Chiloscyllium plagiosum isolate BGI_BamShark_2017 chromosome 40, ASM401019v2, whole genome shotgun sequence.
Chiloscyllium plagiosum (whitespotted bambooshark)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Chondrichthyes; Elasmobranchii; Galeomorphii; Galeoidea; Orectolobiformes; Hemiscylliidae; Chiloscyllium.
REFSEQ INFORMATION: The reference sequence is identical to\nCM012995.1.\nAssembly name: ASM401019v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the BGI on 2019/01/10. The\noriginal whole-genome shotgun project has the accession\nQPFF00000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: BGI\nAssembly Method :: platanus v. 1.2.4; 3ddna v. 170123\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 280.0x\nSequencing Technology :: BGIseq-500\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Chiloscyllium plagiosum Annotation\n Release 100\nAnnotation Version :: 100\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.
probable E3 ubiquitin-protein ligase HERC1
COORDINATES: polyA evidence [ECO:0006239]
F-box and leucine-rich repeat protein 22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
carbonic anhydrase XII, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
carbonic anhydrase XII, transcript variant X3
carbonic anhydrase XII, transcript variant X4
carbonic anhydrase XII, transcript variant X2
death-associated protein kinase 2b, 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 5 samples with support for all annotated introns
death-associated protein kinase 2 isoform X2
death-associated protein kinase 2b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
death-associated protein kinase 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TBC1 domain family, member 2B, transcript variant X1
TBC1 domain family, member 2B, transcript variant X4
TBC1 domain family, member 2B, 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
TBC1 domain family, member 2B, 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
calcium and integrin binding family member 2, 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 4 samples with support for all annotated introns
calcium and integrin binding family member 2, 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
calcium and integrin-binding family member 2 isoform X2
calcium and integrin-binding family member 2 isoform X1
leucine rich repeat containing 61, 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 14 samples with support for all annotated introns
leucine rich repeat containing 61, transcript variant X4
leucine rich repeat containing 61, transcript variant X1
leucine rich repeat containing 61, transcript variant X5
leucine rich repeat containing 61, transcript variant X2
leucine-rich repeat-containing protein 61 isoform X1
leucine-rich repeat-containing protein 61 isoform X4
leucine-rich repeat-containing protein 61 isoform X5
leucine-rich repeat-containing protein 61 isoform X3
leucine-rich repeat-containing protein 61 isoform X2
isocitrate dehydrogenase (NAD(+)) 3 catalytic subunit alpha
isocitrate dehydrogenase [NAD] subunit alpha, mitochondrial
WD repeat domain 61, transcript variant X2
WD repeat domain 61, transcript variant X1
cellular retinoic acid binding protein 1a, transcript variant X2
cellular retinoic acid binding protein 1a, transcript variant X1
cellular retinoic acid-binding protein 1a isoform X1
cellular retinoic acid-binding protein 1a isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
iron-responsive element binding protein 2
iron-responsive element-binding protein 2
hydroxylysine kinase-like, 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 6 samples with support for all annotated introns
hydroxylysine kinase-like, transcript variant X6
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
hydroxylysine kinase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
hydroxylysine kinase-like, transcript variant X4
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 4 samples with support for all annotated introns
hydroxylysine kinase-like, transcript variant X5
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
hydroxylysine kinase-like, 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
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 4 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, 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 2 samples with support for all annotated introns
proteasome 20S subunit alpha 4, transcript variant X1
proteasome 20S subunit alpha 4, transcript variant X4
proteasome 20S subunit alpha 4, transcript variant X2
proteasome 20S subunit alpha 4, transcript variant X3
proteasome 20S subunit alpha 4, transcript variant X6
proteasome 20S subunit alpha 4, transcript variant X5
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 11 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00377
deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial-like, transcript variant X1
deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial-like, transcript variant X2
deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial-like, transcript variant X3
deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial-like isoform X1
deoxyuridine 5'-triphosphate nucleotidohydrolase-like isoform X2
deoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial-like isoform X3
solute carrier family 12 member 1, transcript variant X2
solute carrier family 12 member 1, transcript variant X1
solute carrier family 12 member 1 isoform X2
solute carrier family 12 member 1 isoform X1
GRAM domain-containing protein 2A-like, transcript variant X4
GRAM domain-containing protein 2A-like, transcript variant X3
GRAM domain-containing protein 2A-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 7 samples with support for all annotated introns
GRAM domain-containing protein 2A-like isoform X3
GRAM domain-containing protein 2A-like isoform X1
GRAM domain-containing protein 2A-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 6 samples with support for all annotated introns
GRAM domain-containing protein 2A-like isoform X2
GRAM domain-containing protein 2A-like, transcript variant X5
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
GRAM domain-containing protein 2A-like isoform X4
CD276 antigen-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
CD276 antigen-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CD276 antigen-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
CD276 antigen-like, transcript variant X3
CD276 antigen-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC122542647, transcript variant X2
uncharacterized LOC122542647, 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 8 samples with support for all annotated introns
lysyl oxidase-like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
lysyl oxidase-like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized LOC122542650, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC122542650, transcript variant X2
uncharacterized LOC122542650, transcript variant X1
secretory carrier-associated membrane protein 5, transcript variant X4
secretory carrier-associated membrane protein 5, transcript variant X1
secretory carrier-associated membrane protein 5, transcript variant X2
secretory carrier-associated membrane protein 5, transcript variant X3
secretory carrier-associated membrane protein 5
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
hyperpolarization activated cyclic nucleotide-gated potassium channel 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
pyruvate kinase M1/2a, transcript variant X3
pyruvate kinase M1/2a, transcript variant X4
pyruvate kinase M1/2a, transcript variant X1
pyruvate kinase M1/2a, transcript variant X2
protein mono-ADP-ribosyltransferase PARP6, 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 5 samples with support for all annotated introns
protein mono-ADP-ribosyltransferase PARP6, transcript variant X2
protein mono-ADP-ribosyltransferase PARP6, 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 5 samples with support for all annotated introns
protein mono-ADP-ribosyltransferase PARP6, transcript variant X4
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
protein mono-ADP-ribosyltransferase PARP6, 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 5 samples with support for all annotated introns
protein mono-ADP-ribosyltransferase PARP6, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein mono-ADP-ribosyltransferase PARP6, transcript variant X7
protein mono-ADP-ribosyltransferase PARP6, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein mono-ADP-ribosyltransferase PARP6, transcript variant X10
protein mono-ADP-ribosyltransferase PARP6, transcript variant X11
protein mono-ADP-ribosyltransferase PARP6 isoform X1
protein mono-ADP-ribosyltransferase PARP6 isoform X2
protein mono-ADP-ribosyltransferase PARP6 isoform X3
protein mono-ADP-ribosyltransferase PARP6 isoform X4
protein mono-ADP-ribosyltransferase PARP6 isoform X5
protein mono-ADP-ribosyltransferase PARP6 isoform X6
protein mono-ADP-ribosyltransferase PARP6 isoform X7
protein mono-ADP-ribosyltransferase PARP6 isoform X9
protein mono-ADP-ribosyltransferase PARP6, transcript variant X8
protein mono-ADP-ribosyltransferase PARP6 isoform X8
CUGBP Elav-like family member 6, transcript variant X10
CUGBP Elav-like family member 6, transcript variant X4
CUGBP Elav-like family member 6, transcript variant X3
CUGBP Elav-like family member 6, transcript variant X1
CUGBP Elav-like family member 6, transcript variant X2
CUGBP Elav-like family member 6, transcript variant X6
CUGBP Elav-like family member 6, transcript variant X5
CUGBP Elav-like family member 6, transcript variant X7
CUGBP Elav-like family member 6, transcript variant X9
CUGBP Elav-like family member 6, transcript variant X8
CUGBP Elav-like family member 6, transcript variant X12
CUGBP Elav-like family member 4 isoform X9
CUGBP Elav-like family member 4 isoform X3
CUGBP Elav-like family member 4 isoform X8
CUGBP Elav-like family member 4 isoform X5
CUGBP Elav-like family member 4 isoform X2
CUGBP Elav-like family member 4 isoform X7
CUGBP Elav-like family member 4 isoform X4
CUGBP Elav-like family member 4 isoform X6
CUGBP Elav-like family member 4 isoform X1
CUGBP Elav-like family member 4 isoform X11
CUGBP Elav-like family member 6, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
CUGBP Elav-like family member 4 isoform X10
uncharacterized LOC122542477, transcript variant X2
uncharacterized LOC122542477, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
family with sequence similarity 219 member B
cytochrome c oxidase subunit 5A, mitochondrial-like
ribonuclease P protein subunit p25-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
AT-rich interactive domain-containing protein 3A-like, transcript variant X2
AT-rich interactive domain-containing protein 3A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
AT-rich interactive domain-containing protein 3A-like, 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 3 samples with support for all annotated introns
AT-rich interactive domain-containing protein 3A-like, transcript variant X5
AT-rich interactive domain-containing protein 3A-like, transcript variant X4
AT-rich interactive domain-containing protein 3B-like isoform X1
AT-rich interactive domain-containing protein 3B-like isoform X2
AT-rich interactive domain-containing protein 3A-like isoform X3
AT-rich interactive domain-containing protein 3A-like isoform X4
AT-rich interactive domain-containing protein 3A-like isoform X5
synaptotagmin-4-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
synaptotagmin-4-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
synaptotagmin-4-like, transcript variant X2
synaptotagmin-4-like, transcript variant X6
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 8 samples with support for all annotated introns
synaptotagmin-4-like, transcript variant X7
synaptotagmin-4-like, transcript variant X3
synaptotagmin-4-like, transcript variant X1
synaptotagmin-4-like, transcript variant X8
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
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
enhancer of mRNA decapping 3 homolog (S. cerevisiae), transcript variant X1
enhancer of mRNA decapping 3 homolog (S. cerevisiae), transcript variant X2
collagen and calcium-binding EGF domain-containing protein 1-like, 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 1 sample with support for all annotated introns
collagen and calcium-binding EGF domain-containing protein 1-like, transcript variant X1
collagen and calcium-binding EGF domain-containing protein 1-like isoform X2
collagen and calcium-binding EGF domain-containing protein 1-like isoform X1
C-terminal Src kinase, transcript variant X4
C-terminal Src kinase, transcript variant X2
C-terminal Src kinase, transcript variant X6
C-terminal Src kinase, transcript variant X3
C-terminal Src kinase, transcript variant X7
C-terminal Src kinase, transcript variant X1
C-terminal Src kinase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sorbitol dehydrogenase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
sorbitol dehydrogenase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
sorbitol dehydrogenase-like, transcript variant X3
sorbitol dehydrogenase-like, transcript variant X6
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 18 samples with support for all annotated introns
sorbitol dehydrogenase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
sorbitol dehydrogenase-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dual oxidase maturation factor 2-like, transcript variant X4
dual oxidase maturation factor 2-like isoform X2
dual oxidase maturation factor 2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dual oxidase maturation factor 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dual oxidase maturation factor 2-like, transcript variant X2
dual oxidase maturation factor 1-like isoform 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 2 samples with support for all annotated introns
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
telomere repeat binding bouquet formation protein 2, 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
telomere repeat binding bouquet formation protein 2, transcript variant X1
telomere repeat binding bouquet formation protein 2, transcript variant X2
telomere repeat binding bouquet formation protein 2, transcript variant X3
telomere repeats-binding bouquet formation protein 2 isoform X2
telomere repeats-binding bouquet formation protein 2 isoform X1
cholesterol side-chain cleavage enzyme, mitochondrial-like, 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 3 samples with support for all annotated introns
cholesterol side-chain cleavage enzyme, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cholesterol side-chain cleavage enzyme, mitochondrial-like isoform X2
cholesterol side-chain cleavage enzyme, mitochondrial-like isoform X1
cholesterol side-chain cleavage enzyme, mitochondrial-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cholesterol side-chain cleavage enzyme, mitochondrial-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cholesterol side-chain cleavage enzyme, mitochondrial-like isoform X3
coiled-coil domain containing 33, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
coiled-coil domain containing 33, transcript variant X1
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 3 samples with support for all annotated introns
coiled-coil domain-containing protein 33 isoform X2
coiled-coil domain-containing protein 33 isoform X1
signaling receptor and transporter of retinol STRA6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
signaling receptor and transporter of retinol STRA6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
signaling receptor and transporter of retinol STRA6, transcript variant X3
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 4 samples with support for all annotated introns
receptor for retinol uptake stra6 isoform X1
receptor for retinol uptake stra6 isoform X2
immunoglobulin superfamily containing leucine-rich repeat 2
immunoglobulin superfamily containing leucine-rich repeat protein 2
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
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: stomatin-like protein 1
leucine-rich repeat-containing protein 49, transcript variant X2
leucine-rich repeat-containing protein 49, transcript variant X1
leucine-rich repeat-containing protein 49, transcript variant X4
leucine-rich repeat-containing protein 49, transcript variant X3
leucine-rich repeat-containing protein 49 isoform X2
leucine-rich repeat-containing protein 49 isoform X1
leucine-rich repeat-containing protein 49 isoform X3
La ribonucleoprotein 6, translational regulator a
TM2 domain containing 3, transcript variant X1
TM2 domain-containing protein 3 isoform X1
TM2 domain containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
TM2 domain-containing protein 3 isoform X2
threonine--tRNA ligase 1, cytoplasmic-like
tight junction protein 1a, transcript variant X1
tight junction protein 1a, transcript variant X2
tight junction protein 1a, transcript variant X3
tight junction protein 1a, transcript variant X5
tight junction protein 1a, transcript variant X4
family with sequence similarity 189 member A1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
amyloid beta (A4) precursor protein-binding, family A, member 2b, transcript variant X4
amyloid beta (A4) precursor protein-binding, family A, member 2b, transcript variant X5
amyloid beta (A4) precursor protein-binding, family A, member 2b, transcript variant X1
amyloid beta (A4) precursor protein-binding, family A, member 2b, transcript variant X3
amyloid beta (A4) precursor protein-binding, family A, member 2b, transcript variant X2
amyloid-beta A4 precursor protein-binding family A member 2 isoform X2
amyloid-beta A4 precursor protein-binding family A member 2 isoform X3
amyloid-beta A4 precursor protein-binding family A member 2 isoform X1
M-phase phosphoprotein 10 (U3 small nucleolar ribonucleoprotein)
U3 small nucleolar ribonucleoprotein protein MPP10
FANCD2 and FANCI associated nuclease 1, transcript variant X2
FANCD2 and FANCI associated nuclease 1, transcript variant X1
fanconi-associated nuclease 1 isoform X2
fanconi-associated nuclease 1 isoform X1
myotubularin related protein 10, transcript variant X2
myotubularin related protein 10, transcript variant X1
myotubularin-related protein 10 isoform X2
myotubularin-related protein 10 isoform X1
transient receptor potential cation channel subfamily M member 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transient receptor potential cation channel subfamily M member 1-like, transcript variant X2
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 3 samples with support for all annotated introns
transient receptor potential cation channel subfamily M member 1-like, transcript variant X3
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
transient receptor potential cation channel subfamily M member 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transient receptor potential cation channel subfamily M member 1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transient receptor potential cation channel subfamily M member 1-like isoform X4
transient receptor potential cation channel subfamily M member 1-like isoform X2
transient receptor potential cation channel subfamily M member 1-like isoform X3
transient receptor potential cation channel subfamily M member 1-like isoform X1
transient receptor potential cation channel subfamily M member 1-like isoform X5
transient receptor potential cation channel subfamily M member 1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transient receptor potential cation channel subfamily M member 1-like isoform X6
transient receptor potential cation channel subfamily M member 1-like, transcript variant X7
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
transient receptor potential cation channel subfamily M member 1-like isoform X7
Kruppel-like factor 13, transcript variant X2
Kruppel-like factor 13, transcript variant X1
OTU deubiquitinase 7A, transcript variant X2
OTU deubiquitinase 7A, transcript variant X4
OTU deubiquitinase 7A, transcript variant X1
OTU deubiquitinase 7A, transcript variant X3
beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase 3-like
ADP-dependent glucokinase-like isoform X4
Bardet-Biedl syndrome 4, transcript variant X5
Bardet-Biedl syndrome 4, transcript variant X2
Bardet-Biedl syndrome 4, transcript variant X1
Bardet-Biedl syndrome 4, transcript variant X4
Bardet-Biedl syndrome 4, transcript variant X3
Bardet-Biedl syndrome 4, transcript variant X6
Bardet-Biedl syndrome 4 protein isoform X1
Bardet-Biedl syndrome 4 protein isoform X2
chondroitin sulfate proteoglycan 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chondroitin sulfate proteoglycan 4-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 29 samples with support for all annotated introns
sorting nexin-1-like, transcript variant X2
sorting nexin-1-like, transcript variant X1
peptidylprolyl isomerase B (cyclophilin B)
COORDINATES: nucleotide motif:Rfam:12.0:RF00600
mannose phosphate isomerase, transcript variant X1
mannose phosphate isomerase, transcript variant X2
mannose-6-phosphate isomerase isoform X1
mannose-6-phosphate isomerase isoform X2
secretory carrier-associated membrane protein 2
unc-51 like kinase 3, transcript variant X1
unc-51 like kinase 3, transcript variant X2
unc-51 like kinase 3, transcript variant X3
unc-51 like kinase 3, transcript variant X4
serine/threonine-protein kinase ULK3 isoform X4
serine/threonine-protein kinase ULK3 isoform X1
serine/threonine-protein kinase ULK3 isoform X2
serine/threonine-protein kinase ULK3 isoform X3
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
pro-neuregulin-4, membrane-bound isoform-like, transcript variant X1
pro-neuregulin-4, membrane-bound isoform-like, transcript variant X2
pro-neuregulin-4, membrane-bound isoform-like
transmembrane protein 266, transcript variant X1
transmembrane protein 266, 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 3 samples with support for all annotated introns
electron transfer flavoprotein subunit alpha, transcript variant X1
electron transfer flavoprotein subunit alpha, mitochondrial isoform X1
electron transfer flavoprotein subunit alpha, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
electron transfer flavoprotein subunit alpha, mitochondrial isoform X2
S-phase cyclin A-associated protein in the ER, transcript variant X3
S-phase cyclin A-associated protein in the ER, transcript variant X1
S-phase cyclin A-associated protein in the ER, transcript variant X2
S-phase cyclin A-associated protein in the ER, transcript variant X6
S phase cyclin A-associated protein in the endoplasmic reticulum isoform X2
S phase cyclin A-associated protein in the endoplasmic reticulum isoform X3
S phase cyclin A-associated protein in the endoplasmic reticulum isoform X1
S phase cyclin A-associated protein in the endoplasmic reticulum isoform X6
S-phase cyclin A-associated protein in the ER, transcript variant X4
S-phase cyclin A-associated protein in the ER, transcript variant X5
S phase cyclin A-associated protein in the endoplasmic reticulum isoform X4
S phase cyclin A-associated protein in the endoplasmic reticulum isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
proline-serine-threonine phosphatase interacting protein 1a, transcript variant X1
proline-serine-threonine phosphatase interacting protein 1a, transcript variant X2
proline-serine-threonine phosphatase interacting protein 1a, transcript variant X3
proline-serine-threonine phosphatase-interacting protein 1a isoform X1
proline-serine-threonine phosphatase-interacting protein 1a isoform X2
proline-serine-threonine phosphatase-interacting protein 1a isoform X3
pseudopodium-enriched atypical kinase 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pseudopodium-enriched atypical kinase 1, 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 5 samples with support for all annotated introns
pseudopodium-enriched atypical kinase 1, transcript variant X4
pseudopodium-enriched atypical kinase 1, transcript variant X6
pseudopodium-enriched atypical kinase 1, transcript variant X7
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 9 samples with support for all annotated introns
pseudopodium-enriched atypical kinase 1, transcript variant X1
pseudopodium-enriched atypical kinase 1, transcript variant X3
inactive tyrosine-protein kinase PEAK1 isoform X2
inactive tyrosine-protein kinase PEAK1 isoform X3
inactive tyrosine-protein kinase PEAK1 isoform X1
high mobility group 20A, transcript variant X3
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 3 samples with support for all annotated introns
high mobility group 20A, transcript variant X1
high mobility group 20A, transcript variant X2
high mobility group 20A, transcript variant X4
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
high mobility group 20A, transcript variant X7
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 14 samples with support for all annotated introns
high mobility group 20A, transcript variant X6
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 20 samples with support for all annotated introns
high mobility group 20A, transcript variant X5
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 19 samples with support for all annotated introns
high mobility group 20A, transcript variant X8
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 28 samples with support for all annotated introns
high mobility group protein 20A isoform X1
high mobility group protein 20A isoform X3
high mobility group protein 20A isoform X2
high mobility group protein 20A isoform X4
high mobility group protein 20A isoform X7
high mobility group protein 20A isoform X5
high mobility group protein 20A isoform X6
high mobility group protein 20A isoform X8
ubiquitin-like 7a (bone marrow stromal cell-derived)
neuronal acetylcholine receptor subunit alpha-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
neuronal acetylcholine receptor subunit beta-4-like, 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 3 samples with support for all annotated introns
neuronal acetylcholine receptor subunit beta-4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 114 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
neuronal acetylcholine receptor subunit beta-4-like, transcript variant X3
neuronal acetylcholine receptor subunit beta-4-like isoform X2
neuronal acetylcholine receptor subunit beta-4-like isoform X1
neuronal acetylcholine receptor subunit beta-4-like isoform X3
SH2 domain-containing adapter protein F-like
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 15 samples with support for all annotated introns
pyroglutamyl-peptidase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
pyroglutamyl-peptidase 1-like isoform X2
pyroglutamyl-peptidase 1-like, transcript variant X1
pyroglutamyl-peptidase 1-like isoform X1
insulin-like growth factor 1a receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
insulin-like growth factor 1a receptor, transcript variant X2
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, including 1 sample with support for all annotated introns
insulin-like growth factor 1a receptor isoform X1
insulin-like growth factor 1a receptor isoform X2
transfer RNA valine (anticodon CAC); 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
cocaine- and amphetamine-regulated transcript protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
tubulin, gamma complex associated protein 4, transcript variant X1
tubulin, gamma complex associated protein 4, transcript variant X2
gamma-tubulin complex component 4 isoform X1
gamma-tubulin complex component 4 isoform X2
diphosphoinositol pentakisphosphate kinase 1a, transcript variant X3
diphosphoinositol pentakisphosphate kinase 1a, transcript variant X1
diphosphoinositol pentakisphosphate kinase 1a, transcript variant X2
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
diphosphoinositol pentakisphosphate kinase 1a, transcript variant X8
diphosphoinositol pentakisphosphate kinase 1a, transcript variant X4
diphosphoinositol pentakisphosphate kinase 1a, transcript variant X7
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 15 samples with support for all annotated introns
diphosphoinositol pentakisphosphate kinase 1a, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
diphosphoinositol pentakisphosphate kinase 1a, transcript variant X9
diphosphoinositol pentakisphosphate kinase 1a, transcript variant X6
diphosphoinositol pentakisphosphate kinase 1a, transcript variant X10
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 16 samples with support for all annotated introns
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2 isoform X10
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2 isoform X7
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 1 isoform X5
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2 isoform X2
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2 isoform X9
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2 isoform X8
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2 isoform X3
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2 isoform X6
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2 isoform X4
inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
creatine kinase U-type, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
creatine kinase U-type, mitochondrial-like, transcript variant X1
creatine kinase U-type, mitochondrial-like, transcript variant X3
creatine kinase U-type, mitochondrial-like isoform X2
creatine kinase U-type, mitochondrial-like isoform X1
uncharacterized LOC122542562, transcript variant X1
uncharacterized LOC122542562, transcript variant X2
creatine kinase U-type, mitochondrial, transcript variant X2
creatine kinase U-type, mitochondrial, transcript variant X1
creatine kinase U-type, mitochondrial isoform X1
creatine kinase U-type, mitochondrial, transcript variant X6
creatine kinase U-type, mitochondrial, transcript variant X3
creatine kinase U-type, mitochondrial, transcript variant X5
creatine kinase U-type, mitochondrial, transcript variant X4
creatine kinase U-type, mitochondrial isoform X2
G-protein coupled receptor 161-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
G-protein coupled receptor 161-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 45% coverage of the annotated genomic feature by RNAseq alignments
protein regulator of cytokinesis 1b, transcript variant X3
protein regulator of cytokinesis 1b, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein regulator of cytokinesis 1b, 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 4 samples with support for all annotated introns
protein regulator of cytokinesis 1b isoform X1
protein regulator of cytokinesis 1b isoform X3
protein regulator of cytokinesis 1b isoform X2
VPS33B late endosome and lysosome associated, transcript variant X5
VPS33B late endosome and lysosome associated, transcript variant X3
VPS33B late endosome and lysosome associated, transcript variant X1
VPS33B late endosome and lysosome associated, transcript variant X4
VPS33B late endosome and lysosome associated, transcript variant X7
VPS33B late endosome and lysosome associated, transcript variant X6
VPS33B late endosome and lysosome associated, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
vacuolar protein sorting-associated protein 33B isoform X2
vacuolar protein sorting-associated protein 33B isoform X3
vacuolar protein sorting-associated protein 33B isoform X4
vacuolar protein sorting-associated protein 33B isoform X1
vacuolar protein sorting-associated protein 33B isoform X5
guanosine-3',5'-bis(diphosphate) 3'-pyrophosphohydrolase MESH1
tubulin polyglutamylase ttll6-like, transcript variant X1
tubulin polyglutamylase ttll6-like, transcript variant X4
tubulin polyglutamylase ttll6-like, transcript variant X5
tubulin polyglutamylase ttll6-like, transcript variant X6
tubulin polyglutamylase ttll6-like isoform X4
tubulin polyglutamylase ttll6-like isoform X1
tubulin polyglutamylase ttll6-like isoform X5
tubulin polyglutamylase TTLL13-like isoform X6
tubulin polyglutamylase ttll6-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tubulin polyglutamylase ttll6-like isoform X2
tubulin polyglutamylase ttll6-like, transcript variant X3
tubulin polyglutamylase ttll6-like isoform X3
tubulin polyglutamylase ttll6-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tubulin polyglutamylase ttll6-like isoform X7
RCC1 domain-containing protein 1-like, transcript variant X3
calcium and integrin-binding protein 1-like, transcript variant X1
calcium and integrin-binding protein 1-like, transcript variant X2
RCC1 domain-containing protein 1-like, transcript variant X2
RCC1 domain-containing protein 1-like isoform X2
calcium and integrin-binding protein 1-like, transcript variant X3
calcium and integrin-binding protein 1-like
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
RCC1 domain-containing protein 1-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 10 samples with support for all annotated introns
RCC1 domain-containing protein 1-like, transcript variant X4
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 7 samples with support for all annotated introns
RCC1 domain-containing protein 1-like isoform X1
RCC1 domain-containing protein 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
mannosidase, alpha, class 2A, member 2, transcript variant X1
mannosidase, alpha, class 2A, member 2, transcript variant X2
FES proto-oncogene, tyrosine kinase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
FES proto-oncogene, tyrosine kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
FES proto-oncogene, tyrosine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
FES proto-oncogene, tyrosine kinase, transcript variant X3
furin (paired basic amino acid cleaving enzyme) a, transcript variant X2
furin (paired basic amino acid cleaving enzyme) a, transcript variant X1
furin (paired basic amino acid cleaving enzyme) a isoform X2
furin (paired basic amino acid cleaving enzyme) a isoform X1
uncharacterized LOC122542576, transcript variant X1
uncharacterized LOC122542576, transcript variant X2
serine incorporator 4, transcript variant X1
serine incorporator 4, transcript variant X3
serine incorporator 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
CREB regulated transcription coactivator 3, transcript variant X2
CREB regulated transcription coactivator 3, transcript variant X3
CREB regulated transcription coactivator 3, transcript variant X1
CREB-regulated transcription coactivator 3 isoform X2
CREB-regulated transcription coactivator 3 isoform X3
CREB-regulated transcription coactivator 3 isoform X1
uncharacterized LOC122542583, transcript variant X2
uncharacterized LOC122542583, transcript variant X1
IQ motif containing GTPase activating protein 1
ras GTPase-activating-like protein IQGAP1
SUMO peptidase family member, NEDD8 specific, transcript variant X2
SUMO peptidase family member, NEDD8 specific, transcript variant X1
SUMO peptidase family member, NEDD8 specific, transcript variant X3
nuclear receptor subfamily 2, group E, member 3
leucine rich repeat and Ig domain containing 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 1
probable voltage-dependent R-type calcium channel subunit alpha-1E
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 609-like, transcript variant X7
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 8 samples with support for all annotated introns
zinc finger protein 609-like, 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 5 samples with support for all annotated introns
zinc finger protein 609-like, transcript variant X1
zinc finger protein 609-like, transcript variant X3
zinc finger protein 609-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 609-like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 609-like, transcript variant X6
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 18 samples with support for all annotated introns
zinc finger protein 609-like, transcript variant X5
zinc finger protein 609-like, transcript variant X4
zinc finger protein 609-like, transcript variant X10
zinc finger protein 609-like, transcript variant X11
thyroid hormone receptor interactor 4, transcript variant X2
activating signal cointegrator 1 isoform X2
thyroid hormone receptor interactor 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
thyroid hormone receptor interactor 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
activating signal cointegrator 1 isoform X1
thyroid hormone receptor interactor 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
activating signal cointegrator 1 isoform X3
uncharacterized LOC122542590, transcript variant X2
uncharacterized LOC122542590, 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 20 samples with support for all annotated introns
protein tyrosine phosphatase non-receptor type 9a, transcript variant X1
tyrosine-protein phosphatase non-receptor type 9 isoform X1
protein tyrosine phosphatase non-receptor type 9a, transcript variant X3
tyrosine-protein phosphatase non-receptor type 9 isoform X3
protein tyrosine phosphatase non-receptor type 9a, transcript variant X2
tyrosine-protein phosphatase non-receptor type 9 isoform X2
protein tyrosine phosphatase non-receptor type 9a, transcript variant X4
protein tyrosine phosphatase non-receptor type 9a, transcript variant X5
tyrosine-protein phosphatase non-receptor type 9 isoform X4
SIN3 transcription regulator family member Aa, transcript variant X1
SIN3 transcription regulator family member Aa, transcript variant X4
SIN3 transcription regulator family member Aa, transcript variant X2
SIN3 transcription regulator family member Aa, transcript variant X3
SIN3 transcription regulator family member Aa
mannosidase, alpha, class 2C, member 1, transcript variant X3
mannosidase, alpha, class 2C, member 1, transcript variant X1
mannosidase, alpha, class 2C, member 1, transcript variant X2
ice-structuring glycoprotein-like, transcript variant X1
ice-structuring glycoprotein-like, transcript variant X2
ice-structuring glycoprotein-like isoform X1
ice-structuring glycoprotein-like isoform X2
sorting nexin-27-like, transcript variant X1
sorting nexin-27-like, transcript variant X2
AP-3 complex subunit beta-2, transcript variant X3
AP-3 complex subunit beta-2, transcript variant X6
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 6 samples with support for all annotated introns
AP-3 complex subunit beta-2, transcript variant X4
AP-3 complex subunit beta-2, transcript variant X5
AP-3 complex subunit beta-2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
AP-3 complex subunit beta-2, transcript variant X2
cytoplasmic polyadenylation element-binding protein 1-like, transcript variant X1
cytoplasmic polyadenylation element-binding protein 1-like isoform X1
cytoplasmic polyadenylation element-binding protein 1-like, transcript variant X3
cytoplasmic polyadenylation element-binding protein 1-like, transcript variant X2
cytoplasmic polyadenylation element-binding protein 1-like isoform X3
cytoplasmic polyadenylation element-binding protein 1-like isoform X2
synaptic vesicle glycoprotein 2, transcript variant X2
synaptic vesicle glycoprotein 2, transcript variant X1
synaptic vesicle glycoprotein 2C isoform X2
synaptic vesicle glycoprotein 2C isoform X1
sperm axonemal maintenance protein CFAP97D1-like
casein kinase I-like, transcript variant X8
casein kinase I-like, transcript variant X2
casein kinase I-like, transcript variant X1
casein kinase I-like, transcript variant X7
casein kinase I-like, transcript variant X6
casein kinase I-like, transcript variant X3
casein kinase I-like, transcript variant X5
casein kinase I-like, transcript variant X4
cholesterol 25-hydroxylase-like protein 1, member 1
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
uncharacterized protein LOC100034462 homolog, transcript variant X2
uncharacterized protein LOC100034462 homolog, transcript variant X4
uncharacterized protein LOC100034462 homolog, transcript variant X1
uncharacterized protein LOC100034462 homolog, transcript variant X3
uncharacterized protein si:dkey-24l11.2 isoform X3
uncharacterized protein si:dkey-24l11.2 isoform X1
uncharacterized protein si:dkey-24l11.2 isoform X2
SEC11 homolog A, signal peptidase complex subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
signal peptidase complex catalytic subunit SEC11A
zinc finger protein 592, transcript variant X6
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 13 samples with support for all annotated introns
zinc finger protein 592, transcript variant X1
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 14 samples with support for all annotated introns
zinc finger protein 592, 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 1 sample with support for all annotated introns
zinc finger protein 592, transcript variant X3
zinc finger protein 592, transcript variant X4
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 7 samples with support for all annotated introns
zinc finger protein 592, transcript variant X5
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 4 samples with support for all annotated introns
MALT paracaspase 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
MALT paracaspase 3, transcript variant X2
MALT paracaspase 3, transcript variant X1
mucosa-associated lymphoid tissue lymphoma translocation protein 1 isoform X1
mucosa-associated lymphoid tissue lymphoma translocation protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 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 9 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 99% coverage of the annotated genomic feature by RNAseq alignments
semaphorin-7A-like, transcript variant X2
semaphorin-7A-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 25 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
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 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
interactor of little elongator complex ELL subunit 2, transcript variant X1
interactor of little elongator complex ELL subunit 2, transcript variant X2
interactor of little elongator complex ELL subunit 2, transcript variant X3
little elongation complex subunit 2 isoform X1
little elongation complex subunit 2 isoform X2
RAR-related orphan receptor A, paralog a, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RAR-related orphan receptor A, paralog a, transcript variant X1
RAR-related orphan receptor A, paralog a, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
maestro heat-like repeat-containing protein family member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
vacuolar protein sorting 13 homolog C, transcript variant X2
vacuolar protein sorting 13 homolog C, transcript variant X1
vacuolar protein sorting 13 homolog C, transcript variant X3
vacuolar protein sorting-associated protein 13C isoform X3
vacuolar protein sorting-associated protein 13C isoform X2
vacuolar protein sorting-associated protein 13C isoform X1
vacuolar protein sorting 13 homolog C, transcript variant X4
vacuolar protein sorting-associated protein 13C isoform X4
C2 calcium dependent domain containing 4A
C2 calcium-dependent domain-containing protein 4A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
tropomyosin 1 (alpha), transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
tropomyosin 1 (alpha), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 120 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
tropomyosin 1 (alpha), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
tropomyosin 1 (alpha), transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
tropomyosin 1 (alpha), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 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 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: 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
serine beta-lactamase-like protein LACTB, mitochondrial
armadillo repeat-containing X-linked protein 4-like, transcript variant X1
armadillo repeat-containing X-linked protein 4-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 14 samples with support for all annotated introns
armadillo repeat-containing X-linked protein 4-like
LOW QUALITY PROTEIN: ornithine decarboxylase antizyme 2-like
RNA-binding protein with multiple splicing 2, 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 16 samples with support for all annotated introns
RNA-binding protein with multiple splicing 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
RNA-binding protein, mRNA-processing factor 2a isoform X3
RNA-binding protein, mRNA-processing factor 2a isoform X9
RNA-binding protein with multiple splicing 2, transcript variant X5
RNA-binding protein with multiple splicing 2 isoform X5
RNA-binding protein with multiple splicing 2, transcript variant X4
RNA-binding protein with multiple splicing 2, transcript variant X10
RNA-binding protein with multiple splicing 2, transcript variant X1
RNA-binding protein with multiple splicing 2, 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
RNA-binding protein with multiple splicing 2, transcript variant X2
RNA-binding protein with multiple splicing 2, transcript variant X7
RNA-binding protein with multiple splicing 2, transcript variant X8
RNA-binding protein with multiple splicing 2 isoform X4
RNA-binding protein with multiple splicing 2 isoform X10
RNA-binding protein with multiple splicing 2 isoform X1
RNA-binding protein, mRNA-processing factor 2a isoform X6
RNA-binding protein with multiple splicing 2 isoform X2
RNA-binding protein with multiple splicing 2 isoform X7
RNA-binding protein with multiple splicing 2 isoform X8
nei-like DNA glycosylase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
nei-like DNA glycosylase 1, transcript variant X1
zinc finger CCCH domain-containing protein 10-like
uncharacterized threonine-rich GPI-anchored glycoprotein PJ4664.02-like
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
chromosome 40 C15orf39 homolog, transcript variant X4
chromosome 40 C15orf39 homolog, transcript variant X1
chromosome 40 C15orf39 homolog, transcript variant X3
chromosome 40 C15orf39 homolog, transcript variant X2
chromosome 40 C15orf39 homolog, transcript variant X5
uncharacterized protein C15orf39 homolog isoform X1
chromosome 40 C15orf39 homolog, transcript variant X9
chromosome 40 C15orf39 homolog, transcript variant X6
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
chromosome 40 C15orf39 homolog, transcript variant X7
uncharacterized protein C15orf39 homolog isoform X3
chromosome 40 C15orf39 homolog, transcript variant X8
uncharacterized protein C15orf39 homolog isoform X2
chromosome 40 C15orf39 homolog, transcript variant X10
COORDINATES: nucleotide motif:Rfam:12.0:RF00002
phosphopantothenoylcysteine decarboxylase
circularly permutated Ras protein 1-like, transcript variant X2
circularly permutated Ras protein 1-like, transcript variant X1
circularly permutated Ras protein 1-like
glycogen [starch] synthase, muscle-like, transcript variant X3
glycogen [starch] synthase, muscle-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glycogen [starch] synthase, muscle-like, transcript variant X1
glycogen [starch] synthase, liver-like isoform X3
glycogen [starch] synthase, muscle-like isoform X2
glycogen [starch] synthase, muscle-like isoform X1
tuberoinfundibular peptide of 39 residues
galanin peptides-like, transcript variant X2
galanin peptides-like, transcript variant X1