Rhincodon typus isolate 14 chromosome 23, 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\nCM038820.1.\nAssembly name: sRhiTyp1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Squalomix on 2022/02/03. The\noriginal whole-genome shotgun project has the accession\nJAHMAH000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Squalomix\nAssembly Date :: 22-FEB-2021\nAssembly Method :: Supernova v. 2.1.1; P_RNA_scaffolder v.\n commit 7941e0f; Tigmint v. 1.1.2; ARKS v.\n 1.1.0; 3D-DNA v. 180922\nAssembly Name :: sRhiTyp1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 46.7x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Rhincodon typus Annotation Release\n 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 18 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
(E3-independent) E2 ubiquitin-conjugating enzyme UBE2O-like
COORDINATES: polyA evidence [ECO:0006239]
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
(E3-independent) E2 ubiquitin-conjugating enzyme-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
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 18 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 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
phosphoribosyl pyrophosphate synthase-associated protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 31 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
UTP6 small subunit processome component, transcript variant X2
UTP6 small subunit processome component, transcript variant X1
U3 small nucleolar RNA-associated protein 6 homolog isoform X1
U3 small nucleolar RNA-associated protein 6 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
retinoid-inducible serine carboxypeptidase
ras homolog family member T1, transcript variant X1
ras homolog family member T1, transcript variant X3
ras homolog family member T1, transcript variant X5
ras homolog family member T1, transcript variant X2
ras homolog family member T1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein Njmu-R1-like, 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 16 samples with support for all annotated introns
protein Njmu-R1-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 19 samples with support for all annotated introns
protein Njmu-R1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
zinc finger protein 207, b, transcript variant X10
zinc finger protein 207, b, transcript variant X7
zinc finger protein 207, b, transcript variant X8
zinc finger protein 207, b, transcript variant X9
zinc finger protein 207, b, transcript variant X2
zinc finger protein 207, b, transcript variant X4
zinc finger protein 207, b, transcript variant X5
zinc finger protein 207, b, transcript variant X3
zinc finger protein 207, b, transcript variant X6
zinc finger protein 207, b, transcript variant X1
BUB3-interacting and GLEBS motif-containing protein ZNF207b isoform X1
BUB3-interacting and GLEBS motif-containing protein ZNF207b isoform X2
BUB3-interacting and GLEBS motif-containing protein ZNF207b isoform X3
BUB3-interacting and GLEBS motif-containing protein ZNF207b isoform X4
arf-GAP with dual PH domain-containing protein 1-like
transcription elongation factor, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 long SRA reads, 7 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
transcription elongation factor, mitochondrial isoform X1
transcription elongation factor, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription elongation factor, mitochondrial isoform X2
ATPase family AAA domain-containing protein 5
polycomb protein suz12-like, transcript variant X1
polycomb protein suz12-like, transcript variant X2
exocyst complex component 7, transcript variant X1
exocyst complex component 7, transcript variant X2
exocyst complex component 7, transcript variant X3
exocyst complex component 7, transcript variant X5
exocyst complex component 7, transcript variant X4
exocyst complex component 7, transcript variant X6
exocyst complex component 7, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein NO VEIN-like, transcript variant X2
protein NO VEIN-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 26% coverage of the annotated genomic feature by RNAseq alignments
UTP18 small subunit processome component, transcript variant X2
UTP18 small subunit processome component, transcript variant X1
U3 small nucleolar RNA-associated protein 18 homolog
uncharacterized LOC125485860, transcript variant X2
uncharacterized LOC125485860, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
C-Jun-amino-terminal kinase-interacting protein 4-like
info WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 30 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2
ankyrin repeat domain-containing protein 40
ATP-binding cassette, sub-family C (CFTR/MRP), member 3, transcript variant X1
ATP-binding cassette, sub-family C (CFTR/MRP), member 3, transcript variant X2
ATP-binding cassette, sub-family C (CFTR/MRP), member 3, transcript variant X7
ATP-binding cassette, sub-family C (CFTR/MRP), member 3, transcript variant X8
ATP-binding cassette sub-family C member 3 isoform X1
ATP-binding cassette sub-family C member 3 isoform X2
ATP-binding cassette sub-family C member 3 isoform X7
ATP-binding cassette, sub-family C (CFTR/MRP), member 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATP-binding cassette sub-family C member 3 isoform X6
ATP-binding cassette, sub-family C (CFTR/MRP), member 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ATP-binding cassette, sub-family C (CFTR/MRP), member 3, transcript variant X4
ATP-binding cassette sub-family C member 3 isoform X5
ATP-binding cassette sub-family C member 3 isoform X4
ATP-binding cassette, sub-family C (CFTR/MRP), member 3, transcript variant X3
ATP-binding cassette sub-family C member 3 isoform X3
Ras-associating and dilute domain-containing protein-like, transcript variant X1
Ras-associating and dilute domain-containing protein-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Ras-associating and dilute domain-containing protein-like, transcript variant X2
ras-associating and dilute domain-containing protein-like isoform X1
Ras-associating and dilute domain-containing protein-like, transcript variant X3
ras-associating and dilute domain-containing protein-like isoform X2
monocyte to macrophage differentiation factor-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
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: 9 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and fibronectin type III domain containing 1
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
ankyrin repeat and fibronectin type-III domain-containing protein 1
sodium-coupled monocarboxylate transporter 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
sterile alpha motif domain-containing protein 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
monocyte to macrophage differentiation factor-like, transcript variant X2
monocyte to macrophage differentiation factor-like, transcript variant X1
monocyte to macrophage differentiation factor-like isoform X2
monocyte to macrophage differentiation factor-like isoform X1
serine/threonine-protein kinase/endoribonuclease IRE1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein kinase/endoribonuclease IRE1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
serine/threonine-protein kinase/endoribonuclease IRE1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 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
serine/threonine-protein kinase/endoribonuclease IRE1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 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
sterile alpha motif domain-containing protein 9-like isoform X1
serine/threonine-protein kinase/endoribonuclease IRE1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein kinase/endoribonuclease IRE1, transcript variant X6
serine/threonine-protein kinase/endoribonuclease IRE1, transcript variant X5
serine/threonine-protein kinase/endoribonuclease IRE1 isoform X3
serine/threonine-protein kinase/endoribonuclease IRE1 isoform X2
serine/threonine-protein kinase/endoribonuclease IRE1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
serine/threonine-protein kinase/endoribonuclease IRE1 isoform X4
uncharacterized LOC125485853, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125485853, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 88% 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: 2 long SRA reads, 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myeloid-associated differentiation marker homolog, transcript variant X2
myeloid-associated differentiation marker homolog, transcript variant X1
myeloid-associated differentiation marker homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 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, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
centrosomal protein 112, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
centrosomal protein of 112 kDa isoform X2
centrosomal protein 112, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
centrosomal protein 112, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
centrosomal protein 112, transcript variant X2
centrosomal protein of 112 kDa isoform X3
centrosomal protein of 112 kDa isoform X1
uncharacterized LOC125485852, transcript variant X2
uncharacterized LOC125485852, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
calcium channel, voltage-dependent, gamma subunit 5b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
voltage-dependent calcium channel gamma-5 subunit
voltage-dependent calcium channel gamma-4 subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
calcium channel, voltage-dependent, gamma subunit 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
voltage-dependent calcium channel gamma-1 subunit
helicase with zinc finger, transcript variant X4
helicase with zinc finger, transcript variant X2
helicase with zinc finger, transcript variant X3
helicase with zinc finger, transcript variant X5
helicase with zinc finger, transcript variant X1
helicase with zinc finger, transcript variant X6
probable helicase with zinc finger domain isoform X4
probable helicase with zinc finger domain isoform X2
probable helicase with zinc finger domain isoform X3
probable helicase with zinc finger domain isoform X5
probable helicase with zinc finger domain isoform X1
probable helicase with zinc finger domain isoform X6
26S proteasome non-ATPase regulatory subunit 12
phosphatidylinositol transfer protein cytoplasmic 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 20 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
cytoplasmic phosphatidylinositol transfer protein 1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nucleosome-remodeling factor subunit BPTF-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
karyopherin alpha 2 (RAG cohort 1, importin alpha 1), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 27 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
karyopherin alpha 2 (RAG cohort 1, importin alpha 1), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
karyopherin alpha 2 (RAG cohort 1, importin alpha 1), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 long SRA reads, 27 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: 3 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA arginine (anticodon CCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nucleosome-remodeling factor subunit BPTF, transcript variant X3
nucleosome-remodeling factor subunit BPTF, transcript variant X2
nucleosome-remodeling factor subunit BPTF, transcript variant X1
nucleosome-remodeling factor subunit BPTF isoform X3
nucleosome-remodeling factor subunit BPTF isoform X2
nucleosome-remodeling factor subunit BPTF isoform X1
DEAD (Asp-Glu-Ala-Asp) box helicase 5, 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 18 samples with support for all annotated introns
DEAD (Asp-Glu-Ala-Asp) box helicase 5, transcript variant X1
probable ATP-dependent RNA helicase DDX5
polymerase (DNA directed), gamma 2, accessory subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
polymerase (DNA directed), gamma 2, accessory subunit, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 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
polymerase (DNA directed), gamma 2, accessory subunit, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 long SRA reads, 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
polymerase (DNA directed), gamma 2, accessory subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 long SRA reads, 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
polymerase (DNA directed), gamma 2, accessory subunit, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 long SRA reads, 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DNA polymerase subunit gamma-2, mitochondrial isoform X1
DNA polymerase subunit gamma-2, mitochondrial isoform X2
platelet endothelial cell adhesion molecule-like, transcript variant X3
platelet endothelial cell adhesion molecule-like, transcript variant X4
platelet endothelial cell adhesion molecule-like, transcript variant X1
platelet endothelial cell adhesion molecule-like, transcript variant X6
platelet endothelial cell adhesion molecule-like, transcript variant X5
platelet endothelial cell adhesion molecule-like, transcript variant X2
platelet endothelial cell adhesion molecule-like isoform X4
platelet endothelial cell adhesion molecule-like isoform X3
