Rhincodon typus isolate 14 chromosome 45, 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\nCM038842.1.\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: 97% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
probable E3 ubiquitin-protein ligase ARI8, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
probable E3 ubiquitin-protein ligase ARI8 isoform X1
probable E3 ubiquitin-protein ligase ARI8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized protein LOC109922980 isoform X2
homeobox protein HMX3-like, transcript variant X1
homeobox protein HMX3-like, transcript variant X2
homeobox protein HMX3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transcription factor HES-7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcription factor HES-7-like, transcript variant X2
ceramide-1-phosphate transfer protein, transcript variant X1
ceramide-1-phosphate transfer protein, transcript variant X3
ceramide-1-phosphate transfer protein, transcript variant X2
procollagen C-endopeptidase enhancer 1-like
polyunsaturated fatty acid lipoxygenase ALOX15B-like
calmodulin-binding transcription activator 1-like
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
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
leucine-rich repeats and calponin homology (CH) domain containing 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 25 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 4, transcript variant X6
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
leucine-rich repeats and calponin homology (CH) domain containing 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
leucine-rich repeats and calponin homology (CH) domain containing 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
leucine-rich repeat and calponin homology domain-containing protein 4 isoform X1
leucine-rich repeat and calponin homology domain-containing protein 4 isoform X4
leucine-rich repeat and calponin homology domain-containing protein 4 isoform X2
uncharacterized LOC125487813, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF217-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 12 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF217-like isoform X1
E3 ubiquitin-protein ligase RNF217-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF217-like isoform X2
uncharacterized LOC125487813, transcript variant X1
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
stress-associated endoplasmic reticulum protein 2
serrate RNA effector molecule homolog (Arabidopsis)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
acyl-CoA dehydrogenase very long chain, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
acyl-CoA dehydrogenase very long chain, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
very long-chain specific acyl-CoA dehydrogenase, mitochondrial
uncharacterized protein LOC794943 homolog
ATPase Na+/K+ transporting subunit beta 2b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
sodium/potassium-transporting ATPase subunit beta-2b
uncharacterized LOC109925694, transcript variant X2
uncharacterized LOC109925694, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
DNA-directed RNA polymerase II subunit RPB1
zona pellucida sperm-binding protein 3-like
fragile X mental retardation syndrome-related protein 1 homolog B-like, transcript variant X2
fragile X mental retardation syndrome-related protein 1 homolog B-like, transcript variant X1
fragile X mental retardation syndrome-related protein 1 homolog A-like isoform X2
fragile X mental retardation syndrome-related protein 1 homolog A-like isoform X1
fragile X mental retardation syndrome-related protein 1 homolog B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 124 long SRA reads, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
fragile X mental retardation syndrome-related protein 1 homolog B-like isoform X3
segment polarity protein dishevelled homolog DVL-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC109924736, 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 2 samples with support for all annotated introns
uncharacterized LOC109924736, transcript variant X1
uncharacterized protein LOC109924736 isoform X2
uncharacterized protein LOC109924736 isoform X1
gamma-aminobutyric acid receptor-associated protein
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 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
lipoma-preferred partner homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
lipoma-preferred partner homolog, transcript variant X5
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 3 samples with support for all annotated introns
lipoma-preferred partner homolog, transcript variant X1
lipoma-preferred partner homolog, transcript variant X4
lipoma-preferred partner homolog, transcript variant X3
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
lipoma-preferred partner homolog, transcript variant X6
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 15 samples with support for all annotated introns
lipoma-preferred partner homolog isoform X3
lipoma-preferred partner homolog isoform X1
lipoma-preferred partner homolog isoform X2
lipoma-preferred partner homolog isoform X4
B-cell lymphoma 6 protein homolog, transcript variant X2
B-cell lymphoma 6 protein homolog, transcript variant X3
B-cell lymphoma 6 protein homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like
solute carrier family 16 member 13, transcript variant X5
solute carrier family 16 member 13, transcript variant X1
solute carrier family 16 member 13, transcript variant X3
solute carrier family 16 member 13, transcript variant X4
solute carrier family 16 member 13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 8 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
zona pellucida sperm-binding protein 3-like, transcript variant X2
zona pellucida sperm-binding protein 3-like, transcript variant X1
zona pellucida sperm-binding protein 3-like isoform X1
zona pellucida sperm-binding protein 3-like isoform X2
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: zinc finger HIT domain-containing protein 1
uncharacterized LOC109921778, transcript variant X1
uncharacterized LOC109921778, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
hydroxysteroid (20-beta) dehydrogenase 2
eukaryotic translation initiation factor 4E type 2-like
cholinergic receptor, nicotinic, epsilon
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: acetylcholine receptor subunit epsilon
sperm-egg fusion protein TMEM95, transcript variant X2
sperm-egg fusion protein TMEM95, transcript variant X1
sperm-egg fusion protein TMEM95, transcript variant X4
sperm-egg fusion protein TMEM95, transcript variant X3
sperm-egg fusion protein TMEM95 isoform X4
sperm-egg fusion protein TMEM95 isoform X3
sperm-egg fusion protein TMEM95 isoform X2
sperm-egg fusion protein TMEM95 isoform X1
RPA-related protein RADX-like, transcript variant X1
RPA-related protein RADX-like, transcript variant X2
RPA-related protein RADX-like, transcript variant X3
RPA-related protein RADX-like isoform X1
RPA-related protein RADX-like isoform X2
RPA-related protein RADX-like isoform X3
P2R1A-PPP2R2A-interacting phosphatase regulator 1-like, transcript variant X2
P2R1A-PPP2R2A-interacting phosphatase regulator 1-like, transcript variant X1
P2R1A-PPP2R2A-interacting phosphatase regulator 1-like isoform X2
P2R1A-PPP2R2A-interacting phosphatase regulator 1-like isoform X1
P2Y purinoceptor 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
P2Y purinoceptor 3, transcript variant X1
P2Y purinoceptor 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
WD repeat containing, antisense to TP53, transcript variant X2
WD repeat containing, antisense to TP53, transcript variant X3
WD repeat containing, antisense to TP53, transcript variant X1
telomerase Cajal body protein 1 isoform X2
telomerase Cajal body protein 1 isoform X1
transmembrane protein 217, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protein 217, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane protein 217, transcript variant X3
transmembrane protein 217, transcript variant X4
transmembrane protein 217, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane protein 217, transcript variant X6
tumor necrosis factor ligand superfamily member 13-like, transcript variant X2
tumor necrosis factor ligand superfamily member 13-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC109937884 isoform X2
tumor necrosis factor ligand superfamily member 13-like isoform X1
uncharacterized si:dkey-19b23.8, transcript variant X4
uncharacterized si:dkey-19b23.8, transcript variant X3
uncharacterized si:dkey-19b23.8, transcript variant X1
uncharacterized si:dkey-19b23.8, transcript variant X2
uncharacterized si:dkey-19b23.7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 long SRA reads, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized si:dkey-19b23.7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
trafficking protein particle complex subunit 1, transcript variant X1
trafficking protein particle complex subunit 1, transcript variant X2
trafficking protein particle complex subunit 1
centrobin, centrosomal BRCA2 interacting protein
retinal guanylyl cyclase 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
retinal guanylyl cyclase 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 long SRA reads, 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
retinal guanylyl cyclase 2-like isoform X1
retinal guanylyl cyclase 2-like isoform X2
galactose-3-O-sulfotransferase 2-like, transcript variant X3
galactose-3-O-sulfotransferase 2-like, transcript variant X2
galactose-3-O-sulfotransferase 2-like, transcript variant X4
galactose-3-O-sulfotransferase 2-like, transcript variant X1
galactose-3-O-sulfotransferase 2-like, transcript variant X5
galactose-3-O-sulfotransferase 2-like isoform X1
galactose-3-O-sulfotransferase 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
trafficking protein particle complex subunit 14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
late endosomal/lysosomal adaptor, MAPK and MTOR activator 4
