Catharus ustulatus isolate bCatUst1 chromosome 20, bCatUst1.pri.v2, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Archosauria; Dinosauria; Saurischia; Theropoda; Coelurosauria; Aves; Neognathae; Passeriformes; Turdidae; Catharus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM020355.1.\nAssembly name: bCatUst1.pri.v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2020/12/22. The original whole-genome shotgun project has the\naccession WNMQ00000000.2.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 06-AUG-2020\nAssembly Method :: FALCON v. DX 1.9.0; FALCON-Unzip v.\n 6.0.0.47841; purge_dups github v.\n purge_haplotig (bitbucket v1.0.3+\n 1.Nov.2018); Scaff10x v. 2; Bionano Solve\n v. 3.2.1_04122018; Salsa2 HiC v. 2.2;\n Arrow polishing and gap filling v.\n Smrtlink_6.0.0.47841; Longranger Align v.\n 2.2.2; freebayes v. 1.3.1; gEVAL manual\n curation v. 2020-08-06; VGP assembly\n pipeline v. 1.5\nAssembly Name :: bCatUst1.pri.v2\nDiploid :: Principal pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 60.58x\nSequencing Technology :: PacBio Sequel I CLR; Illumina NovaSeq;\n Arima Genomics Hi-C; Bionano Genomics DLS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Catharus ustulatus Annotation\n Release 101\nAnnotation Version :: 101\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.
protoheme IX farnesyltransferase, mitochondrial, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
protoheme IX farnesyltransferase, mitochondrial, transcript variant X2
protoheme IX farnesyltransferase, mitochondrial isoform X1
protoheme IX farnesyltransferase, mitochondrial, transcript variant X5
protoheme IX farnesyltransferase, mitochondrial, transcript variant X9
protoheme IX farnesyltransferase, mitochondrial, transcript variant X3
protoheme IX farnesyltransferase, mitochondrial, transcript variant X8
protoheme IX farnesyltransferase, mitochondrial, transcript variant X6
protoheme IX farnesyltransferase, mitochondrial, transcript variant X4
protoheme IX farnesyltransferase, mitochondrial isoform X4
protoheme IX farnesyltransferase, mitochondrial isoform X2
protoheme IX farnesyltransferase, mitochondrial, transcript variant X7
protoheme IX farnesyltransferase, mitochondrial isoform X3
protoheme IX farnesyltransferase, mitochondrial, transcript variant X10
protoheme IX farnesyltransferase, mitochondrial isoform X5
heparan sulfate glucosamine 3-O-sulfotransferase 3B1-like
peripheral myelin protein 22, transcript variant X1
peripheral myelin protein 22, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 70% coverage of the annotated genomic feature by RNAseq alignments
Golgi apparatus membrane protein TVP23 homolog B-like, transcript variant X2
Golgi apparatus membrane protein TVP23 homolog B-like, transcript variant X1
Golgi apparatus membrane protein TVP23 homolog B-like isoform X1
Golgi apparatus membrane protein TVP23 homolog B-like isoform X2
F-box/WD repeat-containing protein 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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: 67 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, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 43
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 42
major facilitator superfamily domain containing 6 like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
major facilitator superfamily domain-containing protein 6-like
phosphoinositide-3-kinase regulatory subunit 6, transcript variant X3
phosphoinositide-3-kinase regulatory subunit 6, transcript variant X2
phosphoinositide-3-kinase regulatory subunit 6, transcript variant X1
phosphoinositide 3-kinase regulatory subunit 6 isoform X2
phosphoinositide 3-kinase regulatory subunit 6 isoform X1
phosphoinositide-3-kinase regulatory subunit 5, transcript variant X4
phosphoinositide-3-kinase regulatory subunit 5, transcript variant X1
phosphoinositide-3-kinase regulatory subunit 5, transcript variant X2
phosphoinositide-3-kinase regulatory subunit 5, transcript variant X3
phosphoinositide 3-kinase regulatory subunit 5 isoform X2
phosphoinositide 3-kinase regulatory subunit 5 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 14 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
myosin heavy chain 10, transcript variant X1
myosin heavy chain 10, transcript variant X3
myosin heavy chain 10, transcript variant X2
myosin heavy chain 10, transcript variant X4
nudE neurodevelopment protein 1 like 1, transcript variant X1
nudE neurodevelopment protein 1 like 1, transcript variant X3
nudE neurodevelopment protein 1 like 1, transcript variant X2
nuclear distribution protein nudE-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
phosphoinositide interacting regulator of transient receptor potential channels
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
shisa family member 6, transcript variant X2
shisa family member 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
shisa family member 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
dynein axonemal heavy chain 9, transcript variant X1
dynein axonemal heavy chain 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
mitogen-activated protein kinase kinase 4, transcript variant X1
mitogen-activated protein kinase kinase 4, transcript variant X2
dual specificity mitogen-activated protein kinase kinase 4 isoform X2
dual specificity mitogen-activated protein kinase kinase 4 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
ADP-ribose/CDP-alcohol diphosphatase, manganese dependent
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
manganese-dependent ADP-ribose/CDP-alcohol diphosphatase
protein SCO1 homolog, mitochondrial, transcript variant X1
protein SCO1 homolog, mitochondrial isoform X1
protein SCO1 homolog, mitochondrial, transcript variant X2
protein SCO1 homolog, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 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: 105 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 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: 110 Proteins, and 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: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
myosin heavy chain, skeletal muscle, adult-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 162 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
myosin heavy chain, skeletal muscle, adult-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 147 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
myosin heavy chain, skeletal muscle, adult-like isoform X1
myosin heavy chain, skeletal muscle, adult-like isoform X2
myosin heavy chain, skeletal muscle, adult-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 240 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, 1 EST, 301 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
myosin heavy chain, skeletal muscle, adult, transcript variant X1
myosin heavy chain, skeletal muscle, adult, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
myosin heavy chain, skeletal muscle, adult isoform X2
myosin heavy chain, skeletal muscle, adult isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 250 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 125 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
myosin heavy chain, skeletal muscle, adult-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 117 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
myosin heavy chain, skeletal muscle, adult-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 130 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
myosin heavy chain, skeletal muscle, adult-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 209 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
myosin heavy chain, skeletal muscle, adult-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 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: 95 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: 187 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: 64 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 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: 49 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: 82 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC117005193, 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 1 sample with support for all annotated introns
uncharacterized LOC117005193, transcript variant X8
uncharacterized LOC117005193, transcript variant X9
uncharacterized LOC117005193, transcript variant X4
uncharacterized LOC117005193, transcript variant X1
uncharacterized LOC117005193, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC117005193, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC117005193, transcript variant X6
uncharacterized LOC117005193, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 213 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
growth arrest specific 7, transcript variant X1
growth arrest specific 7, transcript variant X2
growth arrest-specific protein 7 isoform X1
growth arrest-specific protein 7 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
dehydrogenase/reductase 7C, transcript variant X6
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 7 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 7C isoform X4
dehydrogenase/reductase 7C, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 1 EST, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dehydrogenase/reductase 7C, transcript variant X4
dehydrogenase/reductase 7C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 1 EST, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
dehydrogenase/reductase 7C, transcript variant X3
dehydrogenase/reductase 7C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 1 EST, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 7C isoform X2
dehydrogenase/reductase SDR family member 7C isoform X1
dehydrogenase/reductase SDR family member 7C isoform X3
biogenesis of lysosomal organelles complex 1 subunit 3
biogenesis of lysosome-related organelles complex 1 subunit 3
coiled-coil domain containing 61, transcript variant X2
coiled-coil domain containing 61, transcript variant X1
protein ADP-ribosylarginine hydrolase-like, transcript variant X1
protein ADP-ribosylarginine hydrolase-like, transcript variant X2
protein ADP-ribosylarginine hydrolase-like isoform X1
protein ADP-ribosylarginine hydrolase-like isoform X2
ubiquitin carboxyl-terminal hydrolase 17-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
heparan sulfate glucosamine 3-O-sulfotransferase 3A1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
meteorin like, glial cell differentiation regulator
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase like 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase like 1, transcript variant X2
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase like 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1 isoform X1
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase like 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase-like protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 8 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
WD repeat domain 45B, transcript variant X2
WD repeat domain phosphoinositide-interacting protein 3 isoform X2
WD repeat domain 45B, transcript variant X1
WD repeat domain phosphoinositide-interacting protein 3 isoform X1
WD repeat domain 45B, transcript variant X3
WD repeat domain phosphoinositide-interacting protein 3 isoform X3
uncharacterized LOC117005419, transcript variant X5
uncharacterized LOC117005419, transcript variant X2
uncharacterized LOC117005419, transcript variant X6
uncharacterized LOC117005419, transcript variant X4
uncharacterized LOC117005419, transcript variant X1
uncharacterized LOC117005419, transcript variant X7
uncharacterized LOC117005419, transcript variant X3
uncharacterized LOC117005419, transcript variant X8
uncharacterized LOC117005419, transcript variant X9
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nuclear prelamin A recognition factor, transcript variant X2
nuclear prelamin A recognition factor, transcript variant X1
2-oxoglutarate and iron dependent oxygenase domain containing 3, transcript variant X1
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 3 isoform X1
2-oxoglutarate and iron dependent oxygenase domain containing 3, transcript variant X2
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 3 isoform X2
urotensin-2 receptor-like, transcript variant X2
urotensin-2 receptor-like, transcript variant X1
urotensin-2 receptor-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 45% coverage of the annotated genomic feature by RNAseq alignments
trinucleotide repeat containing adaptor 6C, transcript variant X5
trinucleotide repeat containing adaptor 6C, transcript variant X1
trinucleotide repeat containing adaptor 6C, transcript variant X3
trinucleotide repeat containing adaptor 6C, transcript variant X7
trinucleotide repeat containing adaptor 6C, transcript variant X6
trinucleotide repeat containing adaptor 6C, transcript variant X8
trinucleotide repeat containing adaptor 6C, transcript variant X2
trinucleotide repeat containing adaptor 6C, transcript variant X4
trinucleotide repeat-containing gene 6C protein isoform X1
trinucleotide repeat-containing gene 6C protein isoform X5
trinucleotide repeat-containing gene 6C protein isoform X3
trinucleotide repeat-containing gene 6C protein isoform X4
trinucleotide repeat-containing gene 6C protein isoform X7
trinucleotide repeat-containing gene 6C protein isoform X6
trinucleotide repeat-containing gene 6C protein isoform X8
trinucleotide repeat-containing gene 6C protein isoform X2
trinucleotide repeat containing adaptor 6C, transcript variant X9
trinucleotide repeat-containing gene 6C protein isoform X9
basic salivary proline-rich protein 2-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00424
