Cervus canadensis isolate Bull #8, Minnesota chromosome 14, ASM1932006v1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Laurasiatheria; Artiodactyla; Ruminantia; Pecora; Cervidae; Cervinae; Cervus.
A pseudomolecule assembly of the Rocky Mountain elk genome
REFSEQ INFORMATION: The reference sequence is identical to\nCM033204.1.\nAssembly name: ASM1932006v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Iowa State University on\n2021/07/26. The original whole-genome shotgun project has the\naccession JACTMD000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Iowa State University\nAssembly Date :: 24-AUG-2020\nAssembly Method :: MaSuRCA v. MAY-2018\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 686.0x\nSequencing Technology :: PacBio RSII; Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Cervus canadensis Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
antiviral innate immune response receptor RIG-I-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
antiviral innate immune response receptor RIG-I
TOP1 binding arginine/serine rich protein, E3 ubiquitin ligase, transcript variant X2
TOP1 binding arginine/serine rich protein, E3 ubiquitin ligase, transcript variant X1
TOP1 binding arginine/serine rich protein, E3 ubiquitin ligase, transcript variant X3
E3 ubiquitin-protein ligase Topors isoform X2
E3 ubiquitin-protein ligase Topors isoform X1
E3 ubiquitin-protein ligase Topors isoform X3
NADH:ubiquinone oxidoreductase subunit B6, transcript variant X2
NADH:ubiquinone oxidoreductase subunit B6, transcript variant X1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 6 isoform X2
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 6 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane protein 215, transcript variant X1
transmembrane protein 215, transcript variant X2
scavenger receptor class A member 3, transcript variant X1
scavenger receptor class A member 3, transcript variant X2
scavenger receptor class A member 3 isoform X1
scavenger receptor class A member 3 isoform X2
coiled-coil domain containing 25, transcript variant X1
coiled-coil domain containing 25, transcript variant X2
coiled-coil domain containing 25, transcript variant X3
coiled-coil domain containing 25, transcript variant X4
coiled-coil domain-containing protein 25 isoform X1
coiled-coil domain-containing protein 25 isoform X2
coiled-coil domain-containing protein 25 isoform X3
coiled-coil domain-containing protein 25 isoform X4
establishment of sister chromatid cohesion N-acetyltransferase 2
lymphokine-activated killer T-cell-originated protein kinase
glycine cleavage system H protein, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
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: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
nuclear GTPase, germinal center associated, 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 2 samples with support for all annotated introns
nuclear GTPase, germinal center associated, transcript variant X6
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 3 samples with support for all annotated introns
nuclear GTPase, germinal center associated, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
nuclear GTPase, germinal center associated, transcript variant X1
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 4 samples with support for all annotated introns
nuclear GTPase, germinal center associated, 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 3 samples with support for all annotated introns
nuclear GTPase, germinal center associated, transcript variant X3
elongator acetyltransferase complex subunit 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 22% 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 mRNAs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 395, transcript variant X1
zinc finger protein 395, transcript variant X2
zinc finger protein 395, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
frizzled class receptor 3, transcript variant X1
frizzled class receptor 3, transcript variant X2
frizzled class receptor 3, 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 2 samples with support for all annotated introns
exostosin like glycosyltransferase 3, transcript variant X2
exostosin like glycosyltransferase 3, transcript variant X3
exostosin like glycosyltransferase 3, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00191
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA cysteine (anticodon ACA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
homeobox containing 1, transcript variant X3
homeobox containing 1, transcript variant X2
homeobox containing 1, transcript variant X9
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 24 samples with support for all annotated introns
homeobox containing 1, transcript variant X1
homeobox containing 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
homeobox containing 1, transcript variant X7
homeobox containing 1, transcript variant X6
homeobox containing 1, transcript variant X5
homeobox containing 1, transcript variant X4
homeobox-containing protein 1 isoform X1
homeobox-containing protein 1 isoform X4
homeobox-containing protein 1 isoform X2
homeobox-containing protein 1 isoform X5
homeobox-containing protein 1 isoform X3
homeobox-containing protein 1 isoform X6
homeobox-containing protein 1 isoform X7
homeobox-containing protein 1 isoform X8
homeobox-containing protein 1 isoform X9
kinesin family member 13B, transcript variant X2
kinesin family member 13B, transcript variant X1
transfer RNA lysine (anticodon CUU); 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: 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: 9 ESTs, 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
uncharacterized LOC122453362, transcript variant X2
uncharacterized LOC122453362, transcript variant X1
methionine sulfoxide reductase A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
methionine sulfoxide reductase A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
methionine sulfoxide reductase A, transcript variant X2
methionine sulfoxide reductase A, transcript variant X1
mitochondrial peptide methionine sulfoxide reductase isoform X1
mitochondrial peptide methionine sulfoxide reductase isoform X2
mitochondrial peptide methionine sulfoxide reductase isoform X4
mitochondrial peptide methionine sulfoxide reductase isoform X3
uncharacterized LOC122452847, 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
uncharacterized LOC122452847, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
methionine sulfoxide reductase A, transcript variant X5
methionine sulfoxide reductase A, transcript variant X6
mitochondrial peptide methionine sulfoxide reductase isoform X5
methionine sulfoxide reductase A, transcript variant X7
mitochondrial peptide methionine sulfoxide reductase isoform X6
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: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
PIN2 (TERF1) interacting telomerase inhibitor 1
PIN2/TERF1-interacting telomerase inhibitor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59% coverage of the annotated genomic feature by RNAseq alignments
L-threonine 3-dehydrogenase, mitochondrial, transcript variant X1
L-threonine 3-dehydrogenase, mitochondrial, transcript variant X2
L-threonine 3-dehydrogenase, mitochondrial
family with sequence similarity 167 member A, transcript variant X5
family with sequence similarity 167 member A, transcript variant X2
family with sequence similarity 167 member A, transcript variant X4
family with sequence similarity 167 member A, transcript variant X8
family with sequence similarity 167 member A, transcript variant X3
family with sequence similarity 167 member A, transcript variant X7
family with sequence similarity 167 member A, transcript variant X1
family with sequence similarity 167 member A, transcript variant X6
BLK proto-oncogene, Src family tyrosine kinase, transcript variant X2
BLK proto-oncogene, Src family tyrosine kinase, transcript variant X4
BLK proto-oncogene, Src family tyrosine kinase, transcript variant X1
BLK proto-oncogene, Src family tyrosine kinase, transcript variant X3
GATA binding protein 4, transcript variant X2
GATA binding protein 4, transcript variant X1
GATA binding protein 4, transcript variant X3
nei like DNA glycosylase 2, transcript variant X1
nei like DNA glycosylase 2, transcript variant X2
farnesyl-diphosphate farnesyltransferase 1, transcript variant X2
farnesyl-diphosphate farnesyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
small nucleolar RNA SNORA62/SNORA6 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00091
disintegrin and metalloproteinase domain-containing protein 20-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
disintegrin and metalloproteinase domain-containing protein 29-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
glycine receptor alpha 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
glycine receptor alpha 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
glycine receptor subunit alpha-3 isoform X1
glycine receptor subunit alpha-3 isoform X2
aurora kinase A and ninein-interacting protein-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 6 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
