibroblast growth factor receptor 4-like, transcript variant X3
fibroblast growth factor receptor 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
AT-rich interactive domain-containing protein 5B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
AT-rich interactive domain-containing protein 5B-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 2 samples with support for all annotated introns
AT-rich interactive domain-containing protein 5B-like, transcript variant X1
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 4 samples with support for all annotated introns
AT-rich interactive domain-containing protein 5B-like isoform X2
AT-rich interactive domain-containing protein 5B-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
homeodomain-interacting protein kinase 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 9 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
NEDD4 binding protein 3, transcript variant X3
NEDD4 binding protein 3, transcript variant X6
NEDD4 binding protein 3, transcript variant X7
NEDD4 binding protein 3, transcript variant X11
NEDD4 binding protein 3, transcript variant X10
NEDD4 binding protein 3, transcript variant X1
NEDD4 binding protein 3, transcript variant X2
NEDD4 binding protein 3, transcript variant X5
NEDD4 binding protein 3, transcript variant X4
NEDD4 binding protein 3, transcript variant X9
NEDD4 binding protein 3, transcript variant X8
NEDD4 binding protein 3, transcript variant X13
NEDD4 binding protein 3, transcript variant X12
uncharacterized LOC125484525, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 210 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC125484525, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 190 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
required for meiotic nuclear division 5 homolog B
E3 ubiquitin-protein ligase NEURL3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
E3 ubiquitin-protein ligase NEURL3-like, 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 1 sample with support for all annotated introns
E3 ubiquitin-protein ligase NEURL3-like isoform X1
E3 ubiquitin-protein ligase NEURL1-like isoform X2
lysine-specific demethylase 3B-like, transcript variant X3
lysine-specific demethylase 3B-like, transcript variant X2
lysine-specific demethylase 3B-like, transcript variant X1
lysine-specific demethylase 3B-like isoform X3
lysine-specific demethylase 3B-like isoform X2
lysine-specific demethylase 3B-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
receptor expression-enhancing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, 11 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: 1 long SRA read, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
immunoglobulin heavy constant gamma 2-like, 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 2 samples with support for all annotated introns
immunoglobulin heavy constant gamma 2-like isoform X2
Ig heavy chain C region-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 764 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: 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: tRNAscan-SE.
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
CDC23 (cell division cycle 23, yeast, homolog)
GDNF family receptor alpha-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
GDNF family receptor alpha-4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
GDNF family receptor alpha-4-like isoform X2
GDNF family receptor alpha-4-like isoform X1
M-phase inducer phosphatase 1-A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
M-phase inducer phosphatase 1-A-like, transcript variant X1
M-phase inducer phosphatase 1-A-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
M-phase inducer phosphatase 1-A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
M-phase inducer phosphatase 1-A-like isoform X2
M-phase inducer phosphatase 1-B-like isoform X1
M-phase inducer phosphatase 1-A-like isoform X4
M-phase inducer phosphatase 1-B-like isoform X3
C-terminal-binding protein 1-like, transcript variant X2
C-terminal-binding protein 1-like, transcript variant X1
C-terminal-binding protein 1-like, transcript variant X4
C-terminal-binding protein 1-like isoform X1
C-terminal-binding protein 1-like, transcript variant X3
C-terminal-binding protein 1-like isoform X2
C-terminal-binding protein 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
transmembrane emp24 domain-containing protein 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00090
melanin-concentrating hormone receptor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 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: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
janus kinase and microtubule interacting protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
janus kinase and microtubule interacting protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 68% coverage of the annotated genomic feature by RNAseq alignments
janus kinase and microtubule interacting protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
janus kinase and microtubule-interacting protein 2 isoform X2
janus kinase and microtubule-interacting protein 2 isoform X3
janus kinase and microtubule-interacting protein 2 isoform X1
dihydropyrimidinase-related protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 Proteins
myelin-associated glycoprotein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myelin-associated glycoprotein-like, transcript variant X1
myelin-associated glycoprotein-like, transcript variant X3
probable U3 small nucleolar RNA-associated protein 13
regulator of G-protein signaling 14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125484554, transcript variant X6
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
uncharacterized LOC125484554, transcript variant X5
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 LOC125484554, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125484554, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125484554, transcript variant X2
uncharacterized LOC125484554, transcript variant X7
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
uncharacterized LOC125484554, transcript variant X1
sodium-dependent phosphate transport protein 2A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 36% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 32% 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 8% coverage of the annotated genomic feature by RNAseq alignments
disintegrin and metalloproteinase domain-containing protein 19, transcript variant X1
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
disintegrin and metalloproteinase domain-containing protein 19, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
disintegrin and metalloproteinase domain-containing protein 19 isoform X1
disintegrin and metalloproteinase domain-containing protein 19 isoform X2
ubiquitin-like domain containing CTD phosphatase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 20 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ubiquitin-like domain-containing CTD phosphatase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
U7 snRNA-associated Sm-like protein LSm11
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: RING finger protein 145
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform, transcript variant X5
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform isoform X1
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform isoform X2
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform isoform X3
serine/threonine-protein phosphatase 2A 55 kDa regulatory subunit B beta isoform isoform X4
cytokine-like protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cytokine-like protein 1, transcript variant X1
serine/threonine-protein kinase 32B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 59% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
programmed cell death protein 4-like, transcript variant X2
programmed cell death protein 4-like, transcript variant X1
programmed cell death protein 4-like isoform X2
programmed cell death protein 4-like isoform X1
vesicular integral-membrane protein VIP36
eukaryotic peptide chain release factor subunit 1, transcript variant X2
eukaryotic peptide chain release factor subunit 1, transcript variant X1
eukaryotic peptide chain release factor subunit 1 isoform X1
eukaryotic peptide chain release factor subunit 1, transcript variant X3
eukaryotic peptide chain release factor subunit 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
F-box/WD repeat-containing protein 11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
F-box/WD repeat-containing protein 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
F-box/WD repeat-containing protein 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
F-box/WD repeat-containing protein 11 isoform X1
F-box/WD repeat-containing protein 11 isoform X2
nucleophosmin-like, transcript variant X4
nucleophosmin-like, transcript variant X2
nucleophosmin-like, transcript variant X3
nucleophosmin-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 67% 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 48% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
kazal-type serine protease inhibitor domain-containing protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
kazal-type serine protease inhibitor domain-containing protein 1-like, transcript variant X1
kazal-type serine protease inhibitor domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Kv channel-interacting protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Kv channel-interacting protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 58 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
polyadenylate-binding protein-interacting protein 2, transcript variant X2
polyadenylate-binding protein-interacting protein 2, transcript variant X1
polyadenylate-binding protein-interacting protein 2
ubiquitin interaction motif containing 1, 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
ubiquitin interaction motif containing 1, transcript variant X1
ubiquitin interaction motif containing 1, transcript variant X2
BRCA1-A complex subunit RAP80 isoform X1
BRCA1-A complex subunit RAP80 isoform X2
hexokinase HKDC1-like, transcript variant X4
hexokinase HKDC1-like, transcript variant X1
hexokinase HKDC1-like, transcript variant X3
hexokinase HKDC1-like, transcript variant X2
G protein-coupled receptor kinase 6, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 79 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
G protein-coupled receptor kinase 6 isoform X5
G protein-coupled receptor kinase 6, transcript variant X4
G protein-coupled receptor kinase 6, transcript variant X3
G protein-coupled receptor kinase 6, transcript variant X1
G protein-coupled receptor kinase 6, transcript variant X6
G protein-coupled receptor kinase 6, transcript variant X2
G protein-coupled receptor kinase 6, transcript variant X7
G protein-coupled receptor kinase 6 isoform X3
G protein-coupled receptor kinase 6 isoform X1
G protein-coupled receptor kinase 6 isoform X4
G protein-coupled receptor kinase 6 isoform X7
G protein-coupled receptor kinase 6 isoform X6
G protein-coupled receptor kinase 6 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
single-stranded DNA binding protein 1, transcript variant X1
single-stranded DNA binding protein 1, transcript variant X3
single-stranded DNA-binding protein, mitochondrial isoform X1
single-stranded DNA-binding protein, mitochondrial isoform X3
single-stranded DNA binding protein 1, transcript variant X2
single-stranded DNA binding protein 1, transcript variant X4
single-stranded DNA-binding protein, mitochondrial isoform X2
single-stranded DNA-binding protein, mitochondrial isoform X4
uncharacterized LOC125484529, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 long SRA reads, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125484529, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
pantothenate kinase 3, transcript variant X4
pantothenate kinase 3, transcript variant X1
pantothenate kinase 3, transcript variant X2
pantothenate kinase 3, transcript variant X3
uncharacterized LOC125484595, transcript variant X1
uncharacterized LOC125484595, transcript variant X2
uncharacterized LOC125484552, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125484552, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125484552, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC125484552, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC125484552, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
catenin (cadherin-associated protein), alpha 1
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
leucine rich repeat transmembrane neuronal 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins
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: leucine-rich repeat transmembrane neuronal protein 2
uncharacterized LOC125484585, transcript variant X1
uncharacterized LOC125484585, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, and 67% 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: 3 long SRA reads, 14 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC125484598, transcript variant X2
uncharacterized LOC125484598, 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 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
fatty acid binding protein 6, ileal (gastrotropin)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
complement C1q tumor necrosis factor-related protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
SLU7 homolog, splicing factor, transcript variant X1
SLU7 homolog, splicing factor, transcript variant X2
cytoplasmic polyadenylation element binding protein 4b, transcript variant X1
cytoplasmic polyadenylation element binding protein 4b, transcript variant X3
cytoplasmic polyadenylation element binding protein 4b, transcript variant X2
cytoplasmic polyadenylation element-binding protein 4b isoform X3
cytoplasmic polyadenylation element-binding protein 4b isoform X2
cytoplasmic polyadenylation element-binding protein 4b isoform X1
biorientation of chromosomes in cell division 1, transcript variant X2
biorientation of chromosomes in cell division 1, transcript variant X1
biorientation of chromosomes in cell division protein 1 isoform X1
biorientation of chromosomes in cell division protein 1 isoform X2
uncharacterized LOC125484600, transcript variant X1
uncharacterized LOC125484600, transcript variant X2
vesicle transport protein SEC20, transcript variant X3
vesicle transport protein SEC20, transcript variant X2
vesicle transport protein SEC20, transcript variant X1
vesicle transport protein SEC20 isoform X1
vesicle transport protein SEC20 isoform X2
vesicle transport protein SEC20 isoform X3
creb3 regulatory factor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
creb3 regulatory factor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
creb3 regulatory factor, transcript variant X2
creb3 regulatory factor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
PTTG1 regulator of sister chromatid separation, securin, transcript variant X3
PTTG1 regulator of sister chromatid separation, securin, transcript variant X4
PTTG1 regulator of sister chromatid separation, securin, transcript variant X2
PTTG1 regulator of sister chromatid separation, securin, transcript variant X1
PTTG1 regulator of sister chromatid separation, securin, transcript variant X6
PTTG1 regulator of sister chromatid separation, securin, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 96% 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein KIAA0232-like, transcript variant X2
uncharacterized protein KIAA0232-like, transcript variant X4
uncharacterized protein KIAA0232-like, transcript variant X1
uncharacterized protein KIAA0232-like, transcript variant X5
uncharacterized protein KIAA0232-like, transcript variant X3
uncharacterized protein KIAA0232-like isoform X2
uncharacterized protein KIAA0232-like isoform X1
prenylcysteine oxidase-like, transcript variant X2
prenylcysteine oxidase-like, transcript variant X1
grpE protein homolog 2, mitochondrial-like, transcript variant X2
grpE protein homolog 2, mitochondrial-like, transcript variant X1
grpE protein homolog 2, mitochondrial-like isoform X2
grpE protein homolog 2, mitochondrial-like isoform X1
actin filament associated protein 1-like 1a
actin filament-associated protein 1-like 1
actin binding LIM protein family, member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 93% 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.
SH3 domain and tetratricopeptide repeats 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
SH3 domain and tetratricopeptide repeats 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
SH3 domain and tetratricopeptide repeats 2, transcript variant X5
SH3 domain and tetratricopeptide repeats 2, transcript variant X6
SH3 domain and tetratricopeptide repeats 2, transcript variant X7
SH3 domain and tetratricopeptide repeats 2, transcript variant X3
SH3 domain and tetratricopeptide repeats 2, transcript variant X2
SH3 domain and tetratricopeptide repeat-containing protein 2 isoform X1
SH3 domain and tetratricopeptide repeat-containing protein 2 isoform X2
SH3 domain and tetratricopeptide repeat-containing protein 2 isoform X3
SH3 domain and tetratricopeptide repeat-containing protein 2 isoform X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
EF-hand calcium-binding domain-containing protein 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
serine/threonine kinase 10, transcript variant X1
serine/threonine kinase 10, transcript variant X2
serine/threonine-protein kinase 10 isoform X1
serine/threonine-protein kinase 10 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
SH3 and PX domains 2B, transcript variant X1
SH3 and PX domains 2B, transcript variant X2
SH3 and PX domain-containing protein 2B isoform X1
SH3 and PX domain-containing protein 2B isoform X2
neuralized E3 ubiquitin protein ligase 1B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
endoplasmic reticulum-golgi intermediate compartment 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
endoplasmic reticulum-Golgi intermediate compartment protein 1
5-hydroxytryptamine receptor 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
5-hydroxytryptamine receptor 4, transcript variant X1
5-hydroxytryptamine receptor 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
5-hydroxytryptamine receptor 4, transcript variant X3
5-hydroxytryptamine receptor 4, transcript variant X4
5-hydroxytryptamine receptor 4 isoform X1
5-hydroxytryptamine receptor 4 isoform X2
5-hydroxytryptamine receptor 4, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
5-hydroxytryptamine receptor 4 isoform X4
5-hydroxytryptamine receptor 4, transcript variant X6
5-hydroxytryptamine receptor 4 isoform X3
solute carrier family 26 member 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 26 member 2, transcript variant X4
solute carrier family 26 member 2, transcript variant X5
solute carrier family 26 member 2, transcript variant X6
solute carrier family 26 member 2, transcript variant X3
solute carrier family 26 member 2, transcript variant X1
solute carrier family 26 member 2, transcript variant X2
rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase TRIM8-like, transcript variant X2
E3 ubiquitin-protein ligase TRIM8-like, transcript variant X1
peroxisome proliferator-activated receptor gamma coactivator 1-alpha-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 35 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
peroxisome proliferator-activated receptor gamma coactivator 1-alpha-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 7 samples with support for all annotated introns
peroxisome proliferator-activated receptor gamma coactivator 1-alpha-like isoform X2
peroxisome proliferator-activated receptor gamma coactivator 1-alpha-like isoform X1
casein kinase 1, alpha 1, transcript variant X2
casein kinase 1, alpha 1, transcript variant X1
rho guanine nucleotide exchange factor 37-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, 131 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
histamine H2 receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 31 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
histamine H2 receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 long SRA reads, 17 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ADP-ribosylation factor-like protein 9, transcript variant X1
ADP-ribosylation factor-like protein 9, transcript variant X2
ADP-ribosylation factor-like protein 9, transcript variant X3
ADP-ribosylation factor-like protein 9 isoform X1
ADP-ribosylation factor-like protein 9 isoform X2
ADP-ribosylation factor-like protein 9 isoform X3
ring finger protein 44, transcript variant X3
ring finger protein 44, transcript variant X4
ring finger protein 44, transcript variant X2
ring finger protein 44, transcript variant X1
ring finger protein 44, transcript variant X5
ring finger protein 44, transcript variant X7
ring finger protein 44, transcript variant X6
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
G protein-regulated inducer of neurite outgrowth 1-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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
eukaryotic translation initiation factor 4E-1A-like, transcript variant X1
eukaryotic translation initiation factor 4E-1A-like, transcript variant X2
eukaryotic translation initiation factor 4E-1A-like isoform X1
eukaryotic translation initiation factor 4E-1A-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 long SRA reads, 36 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
PDZ and LIM domain 7, transcript variant X1
PDZ and LIM domain 7, transcript variant X6
PDZ and LIM domain 7, transcript variant X3
PDZ and LIM domain 7, transcript variant X4
PDZ and LIM domain 7, transcript variant X5
PDZ and LIM domain 7, transcript variant X2
PDZ and LIM domain 7, transcript variant X7
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
PDZ and LIM domain 7, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
PDZ and LIM domain 7, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, delta-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 27 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: 4 long SRA reads, and 88% coverage of the annotated genomic feature by RNAseq alignments
DNA damage-inducible transcript 4-like protein-like
endothelial cell surface expressed chemotaxis and apoptosis regulator, transcript variant X2
endothelial cell surface expressed chemotaxis and apoptosis regulator, transcript variant X1
endothelial cell-specific chemotaxis regulator isoform X2
endothelial cell-specific chemotaxis regulator isoform X1
stimulator of interferon response cGAMP interactor 1, transcript variant X1
stimulator of interferon response cGAMP interactor 1, transcript variant X2
stimulator of interferon response cGAMP interactor 1, transcript variant X11
stimulator of interferon response cGAMP interactor 1, transcript variant X9
stimulator of interferon response cGAMP interactor 1, transcript variant X4
stimulator of interferon response cGAMP interactor 1, transcript variant X7
stimulator of interferon response cGAMP interactor 1, transcript variant X6
stimulator of interferon response cGAMP interactor 1, transcript variant X3
stimulator of interferon response cGAMP interactor 1, transcript variant X10
stimulator of interferon response cGAMP interactor 1, transcript variant X8
stimulator of interferon response cGAMP interactor 1, transcript variant X5
stimulator of interferon genes protein isoform X1
stimulator of interferon genes protein isoform X2
stimulator of interferon genes protein isoform X3
protein phosphatase 3 catalytic subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
nuclear factor NF-kappa-B p105 subunit-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin-conjugating enzyme E2D 2 (UBC4/5 homolog, yeast), transcript variant X1
ubiquitin-conjugating enzyme E2 D2 isoform X1
