Cottoperca gobio chromosome 20, fCotGob3.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Neoteleostei; Acanthomorphata; Eupercaria; Perciformes; Notothenioidei; Bovichtidae; Cottoperca.
REFSEQ INFORMATION: The reference sequence is identical to\nLR131928.1.\nAssembly name: fCotGob3.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the SC on 2019/02/06. The\noriginal whole-genome shotgun project has the accession\nCAAAFJ000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Cottoperca gobio Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.2\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: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
enhancer of polycomb homolog 1-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 4 samples with support for all annotated introns
enhancer of polycomb homolog 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
enhancer of polycomb homolog 1-like isoform X1
enhancer of polycomb homolog 1-like isoform X2
enhancer of polycomb homolog 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
enhancer of polycomb homolog 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 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: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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.
drosha ribonuclease III, 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 3 samples with support for all annotated introns
drosha ribonuclease III, transcript variant X1
drosha ribonuclease III, 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 2 samples with support for all annotated introns
drosha ribonuclease III, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 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: 59 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 1 sample with support for all annotated introns
ring finger protein 152, transcript variant X2
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 3 samples with support for all annotated introns
ring finger protein 152, transcript variant X1
uncharacterized LOC115025512, 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 1 sample with support for all annotated introns
uncharacterized LOC115025512, transcript variant X1
uncharacterized protein LOC115025512 isoform X2
uncharacterized protein LOC115025512 isoform X1
kelch repeat and BTB domain containing 2
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
kelch repeat and BTB domain-containing protein 2
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
late secretory pathway protein AVL9 homolog
LSM5 homolog, U6 small nuclear RNA and mRNA degradation associated, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
U6 snRNA-associated Sm-like protein LSm5 isoform X1
LSM5 homolog, U6 small nuclear RNA and mRNA degradation associated, transcript variant X2
U6 snRNA-associated Sm-like protein LSm5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ring finger protein 31, 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 3 samples with support for all annotated introns
ring finger protein 31, 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 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF31 isoform X1
E3 ubiquitin-protein ligase RNF31 isoform X2
interferon regulatory factor 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
interferon regulatory factor 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
interferon regulatory factor 4-like isoform X1
interferon regulatory factor 9-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
neutral cholesterol ester hydrolase 1-like
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
tumor necrosis factor ligand superfamily member 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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
A-agglutinin anchorage subunit-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
A-agglutinin anchorage subunit-like, transcript variant X2
A-agglutinin anchorage subunit-like isoform X1
A-agglutinin anchorage subunit-like isoform X2
vasoactive intestinal polypeptide receptor 2-like
disco-interacting protein 2 homolog C-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
disco-interacting protein 2 homolog C-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 1 sample with support for all annotated introns
disco-interacting protein 2 homolog C-like, transcript variant X1
disco-interacting protein 2 homolog C-like isoform X2
disco-interacting protein 2 homolog C-like isoform X1
la-related protein 4B-like, transcript variant X3
la-related protein 4B-like, transcript variant X4
la-related protein 4B-like, transcript variant X1
la-related protein 4B-like, transcript variant X2
la-related protein 4B-like, transcript variant X6
la-related protein 4B-like, transcript variant X5
uncharacterized protein LOC115025743 isoform X4
uncharacterized protein LOC115025743 isoform X2
uncharacterized protein LOC115025743 isoform X3
uncharacterized protein LOC115025743 isoform X1
gamma-aminobutyric acid receptor subunit rho-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ATP binding cassette subfamily D member 3, transcript variant X3
ATP-binding cassette sub-family D member 3 isoform X3
ATP binding cassette subfamily D member 3, transcript variant X2
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 4 samples with support for all annotated introns
ATP binding cassette subfamily D member 3, transcript variant X1
ATP-binding cassette sub-family D member 3 isoform X1
ATP-binding cassette sub-family D member 3 isoform X2
tartrate-resistant acid phosphatase type 5-like
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
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
STEAP2 metalloreductase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ALG14 UDP-N-acetylglucosaminyltransferase subunit
UDP-N-acetylglucosamine transferase subunit ALG14 homolog
STEAP2 metalloreductase, transcript variant X1
STEAP2 metalloreductase, 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 1 sample with support for all annotated introns
STEAP2 metalloreductase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
MOS proto-oncogene, serine/threonine kinase
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
proto-oncogene serine/threonine-protein kinase mos
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
coiled-coil-helix-coiled-coil-helix domain containing 7, 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
coiled-coil-helix-coiled-coil-helix domain containing 7, 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 4 samples with support for all annotated introns
coiled-coil-helix-coiled-coil-helix domain-containing protein 7
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: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC115025287
protein FAM92B-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein FAM92B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein FAM92B-like, transcript variant X1
tripartite motif-containing protein 16-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 Proteins, and 74% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
putative ferric-chelate reductase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
putative ferric-chelate reductase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
putative ferric-chelate reductase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase RNF12-B-like
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: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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.
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: 6 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
neurogenic differentiation factor 6-A-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: neurogenic differentiation factor 6-A-like
protein phosphatase 1 regulatory subunit 17, transcript variant X1
protein phosphatase 1 regulatory subunit 17, transcript variant X2
protein phosphatase 1 regulatory subunit 17
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: 27 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: calcium/calmodulin-dependent 3',5'-cyclic nucleotide phosphodiesterase 1C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tRNA (cytosine(38)-C(5))-methyltransferase
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
phosphodiesterase 7A, transcript variant X1
phosphodiesterase 7A, 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
high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A isoform X1
high affinity cAMP-specific 3',5'-cyclic phosphodiesterase 7A isoform X2
mitochondrial fission regulator 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
mitochondrial fission regulator 1, transcript variant X2
mitochondrial fission regulator 1, 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 1 sample with support for all annotated introns
armadillo repeat-containing protein 1-like, transcript variant X1
armadillo repeat-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 4 samples with support for all annotated introns
armadillo repeat-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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 4 samples with support for all annotated introns
mycophenolic acid acyl-glucuronide esterase, mitochondrial
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
complement C1q and tumor necrosis factor-related protein 9A-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: complement C1q and tumor necrosis factor-related protein 9A-like
spermatogenesis-associated protein 13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: transmembrane protease serine 7
suppressor of tumorigenicity 14 protein homolog
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
fms related tyrosine kinase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
fms related tyrosine kinase 1, transcript variant X2
vascular endothelial growth factor receptor 1 isoform X1
vascular endothelial growth factor receptor 1 isoform X2