15-hydroxyprostaglandin dehydrogenase [NAD(+)]
centrosomal protein 44, transcript variant X5
centrosomal protein 44, transcript variant X2
centrosomal protein 44, transcript variant X4
centrosomal protein 44, transcript variant X10
centrosomal protein 44, transcript variant X1
centrosomal protein 44, transcript variant X6
centrosomal protein 44, transcript variant X3
centrosomal protein 44, transcript variant X7
centrosomal protein of 44 kDa isoform X4
centrosomal protein of 44 kDa isoform X1
centrosomal protein 44, transcript variant X8
centrosomal protein 44, transcript variant X9
centrosomal protein of 44 kDa isoform X2
centrosomal protein of 44 kDa isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 13 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 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00156
heart and neural crest derivatives expressed 2
heart- and neural crest derivatives-expressed protein 2
uncharacterized LOC122453016, transcript variant X4
uncharacterized LOC122453016, transcript variant X3
uncharacterized LOC122453016, 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
uncharacterized LOC122453016, transcript variant X1
stimulator of chondrogenesis 1, transcript variant X1
stimulator of chondrogenesis 1, transcript variant X2
histone deacetylase complex subunit SAP30
polypeptide N-acetylgalactosaminyltransferase 7, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 7, transcript variant X1
N-acetylgalactosaminyltransferase 7 isoform X1
N-acetylgalactosaminyltransferase 7 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 23 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase like 6
polypeptide N-acetylgalactosaminyltransferase-like 6
transfer RNA arginine (anticodon CCU); 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, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
testis expressed 10, transcript variant X1
testis expressed 10, transcript variant X3
testis expressed 10, transcript variant X2
endoplasmic reticulum resident protein 44
nuclear receptor subfamily 4 group A member 3, transcript variant X1
nuclear receptor subfamily 4 group A member 3, transcript variant X2
nuclear receptor subfamily 4 group A member 3 isoform X1
nuclear receptor subfamily 4 group A member 3 isoform X2
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit 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 9 samples with support for all annotated introns
protein transport protein Sec61 subunit beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transforming growth factor beta receptor 1, transcript variant X1
transforming growth factor beta receptor 1, transcript variant X2
collagen type XV alpha 1 chain, transcript variant X2
collagen type XV alpha 1 chain, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 12, transcript variant X2
polypeptide N-acetylgalactosaminyltransferase 12, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 12 isoform X2
polypeptide N-acetylgalactosaminyltransferase 12 isoform X1
ankyrin repeat and sterile alpha motif domain containing 6, transcript variant X6
ankyrin repeat and sterile alpha motif domain containing 6, transcript variant X1
ankyrin repeat and sterile alpha motif domain containing 6, transcript variant X2
ankyrin repeat and sterile alpha motif domain containing 6, transcript variant X4
ankyrin repeat and sterile alpha motif domain containing 6, transcript variant X5
ankyrin repeat and sterile alpha motif domain containing 6, transcript variant X3
ankyrin repeat and SAM domain-containing protein 6 isoform X1
ankyrin repeat and SAM domain-containing protein 6 isoform X2
ankyrin repeat and SAM domain-containing protein 6 isoform X3
ankyrin repeat and SAM domain-containing protein 6 isoform X4
ankyrin repeat and SAM domain-containing protein 6 isoform X5
gamma-aminobutyric acid type B receptor subunit 2
uncharacterized LOC122452806, transcript variant X5
uncharacterized protein LOC122452806 isoform X4
uncharacterized LOC122452806, 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 1 sample with support for all annotated introns
uncharacterized protein LOC122452806 isoform X5
uncharacterized LOC122452806, transcript variant X2
uncharacterized LOC122452806, transcript variant X3
uncharacterized LOC122452806, transcript variant X4
uncharacterized LOC122452806, transcript variant X1
uncharacterized LOC122452806, transcript variant X12
uncharacterized LOC122452806, transcript variant X9
uncharacterized LOC122452806, transcript variant X8
uncharacterized LOC122452806, transcript variant X11
uncharacterized protein LOC122452806 isoform X2
uncharacterized protein LOC122452806 isoform X3
uncharacterized protein LOC122452806 isoform X1
uncharacterized protein LOC122452806 isoform X9
uncharacterized protein LOC122452806 isoform X7
uncharacterized LOC122452806, transcript variant X10
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 5 samples with support for all annotated introns
uncharacterized LOC122452806, 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
uncharacterized protein LOC122452806 isoform X8
uncharacterized protein LOC122452806 isoform X6
uncharacterized LOC122452806, transcript variant X16
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
uncharacterized LOC122452806, transcript variant X17
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 4 samples with support for all annotated introns
uncharacterized LOC122452806, transcript variant X14
uncharacterized LOC122452806, transcript variant X15
uncharacterized LOC122452806, transcript variant X13
TBC1 domain family member 2, transcript variant X3
TBC1 domain family member 2, transcript variant X2
TBC1 domain family member 2, transcript variant X1
TBC1 domain family member 2, transcript variant X4
acidic nuclear phosphoprotein 32 family member B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
acidic leucine-rich nuclear phosphoprotein 32 family member B isoform X2
acidic nuclear phosphoprotein 32 family member B, transcript variant X1
acidic leucine-rich nuclear phosphoprotein 32 family member B isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00548
tRNA methyltransferase O, transcript variant X1
tRNA methyltransferase O, transcript variant X2
tRNA (adenine(37)-N6)-methyltransferase isoform X1
tRNA (adenine(37)-N6)-methyltransferase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 10 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: 54 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
non-histone chromosomal protein HMG-14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
XPA, DNA damage recognition and repair factor, transcript variant X2
XPA, DNA damage recognition and repair factor, transcript variant X1
DNA repair protein complementing XP-A cells
thiosulfate sulfurtransferase like domain containing 2, transcript variant X4
thiosulfate sulfurtransferase like domain containing 2, transcript variant X2
thiosulfate sulfurtransferase like domain containing 2, transcript variant X3
thiosulfate sulfurtransferase like domain containing 2, transcript variant X1
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 2
tudor domain containing 7, transcript variant X1
tudor domain containing 7, transcript variant X3
tudor domain containing 7, transcript variant X2
tudor domain-containing protein 7 isoform X1
tudor domain-containing protein 7 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: coiled-coil domain-containing protein 180
stimulated by retinoic acid gene 6 protein-like
insulin like growth factor binding protein like 1
insulin-like growth factor-binding protein-like 1
aldehyde dehydrogenase 1 family member B1
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: 2 Proteins, and 18% 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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: aldehyde dehydrogenase X, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 25 member 51, transcript variant X5
solute carrier family 25 member 51, transcript variant X1
solute carrier family 25 member 51, transcript variant X3
solute carrier family 25 member 51, transcript variant X4
solute carrier family 25 member 51, transcript variant X2
solute carrier family 25 member 51, transcript variant X6
mitochondrial nicotinamide adenine dinucleotide transporter SLC25A51
DDB1 and CUL4 associated factor 10, transcript variant X2
DDB1 and CUL4 associated factor 10, transcript variant X3
DDB1 and CUL4 associated factor 10, transcript variant X1
DDB1- and CUL4-associated factor 10 isoform X2
DDB1- and CUL4-associated factor 10 isoform X3
DDB1- and CUL4-associated factor 10 isoform X1
DDB1 and CUL4 associated factor 10, transcript variant X4
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 23 samples with support for all annotated introns
DDB1 and CUL4 associated factor 10, 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 7 samples with support for all annotated introns
DDB1- and CUL4-associated factor 10 isoform X4
tRNA methyltransferase 10B, transcript variant X2
tRNA methyltransferase 10B, transcript variant X1
tRNA methyltransferase 10 homolog B isoform X1
tRNA methyltransferase 10B, transcript variant X3
tRNA methyltransferase 10 homolog B isoform X2
FERM and PDZ domain containing 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
FERM and PDZ domain containing 1, transcript variant X2
FERM and PDZ domain containing 1, transcript variant X3
FERM and PDZ domain containing 1, transcript variant X1
FERM and PDZ domain containing 1, transcript variant X5
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 1 sample with support for all annotated introns
FERM and PDZ domain-containing protein 1 isoform X2
FERM and PDZ domain-containing protein 1 isoform X1
transfer RNA glycine (anticodon CCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
translocase of outer mitochondrial membrane 5
mitochondrial import receptor subunit TOM5 homolog
DNA-directed RNA polymerase I subunit RPA49
zinc finger and BTB domain containing 5, transcript variant X1
zinc finger and BTB domain containing 5, transcript variant X2
zinc finger and BTB domain containing 5, transcript variant X3
zinc finger and BTB domain containing 5, transcript variant X4
zinc finger and BTB domain containing 5, transcript variant X5
zinc finger and BTB domain-containing protein 5
glyoxylate and hydroxypyruvate reductase
glyoxylate reductase/hydroxypyruvate reductase
zinc finger CCHC-type containing 7, transcript variant X2
zinc finger CCHC-type containing 7, transcript variant X1
zinc finger CCHC domain-containing protein 7
maternal embryonic leucine zipper kinase, transcript variant X4
maternal embryonic leucine zipper kinase, transcript variant X1
maternal embryonic leucine zipper kinase, transcript variant X2
maternal embryonic leucine zipper kinase, transcript variant X3
maternal embryonic leucine zipper kinase isoform X2
maternal embryonic leucine zipper kinase isoform X1
uncharacterized LOC122453206, 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
uncharacterized LOC122453206, transcript variant X1
ring finger protein 38, transcript variant X1
E3 ubiquitin-protein ligase RNF38 isoform X1
ring finger protein 38, transcript variant X8
ring finger protein 38, transcript variant X6
ring finger protein 38, transcript variant X5
ring finger protein 38, transcript variant X7
ring finger protein 38, transcript variant X4
ring finger protein 38, transcript variant X3
ring finger protein 38, transcript variant X10
ring finger protein 38, transcript variant X9
ring finger protein 38, transcript variant X2
E3 ubiquitin-protein ligase RNF38 isoform X2
E3 ubiquitin-protein ligase RNF38 isoform X3
glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase, transcript variant X1
bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase isoform X1
glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase, transcript variant X5
glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase, transcript variant X3
glucosamine (UDP-N-acetyl)-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 X3
glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase, transcript variant X4
bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase isoform X4
clathrin light chain A, transcript variant X3
clathrin light chain A, transcript variant X2
clathrin light chain A, transcript variant X1
GLI pathogenesis related 2, transcript variant X1
Golgi-associated plant pathogenesis-related protein 1 isoform X1
GLI pathogenesis related 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 75% coverage of the annotated genomic feature by RNAseq alignments
Golgi-associated plant pathogenesis-related protein 1 isoform X2
reversion inducing cysteine rich protein with kazal motifs
reversion-inducing cysteine-rich protein with Kazal motifs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00561
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00265
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 91 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 87 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 90 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
olfactory receptor 13C7-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins
olfactory receptor 13C7-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 84 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 90 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
small regulatory polypeptide of amino acid response
histidine-rich carboxyl terminus protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial-like isoform X1
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
succinate dehydrogenase [ubiquinone] cytochrome b small subunit, mitochondrial-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 17 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 8B, transcript variant X1
transmembrane protein 8B, transcript variant X2
transmembrane protein 8B, transcript variant X3
family with sequence similarity 221 member B
histidine triad nucleotide binding protein 2
histidine triad nucleotide-binding protein 2, mitochondrial
sperm associated antigen 8, transcript variant X1
sperm associated antigen 8, transcript variant X2
natriuretic peptide receptor 2, transcript variant X7
natriuretic peptide receptor 2, transcript variant X6
natriuretic peptide receptor 2, transcript variant X5
natriuretic peptide receptor 2, transcript variant X4
natriuretic peptide receptor 2, transcript variant X2
natriuretic peptide receptor 2, transcript variant X3
natriuretic peptide receptor 2, transcript variant X1
atrial natriuretic peptide receptor 2 isoform X7
atrial natriuretic peptide receptor 2 isoform X6
atrial natriuretic peptide receptor 2 isoform X5
atrial natriuretic peptide receptor 2 isoform X4
atrial natriuretic peptide receptor 2 isoform X2
atrial natriuretic peptide receptor 2 isoform X3
atrial natriuretic peptide receptor 2 isoform X1
natriuretic peptide receptor 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
atrial natriuretic peptide receptor 2 isoform X8
RGP1 homolog, RAB6A GEF complex partner 1, transcript variant X4
RGP1 homolog, RAB6A GEF complex partner 1, transcript variant X11
RGP1 homolog, RAB6A GEF complex partner 1, transcript variant X12
RGP1 homolog, RAB6A GEF complex partner 1, transcript variant X3
RGP1 homolog, RAB6A GEF complex partner 1, transcript variant X2
RGP1 homolog, RAB6A GEF complex partner 1, transcript variant X1
RAB6A-GEF complex partner protein 2 isoform X2
RAB6A-GEF complex partner protein 2 isoform X3
RGP1 homolog, RAB6A GEF complex partner 1, transcript variant X10
RGP1 homolog, RAB6A GEF complex partner 1, transcript variant X9
RGP1 homolog, RAB6A GEF complex partner 1, transcript variant X6
RGP1 homolog, RAB6A GEF complex partner 1, transcript variant X8
RGP1 homolog, RAB6A GEF complex partner 1, transcript variant X5
RGP1 homolog, RAB6A GEF complex partner 1, transcript variant X7
RAB6A-GEF complex partner protein 2 isoform X1
cAMP responsive element binding protein 3, transcript variant X2
cAMP responsive element binding protein 3, transcript variant X1
cyclic AMP-responsive element-binding protein 3 isoform X2
cyclic AMP-responsive element-binding protein 3 isoform X1
carbonic anhydrase 9, transcript variant X4
carbonic anhydrase 9, transcript variant X3
carbonic anhydrase 9, transcript variant X1
carbonic anhydrase 9, transcript variant X2
Rho guanine nucleotide exchange factor 39, transcript variant X2
Rho guanine nucleotide exchange factor 39, transcript variant X1
rho guanine nucleotide exchange factor 39 isoform X1
rho guanine nucleotide exchange factor 39 isoform X2
coiled-coil domain containing 107, transcript variant X2
coiled-coil domain containing 107, transcript variant X3
coiled-coil domain containing 107, transcript variant X1
coiled-coil domain-containing protein 107 isoform X2
coiled-coil domain-containing protein 107 isoform X3
coiled-coil domain-containing protein 107 isoform X1
signaling threshold regulating transmembrane adaptor 1
signaling threshold-regulating transmembrane adapter 1
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
testis associated actin remodelling kinase 1
dual specificity testis-specific protein kinase 1
family with sequence similarity 166 member B, transcript variant X1
family with sequence similarity 166 member B, transcript variant X3
family with sequence similarity 166 member B, transcript variant X2
RUN and SH3 domain containing 2, transcript variant X1
RUN and SH3 domain containing 2, transcript variant X5
RUN and SH3 domain containing 2, transcript variant X3
RUN and SH3 domain containing 2, transcript variant X4
RUN and SH3 domain containing 2, transcript variant X2
RUN and SH3 domain containing 2, transcript variant X6
phospholipid-transporting ATPase FetA-like, transcript variant X3
phospholipid-transporting ATPase FetA-like, transcript variant X2
phospholipid-transporting ATPase FetA-like, transcript variant X1
phospholipid-transporting ATPase FetA-like isoform X3
phospholipid-transporting ATPase FetA-like isoform X2
phospholipid-transporting ATPase FetA-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 216 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 214 member B, transcript variant X1
family with sequence similarity 214 member B, 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 20 samples with support for all annotated introns
family with sequence similarity 214 member B, transcript variant X2
phosphatidylinositol glycan anchor biosynthesis class O, transcript variant X2
GPI ethanolamine phosphate transferase 3 isoform X2
phosphatidylinositol glycan anchor biosynthesis class O, transcript variant X3
phosphatidylinositol glycan anchor biosynthesis class O, transcript variant X1
GPI ethanolamine phosphate transferase 3 isoform X3
GPI ethanolamine phosphate transferase 3 isoform X1
FA complementation group G, transcript variant X1
FA complementation group G, transcript variant X2
FA complementation group G, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
FA complementation group G, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
FA complementation group G, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Fanconi anemia group G protein isoform X1
Fanconi anemia group G protein isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
LOW QUALITY PROTEIN: transitional endoplasmic reticulum ATPase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C9orf131 homolog
26S proteasome regulatory subunit 10B-like
DnaJ heat shock protein family (Hsp40) member B5, transcript variant X3
DnaJ heat shock protein family (Hsp40) member B5, transcript variant X2
DnaJ heat shock protein family (Hsp40) member B5, transcript variant X1
dnaJ homolog subfamily B member 5 isoform X1
dnaJ homolog subfamily B member 5 isoform X2
PHD finger protein 24, transcript variant X2
PHD finger protein 24, transcript variant X3
PHD finger protein 24, transcript variant X1
PHD finger protein 24, transcript variant X4
family with sequence similarity 205 member C, transcript variant X3
family with sequence similarity 205 member C, transcript variant X1
family with sequence similarity 205 member C, transcript variant X2
spermatogenesis-associated protein 31D3-like
spermatogenesis-associated protein 31D1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transducin-like enhancer protein 1, transcript variant X1
transducin-like enhancer protein 1, transcript variant X2
transducin-like enhancer protein 1, transcript variant X3
transducin-like enhancer protein 1, transcript variant X6
transducin-like enhancer protein 1, transcript variant X4
transducin-like enhancer protein 1, transcript variant X8
transducin-like enhancer protein 1, transcript variant X5
transducin-like enhancer protein 1, transcript variant X9
transducin-like enhancer protein 1, transcript variant X7
transducin-like enhancer protein 1 isoform X1
transducin-like enhancer protein 1 isoform X2
transducin-like enhancer protein 1 isoform X3
transducin-like enhancer protein 1 isoform X6
transducin-like enhancer protein 1 isoform X4
transducin-like enhancer protein 1 isoform X8
transducin-like enhancer protein 1 isoform X5
transducin-like enhancer protein 1 isoform X9
transducin-like enhancer protein 1 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 19 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00153
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 6% 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 43% coverage of the annotated genomic feature by RNAseq alignments
TLE family member 4, transcriptional corepressor, transcript variant X6
TLE family member 4, transcriptional corepressor, transcript variant X5
TLE family member 4, transcriptional corepressor, transcript variant X2
TLE family member 4, transcriptional corepressor, transcript variant X1
TLE family member 4, transcriptional corepressor, transcript variant X7
TLE family member 4, transcriptional corepressor, transcript variant X4
TLE family member 4, transcriptional corepressor, transcript variant X3
TLE family member 4, transcriptional corepressor, transcript variant X8
TLE family member 4, transcriptional corepressor, transcript variant X9
transducin-like enhancer protein 4 isoform X6
transducin-like enhancer protein 4 isoform X5
transducin-like enhancer protein 4 isoform X2
transducin-like enhancer protein 4 isoform X1
transducin-like enhancer protein 4 isoform X8
transducin-like enhancer protein 4 isoform X7
transducin-like enhancer protein 4 isoform X4
transducin-like enhancer protein 4 isoform X3
transducin-like enhancer protein 4 isoform X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 13 ESTs, 3 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
centrosomal protein 78, transcript variant X3
centrosomal protein 78, transcript variant X2
centrosomal protein 78, transcript variant X1
centrosomal protein of 78 kDa isoform X3
centrosomal protein of 78 kDa isoform X2
centrosomal protein of 78 kDa isoform X1
guanine nucleotide-binding protein G(q) subunit alpha
guanine nucleotide-binding protein subunit alpha-14
vacuolar protein sorting 13 homolog A, transcript variant X2
vacuolar protein sorting 13 homolog A, transcript variant X1
vacuolar protein sorting-associated protein 13A isoform X2
vacuolar protein sorting-associated protein 13A isoform X1
vacuolar protein sorting 13 homolog A, transcript variant X3
vacuolar protein sorting-associated protein 13A isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 7 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: 6 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: protein prune homolog 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments
glucosaminyl (N-acetyl) transferase 1, transcript variant X2
glucosaminyl (N-acetyl) transferase 1, transcript variant X1
glucosaminyl (N-acetyl) transferase 1, transcript variant X6
glucosaminyl (N-acetyl) transferase 1, transcript variant X4
glucosaminyl (N-acetyl) transferase 1, transcript variant X3
glucosaminyl (N-acetyl) transferase 1, transcript variant X7
glucosaminyl (N-acetyl) transferase 1, transcript variant X9
glucosaminyl (N-acetyl) transferase 1, transcript variant X8
glucosaminyl (N-acetyl) transferase 1, transcript variant X5
beta-1,3-galactosyl-O-glycosyl-glycoprotein beta-1,6-N-acetylglucosaminyltransferase
proprotein convertase subtilisin/kexin type 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 7 ESTs, 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
proprotein convertase subtilisin/kexin type 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 7 ESTs, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
proprotein convertase subtilisin/kexin type 5 isoform X3
proprotein convertase subtilisin/kexin type 5 isoform X2
proprotein convertase subtilisin/kexin type 5, transcript variant X1
proprotein convertase subtilisin/kexin type 5 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
dnaJ homolog subfamily A member 1-like, transcript variant X2
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
dnaJ homolog subfamily A member 1-like, 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
dnaJ homolog subfamily A member 1-like isoform X2
dnaJ homolog subfamily A member 1-like isoform X1
osteoclast stimulating factor 1, transcript variant X2
osteoclast stimulating factor 1, transcript variant X1
osteoclast-stimulating factor 1 isoform X2
osteoclast-stimulating factor 1 isoform X1
nicotinamide riboside kinase 1, transcript variant X2
nicotinamide riboside kinase 1, transcript variant X3
nicotinamide riboside kinase 1, transcript variant X1
nicotinamide riboside kinase 1, transcript variant X4
nicotinamide riboside kinase 1 isoform X1
nicotinamide riboside kinase 1 isoform X3
nicotinamide riboside kinase 1 isoform X2
LOW QUALITY PROTEIN: carnosine N-methyltransferase
transient receptor potential cation channel subfamily M member 6, transcript variant X3
transient receptor potential cation channel subfamily M member 6, transcript variant X4
transient receptor potential cation channel subfamily M member 6 isoform X3
transient receptor potential cation channel subfamily M member 6, transcript variant X1
transient receptor potential cation channel subfamily M member 6, transcript variant X2
transient receptor potential cation channel subfamily M member 6 isoform X1
transient receptor potential cation channel subfamily M member 6 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00494
COORDINATES: nucleotide motif:Rfam:12.0:RF00493
small nucleolar RNA SNORA42/SNORA80 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00406
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 41 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00594
uncharacterized LOC122453370, transcript variant X1
uncharacterized LOC122453370, transcript variant X2
uncharacterized LOC122453370, transcript variant X3
aldehyde dehydrogenase 1 family member A1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: transmembrane channel-like protein 1
uncharacterized LOC122453161, transcript variant X2
uncharacterized LOC122453161, transcript variant X3
uncharacterized LOC122453161, transcript variant X1
guanine deaminase, transcript variant X1
guanine deaminase, transcript variant X2
guanine deaminase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
abhydrolase domain containing 17B, depalmitoylase, transcript variant X1
abhydrolase domain containing 17B, depalmitoylase, transcript variant X5
abhydrolase domain containing 17B, depalmitoylase, transcript variant X2
abhydrolase domain containing 17B, depalmitoylase, transcript variant X3
abhydrolase domain containing 17B, depalmitoylase, transcript variant X4
alpha/beta hydrolase domain-containing protein 17B
transient receptor potential cation channel subfamily M member 3, transcript variant X4
transient receptor potential cation channel subfamily M member 3, transcript variant X6
transient receptor potential cation channel subfamily M member 3 isoform X3
transient receptor potential cation channel subfamily M member 3 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
transient receptor potential cation channel subfamily M member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transient receptor potential cation channel subfamily M member 3, transcript variant X1
transient receptor potential cation channel subfamily M member 3, transcript variant X5
transient receptor potential cation channel subfamily M member 3, transcript variant X3
transient receptor potential cation channel subfamily M member 3, transcript variant X7
transient receptor potential cation channel subfamily M member 3, transcript variant X14
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 10 samples with support for all annotated introns
transient receptor potential cation channel subfamily M member 3, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
transient receptor potential cation channel subfamily M member 3, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transient receptor potential cation channel subfamily M member 3, transcript variant X10
transient receptor potential cation channel subfamily M member 3, transcript variant X12
transient receptor potential cation channel subfamily M member 3, transcript variant X13
transient receptor potential cation channel subfamily M member 3 isoform X9
transient receptor potential cation channel subfamily M member 3 isoform X10
transient receptor potential cation channel subfamily M member 3 isoform X11
transient receptor potential cation channel subfamily M member 3 isoform X1
transient receptor potential cation channel subfamily M member 3 isoform X2
transient receptor potential cation channel subfamily M member 3 isoform X4
transient receptor potential cation channel subfamily M member 3 isoform X6
transient receptor potential cation channel subfamily M member 3 isoform X12
transient receptor potential cation channel subfamily M member 3 isoform X13
transient receptor potential cation channel subfamily M member 3, transcript variant X8
transient receptor potential cation channel subfamily M member 3 isoform X7
transient receptor potential cation channel subfamily M member 3, transcript variant X9
transient receptor potential cation channel subfamily M member 3 isoform X8
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: histone-binding protein RBBP4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
10 kDa heat shock protein, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 94% 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: 14 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
structural maintenance of chromosomes protein 5
structural maintenance of chromosomes protein 5-like
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 37 samples with support for all annotated introns
MAM domain containing 2, transcript variant X1
MAM domain-containing protein 2 isoform X1
MAM domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
MAM domain-containing protein 2 isoform X2
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cilia and flagella associated protein 95
protein prenyltransferase alpha subunit repeat containing 1
protein prenyltransferase alpha subunit repeat-containing protein 1
amyloid beta precursor protein binding family A member 1, transcript variant X2
amyloid beta precursor protein binding family A member 1, transcript variant X1
amyloid beta precursor protein binding family A member 1, transcript variant X4
amyloid beta precursor protein binding family A member 1, transcript variant X3
amyloid-beta A4 precursor protein-binding family A member 1 isoform X1
amyloid-beta A4 precursor protein-binding family A member 1 isoform X2
family with sequence similarity 189 member A2, transcript variant X2
family with sequence similarity 189 member A2, transcript variant X1
tight junction protein 2, transcript variant X4
tight junction protein 2, transcript variant X3
tight junction protein 2, transcript variant X8
tight junction protein 2, transcript variant X6
tight junction protein 2, transcript variant X2
tight junction protein 2, transcript variant X7
tight junction protein 2, transcript variant X5
tight junction protein 2, transcript variant X1
phosphatidylinositol-4-phosphate 5-kinase type 1 beta, transcript variant X2
phosphatidylinositol-4-phosphate 5-kinase type 1 beta, transcript variant X1
phosphatidylinositol 4-phosphate 5-kinase type-1 beta isoform X1
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 5
phosphatidylinositol-4-phosphate 5-kinase type 1 beta, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
phosphatidylinositol 4-phosphate 5-kinase type-1 beta isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF01210
PP2A Aalpha (PPP2R1A) and B55A (PPP2R2A) interacting phosphatase regulator 1
PPP2R1A-PPP2R2A-interacting phosphatase regulator 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 EST, 7 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
COBW domain-containing protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 3 ESTs, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
COBW domain-containing protein 2, transcript variant X5
COBW domain-containing protein 2, transcript variant X2
COBW domain-containing protein 2, transcript variant X1
COBW domain-containing protein 2, transcript variant X3
COBW domain-containing protein 2, transcript variant X8
COBW domain-containing protein 2, transcript variant X7
COBW domain-containing protein 2, transcript variant X6
putative COBW domain-containing protein 7 isoform X2
COBW domain-containing protein 2 isoform X1
putative COBW domain-containing protein 7 isoform X3
dedicator of cytokinesis 8, transcript variant X1
dedicator of cytokinesis 8, transcript variant X3
dedicator of cytokinesis protein 8 isoform X1
dedicator of cytokinesis 8, transcript variant X2
dedicator of cytokinesis 8, transcript variant X4
dedicator of cytokinesis protein 8 isoform X2
KN motif and ankyrin repeat domains 1, transcript variant X3
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
KN motif and ankyrin repeat domain-containing protein 1 isoform X3
KN motif and ankyrin repeat domains 1, transcript variant X2
KN motif and ankyrin repeat domains 1, transcript variant X1
KN motif and ankyrin repeat domains 1, transcript variant X4
KN motif and ankyrin repeat domain-containing protein 1 isoform X1
KN motif and ankyrin repeat domain-containing protein 1 isoform X4
KN motif and ankyrin repeat domains 1, transcript variant X5
KN motif and ankyrin repeat domain-containing protein 1 isoform X2
small ubiquitin-related modifier 2-A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
small ubiquitin-related modifier 2-A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
small ubiquitin-related modifier 2-like isoform X2
small ubiquitin-related modifier 2-A-like isoform X1
doublesex and mab-3 related transcription factor 1
LOW QUALITY PROTEIN: doublesex- and mab-3-related transcription factor 1
doublesex and mab-3 related transcription factor 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
doublesex- and mab-3-related transcription factor 3
doublesex and mab-3 related transcription factor 2, transcript variant X1
doublesex and mab-3 related transcription factor 2, transcript variant X3
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 3 samples with support for all annotated introns
doublesex- and mab-3-related transcription factor 2 isoform X1
doublesex- and mab-3-related transcription factor 2 isoform X3
doublesex and mab-3 related transcription factor 2, transcript variant X2
doublesex- and mab-3-related transcription factor 2 isoform X2
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2, transcript variant X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2, transcript variant X3
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2, transcript variant X4
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2, transcript variant X1
probable global transcription activator SNF2L2 isoform X1
probable global transcription activator SNF2L2 isoform X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2, transcript variant X6
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2, transcript variant X5
probable global transcription activator SNF2L2 isoform X3
uncharacterized LOC122453009, transcript variant X3
uncharacterized LOC122453009, transcript variant X6
uncharacterized LOC122453009, transcript variant X7
uncharacterized LOC122453009, transcript variant X2
uncharacterized LOC122453009, transcript variant X5
uncharacterized LOC122453009, transcript variant X1
uncharacterized LOC122453009, transcript variant X4
potassium voltage-gated channel modifier subfamily V member 2
potassium voltage-gated channel subfamily V member 2
pumilio RNA binding family member 3, transcript variant X5
pumilio RNA binding family member 3, transcript variant X8
pumilio RNA binding family member 3, transcript variant X7
pumilio RNA binding family member 3, transcript variant X3
pumilio RNA binding family member 3, transcript variant X1
pumilio RNA binding family member 3, transcript variant X10
pumilio RNA binding family member 3, transcript variant X6
pumilio RNA binding family member 3, transcript variant X2
pumilio RNA binding family member 3, transcript variant X9
pumilio RNA binding family member 3, transcript variant X4
uncharacterized LOC122453038, transcript variant X2
uncharacterized LOC122453038, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
histone-arginine methyltransferase CARM1-like, transcript variant X2
histone-arginine methyltransferase CARM1-like, transcript variant X1
histone-arginine methyltransferase CARM1-like, transcript variant X4
histone-arginine methyltransferase CARM1-like, transcript variant X5
histone-arginine methyltransferase CARM1-like
histone-arginine methyltransferase CARM1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
regulatory factor X3, transcript variant X2
regulatory factor X3, transcript variant X3
regulatory factor X3, transcript variant X1
regulatory factor X3, transcript variant X4
regulatory factor X3, transcript variant X6
regulatory factor X3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
GLIS family zinc finger 3, transcript variant X4
GLIS family zinc finger 3, transcript variant X3
GLIS family zinc finger 3, transcript variant X6
GLIS family zinc finger 3, transcript variant X8
GLIS family zinc finger 3, transcript variant X5
GLIS family zinc finger 3, transcript variant X1
GLIS family zinc finger 3, transcript variant X2
GLIS family zinc finger 3, transcript variant X7
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
spermatogenesis associated 6 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
spermatogenesis associated 6 like, transcript variant X3
spermatogenesis associated 6 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
spermatogenesis associated 6 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
spermatogenesis associated 6 like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
spermatogenesis associated 6-like protein isoform X3
spermatogenesis associated 6-like protein isoform X1
spermatogenesis associated 6-like protein isoform X4
spermatogenesis associated 6-like protein isoform X2
spermatogenesis associated 6-like protein isoform X5
adenylate kinase 3, transcript variant X3
adenylate kinase 3, transcript variant X2
adenylate kinase 3, transcript variant X1
GTP:AMP phosphotransferase AK3, mitochondrial isoform X1
GTP:AMP phosphotransferase AK3, mitochondrial isoform X2
RNA terminal phosphate cyclase like 1, transcript variant X2
RNA terminal phosphate cyclase like 1, transcript variant X1
RNA 3'-terminal phosphate cyclase-like protein isoform X1
RNA terminal phosphate cyclase like 1, transcript variant X3
RNA 3'-terminal phosphate cyclase-like protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
plasminogen receptor with a C-terminal lysine, transcript variant X1
plasminogen receptor with a C-terminal lysine, transcript variant X2
plasminogen receptor with a C-terminal lysine, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
programmed cell death 1 ligand 1 isoform X2
programmed cell death 1 ligand 1 isoform X1
programmed cell death 1 ligand 2, transcript variant X1
programmed cell death 1 ligand 2, transcript variant X2
programmed cell death 1 ligand 2, transcript variant X4
programmed cell death 1 ligand 2, transcript variant X5
programmed cell death 1 ligand 2, transcript variant X3
programmed cell death 1 ligand 2 isoform X1
programmed cell death 1 ligand 2 isoform X2
programmed cell death 1 ligand 2 isoform X4
programmed cell death 1 ligand 2 isoform X5
programmed cell death 1 ligand 2 isoform X3
RIC1 homolog, RAB6A GEF complex partner 1, transcript variant X1
RIC1 homolog, RAB6A GEF complex partner 1, transcript variant X3
RIC1 homolog, RAB6A GEF complex partner 1, transcript variant X2
guanine nucleotide exchange factor subunit RIC1 isoform X1
guanine nucleotide exchange factor subunit RIC1 isoform X3
guanine nucleotide exchange factor subunit RIC1 isoform X2
RIC1 homolog, RAB6A GEF complex partner 1, transcript variant X4
guanine nucleotide exchange factor subunit RIC1 isoform X4
endoplasmic reticulum metallopeptidase 1, transcript variant X1
endoplasmic reticulum metallopeptidase 1, transcript variant X3
endoplasmic reticulum metallopeptidase 1, transcript variant X4
endoplasmic reticulum metallopeptidase 1, transcript variant X2
endoplasmic reticulum metallopeptidase 1 isoform X4
endoplasmic reticulum metallopeptidase 1 isoform X2
endoplasmic reticulum metallopeptidase 1 isoform X3
endoplasmic reticulum metallopeptidase 1 isoform X1
melanoma antigen recognized by T-cells 1 isoform X1
melanoma antigen recognized by T-cells 1 isoform X2
KIAA2026 ortholog, transcript variant X3
KIAA2026 ortholog, transcript variant X2
KIAA2026 ortholog, transcript variant X1
KIAA2026 ortholog, transcript variant X5
KIAA2026 ortholog, transcript variant X4
uncharacterized protein KIAA2026 homolog isoform X3
uncharacterized protein KIAA2026 homolog isoform X2
uncharacterized protein KIAA2026 homolog isoform X1
uncharacterized protein KIAA2026 homolog isoform X4
uncharacterized protein KIAA2026 homolog isoform X5
RAN binding protein 6, transcript variant X3
RAN binding protein 6, transcript variant X2
RAN binding protein 6, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00319
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 29% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
ubiquitin like with PHD and ring finger domains 2, transcript variant X1
ubiquitin like with PHD and ring finger domains 2, transcript variant X2
E3 ubiquitin-protein ligase UHRF2 isoform X1
E3 ubiquitin-protein ligase UHRF2 isoform X2
glycine dehydrogenase (decarboxylating), mitochondrial
transfer RNA glutamic acid (anticodon UUC); 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, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
distal membrane arm assembly component 1, transcript variant X1
distal membrane arm assembly component 1, transcript variant X2
distal membrane-arm assembly complex protein 1 isoform X1
distal membrane arm assembly component 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
distal membrane-arm assembly complex protein 1 isoform X2
distal membrane-arm assembly complex protein 1 isoform X3
protein tyrosine phosphatase receptor type D, transcript variant X12
protein tyrosine phosphatase receptor type D, transcript variant X9
protein tyrosine phosphatase receptor type D, transcript variant X13
protein tyrosine phosphatase receptor type D, transcript variant X11
protein tyrosine phosphatase receptor type D, transcript variant X2
protein tyrosine phosphatase receptor type D, transcript variant X10
protein tyrosine phosphatase receptor type D, transcript variant X6
protein tyrosine phosphatase receptor type D, transcript variant X5
protein tyrosine phosphatase receptor type D, transcript variant X4
protein tyrosine phosphatase receptor type D, transcript variant X8
protein tyrosine phosphatase receptor type D, transcript variant X1
protein tyrosine phosphatase receptor type D, transcript variant X3
protein tyrosine phosphatase receptor type D, transcript variant X7
receptor-type tyrosine-protein phosphatase delta isoform X12
receptor-type tyrosine-protein phosphatase delta isoform X9
receptor-type tyrosine-protein phosphatase delta isoform X13
receptor-type tyrosine-protein phosphatase delta isoform X11
receptor-type tyrosine-protein phosphatase delta isoform X2
receptor-type tyrosine-protein phosphatase delta isoform X10
receptor-type tyrosine-protein phosphatase delta isoform X6
receptor-type tyrosine-protein phosphatase delta isoform X5
receptor-type tyrosine-protein phosphatase delta isoform X4
receptor-type tyrosine-protein phosphatase delta isoform X8
receptor-type tyrosine-protein phosphatase delta isoform X1
receptor-type tyrosine-protein phosphatase delta isoform X3
receptor-type tyrosine-protein phosphatase delta isoform X7
uncharacterized LOC122453173, transcript variant X1
uncharacterized LOC122453173, transcript variant X2
elongation factor 1-alpha 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
elongation factor 1-alpha 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 14 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
5,6-dihydroxyindole-2-carboxylic acid oxidase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
multiple PDZ domain crumbs cell polarity complex component, transcript variant X3
multiple PDZ domain crumbs cell polarity complex component, transcript variant X9
multiple PDZ domain crumbs cell polarity complex component, transcript variant X6
multiple PDZ domain crumbs cell polarity complex component, transcript variant X4
multiple PDZ domain crumbs cell polarity complex component, transcript variant X1
multiple PDZ domain crumbs cell polarity complex component, transcript variant X2
multiple PDZ domain crumbs cell polarity complex component, transcript variant X8
multiple PDZ domain crumbs cell polarity complex component, transcript variant X7
multiple PDZ domain crumbs cell polarity complex component, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 20% coverage of the annotated genomic feature by RNAseq alignments
flavin containing dimethylaniline monoxygenase 1, transcript variant X1
dimethylaniline monooxygenase [N-oxide-forming] 1
flavin containing dimethylaniline monoxygenase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
flavin containing dimethylaniline monoxygenase 2, transcript variant X4
flavin containing dimethylaniline monoxygenase 2, transcript variant X1
flavin containing dimethylaniline monoxygenase 2, transcript variant X2
flavin containing dimethylaniline monoxygenase 2, transcript variant X3
dimethylaniline monooxygenase [N-oxide-forming] 2 isoform X1
dimethylaniline monooxygenase [N-oxide-forming] 2 isoform X2
dimethylaniline monooxygenase [N-oxide-forming] 2 isoform X3
nuclear factor I B, transcript variant X1
nuclear factor I B, transcript variant X3
nuclear factor I B, transcript variant X6
nuclear factor I B, transcript variant X4
nuclear factor I B, transcript variant X9
nuclear factor I B, transcript variant X5
nuclear factor I B, transcript variant X7
nuclear factor I B, transcript variant X8
nuclear factor I B, transcript variant X2
nuclear factor I B, transcript variant X10
nuclear factor I B, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
zinc finger DHHC-type palmitoyltransferase 21, transcript variant X3
zinc finger DHHC-type palmitoyltransferase 21, transcript variant X1
zinc finger DHHC-type palmitoyltransferase 21, transcript variant X2
zinc finger DHHC-type palmitoyltransferase 21, transcript variant X5
zinc finger DHHC-type palmitoyltransferase 21, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
FRAS1 related extracellular matrix 1, transcript variant X2
FRAS1 related extracellular matrix 1, transcript variant X1
FRAS1 related extracellular matrix 1, transcript variant X3
FRAS1 related extracellular matrix 1, transcript variant X6
FRAS1-related extracellular matrix protein 1 isoform X1
FRAS1-related extracellular matrix protein 1 isoform X2
FRAS1-related extracellular matrix protein 1 isoform X5
FRAS1 related extracellular matrix 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
FRAS1-related extracellular matrix protein 1 isoform X3
FRAS1 related extracellular matrix 1, transcript variant X5
FRAS1-related extracellular matrix protein 1 isoform X4
FRAS1 related extracellular matrix 1, transcript variant X7
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 1 sample with support for all annotated introns
FRAS1-related extracellular matrix protein 1 isoform X6
small nuclear RNA activating complex polypeptide 3, transcript variant X2
small nuclear RNA activating complex polypeptide 3, transcript variant X1
snRNA-activating protein complex subunit 3 isoform X1
snRNA-activating protein complex subunit 3 isoform X2
PC4 and SFRS1-interacting protein, transcript variant X1
PC4 and SFRS1-interacting protein isoform X1
PC4 and SFRS1-interacting protein, transcript variant X3
PC4 and SFRS1-interacting protein, transcript variant X2
PC4 and SFRS1-interacting protein, transcript variant X4
PC4 and SFRS1-interacting protein isoform X2
PC4 and SFRS1-interacting protein isoform X3
PC4 and SFRS1-interacting protein isoform X4
LOW QUALITY PROTEIN: coiled-coil domain-containing protein 171
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC122453305, transcript variant X1
uncharacterized LOC122453305, transcript variant X2
zinc finger protein basonuclin-2 isoform X9
zinc finger protein basonuclin-2 isoform X6
zinc finger protein basonuclin-2 isoform X4
zinc finger protein basonuclin-2 isoform X3
zinc finger protein basonuclin-2 isoform X2
zinc finger protein basonuclin-2 isoform X1
zinc finger protein basonuclin-2 isoform X10
zinc finger protein basonuclin-2 isoform X8
zinc finger protein basonuclin-2 isoform X5
zinc finger protein basonuclin-2 isoform X7
zinc finger protein basonuclin-2 isoform X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein basonuclin-2 isoform X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein basonuclin-2 isoform X15
zinc finger protein basonuclin-2 isoform X12
zinc finger protein basonuclin-2 isoform X13
SH3 domain containing GRB2 like 2, endophilin A1, transcript variant X1
SH3 domain containing GRB2 like 2, endophilin A1, transcript variant 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
LOW QUALITY PROTEIN: PC4 and SFRS1-interacting protein-like
LOW QUALITY PROTEIN: ADAMTS-like protein 1
uncharacterized LOC122453080, transcript variant X1
uncharacterized LOC122453080, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00568
COORDINATES: nucleotide motif:Rfam:12.0:RF00286
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
DENN domain containing 4C, transcript variant X1
DENN domain containing 4C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
DENN domain-containing protein 4C isoform X1
DENN domain-containing protein 4C isoform X2
DENN domain containing 4C, transcript variant X3
DENN domain-containing protein 4C isoform X3
alkaline ceramidase 2, transcript variant X1
alkaline ceramidase 2, transcript variant X2
alkaline ceramidase 2, transcript variant X3
uncharacterized LOC122453138, transcript variant X2
uncharacterized LOC122453138, 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
solute carrier family 24 member 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 24 member 2, 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 4 samples with support for all annotated introns
solute carrier family 24 member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 24 member 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium/potassium/calcium exchanger 2 isoform X2
sodium/potassium/calcium exchanger 2 isoform X3
sodium/potassium/calcium exchanger 2 isoform X4
sodium/potassium/calcium exchanger 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 336 ESTs, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
splicing factor U2AF 65 kDa subunit-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 ESTs, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 ESTs, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 15 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: 2 ESTs, 12 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: 2 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 54% 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 ESTs, 15 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122453393, transcript variant X3
uncharacterized LOC122453393, 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 22 samples with support for all annotated introns
uncharacterized LOC122453393, transcript variant X4
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 15 samples with support for all annotated introns
uncharacterized protein LOC122453393 isoform X2
uncharacterized LOC122453393, transcript variant X5
uncharacterized LOC122453393, transcript variant X1
uncharacterized protein LOC122453393 isoform X3
uncharacterized protein LOC122453393 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 5 ESTs, 10 Proteins, and 16% 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 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 56% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: interferon alpha-3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 45% 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 16% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 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 35% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 82 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 70% 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 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 33% 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, 75 Proteins, and 77% 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 mRNAs, 60 Proteins, and 26% 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 ESTs, 80 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 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: 2 mRNAs, 61 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 55 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 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: 77 Proteins, and 79% 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 mRNAs, 1 EST, 77 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
interferon omega-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 36 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
interferon omega-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 77 Proteins, and 51% 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 mRNA, 73 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
cyclin-dependent kinase 4 inhibitor B-like, transcript variant X1
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 7 samples with support for all annotated introns
cyclin-dependent kinase 4 inhibitor B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
cyclin-dependent kinase inhibitor 2A-like isoform X1
cyclin-dependent kinase 4 inhibitor B-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
doublesex- and mab-3-related transcription factor A1
transfer RNA phenylalanine (anticodon AAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ELAV like RNA binding protein 2, transcript variant X10
ELAV like RNA binding protein 2, transcript variant X8
ELAV like RNA binding protein 2, transcript variant X4
ELAV like RNA binding protein 2, transcript variant X17
ELAV like RNA binding protein 2, transcript variant X15
ELAV like RNA binding protein 2, transcript variant X11
ELAV like RNA binding protein 2, transcript variant X9
ELAV like RNA binding protein 2, transcript variant X6
ELAV like RNA binding protein 2, transcript variant X1
ELAV like RNA binding protein 2, transcript variant X3
ELAV like RNA binding protein 2, transcript variant X16
ELAV like RNA binding protein 2, transcript variant X5
ELAV like RNA binding protein 2, transcript variant X20
ELAV like RNA binding protein 2, transcript variant X19
ELAV like RNA binding protein 2, transcript variant X2
ELAV like RNA binding protein 2, transcript variant X14
ELAV like RNA binding protein 2, transcript variant X12
ELAV like RNA binding protein 2, transcript variant X7
ELAV like RNA binding protein 2, transcript variant X21
ELAV like RNA binding protein 2, transcript variant X13
ELAV like RNA binding protein 2, transcript variant X18
succinate dehydrogenase cytochrome b560 subunit, mitochondrial-like
heterogeneous nuclear ribonucleoprotein K-like
IZUMO family member 3, transcript variant X1
IZUMO family member 3, transcript variant X2
izumo sperm-egg fusion protein 3 isoform X2
izumo sperm-egg fusion protein 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
tumor suppressor candidate gene 1 protein
lipoyltransferase 1, mitochondrial, transcript variant X2
lipoyltransferase 1, mitochondrial, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
caspase activity and apoptosis inhibitor 1
phospholipase A2 activating protein, transcript variant X2
phospholipase A2 activating protein, transcript variant X1
phospholipase A2 activating protein, transcript variant X3
phospholipase A-2-activating protein isoform X2
phospholipase A-2-activating protein isoform X1
phospholipase A-2-activating protein isoform X3
intraflagellar transport 74, transcript variant X1
intraflagellar transport 74, transcript variant X2
intraflagellar transport 74, transcript variant X3
intraflagellar transport 74, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
intraflagellar transport 74, transcript variant X4
intraflagellar transport protein 74 homolog isoform X1
intraflagellar transport protein 74 homolog isoform X2
intraflagellar transport protein 74 homolog isoform X3
leucine rich repeat containing 19, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine rich repeat containing 19, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine-rich repeat-containing protein 19
TEK receptor tyrosine kinase, transcript variant X1
TEK receptor tyrosine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
MOB kinase activator 3B, transcript variant X4
MOB kinase activator 3B, transcript variant X1
MOB kinase activator 3B, transcript variant X3
MOB kinase activator 3B, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
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; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
C9orf72-SMCR8 complex subunit, transcript variant X1
C9orf72-SMCR8 complex subunit, transcript variant X2
guanine nucleotide exchange C9orf72 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
leucine rich repeat and Ig domain containing 2
leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 2
COX assembly mitochondrial protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA arginine (anticodon ACG); 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins
serine/arginine-rich splicing factor 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00614
kynurenine/alpha-aminoadipate aminotransferase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
kynurenine/alpha-aminoadipate aminotransferase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
microfibril associated protein 3 like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
microfibril associated protein 3 like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
microfibril associated protein 3 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
microfibril associated protein 3 like, transcript variant X6
microfibril associated protein 3 like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
microfibril associated protein 3 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
microfibril associated protein 3 like, transcript variant X3
microfibril associated protein 3 like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
microfibril associated protein 3 like, transcript variant X9
microfibrillar-associated protein 3-like
chloride voltage-gated channel 3, transcript variant X5
chloride voltage-gated channel 3, transcript variant X1
chloride voltage-gated channel 3, transcript variant X2
chloride voltage-gated channel 3, transcript variant X3
chloride voltage-gated channel 3, transcript variant X4
chloride voltage-gated channel 3, transcript variant X6
H(+)/Cl(-) exchange transporter 3 isoform X1
H(+)/Cl(-) exchange transporter 3 isoform X2
H(+)/Cl(-) exchange transporter 3 isoform X3
H(+)/Cl(-) exchange transporter 3 isoform X4
NIMA related kinase 1, transcript variant X1
NIMA related kinase 1, transcript variant X4
NIMA related kinase 1, transcript variant X2
NIMA related kinase 1, transcript variant X3
NIMA related kinase 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
NIMA related kinase 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
serine/threonine-protein kinase Nek1 isoform X1
serine/threonine-protein kinase Nek1 isoform X4
serine/threonine-protein kinase Nek1 isoform X2
serine/threonine-protein kinase Nek1 isoform X3
serine/threonine-protein kinase Nek1 isoform X5
serine/threonine-protein kinase Nek1 isoform X6
SH3 domain containing ring finger 1, transcript variant X1
SH3 domain containing ring finger 1, transcript variant X2
SH3 domain containing ring finger 1, transcript variant X3
SH3 domain containing ring finger 1, transcript variant X4
E3 ubiquitin-protein ligase SH3RF1 isoform X1
E3 ubiquitin-protein ligase SH3RF1 isoform X2
E3 ubiquitin-protein ligase SH3RF1 isoform X3
3-oxoacyl-[acyl-carrier-protein] reductase
palladin, cytoskeletal associated protein, transcript variant X7
palladin, cytoskeletal associated protein, transcript variant X1
palladin, cytoskeletal associated protein, transcript variant X3
palladin, cytoskeletal associated protein, transcript variant X4
palladin, cytoskeletal associated protein, transcript variant X5
palladin, cytoskeletal associated protein, transcript variant X6
palladin, cytoskeletal associated protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 3 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
LOW QUALITY PROTEIN: probable ATP-dependent RNA helicase DDX60-like
myosin-binding protein C, fast-type-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: 58 ESTs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: myosin-binding protein C, fast-type-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
major facilitator superfamily domain containing 14B, transcript variant X2
major facilitator superfamily domain containing 14B, transcript variant X1
major facilitator superfamily domain containing 14B, transcript variant X3
hippocampus abundant transcript-like protein 1 isoform X2
hippocampus abundant transcript-like protein 1 isoform X1
hippocampus abundant transcript-like protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 Proteins
mitochondrial import receptor subunit TOM20 homolog
proline-rich receptor-like protein kinase PERK10
wiskott-Aldrich syndrome protein homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122453375, transcript variant X2
uncharacterized LOC122453375, transcript variant X1
endogenous retrovirus group K member 7 Env polyprotein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% 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 92% 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 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase BAP1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 ESTs, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA tyrosine (anticodon AUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
proto-oncogene tyrosine-protein kinase receptor Ret-like
proto-oncogene tyrosine-protein kinase receptor Ret-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
proto-oncogene tyrosine-protein kinase receptor Ret-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 2 samples with support for all annotated introns
proto-oncogene tyrosine-protein kinase receptor Ret-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 6 samples with support for all annotated introns
proto-oncogene tyrosine-protein kinase receptor Ret-like isoform X1
proto-oncogene tyrosine-protein kinase receptor Ret-like isoform X2
uncharacterized LOC122453094, transcript variant X1
uncharacterized LOC122453094, transcript variant X2
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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: proto-oncogene tyrosine-protein kinase receptor Ret-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
WD repeat and FYVE domain-containing protein 3-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 35 samples with support for all annotated introns