Rhincodon typus isolate 14 chromosome 14, 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\nCM038811.1.\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.
COORDINATES: polyA evidence [ECO:0006239]
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
coiled-coil domain containing 160, transcript variant X1
coiled-coil domain containing 160, transcript variant X2
coiled-coil domain-containing protein 160
hypoxanthine phosphoribosyltransferase 1, transcript variant X2
hypoxanthine phosphoribosyltransferase 1, transcript variant X1
hypoxanthine-guanine phosphoribosyltransferase isoform X1
hypoxanthine-guanine phosphoribosyltransferase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 82% 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: 2 long SRA reads, 1 Protein, and 74% coverage of the annotated genomic feature by RNAseq alignments
motile sperm domain containing 1, transcript variant X3
motile sperm domain containing 1, transcript variant X1
motile sperm domain containing 1, transcript variant X2
motile sperm domain-containing protein 1 isoform X2
motile sperm domain-containing protein 1 isoform X1
integrator complex subunit 6-like, transcript variant X1
integrator complex subunit 6-like isoform X1
integrator complex subunit 6-like, transcript variant X2
integrator complex subunit 6-like isoform X2
integrator complex subunit 6-like, transcript variant X3
integrator complex subunit 6-like isoform X3
integrator complex subunit 6-like, transcript variant X4
integrator complex subunit 6-like isoform X4
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon UUC); 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
four and a half LIM domains protein 1-like
adhesion G-protein coupled receptor G2-like
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
transcription cofactor vestigial-like protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription cofactor vestigial-like protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transcription cofactor vestigial-like protein 3, transcript variant X2
transcription cofactor vestigial-like protein 3 isoform X2
transcription cofactor vestigial-like protein 3 isoform X1
uncharacterized protein LOC125484840 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
rho guanine nucleotide exchange factor 6-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 2 bases in 2 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable G-protein coupled receptor 101
transmembrane 9 superfamily member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 long SRA reads, 27 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transmembrane 9 superfamily member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 75% coverage of the annotated genomic feature by RNAseq alignments
RNA-binding motif protein, X chromosome-like, transcript variant X1
RNA-binding motif protein, X chromosome-like, transcript variant X3
RNA-binding motif protein, X chromosome-like, transcript variant X2
RNA-binding motif protein, X chromosome-like
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00270
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 13-like, transcript variant X2
fibroblast growth factor 13-like, transcript variant X1
fibroblast growth factor 13-like isoform X2
fibroblast growth factor 13-like isoform X1
guanine nucleotide exchange factor DBS-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phospholipid-transporting ATPase IG-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 long SRA reads, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 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
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 3 samples with support for all annotated introns
uncharacterized protein LOC321250 homolog
capping protein-inhibiting regulator of actin dynamics
LON peptidase N-terminal domain and RING finger protein 3-like
family with sequence similarity 199, X-linked, transcript variant X2
family with sequence similarity 199, X-linked, transcript variant X1
aristaless-related homeobox protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
interleukin 1 receptor accessory protein-like 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
X-linked interleukin-1 receptor accessory protein-like 2
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 4, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 4 isoform X1
mitogen-activated protein kinase kinase kinase kinase 4 isoform X2
RPA-related protein RADX-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RPA-related protein RADX-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
RPA-related protein RADX-like isoform X1
RPA-related protein RADX-like isoform X2
ring finger protein 128, transcript variant X2
ring finger protein 128, transcript variant X1
E3 ubiquitin-protein ligase RNF128 isoform X1
E3 ubiquitin-protein ligase RNF128 isoform X2
TBC1 domain family member 8B, transcript variant X3
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 5 samples with support for all annotated introns
TBC1 domain family member 8B, transcript variant X2
TBC1 domain family member 8B, transcript variant X1
neuronal PAS domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 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: 4 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins
high mobility group protein B3-like, transcript variant X4
high mobility group protein B3-like, transcript variant X2
high mobility group protein B3-like, transcript variant X1
high mobility group protein B3-like, transcript variant X3
high mobility group protein B3-like isoform X1
high mobility group protein B3-like isoform X2
CD99 molecule-like 2, transcript variant X2
CD99 molecule-like 2, transcript variant X4
CD99 molecule-like 2, transcript variant X5
CD99 molecule-like 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
CD99 molecule-like 2, transcript variant X1
myotubularin related protein 1b, transcript variant X1
myotubularin related protein 1b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 7 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC550336 homolog, transcript variant X2
uncharacterized protein LOC550336 homolog, transcript variant X1
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
heat shock transcription factor, Y-linked-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain-containing protein 46, transcript variant X2
ankyrin repeat domain-containing protein 46, transcript variant X1
ankyrin repeat domain-containing protein 46 isoform X2
ankyrin repeat domain-containing protein 46 isoform X1
membrane-associated progesterone receptor component 2-like
A-kinase anchor protein 17B-like, transcript variant X2
A-kinase anchor protein 17B-like, transcript variant X3
A-kinase anchor protein 17B-like, transcript variant X1
A-kinase anchor protein 17B-like isoform X2
A-kinase anchor protein 17B-like isoform X1
ubiquitin-conjugating enzyme E2A (RAD6 homolog), transcript variant X3
ubiquitin-conjugating enzyme E2A (RAD6 homolog), transcript variant X2
ubiquitin-conjugating enzyme E2A (RAD6 homolog), transcript variant X1
ubiquitin-conjugating enzyme E2 A isoform X1
ubiquitin-conjugating enzyme E2 A isoform X2
ubiquitin-conjugating enzyme E2 A isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 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, 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
sosondowah ankyrin repeat domain family d
ankyrin repeat domain-containing protein SOWAHC
UPF3B regulator of nonsense mediated mRNA decay
NADH:ubiquinone oxidoreductase subunit A1
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 1
NFKB activating protein, transcript variant X2
NFKB activating protein, transcript variant X1
zinc finger and BTB domain containing 33, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger and BTB domain containing 33, transcript variant X4
zinc finger and BTB domain containing 33, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger and BTB domain containing 33, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 4 Proteins, and 97% 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATPase Na+/K+ transporting subunit beta 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATPase Na+/K+ transporting subunit beta 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
transcription factor Dp-1-like, transcript variant X1
transcription factor Dp-1-like, transcript variant X3
transcription factor Dp-1-like, transcript variant X2
relaxin family peptide receptor 2, like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
relaxin family peptide receptor 2, like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
STING1 ER exit protein 1, transcript variant X2
STING1 ER exit protein 1, transcript variant X1
uncharacterized LOC109929980, transcript variant X2
uncharacterized LOC109929980, transcript variant X1
uncharacterized protein LOC109929980 isoform X2
uncharacterized protein LOC109929980 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
androgen receptor-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
androgen receptor-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
androgen receptor-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
androgen receptor-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
androgen receptor-like, transcript variant X5
androgen receptor-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tumor necrosis factor receptor superfamily member 19-like
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 25 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: 51 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 13 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
ectodysplasin-A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ectodysplasin-A-like, transcript variant X1
collagen, type IV, alpha 6, transcript variant X4
collagen, type IV, alpha 6, transcript variant X1
collagen, type IV, alpha 6, transcript variant X3
collagen, type IV, alpha 6, transcript variant X2
collagen, type IV, alpha 6, transcript variant X5
collagen, type IV, alpha 5 (Alport syndrome), transcript variant X2
collagen, type IV, alpha 5 (Alport syndrome), transcript variant X4
collagen, type IV, alpha 5 (Alport syndrome), transcript variant X1
collagen, type IV, alpha 5 (Alport syndrome), transcript variant X5
collagen, type IV, alpha 5 (Alport syndrome), transcript variant X3
collagen, type IV, alpha 5 (Alport syndrome), transcript variant X6
uncharacterized LOC125484804, transcript variant X2
uncharacterized LOC125484804, transcript variant X1
uncharacterized LOC125484804, transcript variant X3
tumor necrosis factor ligand superfamily member 13B-like, transcript variant X4
tumor necrosis factor ligand superfamily member 13B-like, transcript variant X3
tumor necrosis factor ligand superfamily member 13B-like isoform X4
tumor necrosis factor ligand superfamily member 13B-like isoform X3
tumor necrosis factor ligand superfamily member 13B-like, transcript variant X2
tumor necrosis factor ligand superfamily member 13B-like, transcript variant X1
uncharacterized protein LOC109914226 isoform X2
uncharacterized protein LOC109914226 isoform X1
autophagy related 4A, cysteine peptidase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 long SRA reads, 19 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cytokine receptor common subunit gamma-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments
forkhead box protein O1-like, transcript variant X1
forkhead box protein O1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein, LIM domain interacting, transcript variant X1
ring finger protein, LIM domain interacting, transcript variant X2
ring finger protein, LIM domain interacting, transcript variant X3
E3 ubiquitin-protein ligase RLIM isoform X1
E3 ubiquitin-protein ligase RNF12-B isoform X2
E3 ubiquitin-protein ligase RNF12-B isoform X3
neurite extension and migration factor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
ATP-binding cassette, sub-family B (MDR/TAP), member 7
iron-sulfur clusters transporter ABCB7, mitochondrial
uracil phosphoribosyltransferase (FUR1) homolog (S. cerevisiae)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
uracil phosphoribosyltransferase homolog
palmitoyltransferase ZDHHC15B-like, transcript variant X2
palmitoyltransferase ZDHHC15B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 long SRA reads, 27 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: 20 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transforming growth factor beta activator LRRC32-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
transforming growth factor beta activator LRRC33-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: retinal guanylyl cyclase 2-like
nuclear transport factor 2-like export factor 2
potassium voltage-gated channel subfamily E regulatory beta subunit 5
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: potassium voltage-gated channel subfamily E regulatory beta subunit 5
acyl-CoA synthetase long chain family member 4a, transcript variant X5
acyl-CoA synthetase long chain family member 4a, transcript variant X2
acyl-CoA synthetase long chain family member 4a, transcript variant X4
acyl-CoA synthetase long chain family member 4a, transcript variant X1
acyl-CoA synthetase long chain family member 4a, transcript variant X3
long-chain-fatty-acid--CoA ligase 4 isoform X2
long-chain-fatty-acid--CoA ligase 4 isoform X1
long-chain-fatty-acid--CoA ligase 4 isoform X3
transforming growth factor beta activator LRRC32-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transforming growth factor beta activator LRRC32-like isoform X1
transmembrane protein 164, transcript variant X1
transmembrane protein 164, transcript variant X2
transmembrane protein 164, transcript variant X7
transmembrane protein 164, transcript variant X3
transmembrane protein 164, transcript variant X5
transmembrane protein 164, transcript variant X4
transmembrane protein 164, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
AMMECR nuclear protein 1, transcript variant X2
AMMECR nuclear protein 1, transcript variant X1
AMME syndrome candidate gene 1 protein homolog isoform X1
AMME syndrome candidate gene 1 protein homolog isoform X2
serine/threonine-protein kinase PAK 3-like, transcript variant X4
serine/threonine-protein kinase PAK 3-like, transcript variant X3
serine/threonine-protein kinase PAK 3-like, transcript variant X2
serine/threonine-protein kinase PAK 3-like, transcript variant X1
serine/threonine-protein kinase PAK 3-like, transcript variant X5
serine/threonine-protein kinase PAK 3-like isoform X1
serine/threonine-protein kinase PAK 3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
neuronal migration protein doublecortin-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neuronal migration protein doublecortin-like isoform X1
neuronal migration protein doublecortin-like, transcript variant X2
neuronal migration protein doublecortin-like isoform X2
ALG13 UDP-N-acetylglucosaminyltransferase subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 10 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
putative bifunctional UDP-N-acetylglucosamine transferase and deubiquitinase ALG13
short transient receptor potential channel 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA methionine (anticodon CAU); 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: 22 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
phosphoglycerate kinase 1, transcript variant X4
phosphoglycerate kinase 1, transcript variant X1
phosphoglycerate kinase 1, transcript variant X2
phosphoglycerate kinase 1, transcript variant X3
ATPase copper transporting alpha, transcript variant X3
ATPase copper transporting alpha, transcript variant X1
ATPase copper transporting alpha, transcript variant X2
ATPase copper transporting alpha, transcript variant X4
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cytochrome c oxidase subunit 7B, mitochondrial
zinc finger MYM-type protein 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger MYM-type protein 3-like, transcript variant X1
zinc finger MYM-type protein 3-like, transcript variant X4
zinc finger MYM-type protein 3-like, transcript variant X5
zinc finger MYM-type protein 3-like, transcript variant X6
zinc finger MYM-type protein 3-like, transcript variant X2
zinc finger MYM-type protein 3-like isoform X3
zinc finger MYM-type protein 3-like isoform X4
zinc finger MYM-type protein 3-like isoform X1
zinc finger MYM-type protein 3-like isoform X5
zinc finger MYM-type protein 3-like isoform X6
zinc finger MYM-type protein 3-like isoform X2
gap junction alpha-3 protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 110 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gap junction alpha-3 protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 110 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gap junction alpha-3 protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 121 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
serpin peptidase inhibitor, clade H (heat shock protein 47), member 1b
immunoglobulin (CD79A) binding protein 1
wiskott-Aldrich syndrome protein family member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 12-B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 32 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
RAS-like, family 11, member A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
RAS-like, family 11, member A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RAS-like, family 11, member A, 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 4 samples with support for all annotated introns
ras-like protein family member 11A-like isoform X1
ras-like protein family member 11A-like isoform X2
ligand of numb-protein X 2b, transcript variant X1
ligand of numb-protein X 2b, transcript variant X5
ligand of numb-protein X 2b, transcript variant X3
ligand of numb-protein X 2b, transcript variant X2
ligand of numb-protein X 2b, transcript variant X4
pre-mRNA 3'-end-processing factor FIP1-like, transcript variant X3
pre-mRNA 3'-end-processing factor FIP1-like, transcript variant X2
pre-mRNA 3'-end-processing factor FIP1-like, transcript variant X1
pre-mRNA 3'-end-processing factor FIP1-like isoform X2
pre-mRNA 3'-end-processing factor FIP1-like isoform X1
pre-mRNA 3'-end-processing factor FIP1-like isoform X3
cysteine-rich hydrophobic domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
kinase insert domain receptor like, transcript variant X1
vascular endothelial growth factor receptor kdr-like isoform X1
kinase insert domain receptor 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
vascular endothelial growth factor receptor kdr-like isoform X2
glutamate receptor 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase XIAP, transcript variant X1
E3 ubiquitin-protein ligase XIAP, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
E3 ubiquitin-protein ligase XIAP, transcript variant X2
E3 ubiquitin-protein ligase XIAP isoform X1
E3 ubiquitin-protein ligase XIAP isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase MSL2-like, transcript variant X1
E3 ubiquitin-protein ligase MSL2-like, 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 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase MSL2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
E3 ubiquitin-protein ligase MSL2-like, transcript variant X5
E3 ubiquitin-protein ligase MSL2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1, transcript variant X1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1, transcript variant X4
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1, transcript variant X3
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 1, transcript variant X2
probable global transcription activator SNF2L1 isoform X4
probable global transcription activator SNF2L1 isoform X3
probable global transcription activator SNF2L1 isoform X2
probable global transcription activator SNF2L1 isoform X1
GRB2 associated binding protein 3, transcript variant X1
GRB2 associated binding protein 3, transcript variant X2
GRB2-associated-binding protein 3 isoform X1
GRB2-associated-binding protein 3 isoform X2
GRB2 associated binding protein 3, transcript variant X4
GRB2 associated binding protein 3, transcript variant X3
GRB2-associated-binding protein 3 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
GRB2-associated-binding protein 3 isoform X4
Cdc42 guanine nucleotide exchange factor (GEF) 9a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
rho guanine nucleotide exchange factor 9
APC membrane recruitment protein 1, transcript variant X4
APC membrane recruitment protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
APC membrane recruitment protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
APC membrane recruitment protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
APC membrane recruitment protein 1 isoform X1
APC membrane recruitment protein 1 isoform X2
ankyrin repeat and SOCS box-containing 12a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
shisa family member 2a, transcript variant X2
shisa family member 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein C8orf48 homolog, transcript variant X1
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
uncharacterized protein C8orf48 homolog, transcript variant X2
uncharacterized protein C8orf48 homolog, 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
zinc finger, C4H2 domain containing, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 15 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
zinc finger, C4H2 domain containing, 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 5 samples with support for all annotated introns
zinc finger C4H2 domain-containing protein isoform X2
zinc finger C4H2 domain-containing protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 11 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Rho GTPase activating protein 20b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Rho GTPase activating protein 20b, transcript variant X2
Rho GTPase activating protein 20b, transcript variant X3
rho GTPase-activating protein 20 isoform X1
rho GTPase-activating protein 20 isoform X2
rho GTPase-activating protein 20 isoform X3
Rho GTPase activating protein 20b, 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 2 samples with support for all annotated introns
rho GTPase-activating protein 20 isoform X4
paraspeckle component 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 62% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
paraspeckle component 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
paraspeckle component 1-like, transcript variant X5
paraspeckle component 1-like, transcript variant X1
non-POU domain-containing octamer-binding protein-like isoform X1
paraspeckle component 1-like, transcript variant X2
non-POU domain-containing octamer-binding protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
lysosome-associated membrane glycoprotein 2-like, transcript variant X1
lysosome-associated membrane glycoprotein 2-like, transcript variant X2
lysosome-associated membrane glycoprotein 2-like isoform X2
lysosome-associated membrane glycoprotein 2-like isoform X1
heat shock factor protein 1-like, transcript variant X3
heat shock factor protein 1-like, transcript variant X1
heat shock factor protein 1-like, transcript variant X2
heat shock factor protein 1-like isoform X2
heat shock factor protein 1-like isoform X1
V-set and immunoglobulin domain-containing protein 1
uncharacterized protein C21orf140 homolog
ras-related protein Rab-39B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 88 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ras-related protein Rab-39B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphatidylinositol-binding clathrin assembly protein, transcript variant X4
phosphatidylinositol-binding clathrin assembly protein, transcript variant X2
phosphatidylinositol-binding clathrin assembly protein, transcript variant X3
phosphatidylinositol-binding clathrin assembly protein, transcript variant X1
phosphatidylinositol-binding clathrin assembly protein isoform X4
phosphatidylinositol-binding clathrin assembly protein isoform X2
phosphatidylinositol-binding clathrin assembly protein isoform X3
phosphatidylinositol-binding clathrin assembly protein isoform X1
small nuclear ribonucleoprotein 35 (U11/U12)
U11/U12 small nuclear ribonucleoprotein 35 kDa protein
high affinity cationic amino acid transporter 1-like, transcript variant X1
high affinity cationic amino acid transporter 1-like, transcript variant X2
high affinity cationic amino acid transporter 1-like isoform X1
high affinity cationic amino acid transporter 1-like isoform X2
uncharacterized protein LOC445063 homolog
cysteine and histidine-rich domain-containing protein 1
uncharacterized LOC125484794, transcript variant X1
uncharacterized LOC125484794, transcript variant X4
uncharacterized LOC125484794, transcript variant X3
uncharacterized LOC125484794, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 long SRA reads, 4 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 49% coverage of the annotated genomic feature by RNAseq alignments
StAR-related lipid transfer (START) domain containing 8, transcript variant X1
stAR-related lipid transfer protein 8 isoform X1
StAR-related lipid transfer (START) domain containing 8, 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 4 samples with support for all annotated introns
stAR-related lipid transfer protein 8 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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
mediator complex subunit 12, transcript variant X1
mediator complex subunit 12, transcript variant X3
mediator complex subunit 12, transcript variant X2
mediator of RNA polymerase II transcription subunit 12 isoform X1
mediator of RNA polymerase II transcription subunit 12 isoform X2
mediator of RNA polymerase II transcription subunit 12 isoform X3
PDZ domain containing 11, transcript variant X2
PDZ domain-containing protein 11 isoform X2
PDZ domain containing 11, transcript variant X4
PDZ domain containing 11, transcript variant X1
PDZ domain containing 11, 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 3 samples with support for all annotated introns
PDZ domain-containing protein 11 isoform X1
PDZ domain-containing protein 11 isoform X3
kinesin family member 4, transcript variant X1
kinesin family member 4, transcript variant X2
glycerophosphodiester phosphodiesterase domain-containing protein 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
glycerophosphodiester phosphodiesterase domain-containing protein 5, transcript variant X3
glycerophosphodiester phosphodiesterase domain-containing protein 5, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glycerophosphodiester phosphodiesterase domain-containing protein 5, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycerophosphodiester phosphodiesterase domain-containing protein 5, transcript variant X2
glycerophosphodiester phosphodiesterase domain-containing protein 5 isoform X1
glycerophosphodiester phosphodiesterase domain-containing protein 5, transcript variant X6
glycerophosphodiester phosphodiesterase domain-containing protein 5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 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: 33 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: 16 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 56% 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 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: 15 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
discs, large homolog 3 (Drosophila), transcript variant X1
uncharacterized LOC125484787, transcript variant X1
uncharacterized LOC125484787, transcript variant X2
discs, large homolog 3 (Drosophila), transcript variant X2
discs, large homolog 3 (Drosophila), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
testis-expressed protein 11-like, transcript variant X2
testis-expressed protein 11-like, transcript variant X1
germ cell nuclear acidic peptidase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
germ cell nuclear acidic peptidase, 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 6 samples with support for all annotated introns
germ cell nuclear acidic peptidase, transcript variant X4
germ cell nuclear acidic peptidase, transcript variant X5
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 2 samples with support for all annotated introns
germ cell nuclear acidic peptidase, transcript variant X2
germ cell nuclear acidic protein isoform X1
germ cell nuclear acidic protein isoform X2
germ cell nuclear acidic protein isoform X3
germ cell nuclear acidic peptidase, transcript variant X6
germ cell nuclear acidic protein isoform X4
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit, transcript variant X1
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit, transcript variant X2
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform X2
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X6
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X2
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X7
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X4
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X5
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X8
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X1
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X11
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X3
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X10
transcription initiation factor TFIID subunit 1 isoform X2
transcription initiation factor TFIID subunit 1 isoform X1
transcription initiation factor TFIID subunit 1 isoform X4
transcription initiation factor TFIID subunit 1 isoform X3
TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
rho-related GTP-binding protein RhoG-like, transcript variant X1
rho-related GTP-binding protein RhoG-like, transcript variant X2
rho-related GTP-binding protein RhoG-like
FH2 domain containing 2, 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 2 samples with support for all annotated introns
FH2 domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
XK related X-linked, transcript variant X2
XK related X-linked, transcript variant X5
XK related X-linked, transcript variant X1
XK related X-linked, transcript variant X7
XK related X-linked, transcript variant X6
XK related X-linked, transcript variant X3
XK related X-linked, transcript variant X8
XK related X-linked, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 7 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
phosphoribosyl pyrophosphate synthetase 1B
FERM and PDZ domain-containing protein 3
MORC family CW-type zinc finger protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 3 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
RNA binding motif protein 41, transcript variant X1
RNA binding motif protein 41, transcript variant X2
cytochrome c oxidase assembly protein COX11, mitochondrial, 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 5 samples with support for all annotated introns
cytochrome c oxidase assembly protein COX11, mitochondrial, transcript variant X1
cytochrome c oxidase assembly protein COX11, mitochondrial isoform X2
cytochrome c oxidase assembly protein COX11, mitochondrial isoform X1
MORC family CW-type zinc finger protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 long SRA reads, 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Rho GTPase activating protein 36, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Rho GTPase activating protein 36, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 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: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase MID2 isoform X1
probable E3 ubiquitin-protein ligase MID2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NIMA-related kinase 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 19 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
NIMA-related kinase 12, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NIMA-related kinase 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein Shroom4-like, transcript variant X1
protein Shroom4-like, transcript variant X2
protein Shroom4-like, transcript variant X5
protein Shroom4-like, transcript variant X3
protein Shroom4-like, transcript variant X4
chloride channel, voltage-sensitive 5b, transcript variant X1
chloride channel, voltage-sensitive 5b, transcript variant X3
chloride channel, voltage-sensitive 5b, transcript variant X4
chloride channel, voltage-sensitive 5b, transcript variant X7
chloride channel, voltage-sensitive 5b, transcript variant X6
chloride channel, voltage-sensitive 5b, transcript variant X8
chloride channel, voltage-sensitive 5b, transcript variant X9
chloride channel, voltage-sensitive 5b, transcript variant X5
chloride channel, voltage-sensitive 5b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 18 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 18 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
methionyl-tRNA synthetase 2, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 long SRA reads, 7 Proteins, and 97% 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: 51 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
inositol polyphosphate 5-phosphatase OCRL-like
OCRL inositol polyphosphate-5-phosphatase
inositol polyphosphate 5-phosphatase OCRL
X-prolyl aminopeptidase (aminopeptidase P) 2, membrane-bound
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
zinc finger DHHC-type palmitoyltransferase 9, transcript variant X1
zinc finger DHHC-type palmitoyltransferase 9, transcript variant X2
uncharacterized protein LOC553498 homolog
U3 small nucleolar RNA-associated protein 14 homolog A
uncharacterized LOC125484836, transcript variant X3
uncharacterized LOC125484836, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125484836, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
sushi-repeat containing protein X-linked 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC335392 homolog
uncharacterized protein si:ch211-153b23.4
uncharacterized protein LOC321177 homolog
glutamine amidotransferase-like class 1 domain-containing protein 3, mitochondrial
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized protein LOC565650 homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: phytanoyl-CoA dioxygenase domain-containing protein 1
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
uncharacterized protein si:ch211-153b23.3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 long SRA reads, 20 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
BTB/POZ domain-containing protein KCTD8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
TNFAIP3-interacting protein 3, transcript variant X3
TNFAIP3-interacting protein 3, transcript variant X1
TNFAIP3-interacting protein 3, transcript variant X2
Kruppel-like factor 5 like, transcript variant X1
Kruppel-like factor 5 like, transcript variant X2
Kruppel-like factor 8, transcript variant X2
Kruppel-like factor 8, transcript variant X4
Kruppel-like factor 8, transcript variant X7
Kruppel-like factor 8, transcript variant X6
Kruppel-like factor 8, transcript variant X3
Kruppel-like factor 8, transcript variant X1
Kruppel-like factor 8, transcript variant X9
Kruppel-like factor 8, transcript variant X10
Kruppel-like factor 8, transcript variant X8
Kruppel-like factor 8, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glucose-dependent insulinotropic receptor
RNA binding motif protein X-linked 2, transcript variant X2
RNA binding motif protein X-linked 2, transcript variant X1
RNA-binding motif protein, X-linked 2 isoform X2
RNA-binding motif protein, X-linked 2 isoform X1
seven in absentia homolog 2 (Drosophila)-like
ATP-binding cassette sub-family C member 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 29 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
ecto-NOX disulfide-thiol exchanger 2, transcript variant X1
ecto-NOX disulfide-thiol exchanger 2, transcript variant X2
ecto-NOX disulfide-thiol exchanger 2, transcript variant X3
ecto-NOX disulfide-thiol exchanger 2, transcript variant X4
NAD(P) dependent steroid dehydrogenase-like, transcript variant X1
NAD(P) dependent steroid dehydrogenase-like, transcript variant X2
sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating isoform X1
sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating isoform X2
SLAIN motif-containing protein-like, transcript variant X1
SLAIN motif-containing protein-like, transcript variant X2
SLAIN motif-containing protein-like isoform X1
SLAIN motif-containing protein-like isoform X2
synaptobrevin-like 1, transcript variant X1
synaptobrevin-like 1, transcript variant X4
synaptobrevin-like 1, transcript variant X2
synaptobrevin-like 1, transcript variant X3
vesicle-associated membrane protein 7 isoform X1
vesicle-associated membrane protein 7 isoform X2
DNA-directed RNA polymerases I and III subunit RPAC2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 51 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor ligand superfamily member 10-like, transcript variant X1
tumor necrosis factor ligand superfamily member 10-like, transcript variant X2
tumor necrosis factor ligand superfamily member 10-like isoform X1
tumor necrosis factor ligand superfamily member 10-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
brain-specific homeobox/POU domain protein 3-like
protein sprouty homolog 2, transcript variant X3
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 11 samples with support for all annotated introns
protein sprouty homolog 2, transcript variant X5
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
protein sprouty homolog 2, 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 3 samples with support for all annotated introns
protein sprouty homolog 2, transcript variant X2
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
protein sprouty homolog 2, transcript variant X1
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 2 samples with support for all annotated introns
short coiled-coil protein B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
short coiled-coil protein B, 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 2 samples with support for all annotated introns
trimethyllysine hydroxylase, epsilon, transcript variant X1
trimethyllysine dioxygenase, mitochondrial isoform X1
trimethyllysine hydroxylase, epsilon, transcript variant X4
trimethyllysine dioxygenase, mitochondrial isoform X4
trimethyllysine hydroxylase, epsilon, transcript variant X2
trimethyllysine hydroxylase, epsilon, transcript variant X3
trimethyllysine dioxygenase, mitochondrial isoform X2
trimethyllysine dioxygenase, mitochondrial isoform X3
dyskeratosis congenita 1, dyskerin, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
H/ACA ribonucleoprotein complex subunit DKC1 isoform X2
dyskeratosis congenita 1, dyskerin, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
H/ACA ribonucleoprotein complex subunit DKC1 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00567
COORDINATES: nucleotide motif:Rfam:12.0:RF00137
COORDINATES: nucleotide motif:Rfam:12.0:RF00340
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 12 samples with support for all annotated introns
MAGUK p55 scaffold protein 1, transcript variant X1
55 kDa erythrocyte membrane protein isoform X1
MAGUK p55 scaffold protein 1, transcript variant X2
55 kDa erythrocyte membrane protein isoform 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 20 samples with support for all annotated introns
G protein-coupled receptor 34 like, transcript variant X1
G protein-coupled receptor 34 like, transcript variant X3
G protein-coupled receptor 34 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
BRCA1/BRCA2-containing complex, subunit 3
C-x(9)-C motif containing 4 homolog (S. cerevisiae), transcript variant X4
C-x(9)-C motif containing 4 homolog (S. cerevisiae), transcript variant X5
C-x(9)-C motif containing 4 homolog (S. cerevisiae), transcript variant X1
C-x(9)-C motif containing 4 homolog (S. cerevisiae), transcript variant X2
C-x(9)-C motif containing 4 homolog (S. cerevisiae), transcript variant X3
cx9C motif-containing protein 4 isoform X1
cx9C motif-containing protein 4 isoform X2
fun14 domain containing 2, transcript variant X1
fun14 domain containing 2, transcript variant X2
FUN14 domain-containing protein 2 isoform X1
FUN14 domain-containing protein 2 isoform X2
coagulation factor VIII, procoagulant component, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
coagulation factor VIII, procoagulant component, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC125484819, transcript variant X1
uncharacterized LOC125484819, transcript variant X2
uncharacterized LOC125484819, transcript variant X3
uncharacterized LOC125484819, transcript variant X4
uncharacterized protein LOC125484819 isoform X1
uncharacterized protein LOC125484819 isoform X2
uncharacterized protein LOC125484819 isoform X3
uncharacterized protein LOC125484819 isoform X4
cytochrome b-245 heavy chain-like, transcript variant X2
cytochrome b-245 heavy chain-like, transcript variant X3
cytochrome b-245 heavy chain-like, transcript variant X1
cytochrome b-245 heavy chain-like, transcript variant X4
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 3 samples with support for all annotated introns
cytochrome b-245 heavy chain-like isoform X1
cytochrome b-245 heavy chain-like isoform X3
cytochrome b-245 heavy chain-like isoform X2
cleavage stimulation factor subunit 2-like, transcript variant X4
cleavage stimulation factor subunit 2-like, transcript variant X2
cleavage stimulation factor subunit 2-like, transcript variant X3
cleavage stimulation factor subunit 2-like, transcript variant X1
cleavage stimulation factor subunit 2-like isoform X4
cleavage stimulation factor subunit 2-like isoform X2
cleavage stimulation factor subunit 2-like isoform X3
cleavage stimulation factor subunit 2-like isoform X1
tRNA methyltransferase 12 homolog, transcript variant X2
tRNA methyltransferase 12 homolog, transcript variant X1
tRNA wybutosine-synthesizing protein 2 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
transmembrane gamma-carboxyglutamic acid protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
transmembrane gamma-carboxyglutamic acid protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transmembrane gamma-carboxyglutamic acid protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane gamma-carboxyglutamic acid protein 3 isoform X2
transmembrane gamma-carboxyglutamic acid protein 3 isoform X3
transmembrane gamma-carboxyglutamic acid protein 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125484831, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125484831, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC125484831, transcript variant X3
uncharacterized LOC125484831, transcript variant X4
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
phospholipase A2, group XIIA, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phospholipase A2, group XIIA, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 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: 2 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform
protein (peptidylprolyl cis/trans isomerase) NIMA-interacting, 4 (parvulin)
peptidyl-prolyl cis-trans isomerase NIMA-interacting 4
histone deacetylase 8, transcript variant X2
histone deacetylase 8, transcript variant X9
histone deacetylase 8, transcript variant X1
histone deacetylase 8, transcript variant X5
histone deacetylase 8, transcript variant X3
histone deacetylase 8, transcript variant X4
histone deacetylase 8, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
histone deacetylase 8, transcript variant X7
cbp/p300-interacting transactivator 1 isoform X4
histone deacetylase 8, transcript variant X8
cbp/p300-interacting transactivator 1 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10335 long SRA reads, 77 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 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: 1 Protein
ADP-ribosylation factor-like protein 13B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC555281 homolog
zinc finger protein 711, transcript variant X2
zinc finger protein 711, transcript variant X5
zinc finger protein 711, transcript variant X1
zinc finger protein 711, transcript variant X4
zinc finger protein 711, transcript variant X3
rab proteins geranylgeranyltransferase component A 1
transmembrane protein 33-like, transcript variant X1
transmembrane protein 33-like, transcript variant X4
transmembrane protein 33-like, transcript variant X2
transmembrane protein 33-like, transcript variant X6
transmembrane protein 33-like isoform X3
transmembrane protein 33-like isoform X1
transmembrane protein 33-like isoform X5
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
transmembrane protein 33-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 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protein 33-like isoform X2
transmembrane protein 33-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
transmembrane protein 33-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
protocadherin-20-like, transcript variant X2
protocadherin-20-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 6 samples with support for all annotated introns
protein diaphanous homolog 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 6 samples with support for all annotated introns
protein diaphanous homolog 2-like, transcript variant X1
protein diaphanous homolog 2-like isoform X2
protein diaphanous homolog 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 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: 139 long SRA reads, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 85% 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: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E74-like ETS transcription factor 1, transcript variant X5
E74-like ETS transcription factor 1, transcript variant X1
E74-like ETS transcription factor 1, transcript variant X3
E74-like ETS transcription factor 1, transcript variant X2
E74-like ETS transcription factor 1, transcript variant X4
E74-like ETS transcription factor 1, transcript variant X6
ETS-related transcription factor Elf-1 isoform X2
ETS-related transcription factor Elf-1 isoform X1
ETS-related transcription factor Elf-1 isoform X3
apoptosis inducing factor mitochondrion associated 1, transcript variant X1
apoptosis inducing factor mitochondrion associated 1, transcript variant X2
apoptosis inducing factor mitochondrion associated 1, transcript variant X3
apoptosis-inducing factor 1, mitochondrial isoform X1
apoptosis-inducing factor 1, mitochondrial isoform X2
apoptosis-inducing factor 1, mitochondrial isoform X3
fatty-acid amide hydrolase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fatty-acid amide hydrolase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
fatty-acid amide hydrolase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
fatty-acid amide hydrolase 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
urotensin-related peptide 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 75% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
urotensin-related peptide 1, transcript variant X4
urotensin-related peptide 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 76% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
urotensin-related peptide 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chloride intracellular channel 2, transcript variant X1
chloride intracellular channel 2, transcript variant X2
chloride intracellular channel protein 2 isoform X1
chloride intracellular channel protein 2 isoform X2
UAP56-interacting factor-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
UAP56-interacting factor-like, transcript variant X2
UAP56-interacting factor-like, transcript variant X3
UAP56-interacting factor-like isoform X1
UAP56-interacting factor-like isoform X2
UAP56-interacting factor-like isoform X3
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 521 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 521 long SRA reads, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X3
leucine-rich repeats and calponin homology (CH) domain containing 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 4 samples with support for all annotated introns
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X1
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X2
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X3
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X4
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 521 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 521 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X5
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 521 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 2, transcript variant X7
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X5
interleukin-13 receptor subunit alpha-2-like, transcript variant X2
interleukin-13 receptor subunit alpha-2-like, transcript variant X1
interleukin-13 receptor subunit alpha-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
succinate--CoA ligase [ADP-forming] subunit beta, mitochondrial
TAF9 RNA polymerase II, TATA box binding protein (TBP)-associated factor
transcription initiation factor TFIID subunit 9
fibronectin type-III domain-containing protein 3A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 long SRA reads, 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
fibronectin type-III domain-containing protein 3A-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 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
fibronectin type-III domain-containing protein 3A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 long SRA reads, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
fibronectin type-III domain-containing protein 3A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 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
fibronectin type-III domain-containing protein 3A-like, transcript variant X4
fibronectin type-III domain-containing protein 3A-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
cysteinyl leukotriene receptor 1, 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 14 samples with support for all annotated introns
cysteinyl leukotriene receptor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cysteinyl leukotriene receptor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
probable G-protein coupled receptor 174, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
probable G-protein coupled receptor 174, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
2-Hydroxyacid oxidase 2-like, transcript variant X3
2-Hydroxyacid oxidase 2-like, transcript variant X1
2-Hydroxyacid oxidase 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
bromodomain and WD repeat-containing protein 3-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: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
non-histone chromosomal protein HMG-14A-like
SH3 domain binding glutamate-rich protein like
SH3 domain-binding glutamic acid-rich-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 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: 24 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109916234, transcript variant X1
uncharacterized LOC109916234, transcript variant X2
uncharacterized LOC125484789, 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 3 samples with support for all annotated introns
uncharacterized LOC125484789, transcript variant X1
U2 snRNP-associated SURP motif-containing protein-like, transcript variant X1
U2 snRNP-associated SURP motif-containing protein-like, transcript variant X3
U2 snRNP-associated SURP motif-containing protein-like, transcript variant X2
U2 snRNP-associated SURP motif-containing protein-like isoform X1
U2 snRNP-associated SURP motif-containing protein-like isoform X2
plastin 3 (T isoform), transcript variant X1
plastin 3 (T isoform), transcript variant X3
plastin 3 (T isoform), transcript variant X2
connector enhancer of kinase suppressor of ras 2
highly divergent homeobox, transcript variant X4
highly divergent homeobox, transcript variant X6
highly divergent homeobox, transcript variant X5
highly divergent homeobox, transcript variant X12
highly divergent homeobox, transcript variant X1
highly divergent homeobox, transcript variant X8
highly divergent homeobox, transcript variant X7
highly divergent homeobox, transcript variant X13
highly divergent homeobox, transcript variant X9
highly divergent homeobox, transcript variant X11
highly divergent homeobox, transcript variant X10
highly divergent homeobox, transcript variant X2
highly divergent homeobox, transcript variant X3
ribosomal protein S6 kinase alpha-6, transcript variant X2
ribosomal protein S6 kinase alpha-6 isoform X2
ribosomal protein S6 kinase alpha-6, transcript variant X1
ribosomal protein S6 kinase alpha-6 isoform X1
POU domain, class 3, transcription factor 4-B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 80 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
TLR adapter interacting with SLC15A4 on the lysosome-like, transcript variant X2
TLR adapter interacting with SLC15A4 on the lysosome-like, transcript variant X1
TLR adapter interacting with SLC15A4 on the lysosome-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 26% 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 9% 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 16% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125484810, transcript variant X1
uncharacterized LOC125484810, transcript variant X2
uncharacterized LOC125484810, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
tRNA methyltransferase 2 homolog B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
tRNA (uracil-5-)-methyltransferase homolog B isoform X1
tRNA methyltransferase 2 homolog B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tRNA methyltransferase 2 homolog B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tRNA (uracil-5-)-methyltransferase homolog B isoform X2
tRNA methyltransferase 2 homolog B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tRNA (uracil-5-)-methyltransferase homolog B isoform X3
muscleblind-like protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
muscleblind-like protein 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
muscleblind-like protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
muscleblind-like protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
muscleblind-like protein 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
muscleblind-like protein 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
muscleblind-like protein 3, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
muscleblind-like protein 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
muscleblind-like protein 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
muscleblind-like protein 3, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 long SRA reads, 4 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase 26, transcript variant X2
serine/threonine-protein kinase 26, transcript variant X1
serine/threonine-protein kinase 26 isoform X2
serine/threonine-protein kinase 26 isoform X1
uncharacterized LOC125484817, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125484817, transcript variant X2
interleukin-13 receptor subunit alpha-1-like, transcript variant X2
interleukin-13 receptor subunit alpha-1-like, transcript variant X1
interleukin-13 receptor subunit alpha-1-like isoform X2
interleukin-13 receptor subunit alpha-1-like isoform X1
interferon-inducible GTPase 5-like, transcript variant X1
interferon-inducible GTPase 5-like, transcript variant X2
T-cell-specific guanine nucleotide triphosphate-binding protein 2-like, transcript variant X4
T-cell-specific guanine nucleotide triphosphate-binding protein 2-like, transcript variant X3
T-cell-specific guanine nucleotide triphosphate-binding protein 2-like, transcript variant X5
T-cell-specific guanine nucleotide triphosphate-binding protein 2-like, transcript variant X1
T-cell-specific guanine nucleotide triphosphate-binding protein 2-like, transcript variant X2
T-cell-specific guanine nucleotide triphosphate-binding protein 2-like isoform X2
T-cell-specific guanine nucleotide triphosphate-binding protein 2-like isoform X1
T-cell-specific guanine nucleotide triphosphate-binding protein 2-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 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: 13 Proteins, and 28% 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: 28 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
T-cell-specific guanine nucleotide triphosphate-binding protein 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
Bruton agammaglobulinemia tyrosine kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Bruton agammaglobulinemia tyrosine kinase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Bruton agammaglobulinemia tyrosine kinase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 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
Bruton agammaglobulinemia tyrosine kinase, transcript variant X7
Bruton agammaglobulinemia tyrosine kinase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Bruton agammaglobulinemia tyrosine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Bruton agammaglobulinemia tyrosine kinase, transcript variant X3
TAF7 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X1
transcription initiation factor TFIID subunit 7 isoform X1
TAF7 RNA polymerase II, TATA box binding protein (TBP)-associated factor, transcript variant X2
transcription initiation factor TFIID subunit 7 isoform X2
gamma-aminobutyric acid receptor subunit gamma-4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gamma-aminobutyric acid receptor subunit alpha-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gamma-aminobutyric acid receptor subunit beta-4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
nucleoporin 62 like, transcript variant X1
nucleoporin 62 like, transcript variant X3
nucleoporin 62 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cyclic nucleotide-gated olfactory channel-like
solute carrier family 25 member 14, transcript variant X3
solute carrier family 25 member 14, transcript variant X1
solute carrier family 25 member 14, transcript variant X2
brain mitochondrial carrier protein 1 isoform X1
brain mitochondrial carrier protein 1 isoform X2
zinc finger protein 239-like, transcript variant X3
zinc finger protein 239-like, transcript variant X1
zinc finger protein 239-like, transcript variant X4
zinc finger protein 239-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 3 samples with support for all annotated introns
thyrotropin-releasing hormone receptor-like