poly(A) specific ribonuclease subunit PAN3, transcript variant X2
poly(A) specific ribonuclease subunit PAN3, transcript variant X1
poly(A) specific ribonuclease subunit PAN3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
poly(A) specific ribonuclease subunit PAN3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
PAN2-PAN3 deadenylation complex subunit PAN3 isoform X2
PAN2-PAN3 deadenylation complex subunit PAN3 isoform X1
PAN2-PAN3 deadenylation complex subunit PAN3 isoform X3
PAN2-PAN3 deadenylation complex subunit PAN3 isoform X4
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: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: receptor-type tyrosine-protein kinase FLT3
ureidoimidazoline (2-oxo-4-hydroxy-4-carboxy-5-) decarboxylase
putative 2-oxo-4-hydroxy-4-carboxy-5-ureidoimidazoline decarboxylase
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
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
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 4 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 12
G protein-coupled receptor 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
G protein-coupled receptor 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
WASP family member 3, 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
WASP family member 3, transcript variant X1
wiskott-Aldrich syndrome protein family member 3
cyclin dependent kinase 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cyclin dependent kinase 8, transcript variant X1
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: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase RNF6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
BOC cell adhesion associated, oncogene regulated, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
BOC cell adhesion associated, oncogene regulated, transcript variant X1
BOC cell adhesion associated, oncogene regulated, 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 2 samples with support for all annotated introns
BOC cell adhesion associated, oncogene regulated, transcript variant X3
upstream transcription factor family member 3
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: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: basic helix-loop-helix domain-containing protein USF3
N(alpha)-acetyltransferase 50, NatE catalytic subunit, transcript variant X2
N(alpha)-acetyltransferase 50, NatE catalytic subunit, transcript variant X1
ATPase H+ transporting V1 subunit A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ATPase H+ transporting V1 subunit A, transcript variant X1
V-type proton ATPase catalytic subunit A
GRAM domain containing 1C, transcript variant X2
GRAM domain containing 1C, transcript variant X1
zinc finger DHHC-type containing 23, transcript variant X2
zinc finger DHHC-type containing 23, transcript variant X1
zinc finger DHHC-type containing 23, transcript variant X3
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
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: coiled-coil domain-containing protein 191
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X2
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
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X3
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
queuine tRNA-ribosyltransferase accessory subunit 2, transcript variant X1
queuine tRNA-ribosyltransferase accessory subunit 2 isoform X1
queuine tRNA-ribosyltransferase accessory subunit 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
queuine tRNA-ribosyltransferase accessory subunit 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: D(3) dopamine receptor-like
thiosulfate:glutathione sulfurtransferase-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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
leukocyte cysteine proteinase inhibitor 1-like
coiled-coil domain containing 58, 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 4 samples with support for all annotated introns
coiled-coil domain containing 58, transcript variant X2
coiled-coil domain-containing protein 58 isoform X1
coiled-coil domain-containing protein 58 isoform X2
family with sequence similarity 162 member A
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: 34 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: importin subunit alpha-5
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 32% coverage of the annotated genomic feature by RNAseq alignments
proteoglycan 4-like, transcript variant X3
proteoglycan 4-like, transcript variant X2
proteoglycan 4-like, transcript variant X1
vasoactive intestinal peptide receptor 1, 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 1 sample with support for all annotated introns
vasoactive intestinal peptide receptor 1, transcript variant X2
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 1 sample with support for all annotated introns
vasoactive intestinal polypeptide receptor 1 isoform X2
vasoactive intestinal peptide receptor 1, transcript variant X4
vasoactive intestinal peptide receptor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
vasoactive intestinal polypeptide receptor 1 isoform X1
vasoactive intestinal polypeptide receptor 1 isoform X3
SEC22 homolog C, vesicle trafficking protein
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: NK-tumor recognition protein
zinc finger and BTB domain containing 47
zinc finger and BTB domain-containing protein 47
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 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: kelch-like protein 40
protein-cysteine N-palmitoyltransferase HHAT-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 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: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF01229
CTD small phosphatase like, transcript variant X5
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 1 sample with support for all annotated introns
CTD small phosphatase like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CTD small phosphatase like, transcript variant X4
CTD small phosphatase like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CTD small phosphatase like, transcript variant X2
CTD small phosphatase like, transcript variant X6
CTD small phosphatase-like protein isoform X1
CTD small phosphatase-like protein isoform X2
CTD small phosphatase-like protein isoform X3
CTD small phosphatase-like protein isoform X4
CTD small phosphatase-like protein isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
phospholipase C delta 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phospholipase C delta 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phospholipase C delta 1, transcript variant X3
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 isoform X2
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 isoform X3
DLEC1 cilia and flagella associated protein
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: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: deleted in lung and esophageal cancer protein 1
mitogen-activated protein kinase kinase kinase 3-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: cryptochrome DASH-like
MYD88 innate immune signal transduction adaptor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
myeloid differentiation primary response protein MyD88
oxidative stress responsive kinase 1, transcript variant X1
oxidative stress responsive kinase 1, transcript variant X2
serine/threonine-protein kinase OSR1 isoform X1
serine/threonine-protein kinase OSR1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
xin actin-binding repeat-containing protein 1-like
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
cysteine/serine-rich nuclear protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
chymotrypsin-like elastase family member 2A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Golgi reassembly-stacking protein 2-like
solute carrier family 35 member G2-like, transcript variant X2
solute carrier family 35 member G2-like, transcript variant X1
NCK adaptor protein 1, transcript variant X1
NCK adaptor protein 1, transcript variant X2
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
D-beta-hydroxybutyrate dehydrogenase, mitochondrial-like
glycogenin-1-like, transcript variant 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, including 2 samples with support for all annotated introns
glycogenin-1-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
glycogenin-1-like, transcript variant X1
angiotensin II receptor type 1, 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 1 sample with support for all annotated introns
angiotensin II receptor type 1, transcript variant X1
Zic family member 1, transcript variant X1
Zic family member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein ZIC 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein ZIC 4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein ZIC 4-like isoform X1
zinc finger protein ZIC 4-like isoform X2
angiotensin II receptor type 1, transcript variant X3
angiotensin II receptor type 1, transcript variant X5
angiotensin II receptor type 1, transcript variant X4
angiotensin II receptor type 1, transcript variant X7
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: 23 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: phospholipid scramblase 2-like
procollagen-lysine,2-oxoglutarate 5-dioxygenase 2, transcript variant X1
procollagen-lysine,2-oxoglutarate 5-dioxygenase 2, 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 3 samples with support for all annotated introns
procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 isoform X1
procollagen-lysine,2-oxoglutarate 5-dioxygenase 2 isoform X2
angiotensin II receptor type 1, transcript variant X6
sodium/hydrogen exchanger 9-like, transcript variant X1
sodium/hydrogen exchanger 9-like, transcript variant X2
sodium/hydrogen exchanger 9-like, transcript variant X3
sodium/hydrogen exchanger 9-like isoform X1
sodium/hydrogen exchanger 9-like isoform X2
transient receptor potential cation channel subfamily C member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
short transient receptor potential channel 1
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
U2 snRNP associated SURP domain containing, transcript variant X2
U2 snRNP associated SURP domain containing, transcript variant X1
U2 snRNP-associated SURP motif-containing protein isoform X1
U2 snRNP-associated SURP motif-containing protein isoform X2
U2 snRNP associated SURP domain containing, transcript variant X3
U2 snRNP-associated SURP motif-containing protein isoform X3
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 3 samples with support for all annotated introns
ubiquitin like modifier activating enzyme 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ubiquitin like modifier activating enzyme 5, transcript variant X1
ubiquitin like modifier activating enzyme 5, transcript variant X2
ubiquitin-like modifier-activating enzyme 5 isoform X1
ubiquitin-like modifier-activating enzyme 5 isoform X2
ubiquitin-like modifier-activating enzyme 5 isoform X3
uracil nucleotide/cysteinyl leukotriene receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
OTU deubiquitinase 1, 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 1 sample with support for all annotated introns
OTU deubiquitinase 1, transcript variant X2
OTU domain-containing protein 1 isoform X1
OTU domain-containing protein 1 isoform X2
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; 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
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: homeobox protein AKR-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: disks large-associated protein 1-like
5-hydroxytryptamine receptor 5A, transcript variant X2
5-hydroxytryptamine receptor 5A, transcript variant X1
insulin induced gene 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
insulin induced gene 1, 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 4 samples with support for all annotated introns
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 2 samples with support for all annotated introns
RNA binding motif protein 33, transcript variant X6
RNA binding motif protein 33, transcript variant X4
RNA binding motif protein 33, transcript variant X3
RNA binding motif protein 33, transcript variant X5
RNA binding motif protein 33, transcript variant X1
RNA binding motif protein 33, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
limb development membrane protein 1, transcript variant X1
limb development membrane protein 1, transcript variant X2
limb region 1 protein homolog isoform X1
limb region 1 protein homolog isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: nucleolar MIF4G domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
motor neuron and pancreas homeobox protein 1
ubiquitin protein ligase E3C, transcript variant X1
ubiquitin protein ligase E3C, transcript variant X2
DnaJ heat shock protein family (Hsp40) member B6, transcript variant X1
DnaJ heat shock protein family (Hsp40) member B6, 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
protein tyrosine phosphatase receptor type N2
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
receptor-type tyrosine-protein phosphatase N2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: condensin-2 complex subunit G2
extended synaptotagmin 2, transcript variant X3
extended synaptotagmin 2, transcript variant X2
extended synaptotagmin 2, transcript variant X1
extended synaptotagmin 2, transcript variant X4
extended synaptotagmin 2, transcript variant X5
extended synaptotagmin 2, transcript variant X6
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: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: WD repeat-containing protein 60
WD repeat domain 97, transcript variant X1
WD repeat domain 97, transcript variant X2
WD repeat domain 97, transcript variant X3
WD repeat-containing protein 97 isoform X1
WD repeat-containing protein 97 isoform X2
WD repeat-containing protein 97 isoform X3
leucine-rich repeat-containing protein 14-like
MAM and LDL receptor class A domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
MAM and LDL-receptor class A domain-containing protein 1
plexin domain containing 2, transcript variant X1
plexin domain containing 2, transcript variant X2
plexin domain-containing protein 2 isoform X1
plexin domain-containing protein 2 isoform X2
GTPase IMAP family member 4-like, transcript variant X3
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
GTPase IMAP family member 4-like, transcript variant X2
GTPase IMAP family member 4-like isoform X2
GTPase IMAP family member 4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
GTPase IMAP family member 4-like isoform X1
charged multivesicular body protein 4c-like
MAF1 homolog, negative regulator of RNA polymerase III
repressor of RNA polymerase III transcription MAF1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
NOP2/Sun RNA methyltransferase 6, transcript variant X2
NOP2/Sun RNA methyltransferase 6, transcript variant X4
NOP2/Sun RNA methyltransferase 6, transcript variant X1
NOP2/Sun RNA methyltransferase 6, transcript variant X6
NOP2/Sun RNA methyltransferase 6, transcript variant X5
NOP2/Sun RNA methyltransferase 6, transcript variant X3
putative methyltransferase NSUN6 isoform X1
putative methyltransferase NSUN6 isoform X2
putative methyltransferase NSUN6 isoform X3
calcium voltage-gated channel auxiliary subunit beta 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: voltage-dependent L-type calcium channel subunit beta-2
solute carrier family 39 member 12, transcript variant X1
solute carrier family 39 member 12, transcript variant X2
solute carrier family 39 member 12, transcript variant X3
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: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: transmembrane protein 236-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 1
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: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial enolase superfamily member 1
YES proto-oncogene 1, Src family tyrosine kinase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
adenylate cyclase activating polypeptide 1, transcript variant X3
adenylate cyclase activating polypeptide 1, transcript variant X1
adenylate cyclase activating polypeptide 1, transcript variant X2
adenylate cyclase activating polypeptide 1, transcript variant X4
pituitary adenylate cyclase-activating polypeptide isoform X3
pituitary adenylate cyclase-activating polypeptide isoform X1
pituitary adenylate cyclase-activating polypeptide isoform X2
pituitary adenylate cyclase-activating polypeptide isoform X4
structural maintenance of chromosomes flexible hinge domain containing 1
structural maintenance of chromosomes flexible hinge domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
phosphatidate phosphatase LPIN2 isoform X2
phosphatidate phosphatase LPIN2 isoform X1
myosin regulatory light chain 2, smooth muscle minor isoform, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 137 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myosin regulatory light chain 2, smooth muscle minor isoform, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 137 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
myosin regulatory light chain 2, smooth muscle minor isoform
FAST kinase domain-containing protein 3, mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: FAST kinase domain-containing protein 3, mitochondrial-like
charged multivesicular body protein 5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulator of G-protein signaling 20-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulator of G-protein signaling 20-like, transcript variant X3
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
regulator of G-protein signaling 20-like, transcript variant X1
regulator of G-protein signaling 20-like isoform X1
regulator of G-protein signaling 20-like isoform X2
39S ribosomal protein L15, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: COPII coat assembly protein sec16-like
VPS41 subunit of HOPS complex, transcript variant X1
vacuolar protein sorting-associated protein 41 homolog isoform X1
VPS41 subunit of HOPS complex, transcript variant X2
vacuolar protein sorting-associated protein 41 homolog isoform X2
POU class 6 homeobox 2, transcript variant X1
POU class 6 homeobox 2, transcript variant X3
POU domain, class 6, transcription factor 2 isoform X1
POU domain, class 6, transcription factor 2 isoform X3
POU class 6 homeobox 2, transcript variant X2
POU domain, class 6, transcription factor 2 isoform X2
eukaryotic translation initiation factor 5B-like, transcript variant X1
eukaryotic translation initiation factor 5B-like, transcript variant X2
eukaryotic translation initiation factor 5B-like, transcript variant X3
eukaryotic translation initiation factor 5B-like
ANKH inorganic pyrophosphate transport regulator, transcript variant X1
ANKH inorganic pyrophosphate transport regulator, transcript variant X2
progressive ankylosis protein homolog isoform X1
progressive ankylosis protein homolog isoform X2
MYC proto-oncogene, bHLH transcription factor, transcript variant X3
MYC proto-oncogene, bHLH transcription factor, transcript variant X2
MYC proto-oncogene, bHLH transcription factor, transcript variant X4
MYC proto-oncogene, bHLH transcription factor, 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 4 samples with support for all annotated introns
MYC proto-oncogene, bHLH transcription factor, transcript variant X1
MYC proto-oncogene, bHLH transcription factor, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC115025545, transcript variant X1
uncharacterized LOC115025545, transcript variant X2
uncharacterized LOC115025554, transcript variant X3
uncharacterized LOC115025554, transcript variant X4
uncharacterized LOC115025554, transcript variant X2
uncharacterized LOC115025554, transcript variant X1
family with sequence similarity 49 member B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
family with sequence similarity 49 member B, transcript variant X3
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
family with sequence similarity 49 member B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
family with sequence similarity 49 member B, 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 1 sample with support for all annotated introns
family with sequence similarity 49 member B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 219 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X7
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X2
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X6
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X3
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X5
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X1
ArfGAP with SH3 domain, ankyrin repeat and PH domain 1, transcript variant X4
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X7
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X4
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X2
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X6
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X3
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X5
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 1 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: transcriptional repressor NF-X1-like
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3, transcript variant X5
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3 isoform X5
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3, 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 2 samples with support for all annotated introns
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3, 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 2 samples with support for all annotated introns
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3, transcript variant X7
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3, transcript variant X4
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3, transcript variant X6
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3, transcript variant X3
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3, transcript variant X8
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3 isoform X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3 isoform X3
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3 isoform X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3 isoform X4
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3 isoform X6
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3 isoform X7
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3 isoform X8
chondroitin sulfate glucuronyltransferase
ATP binding cassette subfamily F member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ATP binding cassette subfamily F member 2, transcript variant X2
ATP-binding cassette sub-family F member 2
solute carrier family 4 member 2, transcript variant X1
solute carrier family 4 member 2, transcript variant X2
solute carrier family 4 member 2, transcript variant X3
solute carrier family 4 member 2, transcript variant X4
mannose-specific lectin-like, transcript variant X1
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: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: mannose-specific lectin-like
mannose-specific lectin-like, transcript variant X2
poly(U) binding splicing factor 60, transcript variant X1
poly(U) binding splicing factor 60, transcript variant X2
poly(U) binding splicing factor 60, transcript variant X3
poly(U) binding splicing factor 60, transcript variant X6
poly(U) binding splicing factor 60, transcript variant X9
poly(U) binding splicing factor 60, transcript variant X4
poly(U) binding splicing factor 60, transcript variant X8
poly(U) binding splicing factor 60, transcript variant X7
poly(U) binding splicing factor 60, transcript variant X10
poly(U) binding splicing factor 60, transcript variant X5
poly(U)-binding-splicing factor PUF60 isoform X1
poly(U)-binding-splicing factor PUF60 isoform X2
poly(U)-binding-splicing factor PUF60 isoform X3
poly(U)-binding-splicing factor PUF60 isoform X6
poly(U)-binding-splicing factor PUF60 isoform X8
poly(U)-binding-splicing factor PUF60 isoform X9
poly(U)-binding-splicing factor PUF60 isoform X4
poly(U)-binding-splicing factor PUF60 isoform X7
poly(U)-binding-splicing factor PUF60 isoform X10
poly(U)-binding-splicing factor PUF60 isoform X5
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: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: protein scribble homolog
kinesin family member 9, transcript variant X5
kinesin family member 9, transcript variant X6
kinesin family member 9, transcript variant X3
kinesin family member 9, transcript variant X2
kinesin family member 9, transcript variant X1
kinesin family member 9, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 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: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: DNA topoisomerase 2-binding protein 1
DnaJ heat shock protein family (Hsp40) member C13, transcript variant X4
DnaJ heat shock protein family (Hsp40) member C13, transcript variant X3
DnaJ heat shock protein family (Hsp40) member C13, transcript variant X5
DnaJ heat shock protein family (Hsp40) member C13, transcript variant X2
DnaJ heat shock protein family (Hsp40) member C13, transcript variant X1
dnaJ homolog subfamily C member 13 isoform X5
dnaJ homolog subfamily C member 13 isoform X2
dnaJ homolog subfamily C member 13 isoform X1
dnaJ homolog subfamily C member 13 isoform X3
dnaJ homolog subfamily C member 13 isoform X4
leucine zipper transcription factor like 1
leucine zipper transcription factor-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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: 10 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: transcriptional activator GLI3
serine/threonine-protein kinase PRP4 homolog
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: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: serine/threonine-protein kinase PRP4 homolog
thioredoxin related transmembrane protein 3, transcript variant X1
thioredoxin related transmembrane protein 3, transcript variant X2
protein disulfide-isomerase TMX3 isoform X1
protein disulfide-isomerase TMX3 isoform 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
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 91% 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: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ADP-ribosyl cyclase/cyclic ADP-ribose hydrolase 1-like
mediator of RNA polymerase II transcription subunit 1-like, transcript variant X2
mediator of RNA polymerase II transcription subunit 1-like, transcript variant X1
mediator of RNA polymerase II transcription subunit 1-like isoform X2
mediator of RNA polymerase II transcription subunit 1-like isoform X1
RAS like proto-oncogene A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 118 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RAS like proto-oncogene A, transcript variant X2
RAS like proto-oncogene A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 118 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: cyclin-dependent kinase 13
RALY RNA binding protein like, transcript variant X1
RALY RNA binding protein like, transcript variant X2
RALY RNA binding protein like, transcript variant X3
RNA-binding Raly-like protein isoform X1
RNA-binding Raly-like protein isoform X2
RALY RNA binding protein like, transcript variant X4
RNA-binding Raly-like protein isoform X3
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
highly reducing polyketide synthase alnA-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: highly reducing polyketide synthase alnA-like
phthioceranic/hydroxyphthioceranic acid synthase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
ATP-dependent zinc metalloprotease YME1L1-like, transcript variant X3
ATP-dependent zinc metalloprotease YME1L1-like, transcript variant X2
ATP-dependent zinc metalloprotease YME1L1-like, transcript variant X1
ATP-dependent zinc metalloprotease YME1L1-like isoform X2
ATP-dependent zinc metalloprotease YME1L1-like isoform X1
ATP-dependent zinc metalloprotease YME1L1-like, transcript variant X4
microtubule associated serine/threonine kinase like
serine/threonine-protein kinase greatwall
acyl-CoA binding domain containing 5, transcript variant X2
acyl-CoA binding domain containing 5, transcript variant X1
acyl-CoA-binding domain-containing protein 5 isoform X2
acyl-CoA-binding domain-containing protein 5 isoform X1
abl interactor 1, transcript variant X10
decaprenyl diphosphate synthase subunit 1
decaprenyl-diphosphate synthase subunit 1
protein adenylyltransferase SelO-like, transcript variant X2
uncharacterized protein LOC115025444 isoform X2
protein adenylyltransferase SelO-like, transcript variant X1
uncharacterized protein LOC115025444 isoform X1
amyloid beta precursor protein binding family B member 1 interacting protein
amyloid beta A4 precursor protein-binding family B member 1-interacting protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 106-like, transcript variant X3
coiled-coil domain-containing protein 106-like, transcript variant X4
coiled-coil domain-containing protein 106-like, transcript variant X1
coiled-coil domain-containing protein 106-like, transcript variant X2
coiled-coil domain-containing protein 106-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
enkurin, TRPC channel interacting protein
phosphoribosyl transferase domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
phosphoribosyltransferase domain-containing protein 1
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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: rho GTPase-activating protein 21