ubiquitin-conjugating enzyme E2D 2 (UBC4/5 homolog, yeast), transcript variant X2
ubiquitin-conjugating enzyme E2D 2 (UBC4/5 homolog, yeast), transcript variant X4
ubiquitin-conjugating enzyme E2D 2 (UBC4/5 homolog, yeast), transcript variant X3
ubiquitin-conjugating enzyme E2D 2 (UBC4/5 homolog, yeast), transcript variant X5
ubiquitin-conjugating enzyme E2 D2 isoform X2
transfer RNA threonine (anticodon AGU); 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: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC109927557, transcript variant X2
uncharacterized LOC109927557, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
pro-neuregulin-2, membrane-bound isoform-like, 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 1 sample with support for all annotated introns
pro-neuregulin-2, membrane-bound isoform-like, 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 6 samples with support for all annotated introns
pro-neuregulin-2, membrane-bound isoform-like isoform X1
pro-neuregulin-2, membrane-bound isoform-like isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
prostate androgen-regulated mucin-like protein 1, transcript variant X2
prostate androgen-regulated mucin-like protein 1, transcript variant X1
prostate androgen-regulated mucin-like protein 1, transcript variant X3
prostate androgen-regulated mucin-like protein 1 isoform X1
cysteine-rich and transmembrane domain-containing protein 1
RUN and FYVE domain-containing protein 1
proheparin-binding EGF-like growth factor
eukaryotic translation initiation factor 4E-binding protein 3-like
ankyrin repeat and KH domain containing 1
ankyrin repeat and KH domain-containing protein 1
heterogeneous nuclear ribonucleoprotein H1, like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 33 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
electrogenic sodium bicarbonate cotransporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 2-like, transcript variant X1
A disintegrin and metalloproteinase with thrombospondin motifs 2-like, transcript variant X2
A disintegrin and metalloproteinase with thrombospondin motifs 2-like
CCR4-NOT transcription complex subunit 6, transcript variant X2
CCR4-NOT transcription complex subunit 6, transcript variant X4
CCR4-NOT transcription complex subunit 6, transcript variant X3
CCR4-NOT transcription complex subunit 6, transcript variant X1
CCR4-NOT transcription complex subunit 6 isoform X1
CCR4-NOT transcription complex subunit 6 isoform X2
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
mitogen-activated protein kinase 9, transcript variant X7
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 5 samples with support for all annotated introns
mitogen-activated protein kinase 9, transcript variant X6
mitogen-activated protein kinase 9, 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 8 samples with support for all annotated introns
mitogen-activated protein kinase 9, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
mitogen-activated protein kinase 9, transcript variant X4
mitogen-activated protein kinase 9, transcript variant X5
mitogen-activated protein kinase 9, 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 12 samples with support for all annotated introns
mitogen-activated protein kinase 9, transcript variant X8
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
ras-GEF domain-containing family member 1C-like
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
dual specificity protein kinase CLK4-like, transcript variant X1
dual specificity protein kinase CLK4-like isoform X1
dual specificity protein kinase CLK4-like, transcript variant X2
dual specificity protein kinase CLK4-like, transcript variant X3
dual specificity protein kinase CLK4-like isoform X2
collagen alpha-1(XXIII) chain-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 6 samples with support for all annotated introns
collagen alpha-1(XXIII) chain-like, transcript variant X5
collagen alpha-1(XXIII) chain-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
collagen alpha-1(XXIII) chain-like, transcript variant X2
collagen alpha-1(XXIII) chain-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
collagen alpha-1(XXIII) chain-like isoform X1
collagen alpha-1(XXIII) chain-like isoform X5
collagen alpha-1(XXIII) chain-like isoform X4
collagen alpha-1(XXIII) chain-like isoform X2
collagen alpha-1(XXIII) chain-like isoform X3
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
5-phosphohydroxy-L-lysine phospho-lyase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
5-phosphohydroxy-L-lysine phospho-lyase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
5-phosphohydroxy-L-lysine phospho-lyase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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
5-phosphohydroxy-L-lysine phospho-lyase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
5-phosphohydroxy-L-lysine phospho-lyase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
5-phosphohydroxy-L-lysine phospho-lyase isoform X2
5-phosphohydroxy-L-lysine phospho-lyase isoform X1
5-phosphohydroxy-L-lysine phospho-lyase isoform X4
5-phosphohydroxy-L-lysine phospho-lyase isoform X3
heterogeneous nuclear ribonucleoprotein D-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein D-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein D-like
protein Wnt-8-like, transcript variant X1
protein Wnt-8-like, transcript variant X3
protein Wnt-8-like, transcript variant X4
protein Wnt-8-like, transcript variant X2
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
NME/NM23 family member 5, transcript variant X1
NME/NM23 family member 5, transcript variant X2
nucleoside diphosphate kinase homolog 5 isoform X1
nucleoside diphosphate kinase homolog 5 isoform X2
guanine nucleotide-binding protein subunit beta-2-like 1
thymosin beta-11-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
thymosin beta-11-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
polycystic kidney disease 2-like 2 protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein A3-like
uncharacterized LOC125484560, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125484560, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
kelch-like protein 3, transcript variant X1
kelch-like protein 3, transcript variant X3
kelch-like protein 3, transcript variant X6
kelch-like protein 3, transcript variant X11
kelch-like protein 3, transcript variant X2
kelch-like protein 3, transcript variant X10
kelch-like protein 3, transcript variant X8
kelch-like protein 3, transcript variant X4
kelch-like protein 3, transcript variant X5
kelch-like protein 3, transcript variant X7
kelch-like protein 3, transcript variant X9
kelch-like protein 3, transcript variant X12
kelch-like protein 3, transcript variant X13
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 5 samples with support for all annotated introns
SPARC (osteonectin), cwcv and kazal like domains proteoglycan 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SPARC (osteonectin), cwcv and kazal like domains proteoglycan 1, transcript variant X1
short transient receptor potential channel 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 19% coverage of the annotated genomic feature by RNAseq alignments
mothers against decapentaplegic homolog 5, transcript variant X2
mothers against decapentaplegic homolog 5, transcript variant X1
mothers against decapentaplegic homolog 5, transcript variant X3
mothers against decapentaplegic homolog 5, transcript variant X4
mothers against decapentaplegic homolog 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
CCR4-NOT transcription complex, subunit 8, transcript variant X2
CCR4-NOT transcription complex, subunit 8, transcript variant X1
CCR4-NOT transcription complex subunit 7
family with sequence similarity 114 member A2
microfibril-associated glycoprotein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 122 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
microfibril-associated glycoprotein 3-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 112 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
microfibril-associated glycoprotein 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 132 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
microfibril-associated glycoprotein 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 127 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
microfibril-associated glycoprotein 3-like
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 18 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 10-like, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 10-like, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 10-like, transcript variant X4
polypeptide N-acetylgalactosaminyltransferase 10-like isoform X1
polypeptide N-acetylgalactosaminyltransferase 10-like isoform X2
polypeptide N-acetylgalactosaminyltransferase 10-like isoform X4
polypeptide N-acetylgalactosaminyltransferase 10-like, transcript variant X3
polypeptide N-acetylgalactosaminyltransferase 10-like isoform X3
polypeptide N-acetylgalactosaminyltransferase 10-like, transcript variant X5
polypeptide N-acetylgalactosaminyltransferase 10-like, transcript variant X6
polypeptide N-acetylgalactosaminyltransferase 10-like isoform X5
polypeptide N-acetylgalactosaminyltransferase 10-like isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
progesterone receptor, transcript variant X2
progesterone receptor, transcript variant X1
progesterone receptor, transcript variant X4
progesterone receptor, transcript variant X3
progesterone receptor, transcript variant X5
progesterone receptor, transcript variant X6
potassium channel tetramerization domain containing 16b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
BTB/POZ domain-containing protein KCTD16b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
transforming growth factor, beta-induced
transforming growth factor-beta-induced protein ig-h3
uncharacterized LOC125484592, transcript variant X1
uncharacterized LOC125484592, transcript variant X3
uncharacterized LOC125484592, 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 10 samples with support for all annotated introns
solute carrier family 25 member 48, transcript variant X4
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
solute carrier family 25 member 48, transcript variant X1
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
solute carrier family 25 member 48 isoform X3
solute carrier family 25 member 48 isoform X1
solute carrier family 25 member 48, transcript variant X2
solute carrier family 25 member 48, transcript variant X3
solute carrier family 25 member 48 isoform X2
chemokine (C-X-C motif) ligand 14, transcript variant X1
chemokine (C-X-C motif) ligand 14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
core histone macro-H2A.1, transcript variant X1
core histone macro-H2A.1, transcript variant X6
core histone macro-H2A.1, transcript variant X3
core histone macro-H2A.1, transcript variant X4
core histone macro-H2A.1, transcript variant X2
core histone macro-H2A.1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
paired-like homeodomain 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
paired-like homeodomain 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
paired-like homeodomain 1, transcript variant X4
paired-like homeodomain 1, transcript variant X5
paired-like homeodomain 1, transcript variant X2
cation channel sperm-associated protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
pterin-4-alpha-carbinolamine dehydratase 2
UPF0461 protein C5orf24 homolog, transcript variant X8
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
UPF0461 protein C5orf24 homolog, transcript variant X7
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 4 samples with support for all annotated introns
UPF0461 protein C5orf24 homolog isoform X4
UPF0461 protein C5orf24 homolog isoform X3
UPF0461 protein C5orf24 homolog, transcript variant X1
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 11 samples with support for all annotated introns
UPF0461 protein C5orf24 homolog, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
UPF0461 protein C5orf24 homolog, transcript variant X5
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 2 samples with support for all annotated introns
UPF0461 protein C5orf24 homolog, transcript variant X4
UPF0461 protein C5orf24 homolog, transcript variant X2
UPF0461 protein C5orf24 homolog, transcript variant X3
UPF0461 protein C5orf24 homolog isoform X1
UPF0461 protein C5orf24 homolog isoform X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 46, transcript variant X5
DEAD (Asp-Glu-Ala-Asp) box polypeptide 46, transcript variant X4
DEAD (Asp-Glu-Ala-Asp) box polypeptide 46, transcript variant X3
DEAD (Asp-Glu-Ala-Asp) box polypeptide 46, transcript variant X2
DEAD (Asp-Glu-Ala-Asp) box polypeptide 46, transcript variant X1
probable ATP-dependent RNA helicase DDX46 isoform X5
probable ATP-dependent RNA helicase DDX46 isoform X4
probable ATP-dependent RNA helicase DDX46 isoform X3
probable ATP-dependent RNA helicase DDX46 isoform X2
probable ATP-dependent RNA helicase DDX46 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
calcium modulating ligand, transcript variant X2
calcium modulating ligand, transcript variant X1
calcium signal-modulating cyclophilin ligand isoform X2
calcium signal-modulating cyclophilin ligand isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments
secretion associated, Ras related GTPase 1B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 76% 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, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC109921400, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC109921400, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cyclin-dependent kinase-like 2, transcript variant X6
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
cyclin-dependent kinase-like 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cyclin-dependent kinase-like 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclin-dependent kinase-like 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 16 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cyclin-dependent kinase-like 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclin-dependent kinase-like 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CDKN2A interacting protein N-terminal like, transcript variant X2
CDKN2A interacting protein N-terminal like, transcript variant X1
CDKN2AIP N-terminal-like protein isoform X2
CDKN2AIP N-terminal-like protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase 2A catalytic subunit alpha isoform
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 6 samples with support for all annotated introns
cytochrome P450 2U1, transcript variant X3
cytochrome P450 2U1, transcript variant X2
cytochrome P450 2U1, transcript variant X1
cytochrome P450 2U1, transcript variant X4
voltage-dependent anion channel 1, transcript variant X3
voltage-dependent anion channel 1, transcript variant X1