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B, transcript variant X2
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B, transcript variant X1
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B isoform X2
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B isoform X1
major facilitator superfamily domain containing 11
serine and arginine rich splicing factor 2, transcript variant X1
serine and arginine rich splicing factor 2, transcript variant X4
serine and arginine rich splicing factor 2, transcript variant X2
serine and arginine rich splicing factor 2, transcript variant X3
jumonji domain containing 6, arginine demethylase and lysine hydroxylase
bifunctional arginine demethylase and lysyl-hydroxylase JMJD6
matrix remodeling associated 7, transcript variant X1
matrix remodeling associated 7, transcript variant X2
matrix remodeling associated 7, transcript variant X3
matrix remodeling associated 7, transcript variant X4
matrix remodeling associated 7, transcript variant X7
matrix remodeling associated 7, transcript variant X6
matrix remodeling associated 7, transcript variant X5
matrix-remodeling-associated protein 7 isoform X1
matrix-remodeling-associated protein 7 isoform X2
matrix-remodeling-associated protein 7 isoform X5
matrix-remodeling-associated protein 7 isoform X3
matrix-remodeling-associated protein 7 isoform X4
matrix-remodeling-associated protein 7 isoform X6
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 1
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 11 samples with support for all annotated introns
alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 1
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2, transcript variant X2
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2, transcript variant X1
alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 isoform X1
alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 2 isoform X2
uncharacterized LOC117005335, transcript variant X3
uncharacterized LOC117005335, transcript variant X2
uncharacterized LOC117005335, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00213
rhomboid 5 homolog 2, transcript variant X2
rhomboid 5 homolog 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
(E3-independent) E2 ubiquitin-conjugating enzyme
sphingosine kinase 1, transcript variant X2
sphingosine kinase 1, transcript variant X1
phosphoribosyl pyrophosphate synthetase associated protein 1, transcript variant X6
phosphoribosyl pyrophosphate synthetase associated protein 1, transcript variant X4
phosphoribosyl pyrophosphate synthetase associated protein 1, transcript variant X5
phosphoribosyl pyrophosphate synthetase associated protein 1, transcript variant X3
phosphoribosyl pyrophosphate synthase-associated protein 1 isoform X2
phosphoribosyl pyrophosphate synthetase associated protein 1, transcript variant X7
phosphoribosyl pyrophosphate synthetase associated protein 1, transcript variant X1
phosphoribosyl pyrophosphate synthetase associated protein 1, transcript variant X2
phosphoribosyl pyrophosphate synthase-associated protein 1 isoform X3
phosphoribosyl pyrophosphate synthase-associated protein 1 isoform X1
phosphoribosyl pyrophosphate synthase-associated protein 1 isoform X4
uncharacterized LOC117005112, transcript variant X2
uncharacterized LOC117005112, transcript variant X1
uncharacterized LOC117005112, transcript variant X3
uncharacterized protein LOC117005112 isoform X3
uncharacterized protein LOC117005112 isoform X1
uncharacterized protein LOC117005112 isoform X2
ring finger protein 157, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ring finger protein 157, transcript variant X3
ring finger protein 157, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
ring finger protein 157, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
ring finger protein 157, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
ring finger protein 157, 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 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 15 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 15 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
exocyst complex component 7, transcript variant X1
exocyst complex component 7, transcript variant X3
exocyst complex component 7, transcript variant X5
exocyst complex component 7, transcript variant X2
exocyst complex component 7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 14 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
signal recognition particle subunit SRP68
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
TEN1 subunit of CST complex, transcript variant X1
TEN1 subunit of CST complex, transcript variant X2
mitochondrial ribosomal protein L38, transcript variant X3
mitochondrial ribosomal protein L38, transcript variant X4
39S ribosomal protein L38, mitochondrial isoform X3
39S ribosomal protein L38, mitochondrial isoform X4
mitochondrial ribosomal protein L38, transcript variant X1
mitochondrial ribosomal protein L38, transcript variant X2
39S ribosomal protein L38, mitochondrial isoform X1
39S ribosomal protein L38, mitochondrial isoform X2
WW domain binding protein 2, transcript variant X1
WW domain binding protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RING finger protein unkempt homolog isoform X5
RING finger protein unkempt homolog isoform X9
RING finger protein unkempt homolog isoform X8
RING finger protein unkempt homolog isoform X7
RING finger protein unkempt homolog isoform X3
RING finger protein unkempt homolog isoform X6
RING finger protein unkempt homolog isoform X4
RING finger protein unkempt homolog isoform X2
RING finger protein unkempt homolog isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
integrin subunit beta 4, transcript variant X2
integrin subunit beta 4, transcript variant X3
integrin subunit beta 4, transcript variant X1
SAP30 binding protein, transcript variant X2
SAP30 binding protein, transcript variant X1
RecQ like helicase 5, transcript variant X1
RecQ like helicase 5, transcript variant X2
RecQ like helicase 5, 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 7 samples with support for all annotated introns
RecQ like helicase 5, transcript variant X7
ATP-dependent DNA helicase Q5 isoform X1
ATP-dependent DNA helicase Q5 isoform X2
ATP-dependent DNA helicase Q5 isoform X5
ATP-dependent DNA helicase Q5 isoform X6
RecQ like helicase 5, transcript variant X3
RecQ like helicase 5, transcript variant X4
ATP-dependent DNA helicase Q5 isoform X3
RecQ like helicase 5, transcript variant X5
ATP-dependent DNA helicase Q5 isoform X4
small integral membrane protein 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
small integral membrane protein 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
LLGL scribble cell polarity complex component 2
tRNA splicing endonuclease subunit 54, transcript variant X2
tRNA splicing endonuclease subunit 54, transcript variant X1
tRNA-splicing endonuclease subunit Sen54 isoform X2
