Cervus elaphus chromosome 31, mCerEla1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Laurasiatheria; Artiodactyla; Ruminantia; Pecora; Cervidae; Cervinae; Cervus.
REFSEQ INFORMATION: The reference sequence is identical to\nOU343108.1.\nAssembly name: mCerEla1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2021/07/07. The original whole-genome shotgun project has the\naccession CAJVBL000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Cervus elaphus 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.
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
WAS/WASL-interacting protein family member 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 41% coverage of the annotated genomic feature by RNAseq alignments
chloride intracellular channel 6, transcript variant X2
chloride intracellular channel 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: 1 Protein
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 LOC122687589, 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 LOC122687589, 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 LOC122687589, 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 27 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
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
DnaJ heat shock protein family (Hsp40) member C28
transmembrane protein 50B, transcript variant X1
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.
transmembrane protein 50B, transcript variant X2
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 X2
interferon alpha and beta receptor subunit 2, transcript variant X1
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 31 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 31 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 31 C21orf62 homolog, transcript variant X5
chromosome 31 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 4 samples with support for all annotated introns
chromosome 31 C21orf62 homolog, transcript variant X1
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 32% 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, 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, transcript variant X3
cilia- and flagella-associated protein 298 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 LOC122687325, transcript variant X2
uncharacterized LOC122687325, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
TIAM Rac1 associated GEF 1, transcript variant X7
TIAM Rac1 associated GEF 1, transcript variant X1
TIAM Rac1 associated GEF 1, transcript variant X5
TIAM Rac1 associated GEF 1, transcript variant X4
TIAM Rac1 associated GEF 1, transcript variant X2
TIAM Rac1 associated GEF 1, transcript variant X3
TIAM Rac1 associated GEF 1, transcript variant X6
rho guanine nucleotide exchange factor TIAM1 isoform X1
rho guanine nucleotide exchange factor TIAM1 isoform X2
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 X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 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: 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 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
keratin-associated protein 6-1-like, transcript variant X3
keratin-associated protein 6-1-like, transcript variant X2
keratin-associated protein 6-1-like, transcript variant X1
keratin-associated protein 6-1-like, transcript variant X4
keratin-associated protein 6-1-like isoform X3
keratin-associated protein 6-1-like isoform X2
keratin-associated protein 6-1-like isoform X1
keratin-associated protein 6-1-like isoform X4
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 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: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 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: 4 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: 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
glutamate ionotropic receptor kainate type subunit 1, transcript variant X3
glutamate ionotropic receptor kainate type subunit 1, transcript variant X1
glutamate ionotropic receptor kainate type subunit 1, transcript variant X4
glutamate ionotropic receptor kainate type subunit 1, transcript variant X2
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 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, 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
glutamate receptor ionotropic, kainate 1 isoform X8
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, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate receptor ionotropic, kainate 1 isoform X6
glutamate ionotropic receptor kainate type subunit 1, transcript variant X7
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 42% 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.
thioredoxin-dependent peroxide reductase, mitochondrial-like
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
chaperonin containing TCP1 subunit 8, transcript variant X1
chaperonin containing TCP1 subunit 8, transcript variant X2
chaperonin containing TCP1 subunit 8, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 110 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
T-complex protein 1 subunit theta isoform X2
T-complex protein 1 subunit theta isoform X1
T-complex protein 1 subunit theta isoform X3
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: 1 mRNA, 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: 1 mRNA, 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: 1 mRNA, 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: 1 mRNA, 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: 1 mRNA, 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: 1 mRNA, 3 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 36 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
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
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00108
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, transcript variant X2
amyloid beta precursor protein, transcript variant X3
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 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: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
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, 2 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 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, 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: 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: 13 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122687403, transcript variant X2
uncharacterized LOC122687403, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 34% 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: 6 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: 4 mRNAs, 6 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
chromosome 31 C21orf91 homolog, transcript variant X2
chromosome 31 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 14 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 LOC122687327, transcript variant X7
uncharacterized LOC122687327, transcript variant X5
uncharacterized LOC122687327, transcript variant X4
uncharacterized LOC122687327, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC122687327, transcript variant X8
uncharacterized LOC122687327, transcript variant X10
uncharacterized LOC122687327, transcript variant X11
uncharacterized LOC122687327, transcript variant X6
uncharacterized LOC122687327, transcript variant X3
uncharacterized LOC122687327, transcript variant X2
uncharacterized protein LOC122687327 isoform X2
uncharacterized LOC122687327, transcript variant X1
uncharacterized protein LOC122687327 isoform X1
uncharacterized LOC122687327, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC122687327, transcript variant X12
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: 37 Proteins
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
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, 5 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 1 mRNA, 6 ESTs, 3 Proteins, and 91% 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 X1
roundabout guidance receptor 2, transcript variant X2
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: 4 mRNAs, 17 ESTs, 5 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
roundabout guidance receptor 1, transcript variant X2
roundabout guidance receptor 1, transcript variant X5
roundabout guidance receptor 1, transcript variant X3
roundabout guidance receptor 1, transcript variant X4
roundabout guidance receptor 1, transcript variant X1
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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.
late secretory pathway protein AVL9 homolog
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 14% 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, 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: 2 mRNAs, 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: 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 31 C3orf38 homolog, transcript variant X2
chromosome 31 C3orf38 homolog, transcript variant X1
uncharacterized protein C3orf38 homolog isoform X1
uncharacterized protein C3orf38 homolog isoform X2
chromosome 31 C3orf38 homolog, transcript variant X3
uncharacterized protein C3orf38 homolog isoform X3
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
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: 2 Proteins, and 5% 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 mRNAs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
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
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.
pleckstrin homology domain-containing family O member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 4 Proteins, and 73% 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, 11 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
unconventional prefoldin RPB5 interactor-like
crystallin beta-gamma domain containing 3
ribosomal oxygenase 2, transcript variant X4
ribosomal oxygenase 2, transcript variant X3
ribosomal oxygenase 2, transcript variant X2
ribosomal oxygenase 2, transcript variant X1
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 52% 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: 28 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: olfactory receptor 5AC1-like
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: 51 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 52 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, 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: 41 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: 43 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 29 Proteins
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, 27 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 23 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 LOC122687463, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00263
uncharacterized LOC122687463, 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
uncharacterized LOC122687264, transcript variant X1
uncharacterized LOC122687264, transcript variant 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 X1
leukemia NUP98 fusion partner 1, transcript variant X6
leukemia NUP98 fusion partner 1, transcript variant X4
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 24 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 9 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 24 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 X30
ABI family member 3 binding protein, transcript variant X42
ABI family member 3 binding protein, transcript variant X46
ABI family member 3 binding protein, transcript variant X44
ABI family member 3 binding protein, transcript variant X24
ABI family member 3 binding protein, transcript variant X21
ABI family member 3 binding protein, transcript variant X14
ABI family member 3 binding protein, transcript variant X23
ABI family member 3 binding protein, transcript variant X15
ABI family member 3 binding protein, transcript variant X27
ABI family member 3 binding protein, transcript variant X12
ABI family member 3 binding protein, transcript variant X17
ABI family member 3 binding protein, transcript variant X9
ABI family member 3 binding protein, transcript variant X10
ABI family member 3 binding protein, transcript variant X45
ABI family member 3 binding protein, transcript variant X43
ABI family member 3 binding protein, transcript variant X4
ABI family member 3 binding protein, transcript variant X5
ABI family member 3 binding protein, transcript variant X25
ABI family member 3 binding protein, transcript variant X41
ABI family member 3 binding protein, transcript variant X40
ABI family member 3 binding protein, transcript variant X39
ABI family member 3 binding protein, transcript variant X38
ABI family member 3 binding protein, transcript variant X37
ABI family member 3 binding protein, transcript variant X36
ABI family member 3 binding protein, transcript variant X34
ABI family member 3 binding protein, transcript variant X35
ABI family member 3 binding protein, transcript variant X33
ABI family member 3 binding protein, transcript variant X31
ABI family member 3 binding protein, transcript variant X28
ABI family member 3 binding protein, transcript variant X22
ABI family member 3 binding protein, transcript variant X13
ABI family member 3 binding protein, transcript variant X32
ABI family member 3 binding protein, transcript variant X26
ABI family member 3 binding protein, transcript variant X29
ABI family member 3 binding protein, transcript variant X19
ABI family member 3 binding protein, transcript variant X11
ABI family member 3 binding protein, transcript variant X20
ABI family member 3 binding protein, transcript variant X8
ABI family member 3 binding protein, transcript variant X18
ABI family member 3 binding protein, transcript variant X16
ABI family member 3 binding protein, transcript variant X7
ABI family member 3 binding protein, transcript variant X6
ABI family member 3 binding protein, transcript variant X2
ABI family member 3 binding protein, transcript variant X3
ABI family member 3 binding protein, transcript variant X1
small nucleolar RNA SNORA42/SNORA80 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00406
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
transfer RNA tyrosine (anticodon GUA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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 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 X9
SUMO specific peptidase 7, transcript variant X8
putative protein FAM172B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 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, 7 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 X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments
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: 1 EST, 8 Proteins, 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: 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
COORDINATES: nucleotide motif:Rfam:12.0:RF00420
zona pellucida like domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 9% coverage of the annotated genomic feature by RNAseq alignments
zona pellucida-like domain-containing protein 1
COORDINATES: nucleotide motif:Rfam:12.0:RF00066
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
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: uncharacterized protein LOC122687392
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: 1 mRNA, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 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: 6 mRNAs, 48 ESTs, 6 Proteins, and 99% 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: 30 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122687333, transcript variant X7
uncharacterized LOC122687333, transcript variant X2
uncharacterized LOC122687333, transcript variant X5
uncharacterized LOC122687333, transcript variant X6
uncharacterized LOC122687333, transcript variant X1
uncharacterized LOC122687333, transcript variant X3
uncharacterized LOC122687333, transcript variant X4
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 X6
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 X7
BBX high mobility group box domain containing, transcript variant X8
BBX high mobility group box domain containing, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
BBX high mobility group box domain containing, transcript variant X10
HMG box transcription factor BBX isoform X1
HMG box transcription factor BBX isoform X2
uncharacterized LOC122687602, transcript variant X1
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
uncharacterized protein LOC122687602 isoform X1
uncharacterized LOC122687602, transcript variant X2
uncharacterized protein LOC122687602 isoform X2
leukocyte surface antigen CD47 isoform X3
leukocyte surface antigen CD47 isoform X2
leukocyte surface antigen CD47 isoform X1
intraflagellar transport protein 57 homolog
ATP synthase-coupling factor 6, mitochondrial-like
HERV-H LTR-associating 2, transcript variant X9
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 X8
HERV-H LTR-associating 2, transcript variant X11
HERV-H LTR-associating 2, transcript variant X5
HERV-H LTR-associating 2, transcript variant X13
HERV-H LTR-associating 2, transcript variant X3
HERV-H LTR-associating 2, transcript variant X6
HERV-H LTR-associating 2, transcript variant X10
HERV-H LTR-associating 2, transcript variant X2
HERV-H LTR-associating protein 2 isoform X4
HERV-H LTR-associating 2, transcript variant X4
HERV-H LTR-associating 2, transcript variant X12
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 X7
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 84% 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 87% 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 X9
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 X6
DAZ interacting zinc finger protein 3, transcript variant X5
DAZ interacting zinc finger protein 3, transcript variant X8
DAZ interacting zinc finger protein 3, transcript variant X10
DAZ interacting zinc finger protein 3, transcript variant X7
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 X3
E3 ubiquitin-protein ligase DZIP3 isoform X2
E3 ubiquitin-protein ligase DZIP3 isoform X5
E3 ubiquitin-protein ligase DZIP3 isoform X7
E3 ubiquitin-protein ligase DZIP3 isoform X6
E3 ubiquitin-protein ligase DZIP3 isoform X4
DAZ interacting zinc finger protein 3, transcript variant X11
E3 ubiquitin-protein ligase DZIP3 isoform X8
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 10 ESTs, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
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 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: 1 mRNA, 2 Proteins, and 13% 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 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: 3 Proteins, and 81% 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: 12 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 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
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 X3
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 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00156
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 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 11 samples with support for all annotated introns
zinc finger BED-type containing 2, transcript variant X2
zinc finger BED domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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 X9
pleckstrin homology like domain family B member 2, transcript variant X11
pleckstrin homology like domain family B member 2, transcript variant X2
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 86% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: transmembrane protease serine 7
chromosome 31 C3orf52 homolog, transcript variant X2
chromosome 31 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
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 21% 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