interferon-induced very large GTPase 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 long SRA reads, 19 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: interferon-induced very large GTPase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
transcription initiation factor TFIID subunit 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 long SRA reads, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
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: 89% coverage of the annotated genomic feature by RNAseq alignments
arrestin red cell, transcript variant X4
arrestin red cell, transcript variant X3
arrestin red cell, transcript variant X1
arrestin red cell, transcript variant X2
arrestin red cell, transcript variant X5
mediator complex subunit 11, 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 1 sample with support for all annotated introns
mediator complex subunit 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
mediator complex subunit 11, 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 2 samples with support for all annotated introns
mediator complex subunit 11, transcript variant X4
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 19 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 11 isoform X2
mediator of RNA polymerase II transcription subunit 11 isoform X3
mediator of RNA polymerase II transcription subunit 11 isoform X1
mediator of RNA polymerase II transcription subunit 11 isoform X4
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
baculoviral IAP repeat-containing protein 1-like, transcript variant X1
baculoviral IAP repeat-containing protein 1-like, transcript variant X3
baculoviral IAP repeat-containing protein 1-like, transcript variant X2
baculoviral IAP repeat-containing protein 1-like isoform X1
baculoviral IAP repeat-containing protein 1-like isoform X3
baculoviral IAP repeat-containing protein 1-like isoform X2
uncharacterized LOC125487818, transcript variant X2
uncharacterized LOC125487818, transcript variant X1
uncharacterized protein LOC125487818 isoform X2
uncharacterized protein LOC125487818 isoform X1
leukocyte cell-derived chemotaxin-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
paired immunoglobulin-like type 2 receptor alpha
paired immunoglobin like type 2 receptor beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 4 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
paired immunoglobulin-like type 2 receptor beta-2
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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: pentraxin fusion protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
proline, glutamate and leucine rich protein 1
proline-, glutamic acid- and leucine-rich protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 long SRA reads, 19 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
AP-1 complex subunit sigma-1A, transcript variant X2
AP-1 complex subunit sigma-1A isoform X2
AP-1 complex subunit sigma-1A, transcript variant X1
AP-1 complex subunit sigma-1A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
histidine N-acetyltransferase-like, transcript variant X2
histidine N-acetyltransferase-like, transcript variant X1
histidine N-acetyltransferase-like, transcript variant X3
leucine-rich repeat-containing protein 55, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine-rich repeat-containing protein 55, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine-rich repeat-containing protein 55
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: G-protein coupled receptor 83-like
chromatin complexes subunit BAP18, transcript variant X3
chromatin complexes subunit BAP18, transcript variant X1
chromatin complexes subunit BAP18, transcript variant X4
chromatin complexes subunit BAP18, transcript variant X2
chromatin complexes subunit BAP18 isoform X4
chromatin complexes subunit BAP18 isoform X2
chromatin complexes subunit BAP18 isoform X3
chromatin complexes subunit BAP18 isoform X1
polyunsaturated fatty acid 5-lipoxygenase-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: polyunsaturated fatty acid 5-lipoxygenase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC109910527, transcript variant X2
uncharacterized LOC109910527, transcript variant X1
UFM1-specific peptidase 1 (non-functional)
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: chloride channel protein ClC-Kb-like
POP7 homolog, ribonuclease P/MRP subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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 9 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 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, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 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: 2 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: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 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: 2 long SRA reads, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC109910522 isoform X9
uncharacterized protein LOC109910522 isoform X1
uncharacterized protein LOC109910522 isoform X6
uncharacterized protein LOC109910522 isoform X2
uncharacterized protein LOC109910522 isoform X5
uncharacterized protein LOC109910522 isoform X10
uncharacterized protein LOC109910522 isoform X11
uncharacterized protein LOC109910522 isoform X8
uncharacterized protein LOC109910522 isoform X13
uncharacterized protein LOC109910522 isoform X14
uncharacterized protein LOC109910522 isoform X15
uncharacterized protein LOC109910522 isoform X3
uncharacterized protein LOC109910522 isoform X4
uncharacterized protein LOC109910522 isoform X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF217-like, transcript variant X3
E3 ubiquitin-protein ligase RNF217-like, transcript variant X4
E3 ubiquitin-protein ligase RNF217-like isoform X3
uncharacterized protein DDB_G0292642-like isoform X1
mitochondrial 2-oxoglutarate/malate carrier protein
ephrin type-B receptor 1-like, transcript variant X1
ephrin type-B receptor 3-like isoform X1
ephrin type-B receptor 1-like, transcript variant X2
ephrin type-B receptor 1-like, transcript variant X3
ephrin type-B receptor 1-like isoform X2
ephrin type-B receptor 3-like isoform X3
actin-like protein 6B, 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 82% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
actin-like protein 6B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-2
multifunctional procollagen lysine hydroxylase and glycosyltransferase LH3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
protein O-fucosyltransferase 1, transcript variant X4
protein O-fucosyltransferase 1, transcript variant X1
protein O-fucosyltransferase 1, transcript variant X3
protein O-fucosyltransferase 1, transcript variant X2
GDP-fucose protein O-fucosyltransferase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
nucleotidyltransferase MB21D2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nucleotidyltransferase MB21D2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
nucleotidyltransferase MB21D2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
nucleotidyltransferase MB21D2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
nucleotidyltransferase MB21D2-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
nucleotidyltransferase MB21D2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
nucleotidyltransferase MB21D2-like, transcript variant X8
nucleotidyltransferase MB21D2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
LOW QUALITY PROTEIN: polyamine-transporting ATPase 13A3-like
protein phosphatase 1, regulatory subunit 35, transcript variant X2
protein phosphatase 1, regulatory subunit 35, transcript variant X6
protein phosphatase 1, regulatory subunit 35, transcript variant X1
protein phosphatase 1, regulatory subunit 35, transcript variant X3
protein phosphatase 1, regulatory subunit 35, transcript variant X5
protein phosphatase 1, regulatory subunit 35, transcript variant X4
protein phosphatase 1 regulatory subunit 35 isoform X1
protein phosphatase 1 regulatory subunit 35 isoform X2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 28 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform-like
uncharacterized protein LOC777626 homolog, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC777626 homolog, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized protein LOC777626 homolog, 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 4 samples with support for all annotated introns
uncharacterized protein LOC777626 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein LOC777626 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized protein LOC777626 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TSC22 domain family protein 4 isoform X2
TSC22 domain family protein 4 isoform X3
TSC22 domain family protein 4 isoform X5
TSC22 domain family protein 4 isoform X6
TSC22 domain family protein 4 isoform X1
TSC22 domain family protein 4 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
minichromosome maintenance complex component 7, transcript variant X1
minichromosome maintenance complex component 7, transcript variant X2
DNA replication licensing factor MCM7 isoform X1
DNA replication licensing factor MCM7 isoform X2
adaptor related protein complex 4 subunit mu 1, transcript variant X1
adaptor related protein complex 4 subunit mu 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 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, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
solute carrier family 2, facilitated glucose transporter member 4-like
lysophosphatidic acid receptor 6-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
lysophosphatidic acid receptor 6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lysophosphatidic acid receptor 6-like, transcript variant X4
lysophosphatidic acid receptor 6-like, transcript variant X5
lysophosphatidic acid receptor 6-like, transcript variant X3
lysophosphatidic acid receptor 6-like isoform X1
lysophosphatidic acid receptor 6-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
small nuclear RNA activating complex, polypeptide 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 long SRA reads, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
snRNA-activating protein complex subunit 2
mitogen-activated protein kinase kinase kinase kinase 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 80% coverage of the annotated genomic feature by RNAseq alignments
Y-box-binding protein 2-A-like, transcript variant X2
Y-box-binding protein 2-A-like, transcript variant X1
Y-box-binding protein 2-A-like isoform X2
Y-box-binding protein 2-A-like isoform X1
uncharacterized LOC125487825, transcript variant X1
uncharacterized LOC125487825, transcript variant X2
eukaryotic translation initiation factor 5A-1-like, transcript variant X3
eukaryotic translation initiation factor 5A-1-like, transcript variant X1
eukaryotic translation initiation factor 5A-1-like, transcript variant X2
eukaryotic translation initiation factor 5A-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 78% 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, 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
pentraxin-related protein PTX3-like, transcript variant X4
pentraxin-related protein PTX3-like, transcript variant X1
pentraxin-related protein PTX3-like isoform X1
pentraxin-related protein PTX3-like, transcript variant X5
pentraxin-related protein PTX3-like, transcript variant X3
pentraxin-related protein PTX3-like, transcript variant X2
pentraxin-related protein PTX3-like isoform X2
N-alpha-acetyltransferase 38, NatC auxiliary subunit, transcript variant X4
N-alpha-acetyltransferase 38, NatC auxiliary subunit, transcript variant X2
N-alpha-acetyltransferase 38, NatC auxiliary subunit, transcript variant X5
N-alpha-acetyltransferase 38, NatC auxiliary subunit, transcript variant X1
N-alpha-acetyltransferase 38, NatC auxiliary subunit, transcript variant X3
N-alpha-acetyltransferase 38, NatC auxiliary subunit isoform X2
N-alpha-acetyltransferase 38, NatC auxiliary subunit isoform X3
N-alpha-acetyltransferase 38, NatC auxiliary subunit isoform X1
N-alpha-acetyltransferase 38, NatC auxiliary subunit isoform X4
cytochrome b5 domain-containing protein 1
chromodomain-helicase-DNA-binding protein 3-like
protein mono-ADP-ribosyltransferase TIPARP-like
chromodomain-helicase-DNA-binding protein 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59% coverage of the annotated genomic feature by RNAseq alignments
voltage-gated potassium channel subunit beta-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
RAN guanine nucleotide release factor, transcript variant X1
RAN guanine nucleotide release factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
arf-GAP domain and FG repeat-containing protein 1-like, transcript variant X2
arf-GAP domain and FG repeat-containing protein 1-like, transcript variant X5
arf-GAP domain and FG repeat-containing protein 1-like, transcript variant X7
arf-GAP domain and FG repeat-containing protein 1-like, transcript variant X8
arf-GAP domain and FG repeat-containing protein 1-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 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
arf-GAP domain and FG repeat-containing protein 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
arf-GAP domain and FG repeat-containing protein 1-like, transcript variant X6
arf-GAP domain and FG repeat-containing protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
arf-GAP domain and FG repeat-containing protein 1-like isoform X2
arf-GAP domain and FG repeat-containing protein 1-like isoform X5
arf-GAP domain and FG repeat-containing protein 2-like isoform X7
arf-GAP domain and FG repeat-containing protein 1-like isoform X8
arf-GAP domain and FG repeat-containing protein 1-like isoform X1
arf-GAP domain and FG repeat-containing protein 1-like isoform X4
arf-GAP domain and FG repeat-containing protein 2-like isoform X6
arf-GAP domain and FG repeat-containing protein 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 long SRA read, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 long SRA reads, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1 isoform X3
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1 isoform X2
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1 isoform X1
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1 isoform X4
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1, transcript variant X6
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
neuronal tyrosine-phosphorylated phosphoinositide-3-kinase adapter 1, transcript variant X5
neuroligin-1-like, transcript variant X1
neuroligin-1-like, transcript variant X2
neuroligin-1-like, transcript variant X3
neuroligin-1-like, transcript variant X4
phospholipase D2-like, transcript variant X1
phospholipase D2-like, transcript variant X4
phospholipase D2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phospholipase D2-like, transcript variant X3
phospholipase D2-like, transcript variant X2