tRNA-splicing endonuclease subunit Sen54 isoform X1
melanin concentrating hormone receptor 1
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 18 samples with support for all annotated introns
melanin-concentrating hormone receptor 1
CASK interacting protein 2, transcript variant X1
CASK interacting protein 2, transcript variant X4
CASK interacting protein 2, transcript variant X2
CASK interacting protein 2, transcript variant X3
transmembrane protein 94, transcript variant X2
transmembrane protein 94, transcript variant X3
transmembrane protein 94, transcript variant X1
mitochondrial thiamine pyrophosphate carrier
golgi associated, gamma adaptin ear containing, ARF binding protein 3
ADP-ribosylation factor-binding protein GGA3
Jupiter microtubule associated homolog 1
5', 3'-nucleotidase, cytosolic, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
5'(3')-deoxyribonucleotidase, cytosolic type isoform X2
5', 3'-nucleotidase, cytosolic, transcript variant X1
5'(3')-deoxyribonucleotidase, cytosolic type 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 4 samples with support for all annotated introns
solute carrier family 16 member 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
solute carrier family 16 member 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
potassium channel tetramerization domain containing 2
5-hydroxytryptamine receptor 3A-like, transcript variant X2
5-hydroxytryptamine receptor 3A-like, transcript variant X3
5-hydroxytryptamine receptor 3A-like, transcript variant X4
5-hydroxytryptamine receptor 3A-like, transcript variant X1
5-hydroxytryptamine receptor 3A-like isoform X3
5-hydroxytryptamine receptor 3A-like isoform X2
5-hydroxytryptamine receptor 3A-like isoform X1
transfer RNA arginine (anticodon UCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
peptidyl-tRNA hydrolase ICT1, mitochondrial
cerebellar degeneration related protein 2 like
cerebellar degeneration-related protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 8 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 EST, 8 Proteins, and 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: 1 EST, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
USH1 protein network component sans, transcript variant X1
USH1 protein network component sans, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Usher syndrome type-1G protein isoform X1
Usher syndrome type-1G protein isoform X2
NADPH:adrenodoxin oxidoreductase, mitochondrial
glutamate ionotropic receptor NMDA type subunit 2C
transmembrane protein 104, transcript variant X2
transmembrane protein 104, transcript variant X1
Na(+)/H(+) exchange regulatory cofactor NHE-RF1
RAB37, member RAS oncogene family, transcript variant X2
RAB37, member RAS oncogene family, transcript variant X3
RAB37, member RAS oncogene family, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
39S ribosomal protein L27, mitochondrial
essential meiotic structure-specific endonuclease 1
leucine-rich repeat-containing protein 59
medium-chain acyl-CoA ligase ACSF2, mitochondrial
uncharacterized LOC117005347, 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 13 samples with support for all annotated introns
uncharacterized LOC117005347, 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 14 samples with support for all annotated introns
radical S-adenosyl methionine domain containing 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
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: radical S-adenosyl methionine domain-containing protein 1, mitochondrial
MYCBP associated protein, transcript variant X1
MYCBP associated protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
spermatogenesis associated 20, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
spermatogenesis associated 20, transcript variant X2
spermatogenesis associated 20, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
spermatogenesis associated 20, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
spermatogenesis-associated protein 20 isoform X1
spermatogenesis associated 20, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
spermatogenesis-associated protein 20 isoform X2
calcium voltage-gated channel subunit alpha1 G, transcript variant X1
calcium voltage-gated channel subunit alpha1 G, transcript variant X15
calcium voltage-gated channel subunit alpha1 G, transcript variant X16
calcium voltage-gated channel subunit alpha1 G, transcript variant X13
calcium voltage-gated channel subunit alpha1 G, transcript variant X19
calcium voltage-gated channel subunit alpha1 G, transcript variant X4
calcium voltage-gated channel subunit alpha1 G, transcript variant X20
calcium voltage-gated channel subunit alpha1 G, transcript variant X6
calcium voltage-gated channel subunit alpha1 G, transcript variant X2
calcium voltage-gated channel subunit alpha1 G, transcript variant X8
calcium voltage-gated channel subunit alpha1 G, transcript variant X3
calcium voltage-gated channel subunit alpha1 G, transcript variant X9
calcium voltage-gated channel subunit alpha1 G, transcript variant X5
calcium voltage-gated channel subunit alpha1 G, transcript variant X18
calcium voltage-gated channel subunit alpha1 G, transcript variant X11
calcium voltage-gated channel subunit alpha1 G, transcript variant X7
calcium voltage-gated channel subunit alpha1 G, transcript variant X10
calcium voltage-gated channel subunit alpha1 G, transcript variant X14
calcium voltage-gated channel subunit alpha1 G, transcript variant X12
calcium voltage-gated channel subunit alpha1 G, transcript variant X17
calcium voltage-gated channel subunit alpha1 G, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
calcium voltage-gated channel subunit alpha1 G, transcript variant X23
calcium voltage-gated channel subunit alpha1 G, transcript variant X21
voltage-dependent T-type calcium channel subunit alpha-1G isoform X1
voltage-dependent T-type calcium channel subunit alpha-1G isoform X15
voltage-dependent T-type calcium channel subunit alpha-1G isoform X16
voltage-dependent T-type calcium channel subunit alpha-1G isoform X13
voltage-dependent T-type calcium channel subunit alpha-1G isoform X19
voltage-dependent T-type calcium channel subunit alpha-1G isoform X4
voltage-dependent T-type calcium channel subunit alpha-1G isoform X20
voltage-dependent T-type calcium channel subunit alpha-1G isoform X6
voltage-dependent T-type calcium channel subunit alpha-1G isoform X2
voltage-dependent T-type calcium channel subunit alpha-1G isoform X8
voltage-dependent T-type calcium channel subunit alpha-1G isoform X3
voltage-dependent T-type calcium channel subunit alpha-1G isoform X9
voltage-dependent T-type calcium channel subunit alpha-1G isoform X5
voltage-dependent T-type calcium channel subunit alpha-1G isoform X18
voltage-dependent T-type calcium channel subunit alpha-1G isoform X11
voltage-dependent T-type calcium channel subunit alpha-1G isoform X7
voltage-dependent T-type calcium channel subunit alpha-1G isoform X10
voltage-dependent T-type calcium channel subunit alpha-1G isoform X14
voltage-dependent T-type calcium channel subunit alpha-1G isoform X12
voltage-dependent T-type calcium channel subunit alpha-1G isoform X17
voltage-dependent T-type calcium channel subunit alpha-1G isoform X21
ATP binding cassette subfamily C member 3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 52 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: ATP-binding cassette sub-family C member 3
ankyrin repeat domain-containing protein 40
LUC7 like 3 pre-mRNA splicing factor, transcript variant X4
LUC7 like 3 pre-mRNA splicing factor, transcript variant X1
LUC7 like 3 pre-mRNA splicing factor, transcript variant X2
LUC7 like 3 pre-mRNA splicing factor, transcript variant X3
LUC7 like 3 pre-mRNA splicing factor, transcript variant X5
ankyrin repeat domain-containing protein 40-like, transcript variant X2
ankyrin repeat domain-containing protein 40-like, transcript variant X3
ankyrin repeat domain-containing protein 40-like, transcript variant X1
ankyrin repeat domain-containing protein 40-like isoform X2
ankyrin repeat domain-containing protein 40-like isoform X3
ankyrin repeat domain-containing protein 40-like isoform X1
WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, 18 Proteins
WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 2
uncharacterized LOC117005367, transcript variant X4
uncharacterized LOC117005367, transcript variant X2
uncharacterized LOC117005367, transcript variant X3
uncharacterized LOC117005367, transcript variant X1
sperm associated antigen 9, transcript variant X2
sperm associated antigen 9, transcript variant X1
sperm associated antigen 9, transcript variant X6
sperm associated antigen 9, transcript variant X4
sperm associated antigen 9, transcript variant X3
sperm associated antigen 9, transcript variant X5
sperm associated antigen 9, transcript variant X7
sperm associated antigen 9, transcript variant X8
sperm associated antigen 9, transcript variant X9
sperm associated antigen 9, transcript variant X10
sperm associated antigen 9, transcript variant X11
sperm associated antigen 9, transcript variant X12
C-Jun-amino-terminal kinase-interacting protein 4 isoform X6
C-Jun-amino-terminal kinase-interacting protein 4 isoform X4
C-Jun-amino-terminal kinase-interacting protein 4 isoform X2
C-Jun-amino-terminal kinase-interacting protein 4 isoform X3
C-Jun-amino-terminal kinase-interacting protein 4 isoform X5
C-Jun-amino-terminal kinase-interacting protein 4 isoform X1
C-Jun-amino-terminal kinase-interacting protein 4 isoform X12
C-Jun-amino-terminal kinase-interacting protein 4 isoform X9
C-Jun-amino-terminal kinase-interacting protein 4 isoform X10
C-Jun-amino-terminal kinase-interacting protein 4 isoform X11
C-Jun-amino-terminal kinase-interacting protein 4 isoform X8
C-Jun-amino-terminal kinase-interacting protein 4 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
mbt domain containing 1, transcript variant X2
mbt domain containing 1, transcript variant X3
mbt domain containing 1, transcript variant X1
mbt domain containing 1, transcript variant X5
mbt domain containing 1, transcript variant X4
mbt domain containing 1, transcript variant X6
mbt domain containing 1, transcript variant X8
mbt domain containing 1, transcript variant X7
MBT domain-containing protein 1 isoform X6
MBT domain-containing protein 1 isoform X2
MBT domain-containing protein 1 isoform X5
MBT domain-containing protein 1 isoform X3
MBT domain-containing protein 1 isoform X4
MBT domain-containing protein 1 isoform X1
MBT domain-containing protein 1 isoform X7
UTP18 small subunit processome component, transcript variant X1
UTP18 small subunit processome component, transcript variant X2
U3 small nucleolar RNA-associated protein 18 homolog
target of myb1 like 1 membrane trafficking protein
cytochrome c oxidase assembly protein COX11, mitochondrial
syntaxin binding protein 4, transcript variant X2
syntaxin binding protein 4, transcript variant X3
syntaxin binding protein 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
syntaxin binding protein 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
syntaxin binding protein 4, transcript variant X1
HLF transcription factor, PAR bZIP family member
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
monocyte to macrophage differentiation associated
monocyte to macrophage differentiation factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 100, transcript variant X3
transmembrane protein 100, transcript variant X1
transmembrane protein 100, transcript variant X2
phosphatidylcholine transfer protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
phosphatidylcholine transfer protein, transcript variant X1
ankyrin repeat and fibronectin type III domain containing 1, transcript variant X2
ankyrin repeat and fibronectin type III domain containing 1, transcript variant X3
ankyrin repeat and fibronectin type III domain containing 1, transcript variant X1
ankyrin repeat and fibronectin type-III domain-containing protein 1
uncharacterized protein C17orf67 homolog
retinoid-inducible serine carboxypeptidase
RAB11 family interacting protein 4, transcript variant X1
rab11 family-interacting protein 4 isoform X1
RAB11 family interacting protein 4, transcript variant X2
rab11 family-interacting protein 4 isoform X2
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
coordinator of PRMT5 and differentiation stimulator
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 6 samples with support for all annotated introns
U3 small nucleolar RNA-associated protein 6 homolog
SUZ12 polycomb repressive complex 2 subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATPase family AAA domain-containing protein 5
ArfGAP with dual PH domains 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ArfGAP with dual PH domains 2, transcript variant X2
arf-GAP with dual PH domain-containing protein 2 isoform X1
arf-GAP with dual PH domain-containing protein 2 isoform X2
ras homolog family member T1, transcript variant X1
ras homolog family member T1, transcript variant X2
ras homolog family member T1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 16 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: 2 ESTs, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger protein 207, transcript variant X3
zinc finger protein 207, transcript variant X1
zinc finger protein 207, transcript variant X2
zinc finger protein 207, transcript variant X5
zinc finger protein 207, transcript variant X4
zinc finger protein 207, transcript variant X6
BUB3-interacting and GLEBS motif-containing protein ZNF207 isoform X1
BUB3-interacting and GLEBS motif-containing protein ZNF207 isoform X3
BUB3-interacting and GLEBS motif-containing protein ZNF207 isoform X2
BUB3-interacting and GLEBS motif-containing protein ZNF207 isoform X4