voltage-dependent anion channel 1, transcript variant X2
voltage-dependent anion-selective channel protein 1 isoform X1
voltage-dependent anion-selective channel protein 1 isoform X2
voltage-dependent anion-selective channel protein 1 isoform X3
keratinocyte-associated transmembrane protein 2
rap guanine nucleotide exchange factor 6-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
rap guanine nucleotide exchange factor 6-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
rap guanine nucleotide exchange factor 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
rap guanine nucleotide exchange factor 6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
rap guanine nucleotide exchange factor 6-like isoform X4
rap guanine nucleotide exchange factor 6-like isoform X3
rap guanine nucleotide exchange factor 6-like isoform X2
rap guanine nucleotide exchange factor 6-like isoform 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 5 samples with support for all annotated introns
long-chain-fatty-acid--CoA ligase 6-like, transcript variant X1
long-chain-fatty-acid--CoA ligase 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
long-chain-fatty-acid--CoA ligase 6-like isoform X1
long-chain-fatty-acid--CoA ligase 6-like isoform X2
interferon regulatory factor 1-like, transcript variant X1
interferon regulatory factor 1-like, transcript variant X4
interferon regulatory factor 1-like, transcript variant X6
interferon regulatory factor 1-like, transcript variant X5
interferon regulatory factor 1-like, transcript variant X2
interferon regulatory factor 1-like, transcript variant X3
interferon regulatory factor 1-like isoform X1
interferon regulatory factor 1-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 37 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
interferon regulatory factor 1-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, 85 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
interferon regulatory factor 1-like isoform X2
uncharacterized LOC125484587, 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
uncharacterized LOC125484587, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 96% 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: 22 long SRA reads, 48 Proteins, and 98% 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 long SRA reads, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 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: 33 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
sorbin and SH3 domain-containing protein 2-like, transcript variant X3
sorbin and SH3 domain-containing protein 2-like, transcript variant X2
sorbin and SH3 domain-containing protein 2-like, transcript variant X1
sorbin and SH3 domain-containing protein 2-like isoform X2
sorbin and SH3 domain-containing protein 2-like isoform X1
sorbin and SH3 domain-containing protein 2-like isoform X3
gamma-aminobutyric acid type A receptor subunit beta2a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid type A receptor subunit beta2a, transcript variant X4
gamma-aminobutyric acid type A receptor subunit beta2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid type A receptor subunit beta2a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit beta-2a isoform X2
gamma-aminobutyric acid receptor subunit beta-2a isoform X4
gamma-aminobutyric acid receptor subunit beta-2a isoform X1
gamma-aminobutyric acid receptor subunit beta-2a isoform X3
gamma-aminobutyric acid type A receptor subunit alpha6b
gamma-aminobutyric acid receptor subunit alpha-6
gamma-aminobutyric acid receptor subunit alpha-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gamma-aminobutyric acid receptor subunit alpha-1-like isoform X1
gamma-aminobutyric acid receptor subunit alpha-1-like, transcript variant X2
gamma-aminobutyric acid receptor subunit alpha-1-like isoform X2
gamma-aminobutyric acid type A receptor subunit gamma2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit gamma-2
uncharacterized LOC125484564, transcript variant X1
uncharacterized LOC125484564, transcript variant X2
glucosamine-6-phosphate deaminase 1, transcript variant X2
glucosamine-6-phosphate deaminase 1, transcript variant X3
glucosamine-6-phosphate deaminase 1, transcript variant X1
glucosamine-6-phosphate deaminase 1, transcript variant X4
glucosamine-6-phosphate isomerase 1 isoform X1
glucosamine-6-phosphate deaminase 1, transcript variant X5
glucosamine-6-phosphate isomerase 1 isoform X2
ring finger protein 14, transcript variant X2
ring finger protein 14, transcript variant X3
ring finger protein 14, transcript variant X1
ring finger protein 14, transcript variant X5
ring finger protein 14, transcript variant X4
ring finger protein 14, transcript variant X6
E3 ubiquitin-protein ligase RNF14 isoform X2
E3 ubiquitin-protein ligase RNF14 isoform X1
E3 ubiquitin-protein ligase RNF14 isoform X3
E3 ubiquitin-protein ligase RNF14 isoform X4
heat shock 70 kDa protein 4, transcript variant X1
heat shock 70 kDa protein 4, transcript variant X2
sosondowah ankyrin repeat domain family member Ab
ankyrin repeat domain-containing protein SOWAHA
cytochrome b-c1 complex subunit 8, transcript variant X1
cytochrome b-c1 complex subunit 8, transcript variant X2
cytochrome b-c1 complex subunit 8, transcript variant X3
liver-expressed antimicrobial peptide 2-like
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
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
AF4/FMR2 family, member 4, transcript variant X5
AF4/FMR2 family, member 4, transcript variant X4
AF4/FMR2 family, member 4, transcript variant X2
AF4/FMR2 family, member 4, transcript variant X1
AF4/FMR2 family, member 4, transcript variant X3
zinc finger, CCHC domain containing 10, transcript variant X2
zinc finger CCHC domain-containing protein 10 isoform X2
zinc finger, CCHC domain containing 10, transcript variant X1
zinc finger CCHC domain-containing protein 10 isoform X1
sarcoglycan, delta (dystrophin-associated glycoprotein), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 long SRA reads, 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sarcoglycan, delta (dystrophin-associated glycoprotein), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 long SRA reads, 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
sarcoglycan, delta (dystrophin-associated glycoprotein), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 long SRA reads, 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
sarcoglycan, delta (dystrophin-associated glycoprotein), transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 long SRA reads, 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sarcoglycan, delta (dystrophin-associated glycoprotein), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 long SRA reads, 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
rho GTPase-activating protein 7, transcript variant X1
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 3 samples with support for all annotated introns
rho GTPase-activating protein 7 isoform X1
rho GTPase-activating protein 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
rho GTPase-activating protein 7 isoform X2
rho GTPase-activating protein 7, transcript variant X4
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
rho GTPase-activating protein 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
rho GTPase-activating protein 7 isoform X3
rho GTPase-activating protein 7 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 long SRA reads, 9 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
arginine--tRNA ligase, cytoplasmic-like, transcript variant X2
arginine--tRNA ligase, cytoplasmic-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
arginine--tRNA ligase, cytoplasmic-like isoform X1
arginine--tRNA ligase, cytoplasmic-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 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 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
vascular endothelial growth factor C-like, transcript variant X1
vascular endothelial growth factor C-like, transcript variant X2
vascular endothelial growth factor C-like isoform X1
vascular endothelial growth factor C-like isoform X2
HMG box domain containing 3, transcript variant X2
HMG box domain containing 3, transcript variant X5
HMG box domain containing 3, transcript variant X6
HMG box domain containing 3, transcript variant X3
HMG box domain containing 3, transcript variant X9
HMG box domain containing 3, transcript variant X8
HMG box domain containing 3, transcript variant X10
HMG box domain containing 3, transcript variant X1
HMG box domain containing 3, transcript variant X4
HMG box domain containing 3, transcript variant X7
HMG domain-containing protein 3 isoform X3
HMG domain-containing protein 3 isoform X2
HMG domain-containing protein 3 isoform X4
HMG domain-containing protein 3 isoform X1
HMG box domain containing 3, transcript variant X12
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
HMG box domain containing 3, transcript variant X13
HMG box domain containing 3, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
HMG domain-containing protein 3 isoform X5
HMG domain-containing protein 3 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 3 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
NudC domain containing 2, transcript variant X2
NudC domain containing 2, transcript variant X4
NudC domain containing 2, transcript variant X3
NudC domain containing 2, transcript variant X1
leucyl-tRNA synthetase 1b, transcript variant X1
leucine--tRNA ligase, cytoplasmic isoform X1
leucyl-tRNA synthetase 1b, transcript variant X2
leucine--tRNA ligase, cytoplasmic isoform X2
E3 ubiquitin-protein ligase SH3RF2-like, transcript variant X3
E3 ubiquitin-protein ligase SH3RF2-like, transcript variant X2
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 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase SH3RF2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase SH3RF3-like isoform X3
E3 ubiquitin-protein ligase SH3RF2-like isoform X2
E3 ubiquitin-protein ligase SH3RF2-like isoform X1
glutaredoxin domain-containing cysteine-rich protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins
GTPase activating protein (SH3 domain) binding protein 1, transcript variant X2
GTPase activating protein (SH3 domain) binding protein 1, transcript variant X1
GTPase activating protein (SH3 domain) binding protein 1, transcript variant X5
GTPase activating protein (SH3 domain) binding protein 1, transcript variant X3
GTPase activating protein (SH3 domain) binding protein 1, transcript variant X4
ras GTPase-activating protein-binding protein 1
secreted protein, acidic, cysteine-rich (osteonectin), transcript variant X1
secreted protein, acidic, cysteine-rich (osteonectin), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91 Proteins
solute carrier family 36 member 1, transcript variant X1
solute carrier family 36 member 1, transcript variant X2
proton-coupled amino acid transporter 1 isoform X1
proton-coupled amino acid transporter 1 isoform X2
solute carrier family 36 member 1, transcript variant X7
solute carrier family 36 member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
proton-coupled amino acid transporter 1 isoform X5
solute carrier family 36 member 1, transcript variant X6
solute carrier family 36 member 1, transcript variant X5
proton-coupled amino acid transporter 1 isoform X4
proton-coupled amino acid transporter 1 isoform X3
solute carrier family 36 member 1, transcript variant X4
solute carrier family 36 member 1, transcript variant X8
solute carrier family 36 member 1, transcript variant X9
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
microtubule-associated tumor suppressor 1 homolog
platelet-derived growth factor receptor-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
fibroblast growth factor 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sprouty homolog 4 (Drosophila), transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sprouty homolog 4 (Drosophila), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sprouty homolog 4 (Drosophila), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
sprouty homolog 4 (Drosophila), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sprouty homolog 4 (Drosophila), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RNA binding motif protein 27, transcript variant X1
RNA binding motif protein 27, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 156 long SRA reads, 10 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
POU domain, class 4, transcription factor 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
RAD50 homolog, double strand break repair protein
prolyl 4-hydroxylase subunit alpha-2-like, transcript variant X3
prolyl 4-hydroxylase subunit alpha-2-like, transcript variant X2
prolyl 4-hydroxylase subunit alpha-2-like, transcript variant X1
prolyl 4-hydroxylase subunit alpha-2-like isoform X2
prolyl 4-hydroxylase subunit alpha-2-like isoform X3
prolyl 4-hydroxylase subunit alpha-2-like isoform X1
prolyl 4-hydroxylase subunit alpha-2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109927662, transcript variant X5
uncharacterized LOC109927662, transcript variant X3
uncharacterized LOC109927662, transcript variant X1
uncharacterized LOC109927662, transcript variant X2
uncharacterized protein LOC109927662 isoform X3
uncharacterized protein LOC109927662 isoform X2
uncharacterized protein LOC109927662 isoform X1
uncharacterized LOC109927662, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC109927663, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC109927663, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC109927663 isoform X2
uncharacterized protein LOC109927663 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
heart- and neural crest derivatives-expressed protein 1-like
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 3 samples with support for all annotated introns
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 23 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like, transcript variant X6
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like, transcript variant X4
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like, transcript variant X5
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like isoform X1
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like isoform X2
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like isoform X3
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
15-hydroxyprostaglandin dehydrogenase [NAD(+)]-like isoform X4
La ribonucleoprotein 1, translational regulator, transcript variant X1
La ribonucleoprotein 1, translational regulator, transcript variant X2
fatty acid hydroxylase domain containing 2
fatty acid hydroxylase domain-containing protein 2
LON peptidase N-terminal domain and RING finger protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
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 2 samples with support for all annotated introns
glutamate receptor, ionotropic, AMPA 1a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor, ionotropic, AMPA 1a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
methionine adenosyltransferase 2 subunit beta
hyaluronan-mediated motility receptor-like
hyaluronan mediated motility receptor-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
cytoplasmic FMR1-interacting protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 29 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
mediator of RNA polymerase II transcription subunit 7
F-BAR and double SH3 domains protein 2-like
RELT-like protein 2, transcript variant X3
RELT-like protein 2, transcript variant X2
RELT-like protein 2, transcript variant X4
RELT-like protein 2, transcript variant X1
histone deacetylase 3, transcript variant X4
histone deacetylase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
histone deacetylase 3, transcript variant X1
histone deacetylase 3, transcript variant X3
zinc finger HIT domain-containing protein 2
mast/stem cell growth factor receptor Kit-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase TRIM62-like, transcript variant X1
E3 ubiquitin-protein ligase TRIM62-like, transcript variant X2
zinc-binding protein A33-like isoform X1
E3 ubiquitin-protein ligase TRIM62-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
vascular endothelial growth factor receptor 3
vascular endothelial growth factor receptor 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 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 86% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ring finger protein 130, transcript variant X4
ring finger protein 130, transcript variant X6
ring finger protein 130, transcript variant X5
ring finger protein 130, transcript variant X1
ring finger protein 130, transcript variant X2
ring finger protein 130, transcript variant X3
E3 ubiquitin-protein ligase RNF130 isoform X3
E3 ubiquitin-protein ligase RNF130 isoform X4
E3 ubiquitin-protein ligase RNF130 isoform X1
E3 ubiquitin-protein ligase RNF130 isoform X2
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B
mastermind-like transcriptional coactivator 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transmembrane O-methyltransferase homolog, transcript variant X3
transmembrane O-methyltransferase homolog, transcript variant X2
transmembrane O-methyltransferase homolog, transcript variant X1
transmembrane O-methyltransferase homolog isoform X2
transmembrane O-methyltransferase homolog isoform X1
DAP3 binding cell death enhancer 1, transcript variant X2
DAP3 binding cell death enhancer 1, transcript variant X1
platelet-derived growth factor receptor beta-like
caudal type homeobox 1 b, transcript variant X1
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
caudal type homeobox 1 b, transcript variant X2
calcium/calmodulin-dependent protein kinase type II subunit alpha-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
H-2 class II histocompatibility antigen gamma chain
N-deacetylase/N-sulfotransferase (heparan glucosaminyl) 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 long SRA reads, 34 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
bifunctional heparan sulfate N-deacetylase/N-sulfotransferase 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
protein NDNF-like, transcript variant X2
protein NDNF-like, transcript variant X3
protein NDNF-like, transcript variant X4
protein NDNF-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
TNFAIP3 interacting protein 1, transcript variant X2
TNFAIP3 interacting protein 1, transcript variant X1
TNFAIP3-interacting protein 1 isoform X1
TNFAIP3-interacting protein 1 isoform X2
gem (nuclear organelle) associated protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
39S ribosomal protein L22, mitochondrial
amyloid-beta A4 precursor protein-binding family B member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 83% coverage of the annotated genomic feature by RNAseq alignments
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
transmembrane and coiled-coil domains 6, transcript variant X3
transmembrane and coiled-coil domains 6, transcript variant X1
transmembrane and coiled-coil domains 6, transcript variant X2
transmembrane and coiled-coil domain-containing protein 6 isoform X1
transmembrane and coiled-coil domain-containing protein 6 isoform X2
transmembrane and coiled-coil domain-containing protein 6 isoform X3
NADH:ubiquinone oxidoreductase subunit A2
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
histidyl-tRNA synthetase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
histidyl-tRNA synthetase, transcript variant X1
SLC35A4 upstream open reading frame protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
DND microRNA-mediated repression inhibitor 1, transcript variant X2
DND microRNA-mediated repression inhibitor 1, transcript variant X3
DND microRNA-mediated repression inhibitor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 Proteins
uncharacterized protein LOC100537710 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 134 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 235 Proteins, and 42% 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: 26 Proteins
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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protocadherin-10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 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: 29 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 233 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: protocadherin alpha-C2-like
protocadherin beta-15-like, transcript variant X1
protocadherin beta-15-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 202 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 93% 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: 56 Proteins
protocadherin beta-15-like, transcript variant X5
protocadherin beta-15-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
protocadherin beta-15-like, transcript variant X7
protocadherin beta-15-like, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protocadherin beta-15-like, transcript variant X12
protocadherin beta-15-like, transcript variant X13
protocadherin beta-15-like, transcript variant X6
protocadherin beta-15-like, transcript variant X10
protocadherin gamma-A11-like isoform X10
protocadherin gamma-A11-like isoform X12
protocadherin gamma-A11-like isoform X13
protocadherin beta-15-like, transcript variant X3
protocadherin beta-15-like, transcript variant X4
protocadherin beta-15-like, transcript variant X8
protocadherin beta-15-like, transcript variant X14
protocadherin beta-15-like, transcript variant X16
protocadherin beta-15-like, transcript variant X15
protocadherin gamma-A11-like isoform X16
protocadherin gamma-A11-like isoform X14
protocadherin gamma-A11-like isoform X15
uncharacterized LOC125484590, transcript variant X2
uncharacterized LOC125484590, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
StAR-related lipid transfer (START) domain containing 15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
ArfGAP with RhoGAP domain, ankyrin repeat and PH domain 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 3
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 3-like, transcript variant X2
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 14 samples with support for all annotated introns
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 3-like isoform X2
arf-GAP with Rho-GAP domain, ANK repeat and PH domain-containing protein 3-like isoform X1