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
apolipoprotein D-like, 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 1 sample with support for all annotated introns
apolipoprotein D-like, transcript variant X7
apolipoprotein D-like, transcript variant X1
apolipoprotein D-like, transcript variant X3
apolipoprotein D-like, transcript variant X4
apolipoprotein D-like, transcript variant X5
apolipoprotein D-like, transcript variant X8
apolipoprotein D-like, transcript variant X9
apolipoprotein D-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
activated CDC42 kinase 1-like, transcript variant X3
activated CDC42 kinase 1-like, transcript variant X2
activated CDC42 kinase 1-like, transcript variant X1
activated CDC42 kinase 1-like isoform X2
activated CDC42 kinase 1-like isoform X1
activated CDC42 kinase 1-like isoform X3
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: 16 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: transferrin receptor protein 1-like
SH3 domain containing kinase binding protein 1, transcript variant X2
SH3 domain containing kinase binding protein 1, transcript variant X1
SH3 domain-containing kinase-binding protein 1 isoform X1
SH3 domain-containing kinase-binding protein 1 isoform X2
mitogen-activated protein kinase kinase kinase 15, 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 1 sample with support for all annotated introns
mitogen-activated protein kinase kinase kinase 15, transcript variant X2
mitogen-activated protein kinase kinase kinase 15 isoform X1
mitogen-activated protein kinase kinase kinase 15 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
connector enhancer of kinase suppressor of Ras 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
small muscle protein X-linked, transcript variant X2
small muscle protein X-linked, transcript variant X1
uncharacterized mitochondrial protein AtMg00860-like
membrane bound transcription factor peptidase, site 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
membrane-bound transcription factor site-2 protease
phosphate regulating endopeptidase homolog X-linked
phosphate-regulating neutral endopeptidase PHEX
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: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: patched domain-containing protein 1
flocculation protein FLO11-like, transcript variant X2
flocculation protein FLO11-like, transcript variant X1
dipeptidyl peptidase like 6, transcript variant X4
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 1 sample with support for all annotated introns
dipeptidyl aminopeptidase-like protein 6 isoform X4
dipeptidyl peptidase like 6, transcript variant X1
dipeptidyl peptidase like 6, transcript variant X2
dipeptidyl aminopeptidase-like protein 6 isoform X2
dipeptidyl aminopeptidase-like protein 6 isoform X1
dipeptidyl peptidase like 6, transcript variant X3
dipeptidyl aminopeptidase-like protein 6 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
phospholipid phosphatase-related protein type 4
phospholipid phosphatase related 5, transcript variant X2
phospholipid phosphatase-related protein type 5 isoform X2
phospholipid phosphatase related 5, transcript variant X1
phospholipid phosphatase-related protein type 5 isoform X1
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: 8 Proteins, and 90% 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: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
vesicular, overexpressed in cancer, prosurvival protein 1
ribosome biogenesis regulatory protein homolog
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: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: myb-related protein A
serum/glucocorticoid regulated kinase family member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
minichromosome maintenance domain containing 2, transcript variant X1
minichromosome maintenance domain containing 2, transcript variant X2
minichromosome maintenance domain-containing protein 2 isoform X1
minichromosome maintenance domain-containing protein 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
protein phosphatase 1 regulatory subunit 42, transcript variant X4
protein phosphatase 1 regulatory subunit 42, transcript variant X2
protein phosphatase 1 regulatory subunit 42, transcript variant X3
protein phosphatase 1 regulatory subunit 42, transcript variant X1
protein phosphatase 1 regulatory subunit 42
centrosome and spindle pole associated protein 1
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
centrosome and spindle pole-associated protein 1
transfer RNA arginine (anticodon CCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ADP ribosylation factor guanine nucleotide exchange factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ADP ribosylation factor guanine nucleotide exchange factor 1, transcript variant X2
brefeldin A-inhibited guanine nucleotide-exchange protein 1 isoform X2
brefeldin A-inhibited guanine nucleotide-exchange protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2, transcript variant X1
phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 2 protein isoform X1
phosphatidylinositol-3,4,5-trisphosphate dependent Rac exchange factor 2, transcript variant X2
phosphatidylinositol 3,4,5-trisphosphate-dependent Rac exchanger 2 protein isoform X2
chromosome 20 C8orf34 homolog, transcript variant X2
chromosome 20 C8orf34 homolog, transcript variant X1
extracellular sulfatase Sulf-1 isoform X1
extracellular sulfatase Sulf-1 isoform X2
solute carrier organic anion transporter family member 5A1, transcript variant X1
solute carrier organic anion transporter family member 5A1, transcript variant X2
solute carrier organic anion transporter family member 5A1
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: 6 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: PR domain zinc finger protein 14
nuclear receptor coactivator 2, transcript variant X2
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, including 3 samples with support for all annotated introns
nuclear receptor coactivator 2, transcript variant X3
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 3 samples with support for all annotated introns
nuclear receptor coactivator 2, transcript variant X4
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, including 4 samples with support for all annotated introns
nuclear receptor coactivator 2, transcript variant X1
nuclear receptor coactivator 2 isoform X2
nuclear receptor coactivator 2 isoform X3
nuclear receptor coactivator 2 isoform X1
translocation associated membrane protein 1
translocating chain-associated membrane protein 1
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: 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: XK-related protein 9
EYA transcriptional coactivator and phosphatase 1, transcript variant X18
EYA transcriptional coactivator and phosphatase 1, transcript variant X2
EYA transcriptional coactivator and phosphatase 1, transcript variant X17
EYA transcriptional coactivator and phosphatase 1, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
EYA transcriptional coactivator and phosphatase 1, transcript variant X15
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 2 samples with support for all annotated introns
EYA transcriptional coactivator and phosphatase 1, transcript variant X14
EYA transcriptional coactivator and phosphatase 1, transcript variant X13
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
EYA transcriptional coactivator and phosphatase 1, transcript variant X10
EYA transcriptional coactivator and phosphatase 1, transcript variant X12
EYA transcriptional coactivator and phosphatase 1, transcript variant X11
EYA transcriptional coactivator and phosphatase 1, transcript variant X9
EYA transcriptional coactivator and phosphatase 1, transcript variant X5
EYA transcriptional coactivator and phosphatase 1, transcript variant X8
EYA transcriptional coactivator and phosphatase 1, transcript variant X7
EYA transcriptional coactivator and phosphatase 1, transcript variant X6
EYA transcriptional coactivator and phosphatase 1, transcript variant X4
EYA transcriptional coactivator and phosphatase 1, transcript variant X1
EYA transcriptional coactivator and phosphatase 1, transcript variant X3
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transient receptor potential cation channel subfamily A member 1
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: 8 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: transient receptor potential cation channel subfamily A member 1
potassium voltage-gated channel subfamily B member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
somatomedin B and thrombospondin type 1 domain containing
somatomedin-B and thrombospondin type-1 domain-containing protein
uncharacterized LOC115025589, transcript variant X1
uncharacterized LOC115025589, transcript variant X2
uncharacterized protein LOC115025589 isoform X2
uncharacterized protein LOC115025589 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00581
staufen double-stranded RNA binding protein 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: double-stranded RNA-binding protein Staufen homolog 2
ubiquitin conjugating enzyme E2 W, transcript variant X1
ubiquitin conjugating enzyme E2 W, transcript variant X2
ubiquitin-conjugating enzyme E2 W isoform X1
ubiquitin-conjugating enzyme E2 W isoform X2
ganglioside induced differentiation associated protein 1, transcript variant X1
ganglioside induced differentiation associated protein 1, transcript variant X2
ganglioside-induced differentiation-associated protein 1 isoform X1
ganglioside-induced differentiation-associated protein 1 isoform X2
peptidase inhibitor 15, transcript variant X1
peptidase inhibitor 15, transcript variant X2
cysteine rich secretory protein LCCL domain containing 1
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: 18 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: cysteine-rich secretory protein LCCL domain-containing 1
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: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 92% 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: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: suppressor of cytokine signaling 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 83% coverage of the annotated genomic feature by RNAseq alignments
translocase of inner mitochondrial membrane 21
mitochondrial import inner membrane translocase subunit Tim21
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X3
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X2
5-methyltetrahydrofolate-homocysteine methyltransferase reductase, transcript variant X1
methionine synthase reductase isoform X1
methionine synthase reductase isoform X2
carboxymethylenebutenolidase homolog, transcript variant X1
carboxymethylenebutenolidase homolog isoform X1
carboxymethylenebutenolidase homolog, transcript variant X2
carboxymethylenebutenolidase homolog isoform X2
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
membrane associated ring-CH-type finger 6, transcript variant X1
membrane associated ring-CH-type finger 6, transcript variant X2
E3 ubiquitin-protein ligase MARCH6 isoform X1
E3 ubiquitin-protein ligase MARCH6 isoform X2
arylamine N-acetyltransferase, pineal gland isozyme NAT-10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
palmitoyltransferase ZDHHC20-like, transcript variant X1
palmitoyltransferase ZDHHC20-like, transcript variant X2
palmitoyltransferase ZDHHC20-like isoform X1
palmitoyltransferase ZDHHC20-like isoform X2
palmitoyltransferase ZDHHC20-like, transcript variant X3
palmitoyltransferase ZDHHC20-like isoform X3
organic solute transporter subunit alpha-like
pyruvate dehydrogenase kinase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
pyruvate dehydrogenase kinase 3, transcript variant X1
pyruvate dehydrogenase kinase 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
pyruvate dehydrogenase kinase 3, transcript variant X5
pyruvate dehydrogenase kinase 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pyruvate dehydrogenase kinase 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pyruvate dehydrogenase kinase, isozyme 3 isoform X1
pyruvate dehydrogenase kinase, isozyme 3 isoform X2
pyruvate dehydrogenase kinase, isozyme 3 isoform X3
pyruvate dehydrogenase kinase, isozyme 3 isoform X4
phosphate cytidylyltransferase 1, choline, beta, transcript variant X1
phosphate cytidylyltransferase 1, choline, beta, transcript variant X2
choline-phosphate cytidylyltransferase B isoform X1
choline-phosphate cytidylyltransferase B isoform X2
DNA polymerase alpha 1, catalytic subunit, transcript variant X1
DNA polymerase alpha 1, catalytic subunit, transcript variant X2
DNA polymerase alpha catalytic subunit isoform X1
DNA polymerase alpha catalytic subunit isoform X2
aristaless related homeobox, transcript variant X1
aristaless related homeobox, transcript variant X2
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: 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: homogentisate 1,2-dioxygenase
NADH:ubiquinone oxidoreductase subunit B4
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; 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, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: rab effector MyRIP-like
ranBP-type and C3HC4-type zinc finger-containing protein 1
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
forkhead box protein H1-like, transcript variant X5
forkhead box protein H1-like, transcript variant X3
forkhead box protein H1-like, transcript variant X4
forkhead box protein H1-like, transcript variant X1
forkhead box protein H1-like, transcript variant X6
forkhead box protein H1-like, transcript variant X2
protein phosphatase 1 regulatory subunit 16A, transcript variant X1
protein phosphatase 1 regulatory subunit 16A, transcript variant X2
protein phosphatase 1 regulatory subunit 16A
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 4 samples with support for all annotated introns
protein disulfide isomerase family A member 4
polycystin 1 like 1, transient receptor potential channel interacting
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; 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
LOW QUALITY PROTEIN: polycystic kidney disease protein 1-like 1
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: 8 Proteins
LOW QUALITY PROTEIN: complement C1q-like protein 2
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
MLLT10 histone lysine methyltransferase DOT1L cofactor, transcript variant X1
MLLT10 histone lysine methyltransferase DOT1L cofactor, transcript variant X4
MLLT10 histone lysine methyltransferase DOT1L cofactor, transcript variant X2
MLLT10 histone lysine methyltransferase DOT1L cofactor, transcript variant X3
BMI1 proto-oncogene, polycomb ring finger, transcript variant X2
BMI1 proto-oncogene, polycomb ring finger, transcript variant X3
BMI1 proto-oncogene, polycomb ring finger, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: sperm-associated antigen 6
phosphatidylinositol-5-phosphate 4-kinase type 2 alpha, transcript variant X2
phosphatidylinositol-5-phosphate 4-kinase type 2 alpha, transcript variant X1
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha isoform X2
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha isoform X1
armadillo repeat containing 3, transcript variant X2
armadillo repeat containing 3, transcript variant X1
armadillo repeat-containing protein 3 isoform X1
armadillo repeat-containing protein 3 isoform X2
methionine-R-sulfoxide reductase B2, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 55% 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: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: contactin-associated protein-like 2
thiamin pyrophosphokinase 1, transcript variant X1
thiamin pyrophosphokinase 1, transcript variant X4
thiamin pyrophosphokinase 1, transcript variant X3
thiamin pyrophosphokinase 1, transcript variant X2
protein transport protein Sec61 subunit gamma
retinol dehydrogenase 12-like, transcript variant X2
retinol dehydrogenase 12-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
retinol dehydrogenase 12-like isoform X1
retinol dehydrogenase 12-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor receptor superfamily member 11A-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: tumor necrosis factor receptor superfamily member 11A-like
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X1
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X3
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X2
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X5
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X6
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X4
phosphatidylinositol glycan anchor biosynthesis class N
GPI ethanolamine phosphate transferase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
polyamine-modulated factor 1-binding protein 1-like isoform X2
polyamine-modulated factor 1-binding protein 1-like isoform X4
polyamine-modulated factor 1-binding protein 1-like isoform X5
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: peroxisome biogenesis factor 2
zinc finger homeobox 4, transcript variant X3
zinc finger homeobox 4, transcript variant X4
zinc finger homeobox 4, transcript variant X1
zinc finger homeobox 4, transcript variant X2
zinc finger homeobox protein 4 isoform X2
zinc finger homeobox protein 4 isoform 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
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: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: myotubularin-related protein 6-like
ankyrin repeat domain-containing protein 33B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
catenin delta-2-like, transcript variant X1
catenin delta-2-like, transcript variant X2
zinc finger C2HC-type containing 1A, transcript variant X2
zinc finger C2HC-type containing 1A, transcript variant X1
zinc finger C2HC domain-containing protein 1A isoform X2
zinc finger C2HC domain-containing protein 1A isoform X1
beta,beta-carotene 15,15'-dioxygenase-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: beta,beta-carotene 15,15'-dioxygenase-like
transmembrane protein 56-B-like, transcript variant X1
transmembrane protein 56-B-like, transcript variant X2
transmembrane protein 56-B-like isoform X1
transmembrane protein 56-B-like isoform X2
pleckstrin homology-like domain family B member 2, transcript variant X2
pleckstrin homology-like domain family B member 2, transcript variant X4
pleckstrin homology-like domain family B member 2, transcript variant X3
pleckstrin homology-like domain family B member 2, transcript variant X1
pleckstrin homology-like domain family B member 2, transcript variant X5
pleckstrin homology-like domain family B member 1 isoform X2
pleckstrin homology-like domain family B member 2 isoform X4
pleckstrin homology-like domain family B member 2 isoform X3
pleckstrin homology-like domain family B member 2 isoform X1
pleckstrin homology-like domain family B member 2 isoform X5
PI-PLC X domain-containing protein 2-like, transcript variant X1
PI-PLC X domain-containing protein 2-like, transcript variant X2
PI-PLC X domain-containing protein 2-like
male germ cell associated kinase, transcript variant X2
male germ cell associated kinase, transcript variant X7
male germ cell associated kinase, transcript variant X8
male germ cell associated kinase, 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
male germ cell associated kinase, transcript variant X3
male germ cell associated kinase, transcript variant X4
serine/threonine-protein kinase MAK isoform X2
serine/threonine-protein kinase MAK isoform X7
serine/threonine-protein kinase MAK isoform X8
serine/threonine-protein kinase MAK isoform X1
serine/threonine-protein kinase MAK isoform X3
serine/threonine-protein kinase MAK isoform X4
male germ cell associated kinase, transcript variant X6
male germ cell associated kinase, transcript variant X5
serine/threonine-protein kinase MAK isoform X5
serine/threonine-protein kinase MAK isoform X6
transcription factor AP-2 alpha, transcript variant X1
transcription factor AP-2 alpha, transcript variant X2
transcription factor AP-2-alpha isoform X1
transcription factor AP-2-alpha isoform X2
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: 1 Protein, and 21% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: orofacial cleft 1 candidate gene 1 protein
adenosine 3'-phospho 5'-phosphosulfate transporter 2
eukaryotic translation elongation factor 1 epsilon 1
eukaryotic translation elongation factor 1 epsilon-1
biogenesis of lysosomal organelles complex 1 subunit 5
biogenesis of lysosome-related organelles complex 1 subunit 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
programmed cell death 6, transcript variant X1
programmed cell death 6, transcript variant X2
programmed cell death protein 6 isoform X2
programmed cell death protein 6 isoform X1
meiotic recombination protein REC8 homolog
flap structure-specific endonuclease 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
flap structure-specific endonuclease 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
vascular cell adhesion protein 1-like, transcript variant X2
vascular cell adhesion protein 1-like, transcript variant X1
vascular cell adhesion protein 1-like isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: vascular cell adhesion protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% 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: 4 Proteins, and 97% 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: 97% coverage of the annotated genomic feature by RNAseq alignments
vascular cell adhesion protein 1-like, transcript variant X5
vascular cell adhesion protein 1-like, transcript variant X3
vascular cell adhesion protein 1-like, transcript variant X4
sialic acid-binding Ig-like lectin 12 isoform X2
sialic acid-binding Ig-like lectin 12 isoform X1
vascular cell adhesion protein 1-like isoform X3
phosphoenolpyruvate carboxykinase, cytosolic [GTP]-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
LOW QUALITY PROTEIN: phosphoenolpyruvate carboxykinase, cytosolic [GTP]-like
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
fat storage-inducing transmembrane protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
thiamine triphosphatase, transcript variant X5
thiamine triphosphatase, transcript variant X2
thiamine triphosphatase, transcript variant X3
thiamine triphosphatase, transcript variant X6
thiamine triphosphatase, transcript variant X7
thiamine triphosphatase, transcript variant X4
thiamine triphosphatase, transcript variant X1
zinc finger homeobox protein 4-like, transcript variant X3
zinc finger homeobox protein 4-like isoform X3
zinc finger homeobox protein 4-like, transcript variant X2
zinc finger homeobox protein 4-like isoform X2
zinc finger homeobox protein 4-like, transcript variant X1
zinc finger homeobox protein 4-like isoform X1
poly(A) binding protein nuclear 1, transcript variant X1
poly(A) binding protein nuclear 1, transcript variant X2
polyadenylate-binding protein 2 isoform X1
polyadenylate-binding protein 2 isoform X2
poly(A) binding protein nuclear 1, transcript variant X3
polyadenylate-binding protein 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 178 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
receptor activity-modifying protein 3-like, transcript variant X2
receptor activity-modifying protein 3-like isoform X2
receptor activity-modifying protein 3-like, transcript variant X1
receptor activity-modifying protein 3-like isoform X1
uncharacterized protein C11orf65 homolog, transcript variant X2
uncharacterized protein C11orf65 homolog, transcript variant X3
uncharacterized protein C11orf65 homolog, transcript variant X1
uncharacterized protein C11orf65 homolog, transcript variant X4
uncharacterized protein C11orf65 homolog
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 2 samples with support for all annotated introns
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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: 17 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: proteasome maturation protein
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: 21 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LOW QUALITY PROTEIN: matrix metalloproteinase-16-like
cyclic nucleotide-gated cation channel beta-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
neutral sphingomyelinase activation associated factor, transcript variant X2
neutral sphingomyelinase activation associated factor, transcript variant X1
transmembrane protein 241, transcript variant X3
transmembrane protein 241, transcript variant X1
transmembrane protein 241, transcript variant X2
RB binding protein 8, endonuclease, transcript variant X3
RB binding protein 8, endonuclease, transcript variant X5
RB binding protein 8, endonuclease, transcript variant X1
RB binding protein 8, endonuclease, transcript variant X2
RB binding protein 8, endonuclease, transcript variant X4
family with sequence similarity 168 member B, transcript variant X2
family with sequence similarity 168 member B, transcript variant X3
family with sequence similarity 168 member B, transcript variant X1
myelin-associated neurite-outgrowth inhibitor isoform X2
myelin-associated neurite-outgrowth inhibitor isoform X1
negative regulator of reactive oxygen species
transforming growth factor beta activator LRRC33
vav guanine nucleotide exchange factor 3
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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: guanine nucleotide exchange factor VAV3
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
RNA binding region (RNP1, RRM) containing 3
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: 4 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
LOW QUALITY PROTEIN: RNA-binding region-containing protein 3
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: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: collagen alpha-1(XI) chain
very-long-chain enoyl-CoA reductase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein kinase, DNA-activated, catalytic subunit
DNA-dependent protein kinase catalytic subunit
GRB2 associated regulator of MAPK1 subtype 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
GRB2-associated and regulator of MAPK protein 1
neutrophil cytosolic factor 2, transcript variant X6
neutrophil cytosolic factor 2, transcript variant X5
neutrophil cytosolic factor 2, transcript variant X1
neutrophil cytosolic factor 2, 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 3 samples with support for all annotated introns
neutrophil cytosolic factor 2, transcript variant X3
neutrophil cytosolic factor 2, transcript variant X4
diphthamide biosynthesis 2, transcript variant X1
diphthamide biosynthesis 2, transcript variant X2
2-(3-amino-3-carboxypropyl)histidine synthase subunit 2
mitochondrial calcium uniporter regulator 1-like, transcript variant X2
mitochondrial calcium uniporter regulator 1-like, transcript variant X1
mitochondrial calcium uniporter regulator 1-like isoform X1
mitochondrial calcium uniporter regulator 1-like isoform X2
regulator of G-protein signaling 9-binding protein B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 84% 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: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF01277
ankyrin repeat and sterile alpha motif domain containing 6, transcript variant X1
ankyrin repeat and sterile alpha motif domain containing 6, transcript variant X2
ankyrin repeat and SAM domain-containing protein 6 isoform X1
ankyrin repeat and SAM domain-containing protein 6 isoform X2
ankyrin repeat and sterile alpha motif domain containing 6, transcript variant X3
ankyrin repeat and SAM domain-containing protein 6 isoform X3
uncharacterized LOC115025755, transcript variant X1
uncharacterized LOC115025755, transcript variant X2
phosphatidylinositol glycan anchor biosynthesis class M
leukocyte elastase inhibitor-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
leukocyte elastase inhibitor-like, 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 4 samples with support for all annotated introns
leukocyte elastase inhibitor-like, transcript variant X1
leukocyte elastase inhibitor-like, transcript variant X2
leukocyte elastase inhibitor-like isoform X1
leukocyte elastase inhibitor-like isoform X2
SUN domain-containing protein 2-like, transcript variant X2
SUN domain-containing protein 2-like, transcript variant X1
SUN domain-containing protein 2-like isoform X1
SUN domain-containing protein 2-like isoform X2
general transcription factor II-I repeat domain-containing protein 2A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 20% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 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: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
leukocyte elastase inhibitor-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
NEDD4-like E3 ubiquitin-protein ligase WWP1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
regulator of microtubule dynamics protein 1
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 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: 36 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: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
isopentenyl-diphosphate delta isomerase 1, transcript variant X1
isopentenyl-diphosphate delta isomerase 1, transcript variant X2
isopentenyl-diphosphate Delta-isomerase 1 isoform X1
isopentenyl-diphosphate Delta-isomerase 1 isoform X2
WD repeat-containing protein 37-like, transcript variant X2
WD repeat-containing protein 37-like, transcript variant X1
WD repeat-containing protein 37-like, transcript variant X3
WD repeat-containing protein 37-like isoform X1
WD repeat-containing protein 37-like isoform X2
double-stranded RNA-specific editase B2-like, transcript variant X5
double-stranded RNA-specific editase B2-like isoform X5
double-stranded RNA-specific editase B2-like, transcript variant X2
double-stranded RNA-specific editase B2-like, transcript variant X6
double-stranded RNA-specific editase B2-like, transcript variant X1
double-stranded RNA-specific editase B2-like, transcript variant X7
double-stranded RNA-specific editase B2-like, transcript variant X3
double-stranded RNA-specific editase B2-like, transcript variant X8
double-stranded RNA-specific editase B2-like isoform X6
double-stranded RNA-specific editase B2-like isoform X2
double-stranded RNA-specific editase B2-like isoform X1
double-stranded RNA-specific editase B2-like isoform X3
double-stranded RNA-specific editase B2-like isoform X7
double-stranded RNA-specific editase B2-like, transcript variant X4
double-stranded RNA-specific editase B2-like isoform X4
ATP-dependent 6-phosphofructokinase, platelet type-like, transcript variant X4
ATP-dependent 6-phosphofructokinase, platelet type-like, transcript variant X9
ATP-dependent 6-phosphofructokinase, platelet type-like, transcript variant X10
ATP-dependent 6-phosphofructokinase, platelet type-like, transcript variant X2
ATP-dependent 6-phosphofructokinase, platelet type-like, transcript variant X3
ATP-dependent 6-phosphofructokinase, platelet type-like, transcript variant X8
ATP-dependent 6-phosphofructokinase, platelet type-like, transcript variant X1
ATP-dependent 6-phosphofructokinase, platelet type-like, transcript variant X7
ATP-dependent 6-phosphofructokinase, platelet type-like, transcript variant X11
ATP-dependent 6-phosphofructokinase, platelet type-like, transcript variant X5
ATP-dependent 6-phosphofructokinase, platelet type-like, transcript variant X6
ATP-dependent 6-phosphofructokinase, platelet type-like isoform X2
ATP-dependent 6-phosphofructokinase, platelet type-like isoform X4
ATP-dependent 6-phosphofructokinase, platelet type-like isoform X1
ATP-dependent 6-phosphofructokinase, platelet type-like isoform X3
ATP-dependent 6-phosphofructokinase, platelet type-like isoform X9
ATP-dependent 6-phosphofructokinase, platelet type-like isoform X5
ATP-dependent 6-phosphofructokinase, platelet type-like isoform X7
ATP-dependent 6-phosphofructokinase, platelet type-like isoform X11
ATP-dependent 6-phosphofructokinase, platelet type-like isoform X10
ATP-dependent 6-phosphofructokinase, platelet type-like isoform X6
ATP-dependent 6-phosphofructokinase, platelet type-like isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 17% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclic AMP-dependent transcription factor ATF-1-like, transcript variant X1
cyclic AMP-dependent transcription factor ATF-1-like, transcript variant X2
cyclic AMP-dependent transcription factor ATF-1-like isoform X1
cyclic AMP-dependent transcription factor ATF-1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transfer RNA tryptophan (anticodon CCA); 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: 12 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: 23 Proteins, and 95% 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: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RAB18, member RAS oncogene family, transcript variant X2
RAB18, member RAS oncogene family, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 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: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: armadillo repeat-containing protein 4
membrane palmitoylated protein 7, transcript variant X2
membrane palmitoylated protein 7, transcript variant X1
WW domain containing adaptor with coiled-coil, transcript variant X3
WW domain containing adaptor with coiled-coil, transcript variant X1
WW domain containing adaptor with coiled-coil, transcript variant X2
WW domain-containing adapter protein with coiled-coil isoform X1
WW domain-containing adapter protein with coiled-coil isoform X2
WW domain-containing adapter protein with coiled-coil isoform X3
BMP and activin membrane bound inhibitor
BMP and activin membrane-bound inhibitor homolog
mitogen-activated protein kinase kinase kinase 8, transcript variant X1
mitogen-activated protein kinase kinase kinase 8, transcript variant X2
mitogen-activated protein kinase kinase kinase 8
mitochondrial poly(A) polymerase, transcript variant X2
mitochondrial poly(A) polymerase, transcript variant X3
mitochondrial poly(A) polymerase, transcript variant X1
poly(A) RNA polymerase, mitochondrial isoform X1
poly(A) RNA polymerase, mitochondrial isoform X2
poly(A) RNA polymerase, mitochondrial isoform X3
junctional cadherin 5 associated, transcript variant X1
junctional cadherin 5 associated, transcript variant X2
junctional protein associated with coronary artery disease
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon UAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA phenylalanine (anticodon AAA); 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: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 438, transcript variant X2
zinc finger protein 438, transcript variant X1
zinc finger protein 438, transcript variant X3
zinc finger E-box binding homeobox 1, transcript variant X1
zinc finger E-box-binding homeobox 1 isoform X1
zinc finger E-box binding homeobox 1, transcript variant X4
zinc finger E-box binding homeobox 1, transcript variant X3
zinc finger E-box-binding homeobox 1 isoform X3
zinc finger E-box binding homeobox 1, transcript variant X2
zinc finger E-box-binding homeobox 1 isoform X2
zinc finger E-box-binding homeobox 1 isoform X4
Rho GTPase activating protein 12, transcript variant X5
Rho GTPase activating protein 12, transcript variant X2
Rho GTPase activating protein 12, transcript variant X4
Rho GTPase activating protein 12, transcript variant X3
Rho GTPase activating protein 12, transcript variant X1
Rho GTPase activating protein 12, transcript variant X6
rho GTPase-activating protein 12 isoform X5
rho GTPase-activating protein 12 isoform X2
rho GTPase-activating protein 12 isoform X4
rho GTPase-activating protein 12 isoform X3
rho GTPase-activating protein 12 isoform X1
rho GTPase-activating protein 12 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
glucose-fructose oxidoreductase domain-containing protein 1, transcript variant X2
glucose-fructose oxidoreductase domain-containing protein 1, transcript variant X1
glucose-fructose oxidoreductase domain-containing protein 1
solute carrier family 12 member 7-like, transcript variant X2
solute carrier family 12 member 7-like, transcript variant X1
solute carrier family 12 member 7-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 12 member 7-like, transcript variant X3
solute carrier family 12 member 7-like isoform X2
solute carrier family 12 member 7-like isoform X1
solute carrier family 12 member 7-like isoform X4
solute carrier family 12 member 7-like isoform X3
zinc finger protein 239-like, transcript variant X3
zinc finger protein 239-like, transcript variant X1
zinc finger protein 239-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
amiloride-sensitive amine oxidase [copper-containing]
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily H member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
microtubule-associated protein 4-like, transcript variant X2
microtubule-associated protein 4-like, transcript variant X1
microtubule-associated protein 4-like, transcript variant X13
microtubule-associated protein 4-like, transcript variant X5
microtubule-associated protein 4-like, transcript variant X7
microtubule-associated protein 4-like, transcript variant X4
microtubule-associated protein 4-like, transcript variant X9
microtubule-associated protein 4-like, transcript variant X3
microtubule-associated protein 4-like, transcript variant X6
microtubule-associated protein 4-like, transcript variant X8
microtubule-associated protein 4-like, transcript variant X11
microtubule-associated protein 4-like, transcript variant X12
microtubule-associated protein 4-like, transcript variant X15
microtubule-associated protein 4-like isoform X2
microtubule-associated protein 4-like isoform X1
microtubule-associated protein 4-like isoform X7
microtubule-associated protein 4-like isoform X4
microtubule-associated protein 4-like isoform X9
microtubule-associated protein 4-like isoform X3
microtubule-associated protein 4-like isoform X13
microtubule-associated protein 4-like isoform X15
microtubule-associated protein 4-like isoform X6
microtubule-associated protein 4-like isoform X8
microtubule-associated protein 4-like isoform X11
microtubule-associated protein 4-like isoform X5
microtubule-associated protein 4-like isoform X12
microtubule-associated protein 4-like, transcript variant X10
microtubule-associated protein 4-like isoform X10
microtubule-associated protein 4-like, transcript variant X14
microtubule-associated protein 4-like isoform X14
intraflagellar transport 74, transcript variant X1
intraflagellar transport 74, transcript variant X2
intraflagellar transport protein 74 homolog isoform X1
intraflagellar transport protein 74 homolog isoform X2
zinc finger CCHC-type containing 2, transcript variant X2
zinc finger CCHC-type containing 2, transcript variant X1
zinc finger CCHC domain-containing protein 2 isoform X2
zinc finger CCHC domain-containing protein 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA leucine (anticodon CAA); 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 85% coverage of the annotated genomic feature by RNAseq alignments
zinc finger BED domain-containing protein 4-like
V-set and transmembrane domain containing 2A
V-set and transmembrane domain-containing protein 2A
HECT, C2 and WW domain containing E3 ubiquitin protein ligase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments