Lemur catta isolate mLemCat1 chromosome 16, mLemCat1.pri, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Strepsirrhini; Lemuriformes; Lemuridae; Lemur.
REFSEQ INFORMATION: The reference sequence is identical to\nCM036487.1.\nAssembly name: mLemCat1.pri\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2021/11/04. The original whole-genome shotgun project has the\naccession JAJGPY000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 16-JUL-2021\nAssembly Method :: hifiasm v. 0.12-r304; purge_dups v.\n 1.2.5; bionano_solve v.\n Solve3.6.1_11162020; salsa2 v. v2.2;\n gEVAL manual curation v. 2021-07-16\nAssembly Name :: mLemCat1.pri\nDiploid :: Principal Pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 20.81x\nSequencing Technology :: Pacbio Sequel II CCS; 10X Genomics linked\n reads; Bionano Genomics DLS; Arima\n Genomics v1 Hi-C\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Lemur catta Annotation Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
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 LOC123621561, transcript variant X2
uncharacterized LOC123621561, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 13% 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 84% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain-containing protein 47-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 6 bases in 5 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 14% 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 6 bases in 5 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger and BTB domain-containing protein 47-like
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
uncharacterized LOC123621633, transcript variant X2
uncharacterized LOC123621633, transcript variant X1
uncharacterized LOC123621632, transcript variant X5
uncharacterized LOC123621632, transcript variant X1
uncharacterized LOC123621632, transcript variant X4
uncharacterized LOC123621632, transcript variant X2
uncharacterized LOC123621632, transcript variant X3
putative neuroblastoma breakpoint family member 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
neuroblastoma breakpoint family member 4-like, transcript variant X4
neuroblastoma breakpoint family member 4-like, transcript variant X6
neuroblastoma breakpoint family member 4-like, transcript variant X1
neuroblastoma breakpoint family member 4-like, transcript variant X3
neuroblastoma breakpoint family member 4-like, transcript variant X2
neuroblastoma breakpoint family member 4-like, transcript variant X5
neuroblastoma breakpoint family member 4-like isoform X2
neuroblastoma breakpoint family member 4-like isoform X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
fms related receptor tyrosine kinase 4, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fms related receptor tyrosine kinase 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 35 ESTs, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fms related receptor tyrosine kinase 4, transcript variant X5
fms related receptor tyrosine kinase 4, transcript variant X6
fms related receptor tyrosine kinase 4, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 27 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fms related receptor tyrosine kinase 4, transcript variant X9
fms related receptor tyrosine kinase 4, transcript variant X3
fms related receptor tyrosine kinase 4, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 26 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fms related receptor tyrosine kinase 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 26 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fms related receptor tyrosine kinase 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 27 ESTs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
vascular endothelial growth factor receptor 3 isoform X5
vascular endothelial growth factor receptor 3 isoform X6
vascular endothelial growth factor receptor 3 isoform X7
vascular endothelial growth factor receptor 3 isoform X9
vascular endothelial growth factor receptor 3 isoform X1
vascular endothelial growth factor receptor 3 isoform X3
vascular endothelial growth factor receptor 3 isoform X10
vascular endothelial growth factor receptor 3 isoform X4
vascular endothelial growth factor receptor 3 isoform X2
vascular endothelial growth factor receptor 3 isoform X8
CCR4-NOT transcription complex subunit 6, transcript variant X1
CCR4-NOT transcription complex subunit 6, transcript variant X2
CCR4-NOT transcription complex subunit 6, transcript variant X3
CCR4-NOT transcription complex subunit 6 isoform X2
CCR4-NOT transcription complex subunit 6 isoform X1
CCR4-NOT transcription complex subunit 6 isoform X3
glutamine-fructose-6-phosphate transaminase 2
glutamine--fructose-6-phosphate aminotransferase [isomerizing] 2
mitogen-activated protein kinase 9, transcript variant X2
mitogen-activated protein kinase 9, transcript variant X1
mitogen-activated protein kinase 9, transcript variant X4
mitogen-activated protein kinase 9, transcript variant X3
mitogen-activated protein kinase 9, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 45 ESTs, 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitogen-activated protein kinase 9, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 ESTs, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitogen-activated protein kinase 9, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 ESTs, 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitogen-activated protein kinase 9 isoform X2
mitogen-activated protein kinase 9 isoform X1
mitogen-activated protein kinase 9 isoform X4
mitogen-activated protein kinase 9 isoform X3
mitogen-activated protein kinase 9 isoform X5
RasGEF domain family member 1C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 14 Proteins
ras-GEF domain-containing family member 1C isoform X1
RasGEF domain family member 1C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins
ras-GEF domain-containing family member 1C isoform X2
ring finger protein 130, transcript variant X1
ring finger protein 130, transcript variant X2
ring finger protein 130, transcript variant X3
E3 ubiquitin-protein ligase RNF130 isoform X1
E3 ubiquitin-protein ligase RNF130 isoform X2
E3 ubiquitin-protein ligase RNF130 isoform X3
TBC1 domain family member 9B, transcript variant X1
TBC1 domain family member 9B, transcript variant X2
TBC1 domain family member 9B, transcript variant X3
TBC1 domain family member 9B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 173 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TBC1 domain family member 9B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 146 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TBC1 domain family member 9B, transcript variant X6
MRN complex interacting protein, transcript variant X1
MRN complex-interacting protein isoform X1
MRN complex interacting protein, transcript variant X2
MRN complex-interacting protein isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B
leukotriene C4 synthase, transcript variant X1
leukotriene C4 synthase, transcript variant X3
leukotriene C4 synthase, transcript variant X2
leukotriene C4 synthase, transcript variant X5
leukotriene C4 synthase, transcript variant X6
leukotriene C4 synthase, transcript variant X4
mastermind like transcriptional coactivator 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
heterogeneous nuclear ribonucleoprotein H1, transcript variant X4
heterogeneous nuclear ribonucleoprotein H1, transcript variant X1
heterogeneous nuclear ribonucleoprotein H1, transcript variant X3
heterogeneous nuclear ribonucleoprotein H1, transcript variant X6
heterogeneous nuclear ribonucleoprotein H1, transcript variant X2
heterogeneous nuclear ribonucleoprotein H1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 1712 ESTs, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein H1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1642 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein H1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1654 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein H1, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1580 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein H1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1617 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein H isoform X4
heterogeneous nuclear ribonucleoprotein H isoform X1
heterogeneous nuclear ribonucleoprotein H isoform X3
heterogeneous nuclear ribonucleoprotein H isoform X6
heterogeneous nuclear ribonucleoprotein H isoform X2
heterogeneous nuclear ribonucleoprotein H isoform X9
heterogeneous nuclear ribonucleoprotein H isoform X5
heterogeneous nuclear ribonucleoprotein H isoform X8
heterogeneous nuclear ribonucleoprotein H isoform X10
heterogeneous nuclear ribonucleoprotein H isoform X7
heterogeneous nuclear ribonucleoprotein H1, transcript variant X11
heterogeneous nuclear ribonucleoprotein H isoform X11
RUN and FYVE domain containing 1, transcript variant X1
RUN and FYVE domain containing 1, transcript variant X2
RUN and FYVE domain-containing protein 1 isoform X1
RUN and FYVE domain-containing protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
ADAM metallopeptidase with thrombospondin type 1 motif 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 2 isoform X1
ADAM metallopeptidase with thrombospondin type 1 motif 2, transcript variant X2
A disintegrin and metalloproteinase with thrombospondin motifs 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 879, transcript variant X3
zinc finger protein 879, transcript variant X4
zinc finger protein 879, transcript variant X2
zinc finger protein 879, transcript variant X1
zinc finger protein 879, transcript variant X5
zinc finger protein 879, transcript variant X7
zinc finger protein 879, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 454, transcript variant X2
zinc finger protein 454, transcript variant X1
ZFP2 zinc finger protein, transcript variant X6
ZFP2 zinc finger protein, transcript variant X5
ZFP2 zinc finger protein, transcript variant X7
ZFP2 zinc finger protein, transcript variant X1
ZFP2 zinc finger protein, transcript variant X2
ZFP2 zinc finger protein, transcript variant X3
ZFP2 zinc finger protein, transcript variant X4
ZFP2 zinc finger protein, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 10 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
putative ankyrin repeat domain-containing protein 20A5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 37% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
G protein subunit alpha L, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 17 ESTs, 9 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
guanine nucleotide-binding protein G(olf) subunit alpha isoform X1
G protein subunit alpha L, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 30 ESTs, 24 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G protein subunit alpha L, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G protein subunit alpha L, transcript variant X3
G protein subunit alpha L, transcript variant X4
G protein subunit alpha L, transcript variant X6
G protein subunit alpha L, transcript variant X5
G protein subunit alpha L, transcript variant X9
G protein subunit alpha L, transcript variant X7
guanine nucleotide-binding protein G(olf) subunit alpha isoform X2
guanine nucleotide-binding protein G(olf) subunit alpha isoform X5
guanine nucleotide-binding protein G(olf) subunit alpha isoform X3
guanine nucleotide-binding protein G(olf) subunit alpha isoform X4
metallophosphoesterase 1, transcript variant X5
metallophosphoesterase 1, transcript variant X3
metallophosphoesterase 1, transcript variant X2
metallophosphoesterase 1, transcript variant X7
metallophosphoesterase 1, transcript variant X6
metallophosphoesterase 1, transcript variant X1
metallophosphoesterase 1, transcript variant X4
metallophosphoesterase 1, transcript variant X8
metallophosphoesterase 1, transcript variant X9
inositol monophosphatase 2, transcript variant X1
inositol monophosphatase 2, transcript variant X2
inositol monophosphatase 2, transcript variant X3
inositol monophosphatase 2, transcript variant X5
inositol monophosphatase 2, transcript variant X4
cell death inducing DFFA like effector a, transcript variant X1
cell death inducing DFFA like effector a, transcript variant X2
uncharacterized LOC123621833, transcript variant X2
uncharacterized LOC123621833, transcript variant X1
AFG3 like matrix AAA peptidase subunit 2, transcript variant X1
AFG3 like matrix AAA peptidase subunit 2, transcript variant X2
AFG3 like matrix AAA peptidase subunit 2, transcript variant X3
PRELI domain containing 3A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 8 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PRELI domain containing 3A, transcript variant X2
spire type actin nucleation factor 1, transcript variant X2
spire type actin nucleation factor 1, transcript variant X1
spire type actin nucleation factor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 ESTs, 1 Protein, and 87% 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: 1 Protein
protein tyrosine phosphatase non-receptor type 2, transcript variant X2
tyrosine-protein phosphatase non-receptor type 2 isoform X2
protein tyrosine phosphatase non-receptor type 2, transcript variant X1
protein tyrosine phosphatase non-receptor type 2, transcript variant X3
tyrosine-protein phosphatase non-receptor type 2 isoform X1
tyrosine-protein phosphatase non-receptor type 2 isoform X3
SEH1 like nucleoporin, transcript variant X1
SEH1 like nucleoporin, transcript variant X3
SEH1 like nucleoporin, transcript variant X2
SEH1 like nucleoporin, transcript variant X4
centrosomal protein 192, transcript variant X2
centrosomal protein of 192 kDa isoform X2
centrosomal protein 192, transcript variant X1
centrosomal protein of 192 kDa isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
low density lipoprotein receptor class A domain containing 4, transcript variant X2
low density lipoprotein receptor class A domain containing 4, transcript variant X1
low-density lipoprotein receptor class A domain-containing protein 4 isoform X1
low-density lipoprotein receptor class A domain-containing protein 4 isoform X2
low density lipoprotein receptor class A domain containing 4, transcript variant X5
low density lipoprotein receptor class A domain containing 4, transcript variant X3
low density lipoprotein receptor class A domain containing 4, transcript variant X4
low-density lipoprotein receptor class A domain-containing protein 4 isoform X3
low-density lipoprotein receptor class A domain-containing protein 4 isoform X4
low-density lipoprotein receptor class A domain-containing protein 4 isoform X5
family with sequence similarity 210 member A, transcript variant X1
family with sequence similarity 210 member A, transcript variant X2
family with sequence similarity 210 member A, transcript variant X3
family with sequence similarity 210 member A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 EST, 11 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 12 Proteins
60 kDa heat shock protein, mitochondrial-like
piezo type mechanosensitive ion channel component 2, transcript variant X1
piezo type mechanosensitive ion channel component 2, transcript variant X2
piezo-type mechanosensitive ion channel component 2 isoform X1
piezo-type mechanosensitive ion channel component 2 isoform X2
NSF attachment protein gamma, transcript variant X1
NSF attachment protein gamma, transcript variant X2
gamma-soluble NSF attachment protein isoform X1
gamma-soluble NSF attachment protein isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF01210
uncharacterized LOC123621498, transcript variant X2
uncharacterized LOC123621498, transcript variant X3
uncharacterized LOC123621498, transcript variant X1
VAMP associated protein A, transcript variant X2
VAMP associated protein A, transcript variant X1
vesicle-associated membrane protein-associated protein A isoform X2
vesicle-associated membrane protein-associated protein A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 4 regulatory subunit 1, transcript variant X1
protein phosphatase 4 regulatory subunit 1, transcript variant X9
protein phosphatase 4 regulatory subunit 1, transcript variant X4
protein phosphatase 4 regulatory subunit 1, transcript variant X10
protein phosphatase 4 regulatory subunit 1, transcript variant X3
protein phosphatase 4 regulatory subunit 1, transcript variant X7
protein phosphatase 4 regulatory subunit 1, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein phosphatase 4 regulatory subunit 1 isoform X1
serine/threonine-protein phosphatase 4 regulatory subunit 1 isoform X9
serine/threonine-protein phosphatase 4 regulatory subunit 1 isoform X4
serine/threonine-protein phosphatase 4 regulatory subunit 1 isoform X10
serine/threonine-protein phosphatase 4 regulatory subunit 1 isoform X3
serine/threonine-protein phosphatase 4 regulatory subunit 1 isoform X7
serine/threonine-protein phosphatase 4 regulatory subunit 1 isoform X11
protein phosphatase 4 regulatory subunit 1, transcript variant X8
protein phosphatase 4 regulatory subunit 1, transcript variant X6
protein phosphatase 4 regulatory subunit 1, transcript variant X2
protein phosphatase 4 regulatory subunit 1, transcript variant X5
serine/threonine-protein phosphatase 4 regulatory subunit 1 isoform X2
serine/threonine-protein phosphatase 4 regulatory subunit 1 isoform X6
serine/threonine-protein phosphatase 4 regulatory subunit 1 isoform X5
serine/threonine-protein phosphatase 4 regulatory subunit 1 isoform X8
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
ralA binding protein 1, transcript variant X2
ralA binding protein 1, transcript variant X1
ralA binding protein 1, transcript variant X3
twisted gastrulation BMP signaling modulator 1
ankyrin repeat domain 12, transcript variant X4
ankyrin repeat domain 12, transcript variant X2
ankyrin repeat domain 12, transcript variant X6
ankyrin repeat domain 12, transcript variant X8
ankyrin repeat domain 12, transcript variant X5
ankyrin repeat domain 12, transcript variant X7
ankyrin repeat domain 12, transcript variant X1
ankyrin repeat domain 12, transcript variant X3
ankyrin repeat domain 12, transcript variant X9
ankyrin repeat domain 12, transcript variant X11
ankyrin repeat domain 12, transcript variant X10
ankyrin repeat domain-containing protein 12 isoform X4
ankyrin repeat domain-containing protein 12 isoform X3
ankyrin repeat domain-containing protein 12 isoform X2
ankyrin repeat domain-containing protein 12 isoform X1
ankyrin repeat domain-containing protein 12 isoform X6
ankyrin repeat domain-containing protein 12 isoform X5
NADH:ubiquinone oxidoreductase core subunit V2
NADH dehydrogenase [ubiquinone] flavoprotein 2, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
microtubule crosslinking factor 1, transcript variant X1
microtubule crosslinking factor 1, transcript variant X2
microtubule cross-linking factor 1 isoform X1
microtubule cross-linking factor 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
protein tyrosine phosphatase receptor type M, transcript variant X1
protein tyrosine phosphatase receptor type M, transcript variant X4
protein tyrosine phosphatase receptor type M, transcript variant X3
protein tyrosine phosphatase receptor type M, transcript variant X2
protein tyrosine phosphatase receptor type M, transcript variant X5
receptor-type tyrosine-protein phosphatase mu isoform X4
receptor-type tyrosine-protein phosphatase mu isoform X3
receptor-type tyrosine-protein phosphatase mu isoform X2
receptor-type tyrosine-protein phosphatase mu isoform X1
receptor-type tyrosine-protein phosphatase mu isoform X5
leucine-rich repeat-containing protein 30
Rho GTPase activating protein 28, transcript variant X1
Rho GTPase activating protein 28, transcript variant X3
Rho GTPase activating protein 28, transcript variant X2
Rho GTPase activating protein 28, transcript variant X4
Rho GTPase activating protein 28, transcript variant X5
rho GTPase-activating protein 28 isoform X3
rho GTPase-activating protein 28 isoform X1
rho GTPase-activating protein 28 isoform X4
rho GTPase-activating protein 28 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00548
COORDINATES: nucleotide motif:Rfam:12.0:RF00424
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 2% coverage of the annotated genomic feature by RNAseq alignments
L3MBTL histone methyl-lysine binding protein 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
L3MBTL histone methyl-lysine binding protein 4, transcript variant X2
L3MBTL histone methyl-lysine binding protein 4, transcript variant X1
L3MBTL histone methyl-lysine binding protein 4, transcript variant X5
L3MBTL histone methyl-lysine binding protein 4, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
L3MBTL histone methyl-lysine binding protein 4, transcript variant X6
L3MBTL histone methyl-lysine binding protein 4, transcript variant X4
lethal(3)malignant brain tumor-like protein 4 isoform X1
lethal(3)malignant brain tumor-like protein 4 isoform X2
lethal(3)malignant brain tumor-like protein 4 isoform X4
lethal(3)malignant brain tumor-like protein 4 isoform X3
erythrocyte membrane protein band 4.1 like 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 121 ESTs, 58 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
erythrocyte membrane protein band 4.1 like 3, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 111 ESTs, 39 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
erythrocyte membrane protein band 4.1 like 3, transcript variant X7
erythrocyte membrane protein band 4.1 like 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 ESTs, 58 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
erythrocyte membrane protein band 4.1 like 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 102 ESTs, 58 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
erythrocyte membrane protein band 4.1 like 3, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 119 ESTs, 38 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
erythrocyte membrane protein band 4.1 like 3, transcript variant X6
erythrocyte membrane protein band 4.1 like 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 138 ESTs, 39 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
erythrocyte membrane protein band 4.1 like 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 111 ESTs, 37 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
erythrocyte membrane protein band 4.1 like 3, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 134 ESTs, 37 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
erythrocyte membrane protein band 4.1 like 3, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 155 ESTs, 43 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
erythrocyte membrane protein band 4.1 like 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 9% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain containing 14, transcript variant X1
zinc finger and BTB domain containing 14, transcript variant X2
zinc finger and BTB domain-containing protein 14
uncharacterized LOC123621896, transcript variant X1
uncharacterized LOC123621896, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 ESTs, 1 Protein, and 52% coverage of the annotated genomic feature by RNAseq alignments
small nucleolar RNA SNORA42/SNORA80 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00406
uncharacterized LOC123621894, transcript variant X10
uncharacterized LOC123621894, transcript variant X8
uncharacterized LOC123621894, transcript variant X9
uncharacterized LOC123621894, transcript variant X3
uncharacterized LOC123621894, transcript variant X7
uncharacterized LOC123621894, transcript variant X6
uncharacterized LOC123621894, transcript variant X20
uncharacterized LOC123621894, transcript variant X19
uncharacterized LOC123621894, transcript variant X15
uncharacterized LOC123621894, transcript variant X2
uncharacterized LOC123621894, transcript variant X11
uncharacterized LOC123621894, transcript variant X18
uncharacterized LOC123621894, transcript variant X22
uncharacterized LOC123621894, transcript variant X5
uncharacterized LOC123621894, transcript variant X21
uncharacterized LOC123621894, transcript variant X12
uncharacterized LOC123621894, transcript variant X4
uncharacterized LOC123621894, transcript variant X17
uncharacterized LOC123621894, transcript variant X16
uncharacterized LOC123621894, transcript variant X14
uncharacterized LOC123621894, transcript variant X13
uncharacterized protein LOC123621894 isoform X5
uncharacterized protein LOC123621894 isoform X2
uncharacterized protein LOC123621894 isoform X6
uncharacterized protein LOC123621894 isoform X4
uncharacterized protein LOC123621894 isoform X3
uncharacterized LOC123621894, transcript variant X1
uncharacterized protein LOC123621894 isoform X1
uncharacterized LOC123621563, transcript variant X2
uncharacterized LOC123621563, transcript variant X1
TGFB induced factor homeobox 1, transcript variant X1
TGFB induced factor homeobox 1, transcript variant X3
TGFB induced factor homeobox 1, transcript variant X5
TGFB induced factor homeobox 1, transcript variant X4
TGFB induced factor homeobox 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 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: 45 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phosphatidate phosphatase LPIN2 isoform X1
phosphatidate phosphatase LPIN2 isoform X2
phosphatidate phosphatase LPIN2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
structural maintenance of chromosomes flexible hinge domain containing 1, transcript variant X2
structural maintenance of chromosomes flexible hinge domain containing 1, transcript variant X1
structural maintenance of chromosomes flexible hinge domain-containing protein 1 isoform X2
structural maintenance of chromosomes flexible hinge domain-containing protein 1 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
methyltransferase 4, N6-adenosine, transcript variant X1
methyltransferase 4, N6-adenosine, transcript variant X2
methyltransferase 4, N6-adenosine, transcript variant X3
N(6)-adenine-specific methyltransferase METTL4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
iron-sulfur cluster assembly enzyme ISCU, mitochondrial-like
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: iron-sulfur cluster assembly enzyme ISCU, mitochondrial-like
adenylate cyclase activating polypeptide 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 3 ESTs, 8 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
pituitary adenylate cyclase-activating polypeptide
YES proto-oncogene 1, Src family tyrosine kinase
enolase superfamily member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
enolase superfamily member 1, transcript variant X1
enolase superfamily member 1, transcript variant X4
mitochondrial enolase superfamily member 1 isoform X1
mitochondrial enolase superfamily member 1 isoform X3
enolase superfamily member 1, transcript variant X3
mitochondrial enolase superfamily member 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 14 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
collectin subfamily member 12, transcript variant X1
collectin subfamily member 12, transcript variant X2
ubiquitin specific peptidase 14, transcript variant X1
ubiquitin specific peptidase 14, transcript variant X3
ubiquitin specific peptidase 14, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 14 isoform X3
ubiquitin carboxyl-terminal hydrolase 14 isoform X1
ubiquitin carboxyl-terminal hydrolase 14 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Rho associated coiled-coil containing protein kinase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
GREB1 like retinoic acid receptor coactivator, transcript variant X1
GREB1 like retinoic acid receptor coactivator, transcript variant X3
GREB1 like retinoic acid receptor coactivator, transcript variant X4
GREB1 like retinoic acid receptor coactivator, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
GREB1 like retinoic acid receptor coactivator, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00153
establishment of sister chromatid cohesion N-acetyltransferase 1, transcript variant X1
establishment of sister chromatid cohesion N-acetyltransferase 1, transcript variant X2
establishment of sister chromatid cohesion N-acetyltransferase 1, transcript variant X3
establishment of sister chromatid cohesion N-acetyltransferase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
small nuclear ribonucleoprotein D1 polypeptide, transcript variant X1
small nuclear ribonucleoprotein D1 polypeptide, transcript variant X2
small nuclear ribonucleoprotein Sm D1 isoform X1
small nuclear ribonucleoprotein Sm D1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
abhydrolase domain containing 3, phospholipase
uncharacterized LOC123621914, transcript variant X3
uncharacterized LOC123621914, transcript variant X1
uncharacterized LOC123621914, transcript variant X2
uncharacterized LOC123621914, transcript variant X4
glyceraldehyde-3-phosphate dehydrogenase-like
GATA binding protein 6, transcript variant X2
GATA binding protein 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
RB binding protein 8, endonuclease, transcript variant X3
uncharacterized LOC123621487, transcript variant X1
uncharacterized LOC123621487, transcript variant X3
uncharacterized LOC123621487, transcript variant X2
RB binding protein 8, endonuclease, transcript variant X1
RB binding protein 8, endonuclease, transcript variant X2
Cdk5 and Abl enzyme substrate 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 64 ESTs, 10 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CDK5 and ABL1 enzyme substrate 1 isoform X1
Cdk5 and Abl enzyme substrate 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 45 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CDK5 and ABL1 enzyme substrate 1 isoform X2
transmembrane protein 241, 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 1 sample with support for all annotated introns
transmembrane protein 241, transcript variant X4
transmembrane protein 241, transcript variant X10
transmembrane protein 241, transcript variant X11
transmembrane protein 241, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane protein 241, transcript variant X1
transmembrane protein 241, transcript variant X5
transmembrane protein 241, transcript variant X6
transmembrane protein 241, transcript variant X7
COORDINATES: nucleotide motif:Rfam:12.0:RF00066
transmembrane protein 241, transcript variant X3
transmembrane protein 241, transcript variant X12
transmembrane protein 241, transcript variant X9
transmembrane protein 241, transcript variant X13
transmembrane protein 241, transcript variant X14
NPC intracellular cholesterol transporter 1, transcript variant X2
NPC intracellular cholesterol transporter 1, transcript variant X1
NPC intracellular cholesterol transporter 1 isoform X2
NPC intracellular cholesterol transporter 1 isoform X1
NPC intracellular cholesterol transporter 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 150 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NPC intracellular cholesterol transporter 1 isoform X3
ankyrin repeat domain 29, transcript variant X4
ankyrin repeat domain 29, transcript variant X2
ankyrin repeat domain 29, transcript variant X3
ankyrin repeat domain 29, transcript variant X1
ankyrin repeat domain-containing protein 29 isoform X4
ankyrin repeat domain-containing protein 29 isoform X2
ankyrin repeat domain-containing protein 29 isoform X3
ankyrin repeat domain-containing protein 29 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs, and 77% 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: 1 EST, 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
laminin subunit alpha-3-like, transcript variant X1
laminin subunit alpha-3-like, transcript variant X2
calcium binding tyrosine phosphorylation regulated, transcript variant X2
calcium binding tyrosine phosphorylation regulated, transcript variant X1
calcium-binding tyrosine phosphorylation-regulated protein
calcium-binding tyrosine phosphorylation-regulated protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
oxysterol binding protein like 1A, transcript variant X1
oxysterol binding protein like 1A, transcript variant X2
oxysterol binding protein like 1A, transcript variant X5
oxysterol binding protein like 1A, transcript variant X4
oxysterol binding protein like 1A, transcript variant X3
oxysterol-binding protein-related protein 1 isoform X1
oxysterol-binding protein-related protein 1 isoform X2
oxysterol-binding protein-related protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 51% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 521, transcript variant X2
zinc finger protein 521, transcript variant X1
SS18 subunit of BAF chromatin remodeling complex, transcript variant X4
SS18 subunit of BAF chromatin remodeling complex, transcript variant X2
SS18 subunit of BAF chromatin remodeling complex, transcript variant X1
SS18 subunit of BAF chromatin remodeling complex, transcript variant X3
SS18 subunit of BAF chromatin remodeling complex, transcript variant X5
proteasome 20S subunit alpha 8, transcript variant X2
proteasome 20S subunit alpha 8, transcript variant X1
proteasome 20S subunit alpha 8, transcript variant X3
proteasome subunit alpha-type 8 isoform X1
proteasome subunit alpha-type 8 isoform X2
proteasome subunit alpha-type 8 isoform X3
TATA-box binding protein associated factor 4b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 ESTs, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
transcription initiation factor TFIID subunit 4B
potassium channel tetramerization domain containing 1, transcript variant X2
potassium channel tetramerization domain containing 1, transcript variant X3
potassium channel tetramerization domain containing 1, transcript variant X1
BTB/POZ domain-containing protein KCTD1 isoform X1
BTB/POZ domain-containing protein KCTD1 isoform X2
carbohydrate sulfotransferase 9, transcript variant X2
carbohydrate sulfotransferase 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 ESTs, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins
small nucleolar RNA SNORA64/SNORA10 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00264
beta-1,4-galactosyltransferase 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 25 ESTs, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
beta-1,4-galactosyltransferase 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 28 ESTs, 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
beta-1,4-galactosyltransferase 6 isoform X1
beta-1,4-galactosyltransferase 6 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
trafficking protein particle complex subunit 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 125, transcript variant X2
ring finger protein 125, transcript variant X3
ring finger protein 125, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E3 ubiquitin-protein ligase RNF125 isoform X2
E3 ubiquitin-protein ligase RNF125 isoform X3
E3 ubiquitin-protein ligase RNF125 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00324
ring finger protein 138, transcript variant X2
ring finger protein 138, transcript variant X1
ring finger protein 138, transcript variant X3
E3 ubiquitin-protein ligase RNF138 isoform X1
E3 ubiquitin-protein ligase RNF138 isoform X2
E3 ubiquitin-protein ligase RNF138 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 6 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
GRB2 associated regulator of MAPK1 subtype 1, transcript variant X2
GRB2 associated regulator of MAPK1 subtype 1, transcript variant X1
GRB2 associated regulator of MAPK1 subtype 1, transcript variant X3
GRB2-associated and regulator of MAPK protein 1 isoform X2
GRB2-associated and regulator of MAPK protein 1 isoform X1
GRB2-associated and regulator of MAPK protein 1 isoform X3
cytochrome c oxidase subunit 7B, mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
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: cytochrome c oxidase subunit 7B, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 178
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
nucleolar protein 4, transcript variant X1
nucleolar protein 4, transcript variant X2
nucleolar protein 4, transcript variant X4
nucleolar protein 4, transcript variant X3
nucleolar protein 4, transcript variant X6
nucleolar protein 4, transcript variant X5
dystrobrevin alpha, transcript variant X3
dystrobrevin alpha, transcript variant X5
dystrobrevin alpha, transcript variant X12
dystrobrevin alpha, transcript variant X13
dystrobrevin alpha, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dystrobrevin alpha, transcript variant X18
dystrobrevin alpha, transcript variant X20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dystrobrevin alpha, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dystrobrevin alpha, transcript variant X16
dystrobrevin alpha, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dystrobrevin alpha, transcript variant X21
dystrobrevin alpha, transcript variant X23
dystrobrevin alpha, transcript variant X26
dystrobrevin alpha, transcript variant X4
dystrobrevin alpha, transcript variant X2
dystrobrevin alpha, transcript variant X15
dystrobrevin alpha, transcript variant X25
dystrobrevin alpha, transcript variant X28
dystrobrevin alpha, transcript variant X7
dystrobrevin alpha, transcript variant X6
dystrobrevin alpha, transcript variant X9
dystrobrevin alpha, transcript variant X10
dystrobrevin alpha, transcript variant X8
dystrobrevin alpha, transcript variant X1
dystrobrevin alpha, transcript variant X14
dystrobrevin alpha, transcript variant X24
dystrobrevin alpha, transcript variant X27
dystrobrevin alpha, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
microtubule associated protein RP/EB family member 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 232 ESTs, 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
microtubule associated protein RP/EB family member 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 ESTs, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
microtubule associated protein RP/EB family member 2, transcript variant X4
microtubule-associated protein RP/EB family member 2 isoform X4
microtubule-associated protein RP/EB family member 2 isoform X2
microtubule associated protein RP/EB family member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 463 ESTs, 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
microtubule associated protein RP/EB family member 2, transcript variant X3
microtubule-associated protein RP/EB family member 2 isoform X3
microtubule-associated protein RP/EB family member 2 isoform X1
microtubule associated protein RP/EB family member 2, transcript variant X6
microtubule-associated protein RP/EB family member 2 isoform X6
microtubule-associated protein RP/EB family member 2 isoform X5
zinc finger and SCAN domain containing 30, transcript variant X4
zinc finger and SCAN domain containing 30, transcript variant X2
zinc finger and SCAN domain containing 30, transcript variant X3
zinc finger and SCAN domain containing 30, transcript variant X1
zinc finger and SCAN domain-containing protein 30 isoform X1
zinc finger and SCAN domain-containing protein 30 isoform X2
zinc finger and SCAN domain containing 30, transcript variant X5
zinc finger and SCAN domain-containing protein 30 isoform X3
zinc finger protein 271, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 ESTs, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 271, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 ESTs, 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 24, transcript variant X2
zinc finger protein 24, transcript variant X4
zinc finger protein 24, transcript variant X3
zinc finger protein 24, transcript variant X1
zinc finger protein 396, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 396, transcript variant X1
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 1 sample with support for all annotated introns
zinc finger protein 396, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
translationally-controlled tumor protein-like
polypeptide N-acetylgalactosaminyltransferase 1
regulation of nuclear pre-mRNA domain containing 1A, transcript variant X1
regulation of nuclear pre-mRNA domain containing 1A, transcript variant X2
regulation of nuclear pre-mRNA domain containing 1A, transcript variant X5
regulation of nuclear pre-mRNA domain-containing protein 1A isoform X1
regulation of nuclear pre-mRNA domain-containing protein 1A isoform X4
regulation of nuclear pre-mRNA domain containing 1A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 178 ESTs, 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulation of nuclear pre-mRNA domain-containing protein 1A isoform X2
regulation of nuclear pre-mRNA domain containing 1A, transcript variant X4
regulation of nuclear pre-mRNA domain-containing protein 1A isoform X3
solute carrier family 39 member 6, transcript variant X1
solute carrier family 39 member 6, transcript variant X2
elongator acetyltransferase complex subunit 2, transcript variant X1
elongator acetyltransferase complex subunit 2, transcript variant X2
molybdenum cofactor sulfurase, transcript variant X1
molybdenum cofactor sulfurase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
molybdenum cofactor sulfurase isoform X1
molybdenum cofactor sulfurase isoform X2
formin homology 2 domain containing 3, transcript variant X1
formin homology 2 domain containing 3, transcript variant X8
formin homology 2 domain containing 3, transcript variant X10
formin homology 2 domain containing 3, transcript variant X2
formin homology 2 domain containing 3, transcript variant X4
formin homology 2 domain containing 3, transcript variant X3
formin homology 2 domain containing 3, transcript variant X5
formin homology 2 domain containing 3, transcript variant X13
formin homology 2 domain containing 3, transcript variant X6
formin homology 2 domain containing 3, transcript variant X7
formin homology 2 domain containing 3, transcript variant X9
formin homology 2 domain containing 3, transcript variant X11
formin homology 2 domain containing 3, transcript variant X12
FH1/FH2 domain-containing protein 3 isoform X1
FH1/FH2 domain-containing protein 3 isoform X2
FH1/FH2 domain-containing protein 3 isoform X4
FH1/FH2 domain-containing protein 3 isoform X3
FH1/FH2 domain-containing protein 3 isoform X5
FH1/FH2 domain-containing protein 3 isoform X13
FH1/FH2 domain-containing protein 3 isoform X6
FH1/FH2 domain-containing protein 3 isoform X7
FH1/FH2 domain-containing protein 3 isoform X8
FH1/FH2 domain-containing protein 3 isoform X9
FH1/FH2 domain-containing protein 3 isoform X10
FH1/FH2 domain-containing protein 3 isoform X11
FH1/FH2 domain-containing protein 3 isoform X12
tubulin polyglutamylase complex subunit 2
KIAA1328 ortholog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
KIAA1328 ortholog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
CUGBP Elav-like family member 4, transcript variant X49
CUGBP Elav-like family member 4, transcript variant X10
CUGBP Elav-like family member 4, transcript variant X8
CUGBP Elav-like family member 4, transcript variant X7
CUGBP Elav-like family member 4, transcript variant X9
CUGBP Elav-like family member 4, transcript variant X19
CUGBP Elav-like family member 4, transcript variant X5
CUGBP Elav-like family member 4, transcript variant X4
CUGBP Elav-like family member 4, transcript variant X3
CUGBP Elav-like family member 4 isoform X10
CUGBP Elav-like family member 4 isoform X8
CUGBP Elav-like family member 4 isoform X7
CUGBP Elav-like family member 4 isoform X9
CUGBP Elav-like family member 4 isoform X19
CUGBP Elav-like family member 4 isoform X49
CUGBP Elav-like family member 4 isoform X5
CUGBP Elav-like family member 4 isoform X4
CUGBP Elav-like family member 4 isoform X3
CUGBP Elav-like family member 4, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 1 Protein, and 40% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 ESTs, 2 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 ESTs, 1 Protein, and 46% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 21 ESTs, 1 Protein, and 46% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4 isoform X11
CUGBP Elav-like family member 4 isoform X6
CUGBP Elav-like family member 4 isoform X2
CUGBP Elav-like family member 4 isoform X1
CUGBP Elav-like family member 4, transcript variant X26
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 21 ESTs, 16 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X50
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 4 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X41
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 2 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X40
CUGBP Elav-like family member 4, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 4 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X36
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 3 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X39
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 ESTs, 3 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X31
CUGBP Elav-like family member 4, transcript variant X32
CUGBP Elav-like family member 4, transcript variant X29
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 ESTs, 5 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 ESTs, 6 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X37
CUGBP Elav-like family member 4, transcript variant X38
CUGBP Elav-like family member 4, transcript variant X34
CUGBP Elav-like family member 4, transcript variant X48
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 21 ESTs, 3 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X35
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 21 ESTs, 3 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X46
CUGBP Elav-like family member 4, transcript variant X47
CUGBP Elav-like family member 4, transcript variant X30
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 21 ESTs, 3 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X45
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 21 ESTs, 4 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 21 ESTs, 5 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X33
CUGBP Elav-like family member 4, transcript variant X28
CUGBP Elav-like family member 4, transcript variant X24
CUGBP Elav-like family member 4, transcript variant X27
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 ESTs, 2 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X21
CUGBP Elav-like family member 4, transcript variant X20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 ESTs, 4 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 ESTs, 5 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 20 ESTs, 5 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 2 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X44
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 21 ESTs, 2 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X23
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 21 ESTs, 2 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 21 ESTs, 2 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X43
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 21 ESTs, 2 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 21 ESTs, 3 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X42
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 21 ESTs, 3 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 21 ESTs, 6 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
CUGBP Elav-like family member 4 isoform X41
CUGBP Elav-like family member 4 isoform X40
CUGBP Elav-like family member 4 isoform X22
CUGBP Elav-like family member 4 isoform X36
CUGBP Elav-like family member 4 isoform X39
CUGBP Elav-like family member 4 isoform X31
CUGBP Elav-like family member 4 isoform X32
CUGBP Elav-like family member 4 isoform X29
CUGBP Elav-like family member 4 isoform X14
CUGBP Elav-like family member 4 isoform X37
CUGBP Elav-like family member 4 isoform X38
CUGBP Elav-like family member 4 isoform X34
CUGBP Elav-like family member 4 isoform X48
CUGBP Elav-like family member 4 isoform X35
CUGBP Elav-like family member 4 isoform X26
CUGBP Elav-like family member 4 isoform X46
CUGBP Elav-like family member 4 isoform X47
CUGBP Elav-like family member 4 isoform X30
CUGBP Elav-like family member 4 isoform X45
CUGBP Elav-like family member 4 isoform X13
CUGBP Elav-like family member 4 isoform X33
CUGBP Elav-like family member 4 isoform X28
CUGBP Elav-like family member 4 isoform X24
CUGBP Elav-like family member 4 isoform X27
CUGBP Elav-like family member 4 isoform X21
CUGBP Elav-like family member 4 isoform X20
CUGBP Elav-like family member 4 isoform X12
CUGBP Elav-like family member 4 isoform X16
CUGBP Elav-like family member 4 isoform X25
CUGBP Elav-like family member 4 isoform X50
CUGBP Elav-like family member 4 isoform X44
CUGBP Elav-like family member 4 isoform X23
CUGBP Elav-like family member 4 isoform X18
CUGBP Elav-like family member 4 isoform X43
CUGBP Elav-like family member 4 isoform X17
CUGBP Elav-like family member 4 isoform X42
CUGBP Elav-like family member 4 isoform X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 26 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
phosphatidylinositol 3-kinase catalytic subunit type 3, transcript variant X1
phosphatidylinositol 3-kinase catalytic subunit type 3, transcript variant X2
phosphatidylinositol 3-kinase catalytic subunit type 3 isoform X1
phosphatidylinositol 3-kinase catalytic subunit type 3 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00217
SET binding protein 1, transcript variant X2
SET binding protein 1, transcript variant X1
SET binding protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 14 member 1 (Kidd blood group), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 17 ESTs, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 14 member 1 (Kidd blood group), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 17 ESTs, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 14 member 1 (Kidd blood group), transcript variant X2
solute carrier family 14 member 1 (Kidd blood group), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 17 ESTs, 31 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: 4 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
ectopic P-granules autophagy protein 5 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 ESTs, 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ectopic P-granules autophagy protein 5 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ectopic P granules protein 5 homolog isoform X2
ectopic P granules protein 5 homolog isoform X1
ectopic P-granules autophagy protein 5 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 ESTs, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ectopic P granules protein 5 homolog isoform X3
proline-serine-threonine phosphatase interacting protein 2
proline-serine-threonine phosphatase-interacting protein 2
ATP synthase subunit alpha, mitochondrial
HAUS augmin like complex subunit 1, transcript variant X2
HAUS augmin like complex subunit 1, transcript variant X1
HAUS augmin-like complex subunit 1 isoform X1
HAUS augmin-like complex subunit 1 isoform X2
chromosome 16 C18orf25 homolog, transcript variant X1
chromosome 16 C18orf25 homolog, transcript variant X2
uncharacterized protein C18orf25 homolog isoform X1
uncharacterized protein C18orf25 homolog isoform X2
ring finger protein 165, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 8% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 165, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase RNF165 isoform X1
E3 ubiquitin-protein ligase RNF165 isoform X2
lipoxygenase homology PLAT domains 1, transcript variant X2
lipoxygenase homology domain-containing protein 1 isoform X2
lipoxygenase homology PLAT domains 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 13% coverage of the annotated genomic feature by RNAseq alignments
lipoxygenase homology domain-containing protein 1 isoform X1
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5, transcript variant X2
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5, transcript variant X1
alpha-2,8-sialyltransferase 8E isoform X2
alpha-2,8-sialyltransferase 8E isoform X1
uncharacterized LOC123621744, transcript variant X3
uncharacterized LOC123621744, transcript variant X2
uncharacterized LOC123621744, transcript variant X5
uncharacterized LOC123621744, transcript variant X1
uncharacterized LOC123621744, transcript variant X4
protein inhibitor of activated STAT 2, transcript variant X5
protein inhibitor of activated STAT 2, transcript variant X2
protein inhibitor of activated STAT 2, transcript variant X1
protein inhibitor of activated STAT 2, transcript variant X3
protein inhibitor of activated STAT 2, transcript variant X4
protein inhibitor of activated STAT 2, transcript variant X6
katanin catalytic subunit A1 like 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
katanin catalytic subunit A1 like 2, transcript variant X3
katanin catalytic subunit A1 like 2, transcript variant X1
katanin catalytic subunit A1 like 2, transcript variant X4
katanin catalytic subunit A1 like 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
katanin p60 ATPase-containing subunit A-like 2 isoform X1
katanin p60 ATPase-containing subunit A-like 2 isoform X2
katanin p60 ATPase-containing subunit A-like 2 isoform X3
katanin catalytic subunit A1 like 2, transcript variant X7
katanin catalytic subunit A1 like 2, transcript variant X8
katanin catalytic subunit A1 like 2, transcript variant X9
katanin catalytic subunit A1 like 2, transcript variant X6
katanin p60 ATPase-containing subunit A-like 2 isoform X4
katanin p60 ATPase-containing subunit A-like 2 isoform X5
haloacid dehalogenase like hydrolase domain containing 2, transcript variant X1
haloacid dehalogenase like hydrolase domain containing 2, transcript variant X2
haloacid dehalogenase like hydrolase domain containing 2, transcript variant X3
haloacid dehalogenase-like hydrolase domain-containing protein 2
immediate early response 3 interacting protein 1
immediate early response 3-interacting protein 1
SKI family transcriptional corepressor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins
SMAD family member 2, transcript variant X2
SMAD family member 2, transcript variant X1
SMAD family member 2, transcript variant X3
SMAD family member 2, transcript variant X4
SMAD family member 2, transcript variant X5
mothers against decapentaplegic homolog 2
zinc finger and BTB domain containing 7C
zinc finger and BTB domain-containing protein 7C
cap binding complex dependent translation initiation factor
CBP80/20-dependent translation initiation factor
SMAD family member 7, transcript variant X2
SMAD family member 7, transcript variant X1
SMAD family member 7, transcript variant X3
mothers against decapentaplegic homolog 7 isoform X3
mothers against decapentaplegic homolog 7 isoform X2
mothers against decapentaplegic homolog 7 isoform X1
uncharacterized LOC123621785, transcript variant X1
uncharacterized LOC123621785, transcript variant X2
chromosome 16 C18orf32 homolog, transcript variant X2
chromosome 16 C18orf32 homolog, transcript variant X4
chromosome 16 C18orf32 homolog, transcript variant X3
chromosome 16 C18orf32 homolog, transcript variant X1
60S ribosomal protein L17, transcript variant X1
60S ribosomal protein L17, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00151
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 12 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123621944, transcript variant X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00492
COORDINATES: nucleotide motif:Rfam:12.0:RF00283
uncharacterized LOC123621944, transcript variant X3
uncharacterized LOC123621944, transcript variant X5
uncharacterized LOC123621944, transcript variant X1
uncharacterized LOC123621944, transcript variant X2
cilia and flagella associated protein 53
cilia- and flagella-associated protein 53
methyl-CpG binding domain protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 226 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
methyl-CpG-binding domain protein 1 isoform X4
methyl-CpG binding domain protein 1, transcript variant X10
methyl-CpG binding domain protein 1, transcript variant X9
methyl-CpG binding domain protein 1, transcript variant X11
methyl-CpG binding domain protein 1, transcript variant X2
methyl-CpG binding domain protein 1, transcript variant X8
methyl-CpG binding domain protein 1, transcript variant X3
methyl-CpG binding domain protein 1, transcript variant X1
methyl-CpG binding domain protein 1, transcript variant X5
methyl-CpG-binding domain protein 1 isoform X7
methyl-CpG-binding domain protein 1 isoform X2
methyl-CpG-binding domain protein 1 isoform X1
methyl-CpG-binding domain protein 1 isoform X8
methyl-CpG-binding domain protein 1 isoform X3
methyl-CpG binding domain protein 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 228 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
methyl-CpG binding domain protein 1, transcript variant X6
methyl-CpG-binding domain protein 1 isoform X9
methyl-CpG-binding domain protein 1 isoform X6
methyl-CpG-binding domain protein 1 isoform X5
CXXC finger protein 1, transcript variant X5
CXXC finger protein 1, transcript variant X4
CXXC finger protein 1, transcript variant X3
CXXC finger protein 1, transcript variant X2
CXXC finger protein 1, transcript variant X1
CXXC-type zinc finger protein 1 isoform X4
CXXC-type zinc finger protein 1 isoform X3
CXXC-type zinc finger protein 1 isoform X2
CXXC-type zinc finger protein 1 isoform X1
CXXC-type zinc finger protein 1 isoform X5
spindle and kinetochore associated complex subunit 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
spindle and kinetochore associated complex subunit 1, transcript variant X2
spindle and kinetochore-associated protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 29 ESTs, 8 Proteins, and 93% 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: 1 EST, 2 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00554
NAD-dependent malic enzyme, mitochondrial isoform X1
NAD-dependent malic enzyme, mitochondrial isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00157
elaC ribonuclease Z 1, transcript variant X1
elaC ribonuclease Z 1, transcript variant X2
elaC ribonuclease Z 1, transcript variant X3
SMAD family member 4, transcript variant X2
SMAD family member 4, transcript variant X1
SMAD family member 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 ESTs, 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SMAD family member 4, transcript variant X4
mothers against decapentaplegic homolog 4 isoform X1
mothers against decapentaplegic homolog 4 isoform X2
RNA-binding E3 ubiquitin-protein ligase MEX3C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
methyl-CpG binding domain protein 2, transcript variant X1
methyl-CpG-binding domain protein 2 isoform X1
methyl-CpG binding domain protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 ESTs, 2 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
methyl-CpG-binding domain protein 2 isoform X2
DNA polymerase iota, transcript variant X2
DNA polymerase iota, transcript variant X4
DNA polymerase iota, transcript variant X1
DNA polymerase iota, transcript variant X3
DNA polymerase iota, transcript variant X5
DNA polymerase iota, transcript variant X6
DNA polymerase iota, transcript variant X7
StAR related lipid transfer domain containing 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chromosome 16 C18orf54 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
chromosome 16 C18orf54 homolog, transcript variant X1
chromosome 16 C18orf54 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lung adenoma susceptibility protein 2 isoform X1
lung adenoma susceptibility protein 2 isoform X2
chromosome 16 C18orf54 homolog, transcript variant X4
lung adenoma susceptibility protein 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123621783, transcript variant X1
uncharacterized LOC123621783, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins
coiled-coil domain containing 68, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain containing 68, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain-containing protein 68 isoform X1
coiled-coil domain-containing protein 68 isoform X2
transcription factor 4, transcript variant X9
transcription factor 4, transcript variant X3
transcription factor 4, transcript variant X8
transcription factor 4, transcript variant X4
transcription factor 4, transcript variant X15
transcription factor 4, transcript variant X7
transcription factor 4, transcript variant X5
transcription factor 4, transcript variant X2
transcription factor 4, transcript variant X6
transcription factor 4, transcript variant X1
transcription factor 4, transcript variant X12
transcription factor 4, transcript variant X10
transcription factor 4, transcript variant X11
transcription factor 4, transcript variant X14
transcription factor 4, transcript variant X13
transcription factor 4, transcript variant X20
transcription factor 4, transcript variant X19
transcription factor 4, transcript variant X17
transcription factor 4, transcript variant X18
transcription factor 4, transcript variant X16
thioredoxin like 1, transcript variant X3
thioredoxin like 1, transcript variant X1
thioredoxin like 1, transcript variant X2
uncharacterized LOC123621513, transcript variant X1
uncharacterized LOC123621513, transcript variant X2
WD repeat domain 7, transcript variant X2
WD repeat domain 7, transcript variant X1
WD repeat domain 7, transcript variant X5
WD repeat domain 7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
WD repeat domain 7, transcript variant X3
WD repeat-containing protein 7 isoform X4
WD repeat-containing protein 7 isoform X1
WD repeat-containing protein 7 isoform X3
WD repeat-containing protein 7 isoform X2
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 EST, 11 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
sia-alpha-2,3-Gal-beta-1,4-GlcNAc-R:alpha 2,8-sialyltransferase
uncharacterized LOC123621584, transcript variant X2
uncharacterized LOC123621584, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
asparaginyl-tRNA synthetase 1, transcript variant X1
asparaginyl-tRNA synthetase 1, transcript variant X2
asparagine--tRNA ligase, cytoplasmic isoform X2
asparagine--tRNA ligase, cytoplasmic isoform X1
uncharacterized LOC123621588, transcript variant X1
uncharacterized LOC123621588, transcript variant X2
ATPase phospholipid transporting 8B1, transcript variant X1
ATPase phospholipid transporting 8B1, transcript variant X2
phospholipid-transporting ATPase IC isoform X1
phospholipid-transporting ATPase IC isoform X2
NEDD4 like E3 ubiquitin protein ligase, transcript variant X4
NEDD4 like E3 ubiquitin protein ligase, transcript variant X1
NEDD4 like E3 ubiquitin protein ligase, transcript variant X3
NEDD4 like E3 ubiquitin protein ligase, transcript variant X2
E3 ubiquitin-protein ligase NEDD4-like isoform X1
E3 ubiquitin-protein ligase NEDD4-like isoform X2
E3 ubiquitin-protein ligase NEDD4-like isoform X3
E3 ubiquitin-protein ligase NEDD4-like isoform X4
NEDD4 like E3 ubiquitin protein ligase, transcript variant X6
NEDD4 like E3 ubiquitin protein ligase, transcript variant X7
NEDD4 like E3 ubiquitin protein ligase, transcript variant X8
NEDD4 like E3 ubiquitin protein ligase, transcript variant X5
NEDD4 like E3 ubiquitin protein ligase, transcript variant X9
E3 ubiquitin-protein ligase NEDD4-like isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 2 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
MALT1 paracaspase, transcript variant X1
MALT1 paracaspase, transcript variant X2
mucosa-associated lymphoid tissue lymphoma translocation protein 1 isoform X2
mucosa-associated lymphoid tissue lymphoma translocation protein 1 isoform X1
zinc finger protein 532, transcript variant X2
zinc finger protein 532, transcript variant X1
zinc finger protein 532, transcript variant X4
zinc finger protein 532, transcript variant X5
zinc finger protein 532, transcript variant X6
zinc finger protein 532, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
SEC11 homolog C, signal peptidase complex subunit
signal peptidase complex catalytic subunit SEC11C
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 transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: gastrin-releasing peptide
retina and anterior neural fold homeobox
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 EST, 5 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
lectin, mannose binding 1, transcript variant X3
lectin, mannose binding 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 198 ESTs, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lectin, mannose binding 1, transcript variant X1
collagen and calcium binding EGF domains 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
collagen and calcium binding EGF domains 1, transcript variant X2
collagen and calcium-binding EGF domain-containing protein 1 isoform X1
collagen and calcium-binding EGF domain-containing protein 1 isoform X2
phorbol-12-myristate-13-acetate-induced protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 11% 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, 13 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phosphatidylinositol glycan anchor biosynthesis class N
GPI ethanolamine phosphate transferase 1
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X2
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X1
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X3
RAB11 binding and LisH domain, coiled-coil and HEAT repeat containing, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 ESTs, 1 Protein, and 99% 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: 1 mRNA, 1 EST, 4 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor receptor superfamily member 11A
zinc finger CCHC-type containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 35 ESTs, 8 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger CCHC-type containing 2, transcript variant X2
zinc finger CCHC-type containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 ESTs, 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger CCHC-type containing 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 ESTs, 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger CCHC domain-containing protein 2 isoform X1
zinc finger CCHC-type containing 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger CCHC domain-containing protein 2 isoform X2
PH domain and leucine rich repeat protein phosphatase 1
PH domain leucine-rich repeat-containing protein phosphatase 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: serine incorporator 3-like
3-ketodihydrosphingosine reductase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 295 ESTs, 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
3-ketodihydrosphingosine reductase, transcript variant X3
3-ketodihydrosphingosine reductase, transcript variant X1
3-ketodihydrosphingosine reductase isoform X2
3-ketodihydrosphingosine reductase isoform X1
vacuolar protein sorting-associated protein 4B
serpin family B member 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 ESTs, 4 Proteins
serpin family B member 12, transcript variant X2
serpin family B member 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
serpin family B member 13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
serpin family B member 13, transcript variant X4
serpin family B member 13, transcript variant X3
serpin family B member 13, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins
serpin family B member 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
serpin family B member 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00092
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 44 ESTs, 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
thioredoxin related transmembrane protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein disulfide-isomerase TMX3 isoform X3
thioredoxin related transmembrane protein 3, transcript variant X2
thioredoxin related transmembrane protein 3, transcript variant X1
protein disulfide-isomerase TMX3 isoform X2
protein disulfide-isomerase TMX3 isoform X1
thioredoxin related transmembrane protein 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein disulfide-isomerase TMX3 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 8 ESTs, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain-containing protein 102B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 12 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
suppressor of cytokine signaling 6, transcript variant X2
suppressor of cytokine signaling 6, transcript variant X4
suppressor of cytokine signaling 6, transcript variant X3
suppressor of cytokine signaling 6, transcript variant X1
neuropilin and tolloid like 1, transcript variant X2
neuropilin and tolloid like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 20 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
translocase of inner mitochondrial membrane 21
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
mitochondrial import inner membrane translocase subunit Tim21
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein
uncharacterized protein C18orf63 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 ESTs, 4 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 30 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc binding alcohol dehydrogenase domain containing 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein 516
zinc finger protein 236, transcript variant X2
zinc finger protein 236, transcript variant X3
zinc finger protein 236, transcript variant X1
myelin basic protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 189 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myelin basic protein, transcript variant X2
myelin basic protein, transcript variant X3
myelin basic protein, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 4183 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myelin basic protein, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 13831 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myelin basic protein, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myelin basic protein, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myelin basic protein, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
myelin basic protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 197 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123621772, transcript variant X1
uncharacterized LOC123621772, 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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 9 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
spalt like transcription factor 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 9% coverage of the annotated genomic feature by RNAseq alignments
spalt like transcription factor 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
ATPase phospholipid transporting 9B (putative), transcript variant X1
ATPase phospholipid transporting 9B (putative), transcript variant X2
probable phospholipid-transporting ATPase IIB isoform X1
probable phospholipid-transporting ATPase IIB isoform X2
ATPase phospholipid transporting 9B (putative), transcript variant X3
probable phospholipid-transporting ATPase IIB isoform X3
ATPase phospholipid transporting 9B (putative), transcript variant X4
probable phospholipid-transporting ATPase IIB isoform X4
nuclear factor of activated T cells 1, transcript variant X1
nuclear factor of activated T cells 1, transcript variant X3
nuclear factor of activated T cells 1, transcript variant X4
nuclear factor of activated T-cells, cytoplasmic 1 isoform X1
nuclear factor of activated T-cells, cytoplasmic 1 isoform X3
nuclear factor of activated T-cells, cytoplasmic 1 isoform X4
nuclear factor of activated T cells 1, transcript variant X2
nuclear factor of activated T-cells, cytoplasmic 1 isoform X2
nuclear factor of activated T cells 1, transcript variant X5
nuclear factor of activated T-cells, cytoplasmic 1 isoform X5
uncharacterized LOC123621781, transcript variant X1
uncharacterized LOC123621781, transcript variant X2
CTD phosphatase subunit 1, transcript variant X1
CTD phosphatase subunit 1, transcript variant X2
RNA polymerase II subunit A C-terminal domain phosphatase isoform X1
RNA polymerase II subunit A C-terminal domain phosphatase isoform X2
CTD phosphatase subunit 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 3 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RNA polymerase II subunit A C-terminal domain phosphatase isoform X3
solute carrier family 66 member 2, transcript variant X3
solute carrier family 66 member 2, transcript variant X2
solute carrier family 66 member 2, transcript variant X1
solute carrier family 66 member 2 isoform X2
solute carrier family 66 member 2 isoform X1
solute carrier family 66 member 2 isoform X3
heat shock factor binding protein 1 like 1, transcript variant X2
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 1 sample with support for all annotated introns
heat shock factor binding protein 1 like 1, transcript variant X1
heat shock factor-binding protein 1-like protein 1 isoform X2
heat shock factor-binding protein 1-like protein 1 isoform X1
thioredoxin like 4A, transcript variant X1
thioredoxin like 4A, transcript variant X3
thioredoxin like 4A, transcript variant X2
probable 2-ketogluconate reductase, transcript variant X2
probable 2-ketogluconate reductase, transcript variant X3
probable 2-ketogluconate reductase, transcript variant X1
probable 2-ketogluconate reductase isoform X1
probable 2-ketogluconate reductase, transcript variant X4
probable 2-ketogluconate reductase isoform X2
ribosome binding factor A, transcript variant X3
ribosome binding factor A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
putative ribosome-binding factor A, mitochondrial isoform X3
putative ribosome-binding factor A, mitochondrial isoform X1
ribosome binding factor A, transcript variant X2
putative ribosome-binding factor A, mitochondrial isoform X2
activity-dependent neuroprotector homeobox protein 2 isoform X1
activity-dependent neuroprotector homeobox protein 2 isoform X3
activity-dependent neuroprotector homeobox protein 2 isoform X2
activity-dependent neuroprotector homeobox protein 2 isoform X4
uncharacterized LOC123621671, transcript variant X4
par-6 family cell polarity regulator gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 9 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123621671, transcript variant X5
uncharacterized LOC123621671, transcript variant X1
uncharacterized LOC123621671, transcript variant X2
uncharacterized LOC123621671, transcript variant X3
uncharacterized LOC123621786, transcript variant X3
uncharacterized LOC123621786, transcript variant X2
uncharacterized LOC123621786, transcript variant X7
uncharacterized LOC123621786, transcript variant X1
uncharacterized LOC123621786, transcript variant X5
uncharacterized LOC123621786, transcript variant X4
uncharacterized LOC123621786, transcript variant X6
uncharacterized LOC123621787, transcript variant X3
uncharacterized LOC123621787, transcript variant X2
uncharacterized LOC123621787, transcript variant X5
uncharacterized LOC123621787, transcript variant X4
uncharacterized LOC123621787, transcript variant X1
uncharacterized LOC123621865, transcript variant X2
uncharacterized LOC123621865, transcript variant X1
uncharacterized LOC123621866, transcript variant X4
uncharacterized LOC123621866, transcript variant X2
uncharacterized LOC123621866, transcript variant X3
uncharacterized LOC123621866, transcript variant X1