Salmo salar chromosome ssa08, Ssal_v3.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Protacanthopterygii; Salmoniformes; Salmonidae; Salmoninae; Salmo.
REFSEQ INFORMATION: The reference sequence is identical to\nHG993267.1.\nAssembly name: Ssal_v3.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the NORWEGIAN UNIVERSITY OF LIFE\nSCIENCES on 2021/04/21. The original whole-genome shotgun project\nhas the accession CAJNNT000000000.2.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Salmo salar Annotation Release 102\nAnnotation Version :: 102\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
DnaJ homolog subfamily A member 1; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
DnaJ homolog subfamily A member 1, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
DnaJ homolog subfamily A member 1, transcript variant X1
similar to RNA sequence, mRNA (same species):RefSeq:NM_001140191.1
annotated by transcript or proteomic data
The RefSeq transcript has 1 non-frameshifting indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: BestRefSeq.
dnaJ homolog subfamily A member 1 isoform X1
dnaJ homolog subfamily A member 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
protein TBATA-like, transcript variant X1
protein TBATA-like, transcript variant X2
microsomal triglyceride transfer protein-like, transcript variant X3
microsomal triglyceride transfer protein-like, transcript variant X4
microsomal triglyceride transfer protein-like, transcript variant X1
microsomal triglyceride transfer protein-like, transcript variant X2
microsomal triglyceride transfer protein-like isoform X1
microsomal triglyceride transfer protein-like isoform X2
microsomal triglyceride transfer protein-like isoform 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 27 samples with support for all annotated introns
pre-mRNA-splicing factor ATP-dependent RNA helicase DHX15-like
storkhead-box protein 2-like, transcript variant X1
storkhead-box protein 2-like, transcript variant X2
DNA-directed primase/polymerase protein, transcript variant X6
DNA-directed primase/polymerase protein, transcript variant X4
DNA-directed primase/polymerase protein, transcript variant X7
DNA-directed primase/polymerase protein, transcript variant X1
DNA-directed primase/polymerase protein, transcript variant X3
DNA-directed primase/polymerase protein, transcript variant X2
DNA-directed primase/polymerase protein, transcript variant X5
DNA-directed primase/polymerase protein isoform X2
DNA-directed primase/polymerase protein isoform X1
uncharacterized protein LOC106610002 isoform X3
uncharacterized protein LOC106610002 isoform X4
long-chain-fatty-acid--CoA ligase 1-like, transcript variant X1
long-chain-fatty-acid--CoA ligase 1-like, transcript variant X5
long-chain-fatty-acid--CoA ligase 1-like, transcript variant X2
long-chain-fatty-acid--CoA ligase 1-like, transcript variant X3
long-chain-fatty-acid--CoA ligase 1-like, transcript variant X4
long-chain-fatty-acid--CoA ligase 1-like isoform X1
long-chain-fatty-acid--CoA ligase 1-like isoform X4
long-chain-fatty-acid--CoA ligase 1-like isoform X2
long-chain-fatty-acid--CoA ligase 1-like isoform X3
uncharacterized LOC106610004, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC106610004, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
hairy and enhancer of split-related protein helt
solute carrier family 25-2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
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 65 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
guanylate cyclase soluble subunit alpha-1-like, transcript variant X1
guanylate cyclase soluble subunit alpha-1-like, transcript variant X2
guanylate cyclase soluble subunit alpha-1-like isoform X1
guanylate cyclase soluble subunit alpha-1-like isoform X2
guanylate cyclase soluble subunit beta-1, transcript variant X2
guanylate cyclase soluble subunit beta-1, transcript variant X1
guanylate cyclase soluble subunit beta-1 isoform X1
guanylate cyclase soluble subunit beta-1 isoform X2
inactive ubiquitin carboxyl-terminal hydrolase 53-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
inactive ubiquitin carboxyl-terminal hydrolase 53-like, transcript variant X1
inactive ubiquitin carboxyl-terminal hydrolase 53-like isoform X2
inactive ubiquitin carboxyl-terminal hydrolase 53-like isoform X1
nematocyst expressed protein 3-like, transcript variant X1
nematocyst expressed protein 3-like, transcript variant X2
nematocyst expressed protein 3-like isoform X1
sporozoite surface protein 2-like, transcript variant X2
sporozoite surface protein 2-like, transcript variant X1
sporozoite surface protein 2-like isoform X2
uncharacterized LOC106610035, transcript variant X2
uncharacterized LOC106610035, transcript variant X3
uncharacterized LOC106610035, transcript variant X1
uncharacterized protein LOC106610035 isoform X1
uncharacterized protein LOC106610035 isoform X2
SPARC-like protein 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
SPARC-like protein 1, transcript variant X2
glycoprotein hormones alpha chain 2-like
tripartite motif-containing protein 2, transcript variant X3
tripartite motif-containing protein 2, transcript variant X2
tripartite motif-containing protein 2, transcript variant X5
tripartite motif-containing protein 2, transcript variant X6
tripartite motif-containing protein 2, transcript variant X1
tripartite motif-containing protein 2, transcript variant X4
tripartite motif-containing protein 2 isoform X1
tripartite motif-containing protein 2 isoform X2
meiotic nuclear division protein 1 homolog
transmembrane protein 131-like, transcript variant X1
transmembrane protein 131-like, transcript variant X3
transmembrane protein 131-like, transcript variant X2
transmembrane protein 131-like isoform X1
transmembrane protein 131-like isoform X3
transmembrane protein 131-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
CDGSH iron sulfur domain 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001140897.1
CDGSH iron-sulfur domain-containing protein 2B
propagated from UniProtKB/Swiss-Prot (B5X8S2.1); transmembrane region
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial, transcript variant X1
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial, transcript variant X2
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial isoform X1
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial isoform X2
leucine-rich repeat transmembrane neuronal 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 39 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
atrial natriuretic peptide receptor 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
atrial natriuretic peptide receptor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments
atrial natriuretic peptide receptor 1-like
RING finger protein 24, transcript variant X3
RING finger protein 24, transcript variant X1
RING finger protein 24, transcript variant X2
F-box only protein 41-like, transcript variant X1
F-box only protein 41-like, transcript variant X3
F-box only protein 41-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
mannosyl-oligosaccharide glucosidase-like, transcript variant X1
mannosyl-oligosaccharide glucosidase-like, transcript variant X2
mannosyl-oligosaccharide glucosidase-like isoform X1
mannosyl-oligosaccharide glucosidase-like isoform X2
programmed cell death protein 4-like, transcript variant X1
programmed cell death protein 4-like, transcript variant X2
programmed cell death protein 4-like isoform X1
programmed cell death protein 4-like isoform X2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protein PAT1 homolog 1-like, transcript variant X1
protein PAT1 homolog 1-like, transcript variant X2
protein PAT1 homolog 1-like, transcript variant X3
retrovirus-related Pol polyprotein from transposon opus
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 31 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 1 sample with support for all annotated introns
SLAM family member 5-like, transcript variant X1
SLAM family member 5-like, transcript variant X7
SLAM family member 5-like, transcript variant X4
SLAM family member 5-like, transcript variant X5
SLAM family member 5-like, transcript variant X6
SLAM family member 5-like, transcript variant X2
SLAM family member 5-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
ribosomal protein S6 kinase beta-2-like, transcript variant X4
ribosomal protein S6 kinase beta-2-like, transcript variant X2
ribosomal protein S6 kinase beta-2-like, transcript variant X1
ribosomal protein S6 kinase beta-2-like, transcript variant X3
ribosomal protein S6 kinase beta-2-like isoform X2
ribosomal protein S6 kinase beta-2-like isoform X1
LON peptidase N-terminal domain and RING finger protein 1
calcium-binding protein 2-like, transcript variant X1
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 1 sample with support for all annotated introns
calcium-binding protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
calcium-binding protein 2-like, transcript variant X3
calcium-binding protein 2-like isoform X2
calcium-binding protein 2-like isoform X1
double C2-like domain-containing protein beta, transcript variant X1
double C2-like domain-containing protein beta, transcript variant X2
double C2-like domain-containing protein beta, transcript variant X3
double C2-like domain-containing protein beta isoform X1
double C2-like domain-containing protein beta isoform X2
plasma protease C1 inhibitor-like, transcript variant X3
plasma protease C1 inhibitor-like, transcript variant X2
plasma protease C1 inhibitor-like, transcript variant X1
plasma protease C1 inhibitor-like isoform X1
plasma protease C1 inhibitor-like isoform X2
cyclin-dependent kinase 2-associated 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, including 26 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 91 samples with support for all annotated introns
uncharacterized LOC106609955, transcript variant X1
uncharacterized protein LOC106609955 isoform X1
uncharacterized LOC106609955, transcript variant X2
uncharacterized protein LOC106609955 isoform X2
E3 ubiquitin-protein ligase ZFP91-like, transcript variant X3
E3 ubiquitin-protein ligase ZFP91-like, transcript variant X1
E3 ubiquitin-protein ligase ZFP91-like, transcript variant X2
E3 ubiquitin-protein ligase ZFP91-like, transcript variant X4
E3 ubiquitin-protein ligase ZFP91-like isoform X1
zinc finger protein squeeze-like isoform X2
uncharacterized protein DDB_G0283357-like
uncharacterized LOC106609985, transcript variant X1
uncharacterized LOC106609985, transcript variant X2
claudin domain-containing protein 1-like, transcript variant X2
claudin domain-containing protein 1-like, transcript variant X1
claudin domain-containing protein 1-like
N-acyl-aromatic-L-amino acid amidohydrolase (carboxylate-forming) B, transcript variant X1
N-acyl-aromatic-L-amino acid amidohydrolase (carboxylate-forming) B, transcript variant X2
N-acyl-aromatic-L-amino acid amidohydrolase (carboxylate-forming) B, transcript variant X3
N-acyl-aromatic-L-amino acid amidohydrolase (carboxylate-forming) B
neuromedin-K receptor-like, 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 5 samples with support for all annotated introns
neuromedin-K receptor-like, 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 6 samples with support for all annotated introns
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
coiled-coil domain-containing protein 86
oxysterol-binding protein 1-like, transcript variant X3
oxysterol-binding protein 1-like, transcript variant X4
oxysterol-binding protein 1-like, transcript variant X8
oxysterol-binding protein 1-like, transcript variant X14
oxysterol-binding protein 1-like, transcript variant X13
oxysterol-binding protein 1-like, transcript variant X11
oxysterol-binding protein 1-like, transcript variant X12
oxysterol-binding protein 1-like, transcript variant X9
oxysterol-binding protein 1-like, transcript variant X10
oxysterol-binding protein 1-like, transcript variant X1
oxysterol-binding protein 1-like, transcript variant X2
oxysterol-binding protein 1-like, transcript variant X6
oxysterol-binding protein 1-like, transcript variant X7
oxysterol-binding protein 1-like, transcript variant X5
oxysterol-binding protein 1-like isoform X2
oxysterol-binding protein 1-like isoform X8
oxysterol-binding protein 1-like isoform X7
oxysterol-binding protein 1-like isoform X5
oxysterol-binding protein 1-like isoform X6
oxysterol-binding protein 1-like isoform X3
oxysterol-binding protein 1-like isoform X4
oxysterol-binding protein 1-like isoform X1
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: pericentriolar material 1 protein
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00066
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
protocadherin Fat 1-like, transcript variant X2
protocadherin Fat 1-like, transcript variant X1
protocadherin Fat 1-like, transcript variant X3
protocadherin Fat 1-like, transcript variant X5
protocadherin Fat 1-like, transcript variant X4
protocadherin Fat 1-like, transcript variant X6
protocadherin Fat 1-like, transcript variant X7
protocadherin Fat 1-like, transcript variant X8
uncharacterized LOC106609938, transcript variant X1
uncharacterized LOC106609938, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 7% 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
sorbin and SH3 domain-containing protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sorbin and SH3 domain-containing protein 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sorbin and SH3 domain-containing protein 2, transcript variant X1
sorbin and SH3 domain-containing protein 2, transcript variant X6
sorbin and SH3 domain-containing protein 2, transcript variant X7
sorbin and SH3 domain-containing protein 2, transcript variant X2
sorbin and SH3 domain-containing protein 2, transcript variant X11
sorbin and SH3 domain-containing protein 2, transcript variant X8
sorbin and SH3 domain-containing protein 2, transcript variant X9
sorbin and SH3 domain-containing protein 2 isoform X1
sorbin and SH3 domain-containing protein 2 isoform X4
sorbin and SH3 domain-containing protein 2 isoform X5
sorbin and SH3 domain-containing protein 2 isoform X8
sorbin and SH3 domain-containing protein 2 isoform X6
sorbin and SH3 domain-containing protein 2 isoform X3
sorbin and SH3 domain-containing protein 2, transcript variant X10
sorbin and SH3 domain-containing protein 2 isoform X7
sorbin and SH3 domain-containing protein 2, transcript variant X3
sorbin and SH3 domain-containing protein 2 isoform X2
PDZ and LIM domain protein 3; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 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: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Lecithin retinol acyltransferase; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001140926.1
The RefSeq transcript has 4 substitutions, 2 non-frameshifting indels compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 18% 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 86% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: palmitoyltransferase ZDHHC5-A
thioredoxin-related transmembrane protein 2b
thioredoxin-related transmembrane protein 2-B
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 33 samples with support for all annotated introns
DNA polymerase delta 4, accessory subunit; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
DNA polymerase delta 4, accessory subunit, transcript variant X1
DNA polymerase delta 4, accessory subunit
similar to RNA sequence, mRNA (same species):RefSeq:NM_001146625.2
The RefSeq transcript has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
DNA polymerase delta subunit 4 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 84% 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 EST, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transmembrane protein 187
NADH dehydrogenase [ubiquinone] iron-sulfur protein 8, mitochondrial
lysine (K)-specific demethylase 2Aa, transcript variant X1
lysine (K)-specific demethylase 2Aa isoform X1
lysine (K)-specific demethylase 2Aa, transcript variant X2
lysine (K)-specific demethylase 2Aa isoform X2
lysine (K)-specific demethylase 2Aa, transcript variant X3
lysine (K)-specific demethylase 2Aa isoform X3
T cell immune regulator 1, ATPase H+ transporting V0 subunit a3a, transcript variant X2
T cell immune regulator 1, ATPase H+ transporting V0 subunit a3a, transcript variant X1
V-type proton ATPase 116 kDa subunit a3 isoform X1
V-type proton ATPase 116 kDa subunit a3 isoform X2
DNA-directed RNA polymerase II subunit RPB1
membrane-spanning 4-domains subfamily A member 12-like, transcript variant X1
membrane-spanning 4-domains subfamily A member 12-like, transcript variant X2
membrane-spanning 4-domains subfamily A member 12-like, transcript variant X3
membrane-spanning 4-domains subfamily A member 12-like
vacuolar protein sorting-associated protein 37C-like, transcript variant X1
vacuolar protein sorting-associated protein 37C-like, transcript variant X2
vacuolar protein sorting-associated protein 37C-like isoform X1
vacuolar protein sorting-associated protein 37C-like, transcript variant X3
vacuolar protein sorting-associated protein 37C-like isoform X2
transmembrane protein 132A, transcript variant X1
transmembrane protein 132A, transcript variant X2
sodium/potassium/calcium exchanger 2-like, transcript variant X1
sodium/potassium/calcium exchanger 2-like, transcript variant X2
sodium/potassium/calcium exchanger 2-like, transcript variant X3
sodium/potassium/calcium exchanger 2-like, transcript variant X4
sodium/potassium/calcium exchanger 2-like isoform X1
sodium/potassium/calcium exchanger 2-like isoform X2
sodium/potassium/calcium exchanger 2-like isoform X3
sodium/potassium/calcium exchanger 2-like isoform X4
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 30 samples with support for all annotated introns
sialic acid synthase-like, transcript variant X1
sialic acid synthase-like, transcript variant X3
sialic acid synthase-like, transcript variant X2
clathrin, light chain A, transcript variant X1
clathrin, light chain A, transcript variant X2
clathrin, light chain A, transcript variant X3
bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase, transcript variant X3
bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase, transcript variant X1
bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase, transcript variant X5
bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase, transcript variant X4
bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase, transcript variant X2
bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase isoform X2
bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase isoform X1
bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
beta-1,4-galactosyltransferase 1-like, transcript variant X1
beta-1,4-galactosyltransferase 1-like isoform X1
beta-1,4-galactosyltransferase 1-like, transcript variant X2
beta-1,4-galactosyltransferase 1-like isoform X2
beta-1,4-galactosyltransferase 1, transcript variant X1
beta-1,4-galactosyltransferase 1 isoform X1
beta-1,4-galactosyltransferase 1, transcript variant X2
beta-1,4-galactosyltransferase 1 isoform X2
phospholipid-transporting ATPase ABCA1, transcript variant X5
phospholipid-transporting ATPase ABCA1, transcript variant X4
phospholipid-transporting ATPase ABCA1, transcript variant X3
phospholipid-transporting ATPase ABCA1, transcript variant X1
phospholipid-transporting ATPase ABCA1, transcript variant X2
phospholipid-transporting ATPase ABCA1 isoform X4
phospholipid-transporting ATPase ABCA1 isoform X3
phospholipid-transporting ATPase ABCA1 isoform X2
phospholipid-transporting ATPase ABCA1 isoform X1
zinc finger protein 34-like, transcript variant X1
zinc finger protein 34-like, transcript variant X4
zinc finger protein 34-like, transcript variant X3
uncharacterized protein LOC106609873 isoform X1
zinc finger protein 34-like, transcript variant X5
neurotrophin receptor-interacting factor homolog, transcript variant X3
neurotrophin receptor-interacting factor homolog, transcript variant X2
neurotrophin receptor-interacting factor homolog, transcript variant X1
neurotrophin receptor-interacting factor homolog, transcript variant X4
uncharacterized protein LOC106609876 isoform X1
uncharacterized protein LOC106609876 isoform X2
uncharacterized protein LOC106609876 isoform X4
neurotrophin receptor-interacting factor homolog isoform X3
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
zinc finger protein 34-like, transcript variant X2
zinc finger protein ztf-6-like isoform X2
oocyte zinc finger protein XlCOF7.1-like, 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 26 samples with support for all annotated introns
oocyte zinc finger protein XlCOF7.1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
oocyte zinc finger protein XlCOF7.1-like isoform X5
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 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 18-like, transcript variant X2
zinc finger and BTB domain-containing protein 18-like, transcript variant X1
zinc finger and BTB domain-containing protein 18-like isoform X1
zinc finger and BTB domain-containing protein 18-like isoform X2
oocyte zinc finger protein XlCOF7.1-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 8 samples with support for all annotated introns
oocyte zinc finger protein XlCOF7.1-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 56 samples with support for all annotated introns
oocyte zinc finger protein XlCOF7.1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
oocyte zinc finger protein XlCOF7.1-like, transcript variant X7
homeotic protein spalt-major-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
oocyte zinc finger protein XlCOF7.1-like, transcript variant X1
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 68 samples with support for all annotated introns
homeotic protein spalt-major-like isoform X1
zinc finger protein 205-like, transcript variant X3
zinc finger protein 205-like, transcript variant X1
zinc finger protein 205-like, transcript variant X2
zinc finger protein 205-like, transcript variant X7
uncharacterized protein LOC106606466 isoform X3
uncharacterized protein LOC106606466 isoform X1
uncharacterized protein LOC106606466 isoform X2
zinc finger protein 768-like, transcript variant X3
zinc finger protein 768-like, transcript variant X1
neurotrophin receptor-interacting factor homolog isoform X1
zinc finger protein 768-like, transcript variant X2
neurotrophin receptor-interacting factor homolog isoform X2
uncharacterized LOC106610055, transcript variant X2
uncharacterized LOC106610055, transcript variant X1
uncharacterized LOC123744281, transcript variant X1
uncharacterized LOC123744281, transcript variant X2
oocyte zinc finger protein XlCOF7.1-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 37 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 76 samples with support for all annotated introns
zinc finger protein with KRAB and SCAN domains 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 samples with support for all annotated introns
zinc finger protein with KRAB and SCAN domains 1-like isoform X1
zinc finger protein with KRAB and SCAN domains 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger protein with KRAB and SCAN domains 1-like isoform X2
uncharacterized LOC106606470, transcript variant X3
uncharacterized LOC106606470, transcript variant X2
uncharacterized LOC106606470, 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
zinc finger protein 205-like, transcript variant X4
zinc finger protein 205-like, transcript variant X5
uncharacterized protein LOC106606466 isoform X4
zinc finger protein 205-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger protein 205-like, transcript variant X8
uncharacterized protein LOC106606466 isoform X6
transcriptional regulator prz1-like isoform X8
zinc finger protein 205-like, transcript variant X9
uncharacterized protein LOC106606466 isoform X9
C2H2 finger domain transcription factor crzA-like
zinc finger protein 214, transcript variant X1
zinc finger protein 214, transcript variant X3
zinc finger protein 214, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
zinc finger protein 214, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
zinc finger protein 214, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
uncharacterized protein LOC106610073 isoform X1
uncharacterized protein LOC106610073 isoform X2
uncharacterized protein LOC106610073 isoform X7
neurotrophin receptor-interacting factor homolog, transcript variant X7
neurotrophin receptor-interacting factor homolog, transcript variant X10
uncharacterized protein LOC106610117 isoform 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 42 samples with support for all annotated introns
zinc finger protein with KRAB and SCAN domains 8-like, transcript variant X1
zinc finger protein with KRAB and SCAN domains 8-like, transcript variant X2
neurotrophin receptor-interacting factor 1-like isoform X1
zinc finger protein with KRAB and SCAN domains 8-like isoform X2
neurotrophin receptor-interacting factor homolog, transcript variant X9
neurotrophin receptor-interacting factor homolog, transcript variant X11
uncharacterized protein LOC106610072 isoform X9
uncharacterized protein LOC106610072 isoform X4
zinc finger protein with KRAB and SCAN domains 8 isoform X11
zinc finger protein 583-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
uncharacterized protein LOC123744271 isoform X2
zinc finger protein 583-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neurotrophin receptor-interacting factor homolog, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized protein LOC106610072 isoform X6
uncharacterized protein LOC106610072 isoform X1
uncharacterized protein LOC106610072 isoform X2
uncharacterized protein LOC106610072 isoform X3
endothelial zinc finger protein induced by tumor necrosis factor alpha-like, transcript variant X2
endothelial zinc finger protein induced by tumor necrosis factor alpha-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 samples with support for all annotated introns
endothelial zinc finger protein induced by tumor necrosis factor alpha-like isoform X1
neurotrophin receptor-interacting factor homolog
Zinc finger protein Xfin; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001173720.1
The RefSeq transcript has 2 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001167191.1
The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
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 46 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 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
neurotrophin receptor-interacting factor homolog, transcript variant X5
uncharacterized protein LOC106610072 isoform X5
neurotrophin receptor-interacting factor homolog, transcript variant X12
neurotrophin receptor-interacting factor homolog isoform X12
neurotrophin receptor-interacting factor homolog, transcript variant X13
gastrula zinc finger protein XlCGF17.1-like, transcript variant X7
gastrula zinc finger protein XlCGF17.1-like, transcript variant X6
uncharacterized protein LOC106610156 isoform X4
gastrula zinc finger protein XlCGF17.1-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
uncharacterized protein LOC106610156 isoform X3
gastrula zinc finger protein XlCGF17.1-like, transcript variant X3
gastrula zinc finger protein XlCGF17.1-like, transcript variant X2
gastrula zinc finger protein XlCGF17.1-like, transcript variant X1
gastrula zinc finger protein XlCGF17.1-like isoform X1
gastrula zinc finger protein XlCGF17.1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 110 samples with support for all annotated introns
uncharacterized protein LOC106610156 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
zinc finger protein 214, transcript variant X4
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 15 samples with support for all annotated introns
zinc finger protein 214, transcript variant X6
zinc finger protein 214, transcript variant X9
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 31 samples with support for all annotated introns
zinc finger protein 214, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
uncharacterized protein LOC106610073 isoform X4
zinc finger and SCAN domain-containing protein 2 isoform X5
zinc finger protein 214, transcript variant X10
neurotrophin receptor-interacting factor homolog, transcript variant X8
neurotrophin receptor-interacting factor homolog isoform X8
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 20 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 2-like, transcript variant X2
zinc finger and SCAN domain-containing protein 2-like, transcript variant X4
zinc finger and SCAN domain-containing protein 2-like, transcript variant X3
zinc finger and SCAN domain-containing protein 2-like, transcript variant X8
zinc finger and SCAN domain-containing protein 2-like, transcript variant X1
zinc finger and SCAN domain-containing protein 2-like isoform X8
gastrula zinc finger protein XlCGF48.2-like, transcript variant X1
gastrula zinc finger protein XlCGF48.2-like, transcript variant X2
uncharacterized protein LOC106610069 isoform X1
uncharacterized protein LOC106610069 isoform X2
gastrula zinc finger protein XlCGF48.2-like, transcript variant X3
gastrula zinc finger protein XlCGF48.2-like isoform X3
oocyte zinc finger protein XlCOF8.4, transcript variant X1
oocyte zinc finger protein XlCOF8.4, transcript variant X2
endothelial zinc finger protein induced by tumor necrosis factor alpha isoform X1
oocyte zinc finger protein XlCOF8.4 isoform X2
zinc finger and SCAN domain-containing protein 2-like, transcript variant X6
zinc finger protein ZIC 2-B-like isoform X6
oocyte zinc finger protein XlCOF8.4-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 8 samples with support for all annotated introns
zinc finger protein 629-like, transcript variant X1
zinc finger protein 629-like, transcript variant X2
uncharacterized protein LOC106610089 isoform X2
uncharacterized protein LOC106610089 isoform X1
zinc finger and BTB domain-containing protein 18-like, transcript variant X3
zinc finger and BTB domain-containing protein 18-like isoform X3
zinc finger and BTB domain-containing protein 20-like
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 91 samples with support for all annotated introns
zinc finger protein 350-like, transcript variant X2
zinc finger protein 350-like, transcript variant X1
zinc finger protein 350-like, transcript variant X3
zinc finger and SCAN domain-containing protein 2-like, transcript variant X7
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 54 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 18-like isoform X5
zinc finger and BTB domain-containing protein 18-like isoform X7
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 67 samples with support for all annotated introns
zinc finger protein 214-like, transcript variant X1
zinc finger protein 214-like, transcript variant X2
uncharacterized protein LOC106610067 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
zinc finger protein 184-like, transcript variant X3
uncharacterized protein LOC106610094 isoform X3
zinc finger protein 184-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 30-like isoform X2
zinc finger protein 184-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
zinc finger protein 184-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 82 samples with support for all annotated introns
uncharacterized protein LOC106610094 isoform 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 87 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 18-like
zinc finger protein 143-like, transcript variant X1
zinc finger protein 143-like, transcript variant X2
zinc finger protein with KRAB and SCAN domains 1-like, transcript variant X5
zinc finger protein with KRAB and SCAN domains 1-like, transcript variant X3
transcriptional regulator prz1-like isoform X3
zinc finger protein with KRAB and SCAN domains 1-like isoform X5
transcriptional regulator prz1-like isoform X2
zinc finger protein with KRAB and SCAN domains 1-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
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 29 samples with support for all annotated introns
transcriptional regulator prz1-like isoform X1
zinc finger and SCAN domain-containing protein 2-like isoform X4
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 34 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 22-like
zinc finger protein 662-like, transcript variant X1
zinc finger protein 28-like, transcript variant X2
zinc finger protein 28-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
uncharacterized protein LOC106610119 isoform X2
zinc finger protein with KRAB and SCAN domains 7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
zinc finger protein 662-like, transcript variant X2
zinc finger protein 662-like, transcript variant X3
uncharacterized LOC106610137, transcript variant X2
uncharacterized protein LOC106610137 isoform X2
uncharacterized LOC106610137, transcript variant X1
uncharacterized protein LOC106610137 isoform X1
zinc finger protein 662-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
zinc finger protein 554-like, transcript variant X5
zinc finger protein 554-like, transcript variant X1
zinc finger protein 554-like, transcript variant X4
zinc finger protein 554-like, transcript variant X3
zinc finger protein 554-like, transcript variant X2
uncharacterized protein LOC106610090 isoform X1
uncharacterized protein LOC106610090 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71% coverage of the annotated genomic feature by RNAseq alignments
ras-responsive element-binding protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
zinc finger protein 213-like, transcript variant X2
zinc finger protein 213-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
zinc finger protein 235, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
zinc finger protein 235, 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 23 samples with support for all annotated introns
zinc finger protein 235, 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 94 samples with support for all annotated introns
uncharacterized protein LOC106610098 isoform X3
zinc finger protein 25-like, transcript variant X2
zinc finger protein 25-like, transcript variant X1
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
xeroderma pigmentosum, complementation group A; Derived by automated computational analysis using gene prediction method: BestRefSeq.
xeroderma pigmentosum, complementation group A
similar to RNA sequence, mRNA (same species):RefSeq:NM_001141862.2
The RefSeq transcript has 8 substitutions, 1 frameshift compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001135334.1
The RefSeq protein has 3 substitutions, 1 frameshift compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
store-operated calcium entry-associated regulatory factor; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
store-operated calcium entry-associated regulatory factor, transcript variant X1
store-operated calcium entry-associated regulatory factor
similar to RNA sequence, mRNA (same species):RefSeq:NM_001140196.1
The RefSeq transcript has 1 substitution, 1 non-frameshifting indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001133668.1
store-operated calcium entry-associated regulatory factor precursor
COORDINATES: ab initio prediction:SignalP:4.0
store-operated calcium entry-associated regulatory factor isoform X1
protein WWC2-like, transcript variant X2
protein WWC2-like, transcript variant X1
deoxycytidylate deaminase, transcript variant X3
deoxycytidylate deaminase, transcript variant X2
deoxycytidylate deaminase, transcript variant X1
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
signal peptidase complex subunit 3 homolog (S. cerevisiae); Derived by automated computational analysis using gene prediction method: BestRefSeq.
signal peptidase complex subunit 3 homolog (S. cerevisiae)
similar to RNA sequence, mRNA (same species):RefSeq:NM_001140682.2
ankyrin repeat and SOCS box protein 5, transcript variant X1
ankyrin repeat and SOCS box protein 5 isoform X1
ankyrin repeat and SOCS box protein 5, transcript variant X2
ankyrin repeat and SOCS box protein 5 isoform X2
WD repeat-containing protein 17, transcript variant X2
WD repeat-containing protein 17, transcript variant X3
WD repeat-containing protein 17, transcript variant X1
WD repeat-containing protein 17 isoform X2
WD repeat-containing protein 17 isoform X3
WD repeat-containing protein 17 isoform X1
neuronal membrane glycoprotein M6-a, transcript variant X2
neuronal membrane glycoprotein M6-a isoform X2
neuronal membrane glycoprotein M6-a, transcript variant X3
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 32 samples with support for all annotated introns
neuronal membrane glycoprotein M6-a, transcript variant X1
neuronal membrane glycoprotein M6-a isoform X1
neuronal membrane glycoprotein M6-a isoform X3
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 11 samples with support for all annotated introns
15-hydroxyprostaglandin dehydrogenase [NAD(+)]
F-box only protein 8, transcript variant X6
F-box only protein 8, transcript variant X1
F-box only protein 8, transcript variant X5
F-box only protein 8, transcript variant X3
F-box only protein 8, transcript variant X4
F-box only protein 8, transcript variant X2
heart- and neural crest derivatives-expressed protein 2
scrapie-responsive protein 1, transcript variant X5
scrapie-responsive protein 1, transcript variant X2
scrapie-responsive protein 1, transcript variant X4
scrapie-responsive protein 1, transcript variant X3
scrapie-responsive protein 1, transcript variant X1
high-mobility group box 2; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001139698.1
N-acetylgalactosaminyltransferase 7, transcript variant X2
N-acetylgalactosaminyltransferase 7, transcript variant X1
N-acetylgalactosaminyltransferase 7 isoform X1
N-acetylgalactosaminyltransferase 7 isoform X2
polypeptide N-acetylgalactosaminyltransferase-like 6, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase-like 6, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase-like 6
transmembrane protein 154, transcript variant X1
transmembrane protein 154, transcript variant X2
uncharacterized protein LOC106610175 isoform X1
F-box/WD repeat-containing protein 7, transcript variant X2
F-box/WD repeat-containing protein 7, transcript variant X1
F-box/WD repeat-containing protein 7, transcript variant X4
F-box/WD repeat-containing protein 7, transcript variant X3
F-box/WD repeat-containing protein 7 isoform X1
F-box/WD repeat-containing protein 7 isoform X2
F-box/WD repeat-containing protein 7, transcript variant X5
F-box/WD repeat-containing protein 7, transcript variant X6
F-box/WD repeat-containing protein 7, transcript variant X7
F-box/WD repeat-containing protein 7 isoform X3
F-box/WD repeat-containing protein 7 isoform X4
F-box/WD repeat-containing protein 7 isoform X5
F-box/WD repeat-containing protein 7, transcript variant X9
F-box/WD repeat-containing protein 7, transcript variant X8
F-box/WD repeat-containing protein 7 isoform X6
F-box/WD repeat-containing protein 7 isoform X7
dCTP pyrophosphatase 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001141892.1
glutamyl-tRNA(Gln) amidotransferase, subunit B, transcript variant X1
glutamyl-tRNA(Gln) amidotransferase, subunit B, transcript variant X2
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial isoform X1
glutamyl-tRNA(Gln) amidotransferase subunit B, mitochondrial isoform X2
FHF complex subunit HOOK interacting protein 1A-like, transcript variant X2
FHF complex subunit HOOK interacting protein 1A-like, transcript variant X1
FHF complex subunit HOOK interacting protein 1A-like
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ribosomal protein S3A, transcript variant X1
40S ribosomal protein S3a-like isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00560
ribosomal protein S3A, transcript variant X3
ribosomal protein S3A, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00071
40S ribosomal protein S3a-like isoform X2
lipopolysaccharide-responsive and beige-like anchor protein, transcript variant X1
lipopolysaccharide-responsive and beige-like anchor protein, transcript variant X3
lipopolysaccharide-responsive and beige-like anchor protein, transcript variant X4
lipopolysaccharide-responsive and beige-like anchor protein, transcript variant X5
lipopolysaccharide-responsive and beige-like anchor protein, transcript variant X2
lipopolysaccharide-responsive and beige-like anchor protein isoform X1
lipopolysaccharide-responsive and beige-like anchor protein isoform X3
lipopolysaccharide-responsive and beige-like anchor protein isoform X4
lipopolysaccharide-responsive and beige-like anchor protein isoform X5
lipopolysaccharide-responsive and beige-like anchor protein isoform X2
lipopolysaccharide-responsive and beige-like anchor protein, transcript variant X6
lipopolysaccharide-responsive and beige-like anchor protein isoform X6
serine/threonine-protein kinase DCLK2, transcript variant X1
serine/threonine-protein kinase DCLK2, transcript variant X2
serine/threonine-protein kinase DCLK2 isoform X2
serine/threonine-protein kinase DCLK2 isoform X1
serine/threonine-protein kinase DCLK2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
serine/threonine-protein kinase DCLK2, transcript variant X3
serine/threonine-protein kinase DCLK2 isoform X3
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
mineralocorticoid receptor-like, transcript variant X1
mineralocorticoid receptor-like, transcript variant X3
mineralocorticoid receptor-like, transcript variant X2
mineralocorticoid receptor-like isoform X1
mineralocorticoid receptor-like isoform X2
rho GTPase-activating protein 10-like, transcript variant X1
rho GTPase-activating protein 10-like, transcript variant X2
rho GTPase-activating protein 10-like isoform X2
rho GTPase-activating protein 10-like isoform X1
protein arginine N-methyltransferase 9, transcript variant X2
protein arginine N-methyltransferase 9 isoform X2
protein arginine N-methyltransferase 9, transcript variant X3
protein arginine N-methyltransferase 9, transcript variant X1
protein arginine N-methyltransferase 9 isoform X1
protein arginine N-methyltransferase 9 isoform X3
endothelin receptor type B, transcript variant X3
endothelin receptor type B, transcript variant X1
endothelin receptor type B, transcript variant X2
POU domain, class 4, transcription factor 2
U6 snRNA-associated Sm-like protein LSm6
zinc finger protein 827, transcript variant X5
zinc finger protein 827, transcript variant X4
zinc finger protein 827, transcript variant X3
zinc finger protein 827, transcript variant X1
zinc finger protein 827, transcript variant X2
zinc finger protein 827, transcript variant X6
zinc finger protein 827, transcript variant X7
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 22 samples with support for all annotated introns
methylmalonic aciduria type A protein, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
methylmalonic aciduria type A protein, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 62 samples with support for all annotated introns
methylmalonic aciduria type A protein, mitochondrial-like
mothers against decapentaplegic homolog 1, transcript variant X3
mothers against decapentaplegic homolog 1, transcript variant X2
mothers against decapentaplegic homolog 1, transcript variant X1
mothers against decapentaplegic homolog 1 isoform X3
mothers against decapentaplegic homolog 1 isoform X2
mothers against decapentaplegic homolog 1 isoform X1
ATP-binding cassette sub-family E member 1
FRAS1-related extracellular matrix protein 2-like
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily A member 5
ubiquitin carboxyl-terminal hydrolase 38-like
GRB2-associated binding protein 1, transcript variant X9
GRB2-associated binding protein 1, transcript variant X6
GRB2-associated binding protein 1, transcript variant X8
GRB2-associated binding protein 1, transcript variant X3
GRB2-associated binding protein 1, transcript variant X4
GRB2-associated binding protein 1, transcript variant X5
GRB2-associated binding protein 1, transcript variant X1
GRB2-associated binding protein 1, transcript variant X11
GRB2-associated binding protein 1, transcript variant X7
GRB2-associated binding protein 1, transcript variant X13
GRB2-associated binding protein 1, transcript variant X10
GRB2-associated binding protein 1, transcript variant X12
GRB2-associated binding protein 1, transcript variant X14
GRB2-associated binding protein 1, transcript variant X2
GRB2-associated-binding protein 1 isoform X1
GRB2-associated-binding protein 1 isoform X2
GRB2-associated-binding protein 1 isoform X4
GRB2-associated-binding protein 1 isoform X5
GRB2-associated-binding protein 1 isoform X7
GRB2-associated-binding protein 1 isoform X3
GRB2-associated-binding protein 1 isoform X9
GRB2-associated-binding protein 1 isoform X6
GRB2-associated-binding protein 1 isoform X8
GRB2-associated-binding protein 1 isoform X10
GRB2-associated binding protein 1, transcript variant X18
GRB2-associated binding protein 1, transcript variant X16
GRB2-associated binding protein 1, transcript variant X19
GRB2-associated binding protein 1, transcript variant X15
GRB2-associated binding protein 1, transcript variant X17
GRB2-associated binding protein 1, transcript variant X20
GRB2-associated-binding protein 1 isoform X11
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X1
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X3
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X2
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X2
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X1
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X3
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X4
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X5
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X7
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X5
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X7
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X6
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X8
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X6
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X8
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X9
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X10
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X9
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X10
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X13
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X12
type II inositol 3,4-bisphosphate 4-phosphatase-like, transcript variant X11
type II inositol 3,4-bisphosphate 4-phosphatase-like isoform X11
uncharacterized LOC106610234, transcript variant X1
uncharacterized LOC106610234, transcript variant X2
uncharacterized protein LOC106610234 isoform X1
uncharacterized protein LOC106610234 isoform X2
RING finger protein 150, transcript variant X1
RING finger protein 150, 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 39 samples with support for all annotated introns
ELMO domain-containing protein 2, transcript variant X1
ELMO domain-containing protein 2, transcript variant X2
G protein-regulated inducer of neurite outgrowth 3-like
uncharacterized protein LOC555481 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
uncharacterized protein LOC555481 homolog, 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 33 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: 6 Proteins
probable E3 ubiquitin-protein ligase HERC3, transcript variant X1
probable E3 ubiquitin-protein ligase HERC3, transcript variant X2
probable E3 ubiquitin-protein ligase HERC3 isoform X2
probable E3 ubiquitin-protein ligase HERC3 isoform X1
probable E3 ubiquitin-protein ligase HERC3
probable E3 ubiquitin-protein ligase HERC6, transcript variant X2
probable E3 ubiquitin-protein ligase HERC6, transcript variant X1
probable E3 ubiquitin-protein ligase HERC6 isoform X2
probable E3 ubiquitin-protein ligase HERC6 isoform X1
ATP binding cassette subfamily G member 2 (Junior blood group); Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
ATP binding cassette subfamily G member 2 (Junior blood group), transcript variant X3
ATP binding cassette subfamily G member 2 (Junior blood group)
similar to RNA sequence, mRNA (same species):RefSeq:NM_001173655.1
ATP binding cassette subfamily G member 2 (Junior blood group), transcript variant X2
broad substrate specificity ATP-binding cassette transporter ABCG2 isoform X2
ATP binding cassette subfamily G member 2 (Junior blood group), transcript variant X1
broad substrate specificity ATP-binding cassette transporter ABCG2 isoform X1
broad substrate specificity ATP-binding cassette transporter ABCG2 isoform X3
broad substrate specificity ATP-binding cassette transporter ABCG2
ras GTPase-activating protein-binding protein 2, transcript variant X7
ras GTPase-activating protein-binding protein 2, transcript variant X8
ras GTPase-activating protein-binding protein 2, transcript variant X1
ras GTPase-activating protein-binding protein 2, transcript variant X2
ras GTPase-activating protein-binding protein 2, transcript variant X4
ras GTPase-activating protein-binding protein 2, transcript variant X5
ras GTPase-activating protein-binding protein 2, transcript variant X3
ras GTPase-activating protein-binding protein 2, transcript variant X9
ras GTPase-activating protein-binding protein 2, transcript variant X6
ras GTPase-activating protein-binding protein 2 isoform X1
ras GTPase-activating protein-binding protein 2 isoform X2
ras GTPase-activating protein-binding protein 2 isoform X4
ras GTPase-activating protein-binding protein 2 isoform X5
ras GTPase-activating protein-binding protein 2 isoform X3
ras GTPase-activating protein-binding protein 2 isoform X9
ras GTPase-activating protein-binding protein 2 isoform X6
ras GTPase-activating protein-binding protein 2 isoform X7
ras GTPase-activating protein-binding protein 2 isoform X8
general vesicular transport factor p115-like, transcript variant X1
general vesicular transport factor p115-like, transcript variant X3
general vesicular transport factor p115-like, transcript variant X4
general vesicular transport factor p115-like, transcript variant X5
general vesicular transport factor p115-like, transcript variant X7
general vesicular transport factor p115-like, transcript variant X2
general vesicular transport factor p115-like, transcript variant X6
general vesicular transport factor p115-like, transcript variant X8
general vesicular transport factor p115-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
general vesicular transport factor p115-like isoform X1
general vesicular transport factor p115-like isoform X3
general vesicular transport factor p115-like isoform X4
general vesicular transport factor p115-like isoform X5
general vesicular transport factor p115-like isoform X7
general vesicular transport factor p115-like isoform X2
general vesicular transport factor p115-like isoform X6
general vesicular transport factor p115-like isoform X8
general vesicular transport factor p115-like isoform X9
acidic (leucine-rich) nuclear phosphoprotein 32 family, member B, transcript variant X1
acidic (leucine-rich) nuclear phosphoprotein 32 family, member B, transcript variant X2
acidic leucine-rich nuclear phosphoprotein 32 family member B isoform X2
acidic leucine-rich nuclear phosphoprotein 32 family member B isoform X1
mitogen-activated protein kinase 7-like isoform X2
tRNA (adenine(37)-N6)-methyltransferase-like
Acidic leucine-rich nuclear phosphoprotein 32 family member B; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Acidic leucine-rich nuclear phosphoprotein 32 family member B
similar to RNA sequence, mRNA (same species):RefSeq:NM_001141161.1
acidic leucine-rich nuclear phosphoprotein 32 family member B, transcript variant X3
acidic leucine-rich nuclear phosphoprotein 32 family member B, transcript variant X1
acidic leucine-rich nuclear phosphoprotein 32 family member B, transcript variant X2
acidic leucine-rich nuclear phosphoprotein 32 family member B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
acidic leucine-rich nuclear phosphoprotein 32 family member B, transcript variant X5
acidic leucine-rich nuclear phosphoprotein 32 family member B isoform X3
acidic leucine-rich nuclear phosphoprotein 32 family member B-like, transcript variant X4
acidic leucine-rich nuclear phosphoprotein 32 family member B-like, transcript variant X3
acidic leucine-rich nuclear phosphoprotein 32 family member B-like, transcript variant X2
acidic leucine-rich nuclear phosphoprotein 32 family member B-like, transcript variant X1
acidic leucine-rich nuclear phosphoprotein 32 family member B-like, transcript variant X5
acidic leucine-rich nuclear phosphoprotein 32 family member B-like, transcript variant X6
acidic leucine-rich nuclear phosphoprotein 32 family member B-like isoform X4
acidic leucine-rich nuclear phosphoprotein 32 family member B-like isoform X3
acidic leucine-rich nuclear phosphoprotein 32 family member B-like isoform X2
acidic leucine-rich nuclear phosphoprotein 32 family member B-like isoform X1
acidic leucine-rich nuclear phosphoprotein 32 family member B-like isoform X5
acidic leucine-rich nuclear phosphoprotein 32 family member B-like isoform X6
sperm-associated antigen 5, transcript variant X1
sperm-associated antigen 5, transcript variant X5
sperm-associated antigen 5, transcript variant X4
sperm-associated antigen 5, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
sperm-associated antigen 5, transcript variant X2
sperm-associated antigen 5, transcript variant X3
sperm-associated antigen 5, transcript variant X6
uncharacterized protein LOC106610270 isoform X1
uncharacterized protein LOC106610270 isoform X3
uncharacterized protein LOC106610270 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
endophilin-A1-like, transcript variant X8
endophilin-A1-like, transcript variant X6
endophilin-A1-like, transcript variant X2
endophilin-A1-like, transcript variant X7
endophilin-A1-like, transcript variant X5
endophilin-A1-like, transcript variant X4
endophilin-A1-like, transcript variant X3
endophilin-A1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 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 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein basonuclin-2-like
PC4 and SFRS1-interacting protein, transcript variant X1
PC4 and SFRS1-interacting protein, transcript variant X2
PC4 and SFRS1-interacting protein, transcript variant X4
PC4 and SFRS1-interacting protein, transcript variant X3
lens epithelium-derived growth factor isoform X1
lens epithelium-derived growth factor isoform X2
PC4 and SFRS1-interacting protein isoform X4
lens epithelium-derived growth factor isoform X3
snRNA-activating protein complex subunit 3-like
tetratricopeptide repeat protein 39B-like, transcript variant X3
tetratricopeptide repeat protein 39B-like, transcript variant X5
tetratricopeptide repeat protein 39B-like, transcript variant X4
tetratricopeptide repeat protein 39B-like, transcript variant X1
tetratricopeptide repeat protein 39B-like, transcript variant X2
tetratricopeptide repeat protein 39B-like isoform X1
tetratricopeptide repeat protein 39B-like isoform X2
tetratricopeptide repeat protein 39B-like isoform X4
tetratricopeptide repeat protein 39B-like isoform X3
tetratricopeptide repeat protein 39B-like isoform X5
group XIIA secretory phospholipase A2-like, transcript variant X2
group XIIA secretory phospholipase A2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
group XIIA secretory phospholipase A2-like isoform X1
group XIIA secretory phospholipase A2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 74 samples with support for all annotated introns
calcium uniporter protein, mitochondrial, transcript variant X1
calcium uniporter protein, mitochondrial, transcript variant X2
calcium uniporter protein, mitochondrial isoform X2
calcium uniporter protein, mitochondrial isoform X1
lymphoid enhancer-binding factor 1, transcript variant X11
lymphoid enhancer-binding factor 1, transcript variant X7
lymphoid enhancer-binding factor 1, transcript variant X1
lymphoid enhancer-binding factor 1, transcript variant X2
lymphoid enhancer-binding factor 1, transcript variant X3
lymphoid enhancer-binding factor 1, transcript variant X4
lymphoid enhancer-binding factor 1, transcript variant X15
lymphoid enhancer-binding factor 1, transcript variant X20
lymphoid enhancer-binding factor 1, transcript variant X16
lymphoid enhancer-binding factor 1, transcript variant X9
lymphoid enhancer-binding factor 1, transcript variant X8
lymphoid enhancer-binding factor 1, transcript variant X10
lymphoid enhancer-binding factor 1, transcript variant X5
lymphoid enhancer-binding factor 1, transcript variant X17
lymphoid enhancer-binding factor 1, transcript variant X12
lymphoid enhancer-binding factor 1, transcript variant X6
lymphoid enhancer-binding factor 1, transcript variant X18
lymphoid enhancer-binding factor 1, transcript variant X13
lymphoid enhancer-binding factor 1, transcript variant X19
lymphoid enhancer-binding factor 1, transcript variant X14
lymphoid enhancer-binding factor 1 isoform X6
lymphoid enhancer-binding factor 1 isoform X7
lymphoid enhancer-binding factor 1 isoform X8
lymphoid enhancer-binding factor 1 isoform X10
lymphoid enhancer-binding factor 1 isoform X1
lymphoid enhancer-binding factor 1 isoform X11
lymphoid enhancer-binding factor 1 isoform X2
lymphoid enhancer-binding factor 1 isoform X12
lymphoid enhancer-binding factor 1 isoform X4
lymphoid enhancer-binding factor 1 isoform X13
lymphoid enhancer-binding factor 1 isoform X3
lymphoid enhancer-binding factor 1 isoform X5
lymphoid enhancer-binding factor 1 isoform X9
lymphoid enhancer-binding factor 1 isoform X14
hydroxyacyl-coenzyme A dehydrogenase, mitochondrial
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: 2 ESTs, 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
LOW QUALITY PROTEIN: cytochrome P450 2U1
phosphatidylcholine:ceramide cholinephosphotransferase 2
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1
aminoacyl tRNA synthetase complex interacting multifunctional protein 1a, transcript variant X3
aminoacyl tRNA synthetase complex interacting multifunctional protein 1a, transcript variant X4
aminoacyl tRNA synthetase complex interacting multifunctional protein 1a, transcript variant X2
aminoacyl tRNA synthetase complex interacting multifunctional protein 1a, transcript variant X1
aminoacyl tRNA synthase complex-interacting multifunctional protein 1 isoform X2
aminoacyl tRNA synthase complex-interacting multifunctional protein 1 isoform X1
aminoacyl tRNA synthase complex-interacting multifunctional protein 1 isoform X3
TBC domain-containing protein kinase-like protein, transcript variant X1
TBC domain-containing protein kinase-like protein, transcript variant X2
TBC domain-containing protein kinase-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
Epidermis-type lipoxygenase 3; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
Epidermis-type lipoxygenase 3, transcript variant X1
similar to RNA sequence, mRNA (same species):RefSeq:NM_001139774.1
The RefSeq transcript has 3 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001133246.1
The RefSeq protein has 2 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
epidermis-type lipoxygenase 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 35% coverage of the annotated genomic feature by RNAseq alignments
hydroperoxide isomerase ALOXE3-like, transcript variant X1
hydroperoxide isomerase ALOXE3-like isoform X1
hydroperoxide isomerase ALOXE3-like, transcript variant X2
hydroperoxide isomerase ALOXE3-like isoform X2
glutathione S-transferase, C-terminal domain containing; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
glutathione S-transferase, C-terminal domain containing, transcript variant X1
glutathione S-transferase, C-terminal domain containing
similar to RNA sequence, mRNA (same species):RefSeq:NM_001173910.1
glutathione S-transferase, C-terminal domain containing, transcript variant X2
glutathione S-transferase, C-terminal domain containing, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
glutathione S-transferase C-terminal domain-containing protein isoform X1
glutathione S-transferase C-terminal domain-containing protein isoform X2
glutathione S-transferase C-terminal domain-containing protein
integrator complex subunit 12-like, transcript variant X2
integrator complex subunit 12-like, transcript variant X1
integrator complex subunit 12-like isoform X1
integrator complex subunit 12-like isoform X2
Rho guanine nucleotide exchange factor (GEF) 38
rho guanine nucleotide exchange factor 38
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
CXXC-type zinc finger protein 4, transcript variant X2
CXXC-type zinc finger protein 4, transcript variant X1
CXXC-type zinc finger protein 4, transcript variant X3
CXXC-type zinc finger protein 4, transcript variant X4
CXXC-type zinc finger protein 4 isoform X1
CXXC-type zinc finger protein 4 isoform X2
methylthioadenosine phosphorylase; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001140147.1
methylthioadenosine phosphorylase, transcript variant X1
S-methyl-5'-thioadenosine phosphorylase isoform X1
uncharacterized LOC123744198, transcript variant X4
uncharacterized LOC123744198, transcript variant X3
uncharacterized LOC123744198, transcript variant X2
uncharacterized LOC123744198, transcript variant X1
uncharacterized protein LOC123744198 isoform X4
uncharacterized protein LOC123744198 isoform X3
uncharacterized protein LOC123744198 isoform X2
uncharacterized protein LOC123744198 isoform X1
calcium-binding and coiled-coil domain-containing protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase Topors-like, transcript variant X1
E3 ubiquitin-protein ligase Topors-like, transcript variant X2
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 6
PRELI domain-containing protein 1, mitochondrial, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 123 samples with support for all annotated introns
PRELI domain-containing protein 1, mitochondrial, 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 75 samples with support for all annotated introns
PRELI domain-containing protein 1, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 105 samples with support for all annotated introns
PRELI domain-containing protein 1, mitochondrial
MAX dimerization protein 4, transcript variant X1
MAX dimerization protein 4, transcript variant X2
MAX dimerization protein 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 samples with support for all annotated introns
proline-, glutamic acid- and leucine-rich protein 1-like, transcript variant X1
proline-, glutamic acid- and leucine-rich protein 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
proline-, glutamic acid- and leucine-rich protein 1-like isoform X1
proline-, glutamic acid- and leucine-rich protein 1-like isoform X2
ubiquitin carboxyl-terminal hydrolase 37-like
ubiquitin carboxyl-terminal hydrolase 37-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 37-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 37-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 37-like isoform X1
ubiquitin carboxyl-terminal hydrolase 37-like isoform X2
C-type lectin domain family 4 member M-like, transcript variant X1
C-type lectin domain family 4 member M-like isoform X1
C-type lectin domain family 4 member M-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
C-type lectin domain family 4 member M-like, transcript variant X3
C-type lectin domain family 4 member M-like isoform X2
C-type lectin domain family 4 member M-like isoform X3
uncharacterized LOC123744202, transcript variant X2
uncharacterized LOC123744202, transcript variant X1
CD209 antigen-like protein E, transcript variant X1
CD209 antigen-like protein E, transcript variant X3
CD209 antigen-like protein E, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
calcium uptake protein 3, mitochondrial, transcript variant X1
calcium uptake protein 3, mitochondrial, transcript variant X2
calcium uptake protein 3, mitochondrial, transcript variant X3
calcium uptake protein 3, mitochondrial, transcript variant X4
calcium uptake protein 3, mitochondrial isoform X1
calcium uptake protein 3, mitochondrial isoform X2
calcium uptake protein 3, mitochondrial isoform X3
calcium uptake protein 3, mitochondrial isoform X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
VPS37A subunit of ESCRT-I; Derived by automated computational analysis using gene prediction method: BestRefSeq.
vacuolar protein sorting-associated protein 37A
myotubularin-related protein 7, transcript variant X1
myotubularin-related protein 7, transcript variant X2
myotubularin-related protein 7 isoform X1
myotubularin-related protein 7 isoform X2
microtubule associated tumor suppressor 1b, transcript variant X3
microtubule associated tumor suppressor 1b, transcript variant X4
microtubule associated tumor suppressor 1b, transcript variant X5
microtubule associated tumor suppressor 1b, transcript variant X2
microtubule associated tumor suppressor 1b, transcript variant X1
microtubule-associated tumor suppressor 1 homolog isoform X1
microtubule-associated tumor suppressor 1 homolog isoform X2
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 502-like, transcript variant X1
zinc finger protein 502-like, transcript variant X2
zinc finger protein 184, transcript variant X1
zinc finger protein 184, transcript variant X3
zinc finger protein 184, transcript variant X2
uncharacterized LOC106610388, transcript variant X1
uncharacterized LOC106610388, transcript variant X2
uncharacterized LOC106610388, transcript variant X3
uncharacterized LOC106610388, transcript variant X4
uncharacterized LOC106610388, transcript variant X5
uncharacterized protein LOC106610388 isoform X5
uncharacterized protein LOC106610388 isoform X2
uncharacterized protein LOC106610388 isoform X4
uncharacterized protein LOC106610388 isoform X3
uncharacterized protein LOC106610388 isoform X1
uncharacterized LOC123744207, transcript variant X2
uncharacterized LOC123744207, transcript variant X1
uncharacterized protein LOC123744207 isoform X1
uncharacterized protein LOC123744207 isoform X2
zinc finger protein 773-like, transcript variant X1
zinc finger protein 773-like, transcript variant X3
zinc finger protein 773-like, transcript variant X2
zinc finger protein 773-like, transcript variant X4
zinc finger protein 773-like, transcript variant X8
putative zinc finger and SCAN domain-containing protein 5D isoform X1
putative zinc finger and SCAN domain-containing protein 5D isoform X3
putative zinc finger and SCAN domain-containing protein 5D isoform X2
putative zinc finger and SCAN domain-containing protein 5D isoform X4
zinc finger protein 614-like, transcript variant X2
zinc finger protein 614-like, transcript variant X1
zinc finger protein 773-like, transcript variant X6
zinc finger protein 773-like, transcript variant X5
zinc finger protein 773-like, transcript variant X7
zinc-responsive transcriptional regulator ZAP1-like isoform X7
zinc finger protein 91, transcript variant X6
zinc finger protein 91, transcript variant X7
zinc finger protein 91, transcript variant X3
zinc finger protein 91, transcript variant X2
zinc finger protein 91, transcript variant X1
zinc finger protein 91, transcript variant X5
zinc finger protein 91, transcript variant X4
putative zinc finger and SCAN domain-containing protein 5D
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 48 samples with support for all annotated introns
zinc finger and SCAN domain-containing protein 22-like, transcript variant X1
zinc finger and SCAN domain-containing protein 22-like, transcript variant X2
zinc finger and SCAN domain-containing protein 22-like isoform X1
zinc finger and SCAN domain-containing protein 22-like isoform X2
zinc finger protein 236-like, transcript variant X1
zinc finger protein 236-like, transcript variant X2
Zinc finger protein 235; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001139879.1
The RefSeq transcript has 10 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001133351.1
The RefSeq protein has 6 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
zinc finger and BTB domain-containing protein 6
MAP7 domain-containing protein 1; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001140050.1
The RefSeq transcript has 6 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001133522.1
The RefSeq protein has 3 substitutions compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Type-2 ice-structuring protein; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001140809.2
The RefSeq transcript has 2 non-frameshifting indels compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Type-2 ice-structuring protein precursor
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 33 samples with support for all annotated introns
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
E3 ubiquitin-protein ligase DTX4-like, transcript variant X1
E3 ubiquitin-protein ligase DTX4-like, transcript variant X2
E3 ubiquitin-protein ligase DTX4-like, transcript variant X3
E3 ubiquitin-protein ligase DTX4-like isoform X1
E3 ubiquitin-protein ligase DTX4-like isoform X2
E3 ubiquitin-protein ligase DTX4-like isoform X3
fibroblast growth factor receptor 3-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 116 samples with support for all annotated introns
fibroblast growth factor receptor 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 129 samples with support for all annotated introns
uncharacterized protein LOC106610471 isoform X2
fibroblast growth factor receptor 3-like isoform X1
DLC1 Rho GTPase activating protein, transcript variant X2
DLC1 Rho GTPase activating protein, transcript variant X1
DLC1 Rho GTPase activating protein, transcript variant X3
rho GTPase-activating protein 7 isoform X1
rho GTPase-activating protein 7 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
C-type lectin domain family 4 member K-like
C-type lectin domain family 4 member E-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 55 samples with support for all annotated introns
C-type lectin domain family 4 member M-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ecto-ADP-ribosyltransferase 5
fatty-acid amide hydrolase 2-A, transcript variant X2
fatty-acid amide hydrolase 2-A, transcript variant X1
fatty-acid amide hydrolase 2-A isoform X1
fatty-acid amide hydrolase 2-A isoform X2
dual specificity testis-specific protein kinase 2, transcript variant X1
dual specificity testis-specific protein kinase 2, transcript variant X2
dual specificity testis-specific protein kinase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
GTPase IMAP family member 4, transcript variant X1
GTPase IMAP family member 4, transcript variant X2
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
GTPase IMAP family member 9-like, transcript variant X1
GTPase IMAP family member 9-like, transcript variant X3
GTPase IMAP family member 9-like, transcript variant X2
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
sterile alpha motif domain-containing protein 9-like, transcript variant X1
sterile alpha motif domain-containing protein 9-like, transcript variant X2
sterile alpha motif domain-containing protein 9-like isoform X2
sterile alpha motif domain-containing protein 9-like isoform X1
CT027 protein; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001140258.1
zinc finger protein RFP-like, transcript variant X1
zinc finger protein RFP-like, transcript variant X2
zinc finger protein 638-like, transcript variant X1
zinc finger protein 638-like, transcript variant X2
zinc finger protein 638-like, transcript variant X3
zinc finger protein 638-like, transcript variant X4
zinc finger protein 638-like, transcript variant X5
zinc finger protein 638-like, transcript variant X6
polyadenylate-binding protein-interacting protein 2B-like, transcript variant X3
polyadenylate-binding protein-interacting protein 2B-like, transcript variant X1
polyadenylate-binding protein-interacting protein 2B-like isoform X1
polyadenylate-binding protein-interacting protein 2B-like isoform X3
polyadenylate-binding protein-interacting protein 2B-like, transcript variant X2
polyadenylate-binding protein-interacting protein 2B-like isoform X2
semaphorin-4F-like, transcript variant X1
semaphorin-4F-like, transcript variant X2
erythroblast NAD(P)(+)--arginine ADP-ribosyltransferase-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
T-cell ecto-ADP-ribosyltransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
NAD(P)(+)--arginine ADP-ribosyltransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
von Willebrand factor A domain-containing protein 7-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, including 14 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 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
von Willebrand factor A domain containing 10, tandem duplicate 2
von Willebrand factor A domain-containing protein 7
C-type lectin domain family 4 member G-like
C-type lectin domain family 4 member E-like, transcript variant X2
C-type lectin domain family 4 member E-like, transcript variant X3
C-type lectin domain family 4 member E-like, transcript variant X1
sodium/potassium-transporting ATPase subunit alpha-1
LOW QUALITY PROTEIN: sodium/potassium-transporting ATPase subunit alpha-1
zinc finger protein 180-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
zinc finger protein 180-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 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 54 samples with support for all annotated introns
zinc finger protein 37-like, transcript variant X2
zinc finger protein 37-like, transcript variant X1
von Willebrand factor A domain-containing protein 7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 63 samples with support for all annotated introns
von Willebrand factor A domain-containing protein 7-like isoform X1
von Willebrand factor A domain-containing protein 7-like, transcript variant X2
von Willebrand factor A domain-containing protein 7-like isoform X2
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 9 samples with support for all annotated introns
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 8% 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 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
interferon-induced very large GTPase 1-like, transcript variant X1
interferon-induced very large GTPase 1-like, transcript variant X2
interferon-induced very large GTPase 1-like isoform X1
interferon-induced very large GTPase 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
interferon-induced very large GTPase 1-like
tripartite motif-containing protein 29-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC106610491, transcript variant X2
uncharacterized protein LOC106610491 isoform X2
uncharacterized LOC106610491, transcript variant X1
uncharacterized LOC106610491, transcript variant X3
uncharacterized protein LOC106610491 isoform X1
uncharacterized protein LOC106610491 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 2 ESTs, 2 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 12% 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
scavenger receptor cysteine-rich type 1 protein M130-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins
N-acetylaspartate synthetase-like, transcript variant X2
N-acetylaspartate synthetase-like, transcript variant X1
N-acetylaspartate synthetase-like, transcript variant X3
N-acetylaspartate synthetase-like isoform X1
N-acetylaspartate synthetase-like isoform X2
GRIP domain-containing protein RUD3-like
uncharacterized LOC106591358, transcript variant X5
uncharacterized LOC106591358, transcript variant X4
uncharacterized LOC106591358, transcript variant X2
uncharacterized LOC106591358, transcript variant X1
uncharacterized LOC106591358, transcript variant X3
uncharacterized protein LOC106591358 isoform X5
uncharacterized protein LOC106591358 isoform X4
uncharacterized protein LOC106591358 isoform X2
uncharacterized protein LOC106591358 isoform X1
uncharacterized protein LOC106591358 isoform X3
uncharacterized LOC106592304, transcript variant X2
uncharacterized LOC106592304, transcript variant X1
uncharacterized LOC106592304, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
C-type lectin domain family 6 member A-like
FERM and PDZ domain-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 125 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: phosphoglucomutase-2
zinc finger CCHC domain-containing protein 7-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 7-like, transcript variant X2
zinc finger CCHC domain-containing protein 7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 70 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 7-like isoform X2
zinc finger CCHC domain-containing protein 7-like isoform X1
paired box protein Pax-5-like, 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 7 samples with support for all annotated introns
paired box protein Pax-5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
paired box protein Pax-5-like isoform X1
paired box protein Pax-5-like isoform X2
maternal embryonic leucine zipper kinase, 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 34 samples with support for all annotated introns
maternal embryonic leucine zipper kinase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
maternal embryonic leucine zipper kinase, transcript variant X2
maternal embryonic leucine zipper kinase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
maternal embryonic leucine zipper kinase isoform X3
maternal embryonic leucine zipper kinase isoform X2
maternal embryonic leucine zipper kinase isoform X1
maternal embryonic leucine zipper kinase isoform X4
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
thrombospondin type-1 domain-containing protein 4-like
ubiquitin-like modifier-activating enzyme 6
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
glyoxylate reductase/hydroxypyruvate reductase-like, transcript variant X2
glyoxylate reductase/hydroxypyruvate reductase-like, transcript variant X1
glyoxylate reductase/hydroxypyruvate reductase-like, transcript variant X3
glyoxylate reductase/hydroxypyruvate reductase-like isoform X1
glyoxylate reductase/hydroxypyruvate reductase-like isoform X2
glyoxylate reductase/hydroxypyruvate reductase-like isoform X3
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
NACHT, LRR and PYD domains-containing protein 1 homolog
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 5-like isoform X5
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like, 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
NACHT, LRR and PYD domains-containing protein 12-like, 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
NACHT, LRR and PYD domains-containing protein 12-like isoform X2
NACHT, LRR and PYD domains-containing protein 12-like isoform X1
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 32 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized protein LOC106597038 isoform X4
uncharacterized protein LOC106597038 isoform X2
uncharacterized protein LOC106597038 isoform X3
keratin-associated protein 5-1-like, transcript variant X9
keratin-associated protein 5-1-like, transcript variant X12
keratin-associated protein 5-1-like, transcript variant X3
keratin-associated protein 5-1-like, transcript variant X11
keratin-associated protein 5-1-like, transcript variant X10
keratin-associated protein 5-1-like, transcript variant X2
keratin-associated protein 5-1-like, transcript variant X8
keratin-associated protein 5-1-like, transcript variant X7
keratin-associated protein 5-1-like, transcript variant X4
keratin-associated protein 5-1-like, transcript variant X6
keratin-associated protein 5-1-like, transcript variant X5
keratin-associated protein 5-1-like, transcript variant X1
keratin-associated protein 5-1-like, transcript variant X13
NACHT, LRR and PYD domains-containing protein 5-like, transcript variant X1
NACHT, LRR and PYD domains-containing protein 5-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 5-like isoform X1
NACHT, LRR and PYD domains-containing protein 5-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X2
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, including 6 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X1
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, including 4 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 3-like isoform X2
NACHT, LRR and PYD domains-containing protein 3-like isoform X1
NACHT, LRR and PYD domains-containing protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 samples with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 12-like
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
NACHT, LRR and PYD domains-containing protein 5-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 1 sample with support for all annotated introns
calcium/calmodulin-dependent protein kinase type II delta 2 chain
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 24 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: calcium/calmodulin-dependent protein kinase type II delta 2 chain
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123744243, transcript variant X2
uncharacterized LOC123744243, transcript variant X1
uncharacterized LOC123744243, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 68 samples with support for all annotated introns
uncharacterized LOC106597193, transcript variant X2
uncharacterized LOC106597193, transcript variant X1
uncharacterized protein LOC106597193 isoform X1
uncharacterized protein LOC106597193 isoform X2
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 67% coverage of the annotated genomic feature by RNAseq alignments
dihydropyrimidinase-related protein 1, transcript variant X1
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 17 samples with support for all annotated introns
dihydropyrimidinase-related protein 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 20 samples with support for all annotated introns
dihydropyrimidinase-related protein 1 isoform X1
dihydropyrimidinase-related protein 1 isoform X2
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
phosphatidylinositol 4-kinase type 2-beta-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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
LOW QUALITY PROTEIN: serine protease HTRA3a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 58 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 51 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
low density lipoprotein receptor-related protein associated protein 1, transcript variant X1
low density lipoprotein receptor-related protein associated protein 1, transcript variant X2
alpha-2-macroglobulin receptor-associated protein isoform X1
alpha-2-macroglobulin receptor-associated protein isoform X2
docking protein 7b, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
docking protein 7b, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 5 bases in 3 codons; 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, including 17 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 5 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: regulator of G-protein signaling 12
COORDINATES: nucleotide motif:Rfam:12.0:RF00582
G protein-coupled receptor kinase 6, transcript variant X2
G protein-coupled receptor kinase 6, transcript variant X1
G protein-coupled receptor kinase 6 isoform X2
G protein-coupled receptor kinase 5 isoform X1
sodium-dependent phosphate transport protein 2B-like, transcript variant X2
sodium-dependent phosphate transport protein 2B-like isoform X2
sodium-dependent phosphate transport protein 2B-like, transcript variant X1
sodium-dependent phosphate transport protein 2B-like isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
ETS-related transcription factor Elf-2, transcript variant X1
ETS-related transcription factor Elf-2, transcript variant X2
ETS-related transcription factor Elf-2, transcript variant X3
ETS-related transcription factor Elf-2 isoform X1
ETS-related transcription factor Elf-2 isoform X2
ETS-related transcription factor Elf-2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 93 samples with support for all annotated introns
ETS-related transcription factor Elf-2 isoform X3
fibrous sheath CABYR-binding protein-like, transcript variant X2
fibrous sheath CABYR-binding protein-like, transcript variant X1
fibrous sheath CABYR-binding protein-like isoform X2
fibrous sheath CABYR-binding protein-like isoform X1
fibrous sheath CABYR-binding protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
ion-translocating oxidoreductase complex subunit C-like isoform X2
fibrous sheath CABYR-binding protein-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 113 samples with support for all annotated introns
mastermind-like transcriptional coactivator 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC106610477, transcript variant X2
uncharacterized LOC106610477, transcript variant X1
short coiled-coil protein B, transcript variant X2
short coiled-coil protein B, transcript variant X1
short coiled-coil protein B, transcript variant X3
short coiled-coil protein B, transcript variant X4
exosome complex component RRP45, transcript variant X1
exosome complex component RRP45, transcript variant X2
exosome complex component RRP45 isoform X1
exosome complex component RRP45 isoform X2
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon UUG); 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 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 15 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.