platelet endothelial cell adhesion molecule-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
platelet endothelial cell adhesion molecule-like, transcript variant X8
Fc receptor-like protein 5, transcript variant X2
Fc receptor-like protein 5, 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 2 samples with support for all annotated introns
uncharacterized protein LOC109917393 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 16 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 1 regulatory subunit 27
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
MAPK regulated corepressor interacting protein 1
mapk-regulated corepressor-interacting protein 1
hepatocyte growth factor-regulated tyrosine kinase substrate
ADP-ribosylation factor-like 16, transcript variant X3
ADP-ribosylation factor-like 16, transcript variant X2
ADP-ribosylation factor-like 16, transcript variant X1
ADP-ribosylation factor-like protein 16 isoform X1
ADP-ribosylation factor-like 16, transcript variant X4
ADP-ribosylation factor-like protein 16 isoform X2
solute carrier family 26 member 11, transcript variant X2
solute carrier family 26 member 11, transcript variant X1
solute carrier family 26 member 11, transcript variant X3
sodium-independent sulfate anion transporter isoform X1
sodium-independent sulfate anion transporter isoform X2
39S ribosomal protein L12, mitochondrial
guanine nucleotide binding protein (G protein) alpha v1
phosphate cytidylyltransferase 2, ethanolamine
ethanolamine-phosphate cytidylyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 7 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
ASPSCR1 tether for SLC2A4, UBX domain containing, transcript variant X3
ASPSCR1 tether for SLC2A4, UBX domain containing, transcript variant X2
ASPSCR1 tether for SLC2A4, UBX domain containing, transcript variant X1
ASPSCR1 tether for SLC2A4, UBX domain containing, transcript variant X4
ASPSCR1 tether for SLC2A4, UBX domain containing, transcript variant X5
tether containing UBX domain for GLUT4 isoform X3
tether containing UBX domain for GLUT4 isoform X2
tether containing UBX domain for GLUT4 isoform X1
tether containing UBX domain for GLUT4 isoform X5
tether containing UBX domain for GLUT4 isoform X4
notum, palmitoleoyl-protein carboxylesterase a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
palmitoleoyl-protein carboxylesterase notum1a
myeloid-associated differentiation marker-like protein 2
pyrroline-5-carboxylate reductase 1, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
pyrroline-5-carboxylate reductase 1, mitochondrial-like isoform X2
pyrroline-5-carboxylate reductase 1, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
pyrroline-5-carboxylate reductase 1, mitochondrial-like isoform X1
N-sulfoglucosamine sulfohydrolase (sulfamidase)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase, transcript variant X1
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase, transcript variant X3
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase, transcript variant X6
alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 isoform X1
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase, transcript variant X7
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase, transcript variant X5
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase, transcript variant X2
alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 isoform X2
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3)-N-acetylgalactosaminide alpha-2,6-sialyltransferase, transcript variant X4
alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 isoform X3
alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 isoform X4
parvalbumin-like EF-hand-containing protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
parvalbumin-like EF-hand-containing protein, transcript variant X2
parvalbumin-like EF-hand-containing protein
serine/threonine-protein kinase LMTK1-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
BAR/IMD domain containing adaptor protein 2a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
BAR/IMD domain containing adaptor protein 2a, 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 11 samples with support for all annotated introns
brain-specific angiogenesis inhibitor 1-associated protein 2a isoform X1
brain-specific angiogenesis inhibitor 1-associated protein 2a isoform X2
brain-specific angiogenesis inhibitor 1-associated protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
regulatory associated protein of MTOR, complex 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ring finger protein 213a, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 long SRA reads, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ring finger protein 213a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ring finger protein 213a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
E3 ubiquitin-protein ligase rnf213-alpha isoform X1
E3 ubiquitin-protein ligase rnf213-alpha isoform X2
E3 ubiquitin-protein ligase rnf213-alpha isoform X3
BTB (POZ) domain containing 17b, transcript variant X2
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 2 samples with support for all annotated introns
BTB (POZ) domain containing 17b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
BTB/POZ domain-containing protein 17 isoform X2
BTB/POZ domain-containing protein 17 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
G-protein coupled receptor family C group 5 member C, transcript variant X1
G-protein coupled receptor family C group 5 member C, transcript variant X2
G-protein coupled receptor family C group 5 member C
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
coiled-coil domain-containing protein 137
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 23 Proteins, and 96% 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: 15 long SRA reads, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
baculoviral IAP repeat containing 5a, transcript variant X2
baculoviral IAP repeat containing 5a, transcript variant X1
baculoviral IAP repeat-containing protein 5a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
threonine aldolase 1, transcript variant X1
threonine aldolase 1, transcript variant X2
threonine aldolase 1, transcript variant X3
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial, transcript variant X4
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial, transcript variant X5
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial, 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 5 samples with support for all annotated introns
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial, transcript variant X2
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial, transcript variant X1
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial isoform X1
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial isoform X2
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial isoform X4
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin specific peptidase 36, transcript variant X2
ubiquitin specific peptidase 36, transcript variant X1
ubiquitin specific peptidase 36, transcript variant X4
ubiquitin specific peptidase 36, transcript variant X3
ubiquitin specific peptidase 36, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 36 isoform X2
ubiquitin carboxyl-terminal hydrolase 36 isoform X1
ubiquitin carboxyl-terminal hydrolase 36 isoform X3
soluble calcium-activated nucleotidase 1
component of oligomeric golgi complex 1, transcript variant X2
component of oligomeric golgi complex 1, transcript variant X1
conserved oligomeric Golgi complex subunit 1 isoform X1
conserved oligomeric Golgi complex subunit 1 isoform X2
component of oligomeric golgi complex 1, transcript variant X3
conserved oligomeric Golgi complex subunit 1 isoform X3
dual specificity mitogen-activated protein kinase kinase 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
potassium inwardly rectifying channel subfamily J member 16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
potassium inwardly rectifying channel subfamily J member 2a, transcript variant X2
potassium inwardly rectifying channel subfamily J member 2a, transcript variant X1
potassium inwardly rectifying channel subfamily J member 2a, transcript variant X3
potassium inwardly rectifying channel subfamily J member 2a, transcript variant X4
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00563
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 182 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 98% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 39, member 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
solute carrier family 39, member 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 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: 125 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase rnf213-alpha-like, transcript variant X1
E3 ubiquitin-protein ligase rnf213-alpha-like, transcript variant X2
E3 ubiquitin-protein ligase rnf213-alpha-like
transmembrane channel-like protein 7, transcript variant X1
transmembrane channel-like protein 7, transcript variant X2
transmembrane channel-like protein 7 isoform X1
transmembrane channel-like protein 7 isoform X2
uncharacterized LOC109939078, transcript variant X4
uncharacterized LOC109939078, transcript variant X2
uncharacterized LOC109939078, transcript variant X3
uncharacterized LOC109939078, transcript variant X1
uncharacterized LOC125485875, 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 4 samples with support for all annotated introns
uncharacterized LOC125485875, 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 8 samples with support for all annotated introns
uncharacterized LOC109939084, transcript variant X1
uncharacterized LOC109939084, transcript variant X2
uncharacterized protein LOC109939084 isoform X1
uncharacterized protein LOC109939084 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane channel-like 6b, transcript variant X1
transmembrane channel-like 6b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC109913422, transcript variant X1
uncharacterized protein LOC109913422 isoform X1
uncharacterized LOC109913422, transcript variant X2
uncharacterized protein LOC109913422 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphodiesterase 6G, cGMP-specific, rod, gamma, paralog b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma
NAD-dependent protein deacetylase sirtuin-7
fatty acid-binding protein 1, liver-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 18 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC109939087, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC109939087, transcript variant X2
WD repeat domain, phosphoinositide interacting 1, transcript variant X2
WD repeat domain, phosphoinositide interacting 1, transcript variant X5
WD repeat domain, phosphoinositide interacting 1, transcript variant X6
WD repeat domain, phosphoinositide interacting 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
WD repeat domain, phosphoinositide interacting 1, transcript variant X1
WD repeat domain, phosphoinositide interacting 1, transcript variant X3
WD repeat domain phosphoinositide-interacting protein 1 isoform X1
WD repeat domain phosphoinositide-interacting protein 1 isoform X2
WD repeat domain phosphoinositide-interacting protein 1 isoform X3
WD repeat domain phosphoinositide-interacting protein 1 isoform X5
WD repeat domain phosphoinositide-interacting protein 1 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 long SRA reads, 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
archaemetzincin-2, transcript variant X2
archaemetzincin-2, transcript variant X3
archaemetzincin-2, transcript variant X4
archaemetzincin-2, transcript variant X1
archaemetzincin-2, transcript variant X5
monocarboxylate transporter 7, transcript variant X1
monocarboxylate transporter 7, transcript variant X2
monocarboxylate transporter 7, transcript variant X3
monocarboxylate transporter 7 isoform X1
monocarboxylate transporter 7 isoform X2
monocarboxylate transporter 7 isoform X3
guanine nucleotide binding protein (G protein), alpha 13a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 86 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
guanine nucleotide-binding protein subunit alpha-13a
APC11 anaphase promoting complex subunit 11 homolog (yeast)
caspase recruitment domain-containing protein 14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
alpha glucosidase, transcript variant X1
alpha glucosidase, transcript variant X2
coiled-coil domain-containing protein 40
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 79% 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: coiled-coil domain-containing protein 40
chromobox homolog 8b, transcript variant X2
chromobox homolog 8b, transcript variant X1
chromobox homolog 4 (Pc class homolog, Drosophila)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
TBC1 domain family member 16-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TBC1 domain family member 16-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TBC1 domain family member 16-like, transcript variant X1
TBC1 domain family member 16-like, transcript variant X3
TBC1 domain family member 16-like, transcript variant X2
TBC1 domain family member 16-like isoform X1
TBC1 domain family member 16-like isoform X2
cAMP-dependent protein kinase type I-alpha regulatory subunit, transcript variant X2
cAMP-dependent protein kinase type I-alpha regulatory subunit, transcript variant X1
cAMP-dependent protein kinase type I-alpha regulatory subunit
platelet-derived growth factor subunit A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
platelet-derived growth factor subunit A-like, transcript variant X4
platelet-derived growth factor subunit A-like, transcript variant X2
platelet-derived growth factor subunit A-like isoform X1
platelet-derived growth factor subunit A-like isoform X4
platelet-derived growth factor subunit A-like isoform X2
platelet-derived growth factor subunit A-like, transcript variant X3
platelet-derived growth factor subunit A-like isoform X3
FAM20A golgi associated secretory pathway pseudokinase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
NPL4 homolog, ubiquitin recognition factor, transcript variant X1
NPL4 homolog, ubiquitin recognition factor, transcript variant X2
nuclear protein localization protein 4 homolog isoform X1
nuclear protein localization protein 4 homolog isoform X2
uncharacterized LOC125485855, transcript variant X4
uncharacterized LOC125485855, transcript variant X6
uncharacterized LOC125485855, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC125485855, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC125485855, transcript variant X5
uncharacterized protein LOC125485855 isoform X4
uncharacterized protein LOC125485855 isoform X6
uncharacterized protein LOC125485855 isoform X1
uncharacterized protein LOC125485855 isoform X2
uncharacterized protein LOC125485855 isoform X5
uncharacterized LOC125485855, transcript variant X10
uncharacterized LOC125485855, transcript variant X9
uncharacterized LOC125485855, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC125485855, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC125485855, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein LOC125485855 isoform X3
Fanconi anemia core complex-associated protein 100
fascin actin-bundling protein 2b, retinal
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
BAH domain and coiled-coil containing 1b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
BAH and coiled-coil domain-containing protein 1
uncharacterized LOC109910946, transcript variant X1
uncharacterized LOC109910946, transcript variant X2
putative sodium-coupled neutral amino acid transporter 10
NADH:ubiquinone oxidoreductase complex assembly factor 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 8
TEPSIN adaptor related protein complex 4 accessory protein, transcript variant X1
TEPSIN adaptor related protein complex 4 accessory protein, transcript variant X2
AP-4 complex accessory subunit Tepsin isoform X1
AP-4 complex accessory subunit Tepsin isoform X2
uncharacterized protein LOC100150256 homolog
uncharacterized si:dkey-21c1.4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized si:dkey-21c1.4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized si:dkey-21c1.4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized si:dkey-21c1.4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized si:dkey-21c1.4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein si:dkey-21c1.4 isoform X1
uncharacterized protein si:dkey-21c1.4 isoform X2
cleavage and polyadenylation specificity factor subunit 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
CDC42 effector protein (Rho GTPase binding) 4b, transcript variant X3
CDC42 effector protein (Rho GTPase binding) 4b, transcript variant X5
CDC42 effector protein (Rho GTPase binding) 4b, transcript variant X2
CDC42 effector protein (Rho GTPase binding) 4b, transcript variant X1
CDC42 effector protein (Rho GTPase binding) 4b, transcript variant X4
CDC42 effector protein (Rho GTPase binding) 4b, transcript variant X6
tweety family member 2, transcript variant X1
tweety family member 2, transcript variant X2
tweety family member 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
ATP-binding cassette, sub-family A (ABC1), member 5, transcript variant X4
ATP-binding cassette, sub-family A (ABC1), member 5, transcript variant X1
ATP-binding cassette, sub-family A (ABC1), member 5, transcript variant X3
ATP-binding cassette, sub-family A (ABC1), member 5, transcript variant X2
ATP-binding cassette sub-family A member 5 isoform X1
ATP-binding cassette sub-family A member 5 isoform X4
ATP-binding cassette sub-family A member 5 isoform X2
ATP-binding cassette sub-family A member 5 isoform X3
uncharacterized LOC109930940, transcript variant X3
uncharacterized LOC109930940, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC109930940, transcript variant X5
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
uncharacterized LOC109930940, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC109930940, transcript variant X1
leucine rich repeat containing 45, transcript variant X1
leucine-rich repeat-containing protein 45 isoform X1
leucine rich repeat containing 45, transcript variant X2
leucine-rich repeat-containing protein 45 isoform X2
ras-related C3 botulinum toxin substrate 3
RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
beta-1,3-N-acetylglucosaminyltransferase radical fringe isoform X2
beta-1,3-N-acetylglucosaminyltransferase radical fringe isoform X3
beta-1,3-N-acetylglucosaminyltransferase radical fringe isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
dihydrouridine synthase 1-like (S. cerevisiae)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 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: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: coiled-coil domain-containing protein 57
monocarboxylate transporter 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 50 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
monocarboxylate transporter 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 85 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cytosolic endo-beta-N-acetylglucosaminidase
RNA binding fox-1 homolog 3a, 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
RNA binding protein fox-1 homolog 3 isoform X2
RNA binding fox-1 homolog 3a, 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
RNA binding protein fox-1 homolog 3 isoform X1
RNA binding fox-1 homolog 3a, 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 2 samples with support for all annotated introns
RNA binding protein fox-1 homolog 3 isoform X3
ectonucleotide pyrophosphatase/phosphodiesterase family member 7
uncharacterized LOC109934247, transcript variant X1
uncharacterized LOC109934247, transcript variant X2
major facilitator superfamily domain containing 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64% coverage of the annotated genomic feature by RNAseq alignments
jumonji domain containing 6, arginine demethylase and lysine hydroxylase
bifunctional arginine demethylase and lysyl-hydroxylase JMJD6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 68% coverage of the annotated genomic feature by RNAseq alignments
trinucleotide repeat containing adaptor 6C1
trinucleotide repeat-containing gene 6C protein
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
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
uncharacterized LOC109924493, transcript variant X1
uncharacterized LOC109924493, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 long SRA reads, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
neuronal-specific septin-3-like isoform X7
neuronal-specific septin-3-like isoform X8
neuronal-specific septin-3-like isoform X3
neuronal-specific septin-3-like isoform X6
neuronal-specific septin-3-like isoform X2
neuronal-specific septin-3-like isoform X1
neuronal-specific septin-3-like isoform X5
programmed cell death 1 ligand 2-like, transcript variant X2
programmed cell death 1 ligand 2-like, transcript variant X1
programmed cell death 1 ligand 2-like isoform X1
programmed cell death 1 ligand 2-like isoform X2
programmed cell death 1 ligand 2-like, transcript variant X3
programmed cell death 1 ligand 2-like isoform X3
uncharacterized LOC109921572, transcript variant X8
uncharacterized LOC109921572, transcript variant X5
uncharacterized LOC109921572, transcript variant X7
uncharacterized LOC109921572, transcript variant X3
uncharacterized LOC109921572, transcript variant X2
uncharacterized protein LOC109921572 isoform X3
uncharacterized LOC109921572, transcript variant X6
uncharacterized LOC109921572, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized protein LOC109921572 isoform X4
uncharacterized protein LOC109921572 isoform X6
uncharacterized protein LOC109921572 isoform X5
uncharacterized protein LOC109921572 isoform X2
uncharacterized LOC109921572, 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 13 samples with support for all annotated introns
uncharacterized protein LOC109921572 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins
urotensin-2 receptor 2, transcript variant X1
urotensin-2 receptor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
hexosaminidase D-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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
hexosaminidase D-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
hexosaminidase D-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
hexosaminidase D-like, transcript variant X4
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 16 samples with support for all annotated introns
nuclear prelamin A recognition factor, transcript variant X4
nuclear prelamin A recognition factor, transcript variant X2
nuclear prelamin A recognition factor, transcript variant X1
nuclear prelamin A recognition factor, transcript variant X3
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cilia and flagella associated protein 52
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 14 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cilia- and flagella-associated protein 52
ubiquitin specific peptidase 43a, transcript variant X1
ubiquitin specific peptidase 43a, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 43a isoform X1
ubiquitin carboxyl-terminal hydrolase 43a isoform X2
phosphoinositide-3-kinase, regulatory subunit 5, transcript variant X1
phosphoinositide-3-kinase, regulatory subunit 5, transcript variant X2
phosphoinositide 3-kinase regulatory subunit 5 isoform X1
phosphoinositide 3-kinase regulatory subunit 5 isoform X2
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X2
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X1
phosphoinositide 3-kinase regulatory subunit 6, transcript variant X3
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
phosphoinositide 3-kinase regulatory subunit 6
radical S-adenosyl methionine domain containing 1, transcript variant X1
radical S-adenosyl methionine domain containing 1, transcript variant X3
radical S-adenosyl methionine domain containing 1, transcript variant X2
radical S-adenosyl methionine domain-containing protein 1, mitochondrial isoform X3
radical S-adenosyl methionine domain-containing protein 1, mitochondrial isoform X2
radical S-adenosyl methionine domain-containing protein 1, mitochondrial isoform X1
medium-chain acyl-CoA ligase ACSF2, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine-rich repeat-containing protein 59
essential meiotic structure-specific endonuclease 1, transcript variant X1
essential meiotic structure-specific endonuclease 1, transcript variant X2
glutamate receptor ionotropic, NMDA 2C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins
transmembrane protein 104, transcript variant X1
transmembrane protein 104, transcript variant X2
probable ATP-dependent RNA helicase DDX41, transcript variant X1
probable ATP-dependent RNA helicase DDX41, transcript variant X2
probable ATP-dependent RNA helicase DDX41 isoform X1
probable ATP-dependent RNA helicase DDX41 isoform X2
novel acetylcholine receptor chaperone, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 14 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
novel acetylcholine receptor chaperone, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 14 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
novel acetylcholine receptor chaperone, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 long SRA reads, 15 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF01268
transmembrane protein 260, transcript variant X4
transmembrane protein 260, transcript variant X3
transmembrane protein 260, transcript variant X1
transmembrane protein 260, transcript variant X2
LLGL scribble cell polarity complex component 2, transcript variant X2
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 3 samples with support for all annotated introns
LLGL scribble cell polarity complex component 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
LLGL scribble cell polarity complex component 2, 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 14 samples with support for all annotated introns
LLGL scribble cell polarity complex component 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
LLGL scribble cell polarity complex component 2, transcript variant X3
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 11 samples with support for all annotated introns
LLGL scribble cell polarity complex component 2 isoform X1
LLGL scribble cell polarity complex component 2 isoform X2
tripartite motif-containing protein 16-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
Jupiter microtubule associated homolog 1, transcript variant X2
Jupiter microtubule associated homolog 1, transcript variant X1
jupiter microtubule associated homolog 1 isoform X2
jupiter microtubule associated homolog 1 isoform X1
Jupiter microtubule associated homolog 1, 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 20 samples with support for all annotated introns
jupiter microtubule associated homolog 2 isoform X3
nuclear pore complex protein Nup85 isoform X5
nuclear pore complex protein Nup85 isoform X1
nuclear pore complex protein Nup85 isoform X2
nuclear pore complex protein Nup85 isoform X3
nuclear pore complex protein Nup85 isoform X4
golgi associated, gamma adaptin ear containing, ARF binding protein 3b
ADP-ribosylation factor-binding protein GGA3
Na(+)/H(+) exchange regulatory cofactor NHE-RF1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
mycbp associated protein, transcript variant X2
mycbp associated protein, transcript variant X1
mycbp associated protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
major facilitator superfamily domain containing 6-like, transcript variant X1
major facilitator superfamily domain containing 6-like, transcript variant X2
major facilitator superfamily domain containing 6-like, transcript variant X3
major facilitator superfamily domain-containing protein 6-like
uncharacterized protein LOC100151763 homolog, transcript variant X1
bMERB domain-containing protein 1 isoform X1
uncharacterized protein LOC100151763 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
bMERB domain-containing protein 1 isoform X2
nuclear distribution protein nudE-like 1, transcript variant X1
nuclear distribution protein nudE-like 1, transcript variant X2
nuclear distribution protein nudE-like 1 isoform X1
nuclear distribution protein nudE-like 1 isoform X2
RING finger protein 222, transcript variant X2
RING finger protein 222, transcript variant X1
testis-expressed protein 47, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
testis-expressed protein 47, transcript variant X2
testis-expressed protein 47, transcript variant X3
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
transfer RNA glycine (anticodon CCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
F-box and WD repeat domain containing 10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
F-box and WD repeat domain containing protein 10B
trans-golgi network vesicle protein 23 homolog B (S. cerevisiae)
Golgi apparatus membrane protein TVP23 homolog B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 3B1-like
protoheme IX farnesyltransferase, mitochondrial
heparan sulfate glucosamine 3-O-sulfotransferase 3A1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 13 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif-containing protein 16-like protein
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 5 samples with support for all annotated introns
meteorin like, glial cell differentiation regulator a
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1, transcript variant X1
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1, transcript variant X4
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1 isoform X1
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1 isoform X4
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1, transcript variant X2
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1 isoform X2
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1, transcript variant X3
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1, transcript variant X5
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1 isoform X3
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC125485877, transcript variant X1
uncharacterized LOC125485877, transcript variant X2
fructosamine 3 kinase related protein, transcript variant X3
fructosamine 3 kinase related protein, transcript variant X2
fructosamine 3 kinase related protein, transcript variant X1
fructosamine 3 kinase related protein, transcript variant X4
fructosamine 3 kinase related protein, transcript variant X5
ras-related protein Rab-40B, transcript variant X2
ras-related protein Rab-40B, transcript variant X1
WD repeat domain 45B, transcript variant X5
WD repeat domain 45B, transcript variant X6
WD repeat domain 45B, transcript variant X1
WD repeat domain 45B, transcript variant X2
WD repeat domain phosphoinositide-interacting protein 3 isoform X5
WD repeat domain phosphoinositide-interacting protein 3 isoform X1
WD repeat domain phosphoinositide-interacting protein 3 isoform X2
WD repeat domain 45B, transcript variant X4
WD repeat domain 45B, transcript variant X3
WD repeat domain phosphoinositide-interacting protein 3 isoform X3
WD repeat domain phosphoinositide-interacting protein 3 isoform X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 long SRA reads, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 21 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC125485859, transcript variant X2
uncharacterized LOC125485859, transcript variant X1
transmembrane protein 220, transcript variant X1
transmembrane protein 220, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
manganese-dependent ADP-ribose/CDP-alcohol diphosphatase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
manganese-dependent ADP-ribose/CDP-alcohol diphosphatase-like, transcript variant X1
manganese-dependent ADP-ribose/CDP-alcohol diphosphatase-like
manganese-dependent ADP-ribose/CDP-alcohol diphosphatase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
mitogen-activated protein kinase kinase 4a
dual specificity mitogen-activated protein kinase kinase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 512 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins
myosin heavy chain, skeletal muscle, adult
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 697 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 578 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: 551 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
growth arrest-specific 7b, transcript variant X1
growth arrest-specific protein 7 isoform X1
growth arrest-specific 7b, transcript variant X2
growth arrest-specific 7b, transcript variant X3
growth arrest-specific protein 7 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
glucagon-like peptide 2 receptor, transcript variant X2
glucagon-like peptide 2 receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glucagon-like peptide 2 receptor isoform X2
glucagon-like peptide 2 receptor isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
protein NATD1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
protein NATD1-like, transcript variant X2
dehydrogenase/reductase SDR family member 7C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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: 3 long SRA reads, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
COP1-interactive protein 1-like, transcript variant X3
COP1-interactive protein 1-like, transcript variant X1
COP1-interactive protein 1-like, transcript variant X4
COP1-interactive protein 1-like, transcript variant X2
COP1-interactive protein 1-like isoform X1
COP1-interactive protein 1-like isoform X4
COP1-interactive protein 1-like isoform X2
COP1-interactive protein 1-like isoform X3
uncharacterized LOC125485833, transcript variant X3
uncharacterized LOC125485833, transcript variant X2
uncharacterized LOC125485833, transcript variant X1
uncharacterized LOC125485833, transcript variant X4
NADPH:adrenodoxin oxidoreductase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent T-type calcium channel subunit alpha-1G-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
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
TSEN54 tRNA splicing endonuclease subunit, transcript variant X2
TSEN54 tRNA splicing endonuclease subunit, transcript variant X1
tRNA-splicing endonuclease subunit Sen54 isoform X1
tRNA-splicing endonuclease subunit Sen54 isoform X2
melanin-concentrating hormone receptor 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: melanin-concentrating hormone receptor 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane protein 94, transcript variant X1
transmembrane protein 94, transcript variant X2
transmembrane protein 94, 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 5 samples with support for all annotated introns
transmembrane protein 94, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protein 94, 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 2 samples with support for all annotated introns
transmembrane protein 94, transcript variant X6
transient receptor potential cation channel subfamily V member 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
transient receptor potential cation channel subfamily V member 6-like, transcript variant X1
transient receptor potential cation channel subfamily V member 6-like, transcript variant X4
transient receptor potential cation channel subfamily V member 6-like, transcript variant X5
transient receptor potential cation channel subfamily V member 6-like, transcript variant X3
transient receptor potential cation channel subfamily V member 6-like, transcript variant X6
transient receptor potential cation channel subfamily V member 6-like, transcript variant X2
transient receptor potential cation channel subfamily V member 6-like isoform X1
transient receptor potential cation channel subfamily V member 6-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase SBK1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin/ISG15 ligase TRIM25-like, transcript variant X2
E3 ubiquitin/ISG15 ligase TRIM25-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E3 ubiquitin/ISG15 ligase TRIM25-like isoform X2
E3 ubiquitin/ISG15 ligase TRIM25-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif-containing protein 65-like
39S ribosomal protein L38, mitochondrial
fas-binding factor 1 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
fas-binding factor 1 homolog, transcript variant X1
fas-binding factor 1 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 long SRA reads, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
fas-binding factor 1 homolog, transcript variant X4
fas-binding factor 1 homolog, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 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
fas-binding factor 1 homolog, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
phosphatidylinositol-4,5-bisphosphate 3-kinase, catalytic subunit gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit gamma isoform
acyl-CoA oxidase 1, palmitoyl, transcript variant X1
acyl-CoA oxidase 1, palmitoyl, transcript variant X3
acyl-CoA oxidase 1, palmitoyl, transcript variant X2
acyl-CoA oxidase 1, palmitoyl, transcript variant X5
acyl-CoA oxidase 1, palmitoyl, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
peroxisomal acyl-coenzyme A oxidase 1 isoform X1
peroxisomal acyl-coenzyme A oxidase 1 isoform X2
peroxisomal acyl-coenzyme A oxidase 1 isoform X3
peroxisomal acyl-coenzyme A oxidase 1 isoform X4
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
signal recognition particle subunit SRP68
N-acetyltransferase 9 (GCN5-related, putative), transcript variant X1
N-acetyltransferase 9 (GCN5-related, putative), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
N-acetyltransferase 9 (GCN5-related, putative), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
zinc finger protein 239-like, transcript variant X2
zinc finger protein 239-like, transcript variant X1
zinc finger protein 239-like, transcript variant X3
baculoviral IAP repeat-containing protein 7-B-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
signal recognition particle subunit SRP68-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 77% coverage of the annotated genomic feature by RNAseq alignments
proton channel OTOP3-like, transcript variant X2
proton channel OTOP3-like, transcript variant X1
proton channel OTOP3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cerebellar degeneration-related protein 2-like, transcript variant X1
cerebellar degeneration-related protein 2-like, transcript variant X2
cerebellar degeneration-related protein 2-like isoform X1
cerebellar degeneration-related protein 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized si:ch211-250n8.1, transcript variant X1
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 3 samples with support for all annotated introns
uncharacterized si:ch211-250n8.1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized protein si:ch211-250n8.1 isoform X2
uncharacterized protein si:ch211-250n8.1 isoform X1
uncharacterized LOC109922632, transcript variant X3
uncharacterized LOC109922632, transcript variant X2
uncharacterized LOC109922632, transcript variant X1
transfer RNA leucine (anticodon CAG); 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: 1 Protein, and 20% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 25 member 19, transcript variant X1
mitochondrial thiamine pyrophosphate carrier isoform X1
solute carrier family 25 member 19, transcript variant X2
mitochondrial thiamine pyrophosphate carrier isoform X2
ras-related protein Rab-37, transcript variant X3
ras-related protein Rab-37, transcript variant X2
ras-related protein Rab-37, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 2% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 long SRA reads, 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 95% coverage of the annotated genomic feature by RNAseq alignments
ADP-ribosylhydrolase ARH1, transcript variant X2
ADP-ribosylhydrolase ARH1, transcript variant X1
ADP-ribosylhydrolase ARH1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 99% 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 long SRA reads, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
gastrula zinc finger protein XlCGF17.1-like