sterile alpha motif domain-containing protein 9-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sterile alpha motif domain-containing protein 9-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
sterile alpha motif domain-containing protein 9-like, transcript variant X1
sterile alpha motif domain-containing protein 9-like
endoplasmic reticulum to nucleus signaling 1, transcript variant X1
endoplasmic reticulum to nucleus signaling 1, transcript variant X2
serine/threonine-protein kinase/endoribonuclease IRE1 isoform X1
serine/threonine-protein kinase/endoribonuclease IRE1 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00289
COORDINATES: nucleotide motif:Rfam:12.0:RF00407
testis expressed 2, transcript variant X2
testis expressed 2, transcript variant X1
platelet and endothelial cell adhesion molecule 1, transcript variant X9
platelet and endothelial cell adhesion molecule 1, transcript variant X8
platelet and endothelial cell adhesion molecule 1, transcript variant X7
platelet and endothelial cell adhesion molecule 1, transcript variant X6
platelet and endothelial cell adhesion molecule 1, transcript variant X5
platelet and endothelial cell adhesion molecule 1, transcript variant X4
platelet and endothelial cell adhesion molecule 1, transcript variant X3
platelet and endothelial cell adhesion molecule 1, transcript variant X2
platelet and endothelial cell adhesion molecule 1, transcript variant X1
platelet endothelial cell adhesion molecule isoform X9
platelet endothelial cell adhesion molecule isoform X8
platelet endothelial cell adhesion molecule isoform X5
platelet endothelial cell adhesion molecule isoform X4
platelet endothelial cell adhesion molecule isoform X2
platelet endothelial cell adhesion molecule isoform X1
platelet endothelial cell adhesion molecule isoform X7
platelet endothelial cell adhesion molecule isoform X6
platelet endothelial cell adhesion molecule isoform X3
mast cell immunoglobulin like receptor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
DNA polymerase gamma 2, accessory subunit
DNA polymerase subunit gamma-2, mitochondrial
probable ATP-dependent RNA helicase DDX5
centrosomal protein 95, transcript variant X2
centrosomal protein 95, transcript variant X1
centrosomal protein of 95 kDa isoform X2
centrosomal protein of 95 kDa isoform X1
SMAD specific E3 ubiquitin protein ligase 2, transcript variant X2
SMAD specific E3 ubiquitin protein ligase 2, transcript variant X1
E3 ubiquitin-protein ligase SMURF2 isoform X2
E3 ubiquitin-protein ligase SMURF2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 13 ESTs, 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transfer RNA arginine (anticodon CCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
chromosome 20 C17orf58 homolog, transcript variant X4
chromosome 20 C17orf58 homolog, transcript variant X1
chromosome 20 C17orf58 homolog, transcript variant X3
UPF0450 protein C17orf58 homolog isoform X1
UPF0450 protein C17orf58 homolog isoform X3
chromosome 20 C17orf58 homolog, transcript variant X2
UPF0450 protein C17orf58 homolog isoform X2
UPF0450 protein C17orf58 homolog isoform X4
bromodomain PHD finger transcription factor, transcript variant X3
bromodomain PHD finger transcription factor, transcript variant X1
bromodomain PHD finger transcription factor, transcript variant X9
bromodomain PHD finger transcription factor, transcript variant X6
bromodomain PHD finger transcription factor, transcript variant X8
bromodomain PHD finger transcription factor, transcript variant X7
bromodomain PHD finger transcription factor, transcript variant X5
bromodomain PHD finger transcription factor, transcript variant X4
nucleosome-remodeling factor subunit BPTF isoform X3
nucleosome-remodeling factor subunit BPTF isoform X1
nucleosome-remodeling factor subunit BPTF isoform X6
nucleosome-remodeling factor subunit BPTF isoform X9
nucleosome-remodeling factor subunit BPTF isoform X8
nucleosome-remodeling factor subunit BPTF isoform X7
nucleosome-remodeling factor subunit BPTF isoform X5
nucleosome-remodeling factor subunit BPTF isoform X4
bromodomain PHD finger transcription factor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 ESTs, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
nucleosome-remodeling factor subunit BPTF isoform X2
nucleolar protein 11, transcript variant X2
nucleolar protein 11, transcript variant X1
phosphatidylinositol transfer protein cytoplasmic 1, transcript variant X2
phosphatidylinositol transfer protein cytoplasmic 1, transcript variant X1
phosphatidylinositol transfer protein cytoplasmic 1, transcript variant X3
cytoplasmic phosphatidylinositol transfer protein 1 isoform X1
cytoplasmic phosphatidylinositol transfer protein 1 isoform X2
cytoplasmic phosphatidylinositol transfer protein 1 isoform X3
proteasome 26S subunit, non-ATPase 12, transcript variant X1
proteasome 26S subunit, non-ATPase 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 12 isoform X1
26S proteasome non-ATPase regulatory subunit 12 isoform X2
helicase with zinc finger, transcript variant X1
helicase with zinc finger, transcript variant X3
helicase with zinc finger, transcript variant X2
helicase with zinc finger, transcript variant X4
probable helicase with zinc finger domain isoform X4
probable helicase with zinc finger domain isoform X1
probable helicase with zinc finger domain isoform X3
probable helicase with zinc finger domain isoform X2
calcium voltage-gated channel auxiliary subunit gamma 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: voltage-dependent calcium channel gamma-1 subunit
calcium voltage-gated channel auxiliary subunit gamma 4
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; deleted 1 base in 1 codon
LOW QUALITY PROTEIN: voltage-dependent calcium channel gamma-4 subunit
calcium voltage-gated channel auxiliary subunit gamma 5, transcript variant X3
calcium voltage-gated channel auxiliary subunit gamma 5, transcript variant X1
calcium voltage-gated channel auxiliary subunit gamma 5, transcript variant X2
voltage-dependent calcium channel gamma-5 subunit
protein kinase C alpha, transcript variant X1
protein kinase C alpha, transcript variant X2
centrosomal protein 112, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
centrosomal protein 112, transcript variant X1
centrosomal protein 112, transcript variant X3
centrosomal protein 112, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
centrosomal protein of 112 kDa isoform X2
centrosomal protein of 112 kDa isoform X1
regulator of G-protein signaling 9-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 ESTs, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
regulator of G-protein signaling 9-like isoform X1
regulator of G-protein signaling 9-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
regulator of G-protein signaling 9-like isoform X2
guanine nucleotide-binding protein subunit alpha-13
WD repeat domain, phosphoinositide interacting 1
WD repeat domain phosphoinositide-interacting protein 1
protein kinase cAMP-dependent type I regulatory subunit alpha, transcript variant X2
protein kinase cAMP-dependent type I regulatory subunit alpha, transcript variant X1
cAMP-dependent protein kinase type I-alpha regulatory subunit
FAM20A golgi associated secretory pathway pseudokinase
ATP-binding cassette sub-family A member 10-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ATP-binding cassette sub-family A member 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
ATP binding cassette subfamily A member 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
ATP binding cassette subfamily A member 5, transcript variant X1
ATP binding cassette subfamily A member 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
cholesterol transporter ABCA5 isoform X1
cholesterol transporter ABCA5 isoform X2
mitogen-activated protein kinase kinase 6
dual specificity mitogen-activated protein kinase kinase 6
potassium inwardly rectifying channel subfamily J member 16, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
potassium inwardly rectifying channel subfamily J member 16, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
potassium inwardly rectifying channel subfamily J member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 3 ESTs, 85 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
solute carrier family 39 member 11, transcript variant X2
solute carrier family 39 member 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
component of oligomeric golgi complex 1, transcript variant X4
component of oligomeric golgi complex 1, transcript variant X2
component of oligomeric golgi complex 1, transcript variant X1
conserved oligomeric Golgi complex subunit 1 isoform X3
conserved oligomeric Golgi complex subunit 1 isoform X1
component of oligomeric golgi complex 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
conserved oligomeric Golgi complex subunit 1 isoform X2
family with sequence similarity 104 member A, transcript variant X2
family with sequence similarity 104 member A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized protein C17orf80 homolog
cleavage and polyadenylation specific factor 4 like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
putative cleavage and polyadenylation specificity factor subunit 4-like protein
sidekick cell adhesion molecule 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 ESTs, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
sidekick cell adhesion molecule 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
sidekick cell adhesion molecule 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ribosomal protein L38, transcript variant X1
ribosomal protein L38, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: BTB/POZ domain-containing protein 17
G protein-coupled receptor 142, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
G protein-coupled receptor 142, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
probable G-protein coupled receptor 142 isoform X1
probable G-protein coupled receptor 142 isoform X2
G protein-coupled receptor class C group 5 member C, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
G protein-coupled receptor class C group 5 member C, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
G protein-coupled receptor class C group 5 member C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
G protein-coupled receptor class C group 5 member C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G-protein coupled receptor family C group 5 member C isoform X1
G-protein coupled receptor family C group 5 member C isoform X2
coiled-coil domain containing 137, 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
coiled-coil domain containing 137, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
coiled-coil domain-containing protein 137 isoform X2
coiled-coil domain-containing protein 137 isoform X1
oxidoreductase-like domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
retinal rod rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
NPL4 homolog, ubiquitin recognition factor
nuclear protein localization protein 4 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
FA core complex associated protein 100, transcript variant X2
FA core complex associated protein 100, transcript variant X1
Fanconi anemia core complex-associated protein 100
fascin actin-bundling protein 2, retinal
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 12 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
BAH domain and coiled-coil containing 1, transcript variant X2
BAH domain and coiled-coil containing 1, transcript variant X3
BAH domain and coiled-coil containing 1, transcript variant X1
BAH and coiled-coil domain-containing protein 1 isoform X2
BAH and coiled-coil domain-containing protein 1 isoform X3
BAH and coiled-coil domain-containing protein 1 isoform X1
putative sodium-coupled neutral amino acid transporter 10
NADH:ubiquinone oxidoreductase complex assembly factor 8
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 8
TEPSIN adaptor related protein complex 4 accessory protein, transcript variant X1
TEPSIN adaptor related protein complex 4 accessory protein, transcript variant X2
TEPSIN adaptor related protein complex 4 accessory protein, transcript variant X3
AP-4 complex accessory subunit tepsin isoform X1
AP-4 complex accessory subunit tepsin isoform X2
AP-4 complex accessory subunit tepsin isoform X3
centrosomal protein 131, transcript variant X1
centrosomal protein 131, transcript variant X4
centrosomal protein 131, transcript variant X3
centrosomal protein 131, transcript variant X5
centrosomal protein 131, transcript variant X2
centrosomal protein of 131 kDa isoform X1
centrosomal protein of 131 kDa isoform X3
centrosomal protein of 131 kDa isoform X2
centrosomal protein of 131 kDa isoform X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 6 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
LOW QUALITY PROTEIN: serine/threonine-protein kinase LMTK1
BAR/IMD domain containing adaptor protein 2, transcript variant X6
BAR/IMD domain containing adaptor protein 2, transcript variant X5
BAR/IMD domain containing adaptor protein 2, transcript variant X8
BAR/IMD domain containing adaptor protein 2, transcript variant X1
BAR/IMD domain containing adaptor protein 2, transcript variant X3
BAR/IMD domain containing adaptor protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
brain-specific angiogenesis inhibitor 1-associated protein 2 isoform X5
brain-specific angiogenesis inhibitor 1-associated protein 2 isoform X4
brain-specific angiogenesis inhibitor 1-associated protein 2 isoform X1
brain-specific angiogenesis inhibitor 1-associated protein 2 isoform X7
brain-specific angiogenesis inhibitor 1-associated protein 2 isoform X3
BAR/IMD domain containing adaptor protein 2, transcript variant X9
BAR/IMD domain containing adaptor protein 2, transcript variant X7
BAR/IMD domain containing adaptor protein 2, transcript variant X2
brain-specific angiogenesis inhibitor 1-associated protein 2 isoform X8
brain-specific angiogenesis inhibitor 1-associated protein 2 isoform X6
brain-specific angiogenesis inhibitor 1-associated protein 2 isoform X2
regulatory associated protein of MTOR complex 1, transcript variant X2
regulatory associated protein of MTOR complex 1, transcript variant X1
regulatory associated protein of MTOR complex 1, transcript variant X4
regulatory associated protein of MTOR complex 1, transcript variant X3
regulatory-associated protein of mTOR isoform X4
regulatory-associated protein of mTOR isoform X2
regulatory-associated protein of mTOR isoform X3
regulatory-associated protein of mTOR isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 26 member 11, transcript variant X2
solute carrier family 26 member 11, transcript variant X3
solute carrier family 26 member 11, transcript variant X1
sodium-independent sulfate anion transporter isoform X2
sodium-independent sulfate anion transporter isoform X3
sodium-independent sulfate anion transporter isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 40
TBC1 domain family member 16, transcript variant X1
TBC1 domain family member 16, transcript variant X2
TBC1 domain family member 16, transcript variant X3
TBC1 domain family member 16, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
ectonucleotide pyrophosphatase/phosphodiesterase 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
ectonucleotide pyrophosphatase/phosphodiesterase family member 7
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
LOW QUALITY PROTEIN: RNA binding protein fox-1 homolog 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
cytosolic endo-beta-N-acetylglucosaminidase
C1q and TNF related 1, transcript variant X3
C1q and TNF related 1, transcript variant X1
C1q and TNF related 1, transcript variant X2
complement C1q tumor necrosis factor-related protein 1
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; 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: inserted 2 bases in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: soluble calcium-activated nucleotidase 1
ubiquitin specific peptidase 36, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 36 isoform X1
ubiquitin specific peptidase 36, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 36 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 14 ESTs, 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
CDP-diacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase, mitochondrial
probable low-specificity L-threonine aldolase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane channel like 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
transmembrane channel like 6, transcript variant X2
hepatocyte growth factor-regulated tyrosine kinase substrate, transcript variant X1
hepatocyte growth factor-regulated tyrosine kinase substrate, transcript variant X2
hepatocyte growth factor-regulated tyrosine kinase substrate isoform X1
hepatocyte growth factor-regulated tyrosine kinase substrate isoform X2
mitochondrial ribosomal protein L12, transcript variant X1
mitochondrial ribosomal protein L12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L12, mitochondrial
solute carrier family 25 member 10, transcript variant X1
solute carrier family 25 member 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
MAPK regulated corepressor interacting protein 1
mapk-regulated corepressor-interacting protein 1
protein phosphatase 1 regulatory subunit 27
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
anaphase promoting complex subunit 11, transcript variant X1
anaphase promoting complex subunit 11, transcript variant X2
anaphase promoting complex subunit 11, transcript variant X4
anaphase promoting complex subunit 11, transcript variant X3
anaphase-promoting complex subunit 11 isoform X1
anaphase-promoting complex subunit 11 isoform X2
anaphase-promoting complex subunit 11 isoform X4
anaphase-promoting complex subunit 11 isoform X3
phosphate cytidylyltransferase 2, ethanolamine, transcript variant X1
phosphate cytidylyltransferase 2, ethanolamine, transcript variant X2
ethanolamine-phosphate cytidylyltransferase isoform X2
ethanolamine-phosphate cytidylyltransferase isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 ESTs, 6 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
NAD-dependent protein deacetylase sirtuin-7
MAF bZIP transcription factor G, transcript variant X1
MAF bZIP transcription factor G, transcript variant X4
MAF bZIP transcription factor G, transcript variant X3
MAF bZIP transcription factor G, transcript variant X2
pyrroline-5-carboxylate reductase 1, mitochondrial
myeloid associated differentiation marker like 2
myeloid-associated differentiation marker-like protein 2
notum, palmitoleoyl-protein carboxylesterase
palmitoleoyl-protein carboxylesterase NOTUM
ASPSCR1 tether for SLC2A4, UBX domain containing, transcript variant X2
ASPSCR1 tether for SLC2A4, UBX domain containing, transcript variant X1
tether containing UBX domain for GLUT4 isoform X1
tether containing UBX domain for GLUT4 isoform X2
leucine rich repeat containing 45, transcript variant X1
leucine rich repeat containing 45, transcript variant X2
leucine rich repeat containing 45, transcript variant X3
leucine-rich repeat-containing protein 45 isoform X1
leucine-rich repeat-containing protein 45 isoform X2
ras-related C3 botulinum toxin substrate 3
RFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
beta-1,3-N-acetylglucosaminyltransferase radical fringe
dihydrouridine synthase 1 like, transcript variant X2
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like isoform X2
dihydrouridine synthase 1 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
dihydrouridine synthase 1 like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like isoform X3
tRNA-dihydrouridine(16/17) synthase [NAD(P)(+)]-like isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: fatty acid synthase
coiled-coil domain-containing protein 57-like, transcript variant X2
coiled-coil domain-containing protein 57-like, transcript variant X1
uncharacterized protein LOC117005221 isoform X2
coiled-coil domain-containing protein 57-like isoform X1
coiled-coil domain-containing protein 57-like, transcript variant X3
coiled-coil domain-containing protein 57-like isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 9 bases in 8 codons; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 10 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 9 bases in 8 codons; deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: fatty acid synthase-like
casein kinase 1 delta, transcript variant X2
casein kinase 1 delta, transcript variant X1
casein kinase 1 delta, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
casein kinase 1 delta, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments