Cervus canadensis isolate Bull #8, Minnesota chromosome 27, 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\nCM033217.1.\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.
chloride intracellular channel protein 6, transcript variant X2
COORDINATES: polyA evidence [ECO:0006239]
chloride intracellular channel protein 6, transcript variant X1
chloride intracellular channel protein 6 isoform X1
chloride intracellular channel protein 6 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
regulator of calcineurin 1, transcript variant X1
regulator of calcineurin 1, transcript variant X2
potassium voltage-gated channel subfamily E regulatory subunit 1, transcript variant X4
potassium voltage-gated channel subfamily E regulatory subunit 1, transcript variant X5
potassium voltage-gated channel subfamily E regulatory subunit 1, transcript variant X1
potassium voltage-gated channel subfamily E regulatory subunit 1, transcript variant X8
potassium voltage-gated channel subfamily E regulatory subunit 1, transcript variant X9
potassium voltage-gated channel subfamily E regulatory subunit 1, transcript variant X3
potassium voltage-gated channel subfamily E regulatory subunit 1, transcript variant X6
potassium voltage-gated channel subfamily E regulatory subunit 1, transcript variant X2
potassium voltage-gated channel subfamily E regulatory subunit 1, transcript variant X7
potassium voltage-gated channel subfamily E member 1
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
small integral membrane protein 11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
small integral membrane protein 11, transcript variant X2
small integral membrane protein 11, transcript variant X1
small integral membrane protein 11, transcript variant X4
potassium voltage-gated channel subfamily E regulatory subunit 2, transcript variant X2
potassium voltage-gated channel subfamily E regulatory subunit 2, transcript variant X1
potassium voltage-gated channel subfamily E member 2
uncharacterized LOC122428959, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC122428959, 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 3 samples with support for all annotated introns
uncharacterized LOC122428959, 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
solute carrier family 5 member 3, transcript variant X3
solute carrier family 5 member 3, transcript variant X1
solute carrier family 5 member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
ATP synthase peripheral stalk subunit OSCP
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 14 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
crystallin zeta like 1, transcript variant X3
crystallin zeta like 1, transcript variant X5
crystallin zeta like 1, transcript variant X2
crystallin zeta like 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
crystallin zeta like 1, transcript variant X1
quinone oxidoreductase-like protein 1 isoform X4
quinone oxidoreductase-like protein 1 isoform X1
quinone oxidoreductase-like protein 1 isoform X2
quinone oxidoreductase-like protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
DNA replication fork stabilization factor DONSON
SON DNA and RNA binding protein, transcript variant X1
SON DNA and RNA binding protein, transcript variant X2
SON DNA and RNA binding protein, transcript variant X3
SON DNA and RNA binding protein, transcript variant X4
SON DNA and RNA binding protein, transcript variant X5
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X6
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X1
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X5
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X7
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X2
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X3
phosphoribosylglycinamide formyltransferase, phosphoribosylglycinamide synthetase, phosphoribosylaminoimidazole synthetase, transcript variant X4
trifunctional purine biosynthetic protein adenosine-3
DnaJ heat shock protein family (Hsp40) member C28
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon CUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
interferon gamma receptor 2, transcript variant X2
interferon gamma receptor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
interferon alpha and beta receptor subunit 1, transcript variant X1
interferon alpha and beta receptor subunit 1, transcript variant X2
interferon alpha/beta receptor 1 isoform X1
interferon alpha/beta receptor 1 isoform X2
interleukin 10 receptor subunit beta, transcript variant X1
interleukin-10 receptor subunit beta isoform X1
interleukin 10 receptor subunit beta, transcript variant X3
interleukin 10 receptor subunit beta, transcript variant X2
interleukin-10 receptor subunit beta isoform X3
interleukin-10 receptor subunit beta isoform X2
interferon alpha and beta receptor subunit 2, transcript variant X1
interferon alpha and beta receptor subunit 2, transcript variant X2
interferon alpha and beta receptor subunit 2, transcript variant X3
interferon alpha/beta receptor 2 isoform X2
interferon alpha/beta receptor 2 isoform X1
interferon alpha/beta receptor 2 isoform X3
interferon alpha and beta receptor subunit 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 33 samples with support for all annotated introns
interferon alpha/beta receptor 2 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins
oligodendrocyte transcription factor 2, transcript variant X2
oligodendrocyte transcription factor 2, transcript variant X1
chromosome 27 C21orf62 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 17 ESTs, 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
chromosome 27 C21orf62 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 ESTs, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chromosome 27 C21orf62 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 ESTs, 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
chromosome 27 C21orf62 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 ESTs, 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein C21orf62 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 ESTs, 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: 15 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 ESTs, 4 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: 10 ESTs, 3 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: 24 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: 2 ESTs, and 82% coverage of the annotated genomic feature by RNAseq alignments
cilia and flagella associated protein 298, transcript variant X1
cilia- and flagella-associated protein 298 isoform X1
cilia and flagella associated protein 298, transcript variant X2
cilia- and flagella-associated protein 298 isoform X2
cilia- and flagella-associated protein 298-like, transcript variant X2
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 3 samples with support for all annotated introns
cilia- and flagella-associated protein 298-like, transcript variant X1
cilia- and flagella-associated protein 298-like isoform X1
cilia- and flagella-associated protein 298-like isoform X2
cilia- and flagella-associated protein 298-like, transcript variant X3
cilia- and flagella-associated protein 298-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122428691, 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 LOC122428691, 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 9 samples with support for all annotated introns
URB1 ribosome biogenesis homolog, transcript variant X1
URB1 ribosome biogenesis homolog, transcript variant X2
URB1 ribosome biogenesis homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
nucleolar pre-ribosomal-associated protein 1 isoform X1
nucleolar pre-ribosomal-associated protein 1 isoform X2
nucleolar pre-ribosomal-associated protein 1 isoform X3
melanocortin 2 receptor accessory protein
melanocortin-2 receptor accessory protein
MIS18 kinetochore protein A, transcript variant X1
MIS18 kinetochore protein A, transcript variant X2
hormonally up-regulated Neu-associated kinase, transcript variant X2
hormonally up-regulated Neu-associated kinase, transcript variant X1
hormonally up-regulated neu tumor-associated kinase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73% coverage of the annotated genomic feature by RNAseq alignments
SR-related CTD associated factor 4, transcript variant X1
SR-related CTD associated factor 4, transcript variant X3
SR-related CTD associated factor 4, transcript variant X2
SR-related CTD associated factor 4, transcript variant X4
SR-related and CTD-associated factor 4 isoform X1
SR-related and CTD-associated factor 4 isoform X3
SR-related and CTD-associated factor 4 isoform X2
SR-related and CTD-associated factor 4 isoform X4
TIAM Rac1 associated GEF 1, transcript variant X1
TIAM Rac1 associated GEF 1, transcript variant X5
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
TIAM Rac1 associated GEF 1, transcript variant X4
TIAM Rac1 associated GEF 1, transcript variant X2
TIAM Rac1 associated GEF 1, transcript variant X7
TIAM Rac1 associated GEF 1, transcript variant X3
TIAM Rac1 associated GEF 1, transcript variant X6
rho guanine nucleotide exchange factor TIAM1 isoform X1
transfer RNA serine (anticodon GGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
TIAM Rac1 associated GEF 1, transcript variant X8
rho guanine nucleotide exchange factor TIAM1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 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 mRNA, 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: 9 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 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 21 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
small nucleolar RNA SNORA62/SNORA6 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00091
glutamate ionotropic receptor kainate type subunit 1, transcript variant X1
glutamate ionotropic receptor kainate type subunit 1, transcript variant X3
glutamate ionotropic receptor kainate type subunit 1, transcript variant X2
glutamate ionotropic receptor kainate type subunit 1, transcript variant X4
glutamate ionotropic receptor kainate type subunit 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
glutamate ionotropic receptor kainate type subunit 1, transcript variant X6
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 1 sample with support for all annotated introns
glutamate ionotropic receptor kainate type subunit 1, transcript variant X7
glutamate ionotropic receptor kainate type subunit 1, transcript variant X5
glutamate receptor ionotropic, kainate 1 isoform X1
glutamate receptor ionotropic, kainate 1 isoform X3
glutamate receptor ionotropic, kainate 1 isoform X2
glutamate receptor ionotropic, kainate 1 isoform X4
glutamate receptor ionotropic, kainate 1 isoform X5
glutamate receptor ionotropic, kainate 1 isoform X8
glutamate receptor ionotropic, kainate 1 isoform X6
glutamate receptor ionotropic, kainate 1 isoform X7
transfer RNA cysteine (anticodon ACA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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 41% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
BTB domain and CNC homolog 1, transcript variant X1
BTB domain and CNC homolog 1, transcript variant X2
MAP3K7 C-terminal like, transcript variant X4
MAP3K7 C-terminal like, transcript variant X3
MAP3K7 C-terminal like, transcript variant X2
MAP3K7 C-terminal like, transcript variant X1
MAP3K7 C-terminal-like protein isoform X1
MAP3K7 C-terminal-like protein isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: T-complex protein 1 subunit theta
ubiquitin specific peptidase 16, transcript variant X3
ubiquitin specific peptidase 16, transcript variant X1
ubiquitin specific peptidase 16, transcript variant X4
ubiquitin specific peptidase 16, transcript variant X2
ubiquitin specific peptidase 16, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 16 isoform X4
ubiquitin carboxyl-terminal hydrolase 16 isoform X3
ubiquitin carboxyl-terminal hydrolase 16 isoform X2
ubiquitin carboxyl-terminal hydrolase 16 isoform X1
RWD domain containing 2B, transcript variant X1
RWD domain containing 2B, transcript variant X2
listerin E3 ubiquitin protein ligase 1, transcript variant X1
listerin E3 ubiquitin protein ligase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 10 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
E3 ubiquitin-protein ligase listerin isoform X1
E3 ubiquitin-protein ligase listerin isoform X2
N-6 adenine-specific DNA methyltransferase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
N-6 adenine-specific DNA methyltransferase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
N-6 adenine-specific DNA methyltransferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
N-6 adenine-specific DNA methyltransferase 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
N-6 adenine-specific DNA methyltransferase 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
N-6 adenine-specific DNA methyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00432
ADAM metallopeptidase with thrombospondin type 1 motif 5
A disintegrin and metalloproteinase with thrombospondin motifs 5
ADAM metallopeptidase with thrombospondin type 1 motif 1
A disintegrin and metalloproteinase with thrombospondin motifs 1
uncharacterized protein LOC122428944 isoform X3
uncharacterized protein LOC122428944 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 5 samples with support for all annotated introns
uncharacterized LOC122428627, transcript variant X2
uncharacterized LOC122428627, transcript variant X3
uncharacterized LOC122428627, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00108
amyloid beta precursor protein, transcript variant X2
amyloid beta precursor protein, transcript variant X3
amyloid beta precursor protein, transcript variant X4
amyloid beta precursor protein, transcript variant X5
amyloid beta precursor protein, transcript variant X6
amyloid beta precursor protein, transcript variant X7
amyloid beta precursor protein, transcript variant X1
amyloid-beta precursor protein isoform X1
amyloid-beta precursor protein isoform X2
amyloid-beta precursor protein isoform X3
amyloid-beta precursor protein isoform X4
amyloid-beta precursor protein isoform X5
amyloid-beta precursor protein isoform X6
amyloid-beta precursor protein isoform X7
GA binding protein transcription factor subunit alpha, transcript variant X2
GA binding protein transcription factor subunit alpha, transcript variant X1
GA binding protein transcription factor subunit alpha, transcript variant X3
GA binding protein transcription factor subunit alpha, transcript variant X5
GA binding protein transcription factor subunit alpha, transcript variant X6
GA binding protein transcription factor subunit alpha, transcript variant X4
ATP synthase peripheral stalk subunit F6, transcript variant X4
ATP synthase peripheral stalk subunit F6, transcript variant X3
ATP synthase peripheral stalk subunit F6, transcript variant X2
ATP synthase peripheral stalk subunit F6, transcript variant X1
ATP synthase-coupling factor 6, mitochondrial isoform X1
ATP synthase-coupling factor 6, mitochondrial isoform X2
39S ribosomal protein L39, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
2-iminobutanoate/2-iminopropanoate deaminase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 ESTs, 3 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: 13 Proteins
double-stranded RNA-binding protein Staufen homolog 2, transcript variant X1
double-stranded RNA-binding protein Staufen homolog 2, transcript variant X2
double-stranded RNA-binding protein Staufen homolog 2 isoform X2
double-stranded RNA-binding protein Staufen homolog 2 isoform X1
neural cell adhesion molecule 2, transcript variant X1
neural cell adhesion molecule 2 isoform X1
neural cell adhesion molecule 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
neural cell adhesion molecule 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 52% 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, and 25% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122428977, transcript variant X2
uncharacterized LOC122428977, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 39% coverage of the annotated genomic feature by RNAseq alignments
transmembrane serine protease 15, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 7 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
transmembrane serine protease 15, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
chromosome 27 C21orf91 homolog, transcript variant X2
chromosome 27 C21orf91 homolog, transcript variant X1
BTG anti-proliferation factor 3, transcript variant X1
BTG anti-proliferation factor 3, transcript variant X2
CXADR Ig-like cell adhesion molecule, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 3 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
coxsackievirus and adenovirus receptor isoform X2
CXADR Ig-like cell adhesion molecule, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 3 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
coxsackievirus and adenovirus receptor isoform X3
CXADR Ig-like cell adhesion molecule, transcript variant X1
coxsackievirus and adenovirus receptor isoform X1
uncharacterized LOC122428683, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
uncharacterized LOC122428683, transcript variant X4
uncharacterized LOC122428683, transcript variant X6
uncharacterized LOC122428683, transcript variant X7
uncharacterized LOC122428683, transcript variant X3
uncharacterized LOC122428683, transcript variant X2
uncharacterized protein LOC122428683 isoform X2
uncharacterized LOC122428683, transcript variant X1
uncharacterized protein LOC122428683 isoform X1
ubiquitin specific peptidase 25, transcript variant X4
ubiquitin specific peptidase 25, transcript variant X2
ubiquitin specific peptidase 25, transcript variant X1
ubiquitin specific peptidase 25, transcript variant X3
ubiquitin specific peptidase 25, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 25 isoform X4
ubiquitin carboxyl-terminal hydrolase 25 isoform X2
ubiquitin carboxyl-terminal hydrolase 25 isoform X1
ubiquitin carboxyl-terminal hydrolase 25 isoform X3
ubiquitin carboxyl-terminal hydrolase 25 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins
dimethylaniline monooxygenase [N-oxide-forming] 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: dimethylaniline monooxygenase [N-oxide-forming] 1-like
COORDINATES: nucleotide motif:Rfam:12.0:RF01210
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
putative uncharacterized protein ENSP00000383407
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
SAM domain, SH3 domain and nuclear localization signals 1, transcript variant X2
SAM domain-containing protein SAMSN-1 isoform X2
SAM domain, SH3 domain and nuclear localization signals 1, transcript variant X1
SAM domain-containing protein SAMSN-1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
heat shock protein family A (Hsp70) member 13
multidrug resistance-associated protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
glyceraldehyde-3-phosphate dehydrogenase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, 7 Proteins, and 97% 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, 3 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
roundabout guidance receptor 2, transcript variant X4
roundabout guidance receptor 2, transcript variant X3
roundabout guidance receptor 2, transcript variant X5
roundabout guidance receptor 2, transcript variant X2
roundabout guidance receptor 2, transcript variant X1
roundabout guidance receptor 2, transcript variant X6
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, 2 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
roundabout guidance receptor 1, transcript variant X2
roundabout guidance receptor 1, transcript variant X1
roundabout guidance receptor 1, transcript variant X5
roundabout guidance receptor 1, transcript variant X3
roundabout guidance receptor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00548
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cell adhesion molecule 2, transcript variant X3
cell adhesion molecule 2, transcript variant X1
cell adhesion molecule 2, transcript variant X2
cell adhesion molecule 2, transcript variant X4
cell adhesion molecule 2, transcript variant X5
tRNA selenocysteine 1-associated protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
vestigial like family member 3, transcript variant X2
vestigial like family member 3, transcript variant X3
vestigial like family member 3, transcript variant X1
transcription cofactor vestigial-like protein 3 isoform X3
transcription cofactor vestigial-like protein 3 isoform X2
transcription cofactor vestigial-like protein 3 isoform X1
charged multivesicular body protein 2B, transcript variant X1
charged multivesicular body protein 2B, transcript variant X2
charged multivesicular body protein 2b isoform X1
charged multivesicular body protein 2b isoform X2
POU class 1 homeobox 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 3 ESTs, 15 Proteins
POU class 1 homeobox 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 5 Proteins
pituitary-specific positive transcription factor 1 isoform X2
pituitary-specific positive transcription factor 1 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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 19 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
CGG triplet repeat binding protein 1, transcript variant X1
CGG triplet repeat binding protein 1, transcript variant X2
CGG triplet repeat binding protein 1, transcript variant X3
zinc finger protein 654, transcript variant X2
zinc finger protein 654, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
zinc finger protein 654, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
chromosome 27 C3orf38 homolog, transcript variant X2
chromosome 27 C3orf38 homolog, transcript variant X1
uncharacterized protein C3orf38 homolog isoform X1
uncharacterized protein C3orf38 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
ASNSD1 upstream open reading frame protein-like
asparagine synthetase domain-containing protein 1-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
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: asparagine synthetase domain-containing protein 1-like
casein kinase 2 subunit alpha' interacting protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
casein kinase 2 subunit alpha' interacting protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
casein kinase II subunit alpha'-interacting protein
ADP ribosylation factor like GTPase 13B, transcript variant X2
ADP ribosylation factor like GTPase 13B, transcript variant X1
ADP ribosylation factor like GTPase 13B, transcript variant X4
ADP ribosylation factor like GTPase 13B, transcript variant X5
ADP-ribosylation factor-like protein 13B isoform X1
ADP-ribosylation factor-like protein 13B isoform X4
ADP ribosylation factor like GTPase 13B, transcript variant X3
ADP-ribosylation factor-like protein 13B isoform X2
ADP-ribosylation factor-like protein 13B isoform X3
DAZ-associated protein 2-like, transcript variant X1
DAZ-associated protein 2-like, transcript variant X2
uncharacterized protein LOC122428623 isoform X2
DAZ-associated protein 2-like isoform X1
NOP2/Sun RNA methyltransferase 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
NOP2/Sun RNA methyltransferase 3, transcript variant X1
NOP2/Sun RNA methyltransferase 3, transcript variant X2
tRNA (cytosine(34)-C(5))-methyltransferase, mitochondrial isoform X1
tRNA (cytosine(34)-C(5))-methyltransferase, mitochondrial isoform X2
tRNA (cytosine(34)-C(5))-methyltransferase, mitochondrial isoform X3
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
polypeptide N-acetylgalactosaminyltransferase 11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 29 ESTs, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
pleckstrin homology domain-containing family O member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 4 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, 16 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
crystallin beta-gamma domain containing 3
ribosomal oxygenase 2, transcript variant X7
ribosomal oxygenase 2, transcript variant X6
ribosomal oxygenase 2, transcript variant X3
ribosomal oxygenase 2, transcript variant X5
ribosomal oxygenase 2, transcript variant X4
ribosomal oxygenase 2, transcript variant X2
ribosomal oxygenase 2, transcript variant X1
ribosomal oxygenase 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gamma-aminobutyric acid type A receptor subunit rho3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit rho-3
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: 34 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 56 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 57 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 22 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 41 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: 40 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 41% 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: 42 Proteins
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: 13 Proteins
LOW QUALITY PROTEIN: olfactory receptor 5K4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 31 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 30 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 27 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
claudin domain containing 1, transcript variant X2
claudin domain containing 1, transcript variant X4
claudin domain containing 1, transcript variant X1
claudin domain containing 1, transcript variant X3
claudin domain-containing protein 1 isoform X3
claudin domain-containing protein 1 isoform X2
claudin domain-containing protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
oxygen-dependent coproporphyrinogen-III oxidase, mitochondrial
uncharacterized LOC122428840, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00263
uncharacterized LOC122428840, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ST3 beta-galactoside alpha-2,3-sialyltransferase 6, transcript variant X1
ST3 beta-galactoside alpha-2,3-sialyltransferase 6, transcript variant X5
ST3 beta-galactoside alpha-2,3-sialyltransferase 6, transcript variant X2
ST3 beta-galactoside alpha-2,3-sialyltransferase 6, transcript variant X6
ST3 beta-galactoside alpha-2,3-sialyltransferase 6, transcript variant X3
ST3 beta-galactoside alpha-2,3-sialyltransferase 6, transcript variant X7
ST3 beta-galactoside alpha-2,3-sialyltransferase 6, transcript variant X4
type 2 lactosamine alpha-2,3-sialyltransferase isoform X1
ST3 beta-galactoside alpha-2,3-sialyltransferase 6, transcript variant X8
type 2 lactosamine alpha-2,3-sialyltransferase isoform X2
discoidin, CUB and LCCL domain containing 2, transcript variant X2
discoidin, CUB and LCCL domain containing 2, transcript variant X1
discoidin, CUB and LCCL domain-containing protein 2 isoform X2
discoidin, CUB and LCCL domain-containing protein 2 isoform X1
collagen type VIII alpha 1 chain, transcript variant X3
collagen type VIII alpha 1 chain, transcript variant X1
collagen type VIII alpha 1 chain, transcript variant X4
collagen type VIII alpha 1 chain, transcript variant X2
cms1 ribosomal small subunit homolog, transcript variant X1
cms1 ribosomal small subunit homolog, transcript variant X3
filamin A interacting protein 1 like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 24 ESTs, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
filamin A-interacting protein 1-like isoform X3
filamin A interacting protein 1 like, transcript variant X1
filamin A interacting protein 1 like, transcript variant X2
filamin A-interacting protein 1-like isoform X1
filamin A-interacting protein 1-like isoform X2
cms1 ribosomal small subunit homolog, transcript variant X2
cell cycle control protein 50C, transcript variant X1
cell cycle control protein 50C isoform X1
cell cycle control protein 50C, transcript variant X2
cell cycle control protein 50C isoform X2
TBC1 domain family member 23, transcript variant X2
TBC1 domain family member 23, transcript variant X1
nitrilase family member 2, transcript variant X2
nitrilase family member 2, transcript variant X1
nitrilase family member 2, transcript variant X3
translocase of outer mitochondrial membrane 70
mitochondrial import receptor subunit TOM70
leukemia NUP98 fusion partner 1, transcript variant X4
leukemia NUP98 fusion partner 1, transcript variant X6
leukemia NUP98 fusion partner 1, transcript variant X1
leukemia NUP98 fusion partner 1, transcript variant X5
leukemia NUP98 fusion partner 1, transcript variant X2
leukemia NUP98 fusion partner 1, transcript variant X3
leukemia NUP98 fusion partner 1 isoform X1
leukemia NUP98 fusion partner 1 isoform X2
leukemia NUP98 fusion partner 1 isoform X3
mitochondrial inner membrane protease subunit 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 45A-like, transcript variant X3
transmembrane protein 45A-like isoform X3
transmembrane protein 45A-like, transcript variant X5
transmembrane protein 45A-like, transcript variant X2
transmembrane protein 45A-like isoform X2
transmembrane protein 45A-like, transcript variant X4
transmembrane protein 45A-like, transcript variant X1
transmembrane protein 45A-like isoform X1
transmembrane protein 45A-like isoform X4
non-histone chromosomal protein HMG-14-like
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 23 samples with support for all annotated introns
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 8 samples with support for all annotated introns
adhesion G protein-coupled receptor G7, transcript variant X1
adhesion G-protein coupled receptor G7 isoform X1
transfer RNA glycine (anticodon CCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
adhesion G protein-coupled receptor G7, transcript variant X2
adhesion G-protein coupled receptor G7 isoform X2
trafficking from ER to golgi regulator, transcript variant X1
trafficking from ER to golgi regulator, transcript variant X2
trafficking from ER to golgi regulator, transcript variant X5
trafficking from ER to golgi regulator, transcript variant X3
trafficking from ER to golgi regulator, transcript variant X4
trafficking from ER to golgi regulator, transcript variant X6
ABI family member 3 binding protein, transcript variant X7
ABI family member 3 binding protein, transcript variant X9
ABI family member 3 binding protein, transcript variant X5
ABI family member 3 binding protein, transcript variant X6
ABI family member 3 binding protein, transcript variant X4
ABI family member 3 binding protein, transcript variant X3
ABI family member 3 binding protein, transcript variant X8
ABI family member 3 binding protein, transcript variant X2
ABI family member 3 binding protein, transcript variant X1
interphotoreceptor matrix proteoglycan 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
SUMO specific peptidase 7, transcript variant X2
SUMO specific peptidase 7, transcript variant X3
SUMO specific peptidase 7, transcript variant X4
SUMO specific peptidase 7, transcript variant X9
SUMO specific peptidase 7, transcript variant X6
SUMO specific peptidase 7, transcript variant X7
SUMO specific peptidase 7, transcript variant X5
SUMO specific peptidase 7, transcript variant X1
SUMO specific peptidase 7, transcript variant X8
putative protein FAM172B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
putative protein FAM172B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
putative protein FAM172B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
putative protein FAM172B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
putative protein FAM172B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
tRNA methyltransferase 10C, mitochondrial RNase P subunit
PEST proteolytic signal containing nuclear protein, transcript variant X1
PEST proteolytic signal-containing nuclear protein isoform X1
PEST proteolytic signal containing nuclear protein, transcript variant X2
PEST proteolytic signal-containing nuclear protein isoform X2
zinc finger and BTB domain containing 11
zinc finger and BTB domain-containing protein 11
centrosomal protein 97, transcript variant X1
centrosomal protein 97, transcript variant X2
neurexophilin and PC-esterase domain family member 3, transcript variant X3
neurexophilin and PC-esterase domain family member 3, transcript variant X1
neurexophilin and PC-esterase domain family member 3, transcript variant X4
neurexophilin and PC-esterase domain family member 3, transcript variant X2
neurexophilin and PC-esterase domain family member 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
zona pellucida like domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00420
zona pellucida like domain containing 1, transcript variant X2
zona pellucida-like domain-containing protein 1
coiled-coil domain-containing protein 127
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 ESTs, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00066
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ubiquitin-associated protein 1-like
activated leukocyte cell adhesion molecule, transcript variant X1
activated leukocyte cell adhesion molecule, transcript variant X2
activated leukocyte cell adhesion molecule, transcript variant X3
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 29 samples with support for all annotated introns
Cbl proto-oncogene B, transcript variant X2
Cbl proto-oncogene B, transcript variant X7
Cbl proto-oncogene B, transcript variant X6
Cbl proto-oncogene B, transcript variant X5
Cbl proto-oncogene B, transcript variant X4
Cbl proto-oncogene B, transcript variant X1
Cbl proto-oncogene B, transcript variant X9
Cbl proto-oncogene B, transcript variant X8
Cbl proto-oncogene B, transcript variant X3
E3 ubiquitin-protein ligase CBL-B isoform X4
E3 ubiquitin-protein ligase CBL-B isoform X3
E3 ubiquitin-protein ligase CBL-B isoform X2
E3 ubiquitin-protein ligase CBL-B isoform X1
transcription initiation factor TFIID subunit 13-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 42 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA arginine (anticodon GCG); 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: 29 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122428703, transcript variant X5
uncharacterized LOC122428703, transcript variant X1
uncharacterized LOC122428703, transcript variant X3
uncharacterized LOC122428703, transcript variant X6
uncharacterized LOC122428703, transcript variant X2
uncharacterized LOC122428703, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
coiled-coil domain-containing protein 54
COORDINATES: nucleotide motif:Rfam:12.0:RF00554
BBX high mobility group box domain containing, transcript variant X1
BBX high mobility group box domain containing, transcript variant X13
BBX high mobility group box domain containing, transcript variant X2
BBX high mobility group box domain containing, transcript variant X3
BBX high mobility group box domain containing, transcript variant X7
BBX high mobility group box domain containing, transcript variant X11
BBX high mobility group box domain containing, transcript variant X5
BBX high mobility group box domain containing, transcript variant X9
BBX high mobility group box domain containing, transcript variant X4
BBX high mobility group box domain containing, transcript variant X6
BBX high mobility group box domain containing, transcript variant X8
BBX high mobility group box domain containing, transcript variant X12
BBX high mobility group box domain containing, transcript variant X10
HMG box transcription factor BBX isoform X1
HMG box transcription factor BBX isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
leukocyte surface antigen CD47 isoform X4
leukocyte surface antigen CD47 isoform X3
leukocyte surface antigen CD47 isoform X2
leukocyte surface antigen CD47 isoform X1
intraflagellar transport 57, transcript variant X2
intraflagellar transport 57, transcript variant X1
intraflagellar transport protein 57 homolog
ATP synthase-coupling factor 6, mitochondrial-like
HERV-H LTR-associating 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
HERV-H LTR-associating 2, transcript variant X1
HERV-H LTR-associating 2, transcript variant X7
HERV-H LTR-associating 2, transcript variant X9
HERV-H LTR-associating 2, transcript variant X5
HERV-H LTR-associating 2, transcript variant X12
HERV-H LTR-associating 2, transcript variant X2
HERV-H LTR-associating 2, transcript variant X4
HERV-H LTR-associating 2, transcript variant X10
HERV-H LTR-associating protein 2 isoform X4
HERV-H LTR-associating 2, transcript variant X3
HERV-H LTR-associating 2, transcript variant X11
HERV-H LTR-associating protein 2 isoform X5
HERV-H LTR-associating protein 2 isoform X1
HERV-H LTR-associating protein 2 isoform X3
HERV-H LTR-associating 2, transcript variant X6
HERV-H LTR-associating protein 2 isoform X2
myosin heavy chain 15, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
myosin heavy chain 15, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 12 Proteins, and 86% 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 7% coverage of the annotated genomic feature by RNAseq alignments
cellular inhibitor of PP2A, transcript variant X1
cellular inhibitor of PP2A, transcript variant X2
DAZ interacting zinc finger protein 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
DAZ interacting zinc finger protein 3, transcript variant X1
DAZ interacting zinc finger protein 3, transcript variant X5
DAZ interacting zinc finger protein 3, transcript variant X7
DAZ interacting zinc finger protein 3, transcript variant X9
DAZ interacting zinc finger protein 3, transcript variant X6
DAZ interacting zinc finger protein 3, transcript variant X3
DAZ interacting zinc finger protein 3, transcript variant X2
DAZ interacting zinc finger protein 3, transcript variant X4
E3 ubiquitin-protein ligase DZIP3 isoform X1
E3 ubiquitin-protein ligase DZIP3 isoform X2
E3 ubiquitin-protein ligase DZIP3 isoform X4
E3 ubiquitin-protein ligase DZIP3 isoform X6
E3 ubiquitin-protein ligase DZIP3 isoform X5
E3 ubiquitin-protein ligase DZIP3 isoform X3
DAZ interacting zinc finger protein 3, transcript variant X10
E3 ubiquitin-protein ligase DZIP3 isoform X7
T-cell receptor-associated transmembrane adapter 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
T-cell receptor-associated transmembrane adapter 1, transcript variant X2
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 3 samples with support for all annotated introns
T-cell receptor-associated transmembrane adapter 1 isoform X1
T-cell receptor-associated transmembrane adapter 1 isoform X2
cyclin-dependent kinase 2-associated protein 1-like
MORC family CW-type zinc finger 1, transcript variant X3
MORC family CW-type zinc finger 1, transcript variant X2
MORC family CW-type zinc finger 1, transcript variant X1
MORC family CW-type zinc finger protein 1 isoform X3
MORC family CW-type zinc finger protein 1 isoform X2
MORC family CW-type zinc finger protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 38% 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, 2 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
developmental pluripotency-associated protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 3 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
developmental pluripotency-associated protein 4
nectin cell adhesion molecule 3, transcript variant X1
nectin cell adhesion molecule 3, transcript variant X2
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 3 samples with support for all annotated introns
nectin cell adhesion molecule 3, transcript variant X4
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
nectin cell adhesion molecule 3, transcript variant X5
nectin cell adhesion molecule 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
T-cell surface protein tactile isoform X1
T-cell surface protein tactile isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00156
zinc finger BED-type containing 2, transcript variant X6
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, including 2 samples with support for all annotated introns
zinc finger BED-type containing 2, transcript variant X3
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, including 1 sample with support for all annotated introns
zinc finger BED-type containing 2, transcript variant X2
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, including 10 samples with support for all annotated introns
zinc finger BED-type containing 2, transcript variant X4
zinc finger BED-type containing 2, transcript variant X1
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, including 3 samples with support for all annotated introns
zinc finger BED-type containing 2, transcript variant X5
zinc finger BED domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
phosphatidylinositol specific phospholipase C X domain containing 2, transcript variant X1
phosphatidylinositol specific phospholipase C X domain containing 2, transcript variant X2
phosphatidylinositol specific phospholipase C X domain containing 2, transcript variant X3
pleckstrin homology like domain family B member 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
pleckstrin homology like domain family B member 2, transcript variant X1
pleckstrin homology like domain family B member 2, transcript variant X5
pleckstrin homology like domain family B member 2, transcript variant X2
pleckstrin homology like domain family B member 2, transcript variant X9
pleckstrin homology like domain family B member 2, transcript variant X11
pleckstrin homology like domain family B member 2, transcript variant X6
pleckstrin homology like domain family B member 2, transcript variant X12
pleckstrin homology like domain family B member 2, transcript variant X8
pleckstrin homology like domain family B member 2, transcript variant X10
pleckstrin homology-like domain family B member 2 isoform X1
pleckstrin homology-like domain family B member 2 isoform X2
pleckstrin homology-like domain family B member 2 isoform X5
pleckstrin homology-like domain family B member 2 isoform X7
pleckstrin homology-like domain family B member 2 isoform X8
pleckstrin homology-like domain family B member 2 isoform X10
pleckstrin homology-like domain family B member 2 isoform X11
pleckstrin homology-like domain family B member 2 isoform X4
pleckstrin homology-like domain family B member 2 isoform X9
pleckstrin homology-like domain family B member 2 isoform X6
pleckstrin homology like domain family B member 2, transcript variant X4
pleckstrin homology like domain family B member 2, transcript variant X3
pleckstrin homology like domain family B member 2, transcript variant X13
pleckstrin homology-like domain family B member 2 isoform X3
pleckstrin homology-like domain family B member 2 isoform X12
abhydrolase domain containing 10, depalmitoylase
palmitoyl-protein thioesterase ABHD10, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 8 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
chromosome 27 C3orf52 homolog, transcript variant X2
chromosome 27 C3orf52 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
TPA-induced transmembrane protein isoform X2
TPA-induced transmembrane protein isoform X1
germinal center associated signaling and motility, 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 8 samples with support for all annotated introns
germinal center associated signaling and motility, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
germinal center-associated signaling and motility protein isoform X2
germinal center-associated signaling and motility protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments