Catharus ustulatus isolate bCatUst1 chromosome 14, bCatUst1.pri.v2, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Archosauria; Dinosauria; Saurischia; Theropoda; Coelurosauria; Aves; Neognathae; Passeriformes; Turdidae; Catharus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM020349.1.\nAssembly name: bCatUst1.pri.v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2020/12/22. The original whole-genome shotgun project has the\naccession WNMQ00000000.2.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 06-AUG-2020\nAssembly Method :: FALCON v. DX 1.9.0; FALCON-Unzip v.\n 6.0.0.47841; purge_dups github v.\n purge_haplotig (bitbucket v1.0.3+\n 1.Nov.2018); Scaff10x v. 2; Bionano Solve\n v. 3.2.1_04122018; Salsa2 HiC v. 2.2;\n Arrow polishing and gap filling v.\n Smrtlink_6.0.0.47841; Longranger Align v.\n 2.2.2; freebayes v. 1.3.1; gEVAL manual\n curation v. 2020-08-06; VGP assembly\n pipeline v. 1.5\nAssembly Name :: bCatUst1.pri.v2\nDiploid :: Principal pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 60.58x\nSequencing Technology :: PacBio Sequel I CLR; Illumina NovaSeq;\n Arima Genomics Hi-C; Bionano Genomics DLS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Catharus ustulatus Annotation\n Release 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
centromere protein A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
centromere protein A, transcript variant X1
centromere protein A, transcript variant X2
centromere protein A, transcript variant X5
centromere protein A, transcript variant X6
centromere protein A, transcript variant X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 2 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: splicing regulator RBM11
histone deacetylase 8, transcript variant X3
histone deacetylase 8, transcript variant X1
histone deacetylase 8, transcript variant X2
histone deacetylase 8, transcript variant X7
histone deacetylase 8, transcript variant X8
histone deacetylase 8, transcript variant X9
histone deacetylase 8, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
histone deacetylase 8, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
histone deacetylase 8, transcript variant X4
phosphorylase kinase regulatory subunit alpha 1, transcript variant X2
phosphorylase kinase regulatory subunit alpha 1, transcript variant X3
phosphorylase kinase regulatory subunit alpha 1, transcript variant X1
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform isoform X3
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform isoform X2
phosphorylase b kinase regulatory subunit alpha, skeletal muscle isoform isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 78% 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
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.
diacylglycerol kinase kappa, transcript variant X1
diacylglycerol kinase kappa, transcript variant X2
diacylglycerol kinase kappa, transcript variant X3
diacylglycerol kinase kappa, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G2/mitotic-specific cyclin-B3 isoform X2
G2/mitotic-specific cyclin-B3 isoform X1
protein eva-1 homolog C-like, transcript variant X2
protein eva-1 homolog C-like, transcript variant X3
protein eva-1 homolog C-like, transcript variant X1
chloride intracellular channel protein 2-like
interferon gamma receptor 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
interferon gamma receptor 1-like isoform X3
interferon gamma receptor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
interferon gamma receptor 1-like, 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 12 samples with support for all annotated introns
uncharacterized protein LOC117003041 isoform X1
uncharacterized protein LOC117003041 isoform X2
TSC22 domain family member 3, transcript variant X2
TSC22 domain family member 3, transcript variant X1
TSC22 domain family protein 3 isoform X2
TSC22 domain family protein 3 isoform X1
probable E3 ubiquitin-protein ligase MID2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
peptidylprolyl cis/trans isomerase, NIMA-interacting 4
peptidyl-prolyl cis-trans isomerase NIMA-interacting 4
ERCC excision repair 6 like, spindle assembly checkpoint helicase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
OCRL inositol polyphosphate-5-phosphatase, transcript variant X1
OCRL inositol polyphosphate-5-phosphatase, transcript variant X2
inositol polyphosphate 5-phosphatase OCRL
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
SAM and SH3 domain containing 3, transcript variant X1
SAM and SH3 domain containing 3, transcript variant X3
SAM and SH3 domain containing 3, transcript variant X2
SAM and SH3 domain-containing protein 3 isoform X1
SAM and SH3 domain-containing protein 3 isoform X3
SAM and SH3 domain-containing protein 3 isoform X2
zinc finger DHHC-type palmitoyltransferase 9
UTP14A small subunit processome component
U3 small nucleolar RNA-associated protein 14 homolog A
uncharacterized protein DKFZp434B061-like
apoptosis inducing factor mitochondria associated 1, transcript variant X3
apoptosis inducing factor mitochondria associated 1, transcript variant X1
apoptosis inducing factor mitochondria associated 1, transcript variant X2
apoptosis-inducing factor 1, mitochondrial isoform X3
apoptosis-inducing factor 1, mitochondrial isoform X1
apoptosis-inducing factor 1, mitochondrial isoform X2
methionyl-tRNA synthetase 2, mitochondrial
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
glucose-dependent insulinotropic receptor
ecto-NOX disulfide-thiol exchanger 2, transcript variant X3
ecto-NOX disulfide-thiol exchanger 2, transcript variant X4
ecto-NOX disulfide-thiol exchanger 2, transcript variant X2
ecto-NOX disulfide-thiol exchanger 2, transcript variant X1
ecto-NOX disulfide-thiol exchanger 2 isoform X1
ecto-NOX disulfide-thiol exchanger 2 isoform X2
Rho GTPase activating protein 36, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Rho GTPase activating protein 36, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
H(+)/Cl(-) exchange transporter 5, transcript variant X9
H(+)/Cl(-) exchange transporter 5, transcript variant X10
H(+)/Cl(-) exchange transporter 5, transcript variant X3
H(+)/Cl(-) exchange transporter 5, transcript variant X7
H(+)/Cl(-) exchange transporter 5, transcript variant X5
H(+)/Cl(-) exchange transporter 5, transcript variant X8
H(+)/Cl(-) exchange transporter 5, transcript variant X4
H(+)/Cl(-) exchange transporter 5, transcript variant X6
H(+)/Cl(-) exchange transporter 5 isoform X3
H(+)/Cl(-) exchange transporter 5 isoform X4
H(+)/Cl(-) exchange transporter 5, transcript variant X1
H(+)/Cl(-) exchange transporter 5, transcript variant X2
H(+)/Cl(-) exchange transporter 5 isoform X1
H(+)/Cl(-) exchange transporter 5 isoform X2
tumor necrosis factor ligand superfamily member 10-like
uncharacterized LOC117002885, transcript variant X2
uncharacterized LOC117002885, transcript variant X1
uncharacterized protein LOC117002885 isoform X2
uncharacterized protein LOC117002885 isoform X1
trimethyllysine hydroxylase, epsilon, transcript variant X1
trimethyllysine hydroxylase, epsilon, transcript variant X2
trimethyllysine dioxygenase, mitochondrial
sprouty RTK signaling antagonist 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sprouty RTK signaling antagonist 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sprouty RTK signaling antagonist 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
sprouty RTK signaling antagonist 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
brain-specific homeobox/POU domain protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
DNA-directed RNA polymerases I and III subunit RPAC2-like
vesicle associated membrane protein 7, transcript variant X1
vesicle associated membrane protein 7, transcript variant X2
vesicle associated membrane protein 7, transcript variant X3
SLAIN motif-containing protein-like, transcript variant X2
SLAIN motif-containing protein-like, transcript variant X1
SLAIN motif-containing protein-like isoform X2
SLAIN motif-containing protein-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
NAD(P) dependent steroid dehydrogenase-like
sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating
glutamine amidotransferase-like class 1 domain-containing protein 3B, mitochondrial
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 5 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 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
TBC1 domain family member 8B, transcript variant X1
TBC1 domain family member 8B, transcript variant X2
PAS domain containing repressor 1, transcript variant X2
PAS domain containing repressor 1, transcript variant X4
PAS domain containing repressor 1, transcript variant X1
PAS domain containing repressor 1, transcript variant X3
PAS domain containing repressor 1, transcript variant X5
circadian clock protein PASD1 isoform X2
circadian clock protein PASD1 isoform X1
circadian clock protein PASD1 isoform X3
vacuolar ATPase assembly integral membrane protein VMA21
high mobility group box 3, transcript variant X1
high mobility group box 3, transcript variant X2
CD99 molecule like 2, transcript variant X2
CD99 molecule like 2, transcript variant X1
myotubularin related protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 ESTs, 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
myotubularin related protein 1, transcript variant X2
myotubularin related protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 ESTs, 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
myotubularin related protein 1, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 ESTs, 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
myotubularin related protein 1, transcript variant X9
myotubularin related protein 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 ESTs, 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
myotubularin related protein 1, transcript variant X7
myotubularin related protein 1, transcript variant X6
myotubularin related protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 ESTs, 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
myotubularin related protein 1, transcript variant X4
myotubularin-related protein 1 isoform X3
myotubularin-related protein 1 isoform X2
myotubularin-related protein 1 isoform X1
mastermind-like domain-containing protein 1
uncharacterized LOC117003063, 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 16 samples with support for all annotated introns
uncharacterized LOC117003063, transcript variant X3
uncharacterized LOC117003063, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
iduronate 2-sulfatase, transcript variant X2
iduronate 2-sulfatase, transcript variant X1
AF4/FMR2 family member 2, transcript variant X3
AF4/FMR2 family member 2, transcript variant X2
AF4/FMR2 family member 2, transcript variant X5
AF4/FMR2 family member 2, transcript variant X1
AF4/FMR2 family member 2, transcript variant X4
fragile X mental retardation 1 neighbor protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% coverage of the annotated genomic feature by RNAseq alignments
FMRP translational regulator 1, transcript variant X4
FMRP translational regulator 1, transcript variant X2
FMRP translational regulator 1, transcript variant X3
FMRP translational regulator 1, transcript variant X1
synaptic functional regulator FMR1 isoform X2
synaptic functional regulator FMR1 isoform X3
synaptic functional regulator FMR1 isoform X1
synaptic functional regulator FMR1 isoform X4
testis-specific serine/threonine-protein kinase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SLIT and NTRK like family member 2, transcript variant X2
SLIT and NTRK like family member 2, transcript variant X1
SLIT and NTRK like family member 4, transcript variant X4
SLIT and NTRK like family member 4, transcript variant X1
SLIT and NTRK like family member 4, transcript variant X3
SLIT and NTRK like family member 4, transcript variant X2
cyclin-dependent kinase inhibitor 1C-like
UAP56-interacting factor-like, transcript variant X3
UAP56-interacting factor-like, transcript variant X2
UAP56-interacting factor-like, transcript variant X1
UAP56-interacting factor-like isoform X3
UAP56-interacting factor-like isoform X2
UAP56-interacting factor-like isoform X1
leucine rich repeats and calponin homology domain containing 2, transcript variant X1
leucine rich repeats and calponin homology domain containing 2, transcript variant X2
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X1
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X2
leucine rich repeats and calponin homology domain containing 2, transcript variant X3
leucine-rich repeat and calponin homology domain-containing protein 2 isoform X3
interleukin 13 receptor subunit alpha 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
interleukin 13 receptor subunit alpha 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
interleukin-13 receptor subunit alpha-2 isoform X2
interleukin-13 receptor subunit alpha-2 isoform X1
5-hydroxytryptamine receptor 2C, transcript variant X3
5-hydroxytryptamine receptor 2C, transcript variant X1
5-hydroxytryptamine receptor 2C, transcript variant X2
glycerophosphodiester phosphodiesterase domain containing 2, transcript variant X1
glycerophosphodiester phosphodiesterase domain containing 2, transcript variant X2
glycerophosphoinositol inositolphosphodiesterase GDPD2 isoform X2
glycerophosphoinositol inositolphosphodiesterase GDPD2 isoform X1
discs large MAGUK scaffold protein 3, transcript variant X1
discs large MAGUK scaffold protein 3, transcript variant X2
discs large MAGUK scaffold protein 3, transcript variant X3
discs large MAGUK scaffold protein 3, transcript variant X5
discs large MAGUK scaffold protein 3, transcript variant X4
discs large MAGUK scaffold protein 3, transcript variant X6
discs large MAGUK scaffold protein 3, transcript variant X8
discs large MAGUK scaffold protein 3, transcript variant X7
solute carrier family 7 member 3, transcript variant X4
solute carrier family 7 member 3, transcript variant X2
solute carrier family 7 member 3, transcript variant X6
solute carrier family 7 member 3, transcript variant X5
solute carrier family 7 member 3, transcript variant X3
solute carrier family 7 member 3, transcript variant X1
solute carrier family 7 member 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
mediator complex subunit 12, transcript variant X3
mediator complex subunit 12, transcript variant X4
mediator complex subunit 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 19 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
mediator complex subunit 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 19 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 12 isoform X1
mediator of RNA polymerase II transcription subunit 12 isoform X2
zinc finger MYM-type containing 3, transcript variant X6
zinc finger MYM-type containing 3, transcript variant X1
zinc finger MYM-type containing 3, transcript variant X2
zinc finger MYM-type containing 3, transcript variant X4
zinc finger MYM-type containing 3, transcript variant X5
zinc finger MYM-type containing 3, transcript variant X3
zinc finger MYM-type protein 3 isoform X2
zinc finger MYM-type protein 3 isoform X1
non-POU domain containing octamer binding, transcript variant X6
non-POU domain containing octamer binding, transcript variant X7
non-POU domain containing octamer binding, transcript variant X2
non-POU domain containing octamer binding, transcript variant X1
non-POU domain containing octamer binding, transcript variant X3
non-POU domain containing octamer binding, transcript variant X4
non-POU domain containing octamer binding, transcript variant X5
non-POU domain-containing octamer-binding protein isoform X1
non-POU domain-containing octamer-binding protein isoform X2
non-POU domain-containing octamer-binding protein isoform X3
non-POU domain-containing octamer-binding protein isoform X4
integrin subunit beta 1 binding protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
rho-related GTP-binding protein RhoG-like, transcript variant X2
rho-related GTP-binding protein RhoG-like, transcript variant X1
rho-related GTP-binding protein RhoG-like, transcript variant X3
rho-related GTP-binding protein RhoG-like, transcript variant X5
rho-related GTP-binding protein RhoG-like, transcript variant X4
rho-related GTP-binding protein RhoG-like, transcript variant X7
rho-related GTP-binding protein RhoG-like, transcript variant X6
rho-related GTP-binding protein RhoG-like
TATA-box binding protein associated factor 1, transcript variant X1
TATA-box binding protein associated factor 1, transcript variant X2
TATA-box binding protein associated factor 1, transcript variant X3
TATA-box binding protein associated factor 1, transcript variant X4
transcription initiation factor TFIID subunit 1 isoform X1
transcription initiation factor TFIID subunit 1 isoform X2
transcription initiation factor TFIID subunit 1 isoform X3
transcription initiation factor TFIID subunit 1 isoform X4
O-linked N-acetylglucosamine (GlcNAc) transferase, transcript variant X3
O-linked N-acetylglucosamine (GlcNAc) transferase, transcript variant X1
O-linked N-acetylglucosamine (GlcNAc) transferase, transcript variant X2
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform X1
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform X2
UDP-N-acetylglucosamine--peptide N-acetylglucosaminyltransferase 110 kDa subunit isoform X3
BRCA1/BRCA2-containing complex subunit 3
C-X9-C motif containing 4, transcript variant X4
C-X9-C motif containing 4, transcript variant X6
C-X9-C motif containing 4, transcript variant X3
cx9C motif-containing protein 4 isoform X3
C-X9-C motif containing 4, transcript variant X1
C-X9-C motif containing 4, transcript variant X2
cx9C motif-containing protein 4 isoform X1
cx9C motif-containing protein 4 isoform X2
C-X9-C motif containing 4, transcript variant X5
cx9C motif-containing protein 4 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
membrane palmitoylated protein 1, transcript variant X1
membrane palmitoylated protein 1, transcript variant X2
55 kDa erythrocyte membrane protein isoform X1
55 kDa erythrocyte membrane protein isoform X2
H/ACA ribonucleoprotein complex subunit DKC1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00137
COORDINATES: nucleotide motif:Rfam:12.0:RF00567
COORDINATES: nucleotide motif:Rfam:12.0:RF00340
tRNA (uracil(54)-C(5))-methyltransferase homolog
aryl-hydrocarbon-interacting protein-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
TATA-box binding protein associated factor 7 like
transcription initiation factor TFIID subunit 7-like
translocase of inner mitochondrial membrane 8A
mitochondrial import inner membrane translocase subunit Tim8 A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 12 ESTs, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
glycine receptor subunit alpha-4, transcript variant X2
glycine receptor subunit alpha-4, transcript variant X1
glycine receptor subunit alpha-4 isoform X2
glycine receptor subunit alpha-4 isoform X1
proteolipid protein 1, transcript variant X1
proteolipid protein 1, transcript variant X2
RAB9B, member RAS oncogene family, transcript variant X2
RAB9B, member RAS oncogene family, transcript variant X1
RAB9B, member RAS oncogene family, transcript variant X3
RAB9B, member RAS oncogene family, transcript variant X4
phosphoribosyl pyrophosphate synthetase 1
FERM and PDZ domain containing 3, transcript variant X1
FERM and PDZ domain containing 3, transcript variant X2
FERM and PDZ domain-containing protein 3 isoform X1
FERM and PDZ domain-containing protein 3 isoform X2
dynein axonemal assembly factor 6, transcript variant X3
dynein axonemal assembly factor 6, transcript variant X1
dynein axonemal assembly factor 6, transcript variant X8
dynein axonemal assembly factor 6, transcript variant X4
dynein axonemal assembly factor 6, transcript variant X7
dynein axonemal assembly factor 6, transcript variant X5
dynein axonemal assembly factor 6, transcript variant X6
dynein axonemal assembly factor 6, transcript variant X2
RNA binding motif protein 41, transcript variant X3
RNA binding motif protein 41, transcript variant X2
RNA binding motif protein 41, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 ESTs, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ripply transcriptional repressor 1, transcript variant X4
ripply transcriptional repressor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ripply transcriptional repressor 1, transcript variant X1
ripply transcriptional repressor 1, 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
ripply transcriptional repressor 1, transcript variant X5
proline rich and Gla domain 3, transcript variant X2
proline rich and Gla domain 3, transcript variant X1
proline rich and Gla domain 3, transcript variant X3
proline rich and Gla domain 3, transcript variant X4
transmembrane gamma-carboxyglutamic acid protein 3 isoform X1
transmembrane gamma-carboxyglutamic acid protein 3 isoform X2
fetal and adult testis-expressed transcript protein
cyclic nucleotide gated channel subunit alpha 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cyclic nucleotide gated channel subunit alpha 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
cyclic nucleotide-gated olfactory channel
zona pellucida sperm-binding protein 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
gamma-aminobutyric acid receptor subunit gamma-4
gamma-aminobutyric acid type A receptor subunit alpha3
gamma-aminobutyric acid receptor subunit alpha-3
gamma-aminobutyric acid receptor subunit beta-4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, 36 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
gamma-aminobutyric acid receptor subunit beta-4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 ESTs, 33 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
gamma-aminobutyric acid receptor subunit beta-4 isoform X1
gamma-aminobutyric acid receptor subunit beta-4 isoform X2
serine/threonine-protein kinase PAK 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
neuronal migration protein doublecortin isoform X4
neuronal migration protein doublecortin isoform X3
neuronal migration protein doublecortin isoform X2
neuronal migration protein doublecortin isoform X1
serine rich and transmembrane domain containing 2
serine-rich and transmembrane domain-containing 2
UDP-N-acetylglucosamine transferase subunit ALG13 homolog
putative bifunctional UDP-N-acetylglucosamine transferase and deubiquitinase ALG13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
transient receptor potential cation channel subfamily C member 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
transient receptor potential cation channel subfamily C member 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
short transient receptor potential channel 5
cytochrome c oxidase subunit 7B, mitochondrial
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: magnesium transporter protein 1
ATRX chromatin remodeler, transcript variant X1
ATRX chromatin remodeler, transcript variant X2
transcriptional regulator ATRX isoform X1
transcriptional regulator ATRX isoform X2
zinc finger DHHC-type palmitoyltransferase 15
uracil phosphoribosyltransferase homolog, transcript variant X3
uracil phosphoribosyltransferase homolog, transcript variant X4
uracil phosphoribosyltransferase homolog, transcript variant X5
uracil phosphoribosyltransferase homolog, transcript variant X2
uracil phosphoribosyltransferase homolog, transcript variant X6
uracil phosphoribosyltransferase homolog, transcript variant X1
uracil phosphoribosyltransferase homolog isoform X3
uracil phosphoribosyltransferase homolog isoform X4
uracil phosphoribosyltransferase homolog isoform X2
uracil phosphoribosyltransferase homolog isoform X5
uracil phosphoribosyltransferase homolog isoform X1
ATP binding cassette subfamily B member 7
iron-sulfur clusters transporter ABCB7, mitochondrial
neurite extension and migration factor, transcript variant X1
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 4 samples with support for all annotated introns
neurite extension and migration factor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
neurite extension and migration factor, transcript variant X2
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 2 samples with support for all annotated introns
neurite extension and migration factor, transcript variant X3
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
neurite extension and migration factor isoform X2
neurite extension and migration factor isoform X1
ring finger protein, LIM domain interacting, transcript variant X2
ring finger protein, LIM domain interacting, transcript variant X3
ring finger protein, LIM domain interacting, transcript variant X1
E3 ubiquitin-protein ligase RLIM isoform X1
E3 ubiquitin-protein ligase RLIM isoform X2
wiskott-Aldrich syndrome protein family member 3-like, transcript variant X1
wiskott-Aldrich syndrome protein family member 3-like, transcript variant X2
wiskott-Aldrich syndrome protein family member 3-like isoform X1
wiskott-Aldrich syndrome protein family member 3-like isoform X2
wiskott-Aldrich syndrome protein family member 3-like, transcript variant X3
wiskott-Aldrich syndrome protein family member 3-like isoform X3
G-protein coupled receptor 12-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 18 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
G-protein coupled receptor 12-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 18 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
G-protein coupled receptor 12-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 18 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
G-protein coupled receptor 12-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 18 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 12-like
ligand of Numb protein X 2-like, transcript variant X2
ligand of Numb protein X 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ligand of Numb protein X 2-like isoform X2
ligand of Numb protein X 2-like isoform X1
pre-mRNA 3'-end-processing factor FIP1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 3 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: pre-mRNA 3'-end-processing factor FIP1-like
cysteine-rich hydrophobic domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 13 Proteins
vascular endothelial growth factor receptor kdr-like
Cdc42 guanine nucleotide exchange factor 9, transcript variant X4
Cdc42 guanine nucleotide exchange factor 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 ESTs, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Cdc42 guanine nucleotide exchange factor 9, transcript variant X10
Cdc42 guanine nucleotide exchange factor 9, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 ESTs, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Cdc42 guanine nucleotide exchange factor 9, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Cdc42 guanine nucleotide exchange factor 9, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 ESTs, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
Cdc42 guanine nucleotide exchange factor 9, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Cdc42 guanine nucleotide exchange factor 9, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Cdc42 guanine nucleotide exchange factor 9, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Cdc42 guanine nucleotide exchange factor 9, transcript variant X12
rho guanine nucleotide exchange factor 9 isoform X4
rho guanine nucleotide exchange factor 9 isoform X9
rho guanine nucleotide exchange factor 9 isoform X7
rho guanine nucleotide exchange factor 9 isoform X10
rho guanine nucleotide exchange factor 9 isoform X11
rho guanine nucleotide exchange factor 9 isoform X8
rho guanine nucleotide exchange factor 9 isoform X1
Cdc42 guanine nucleotide exchange factor 9, transcript variant X5
Cdc42 guanine nucleotide exchange factor 9, transcript variant X3
Cdc42 guanine nucleotide exchange factor 9, transcript variant X2
rho guanine nucleotide exchange factor 9 isoform X5
rho guanine nucleotide exchange factor 9 isoform X3
rho guanine nucleotide exchange factor 9 isoform X2
Cdc42 guanine nucleotide exchange factor 9, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
rho guanine nucleotide exchange factor 9 isoform X6
APC membrane recruitment protein 1, transcript variant X2
APC membrane recruitment protein 1, transcript variant X1
ankyrin repeat and SOCS box containing 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein C8orf48 homolog
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Kruppel like factor 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Kruppel like factor 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Kruppel like factor 8, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Kruppel like factor 8, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
BTB/POZ domain-containing protein KCTD8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
serine/threonine-protein kinase PAK 3, transcript variant X1
serine/threonine-protein kinase PAK 3, transcript variant X2
serine/threonine-protein kinase PAK 3, transcript variant X3
serine/threonine-protein kinase PAK 3, transcript variant X4
AMMECR nuclear protein 1, transcript variant X1
AMMECR nuclear protein 1, transcript variant X2
AMME syndrome candidate gene 1 protein isoform X1
AMME syndrome candidate gene 1 protein isoform X2
transmembrane protein 164, transcript variant X1
transmembrane protein 164, transcript variant X2
transmembrane protein 164, transcript variant X3
uncharacterized LOC117002805, transcript variant X2
uncharacterized LOC117002805, transcript variant X1
acyl-CoA synthetase long chain family member 4, transcript variant X1
acyl-CoA synthetase long chain family member 4, transcript variant X3
acyl-CoA synthetase long chain family member 4, transcript variant X2
acyl-CoA synthetase long chain family member 4, transcript variant X4
long-chain-fatty-acid--CoA ligase 4 isoform X1
long-chain-fatty-acid--CoA ligase 4 isoform X2
nuclear transport factor 2 like export factor 2, transcript variant X2
nuclear transport factor 2 like export factor 2, transcript variant X1
NTF2-related export protein 2 isoform X2
NTF2-related export protein 2 isoform X1
collagen type IV alpha 5 chain, transcript variant X4
collagen type IV alpha 5 chain, transcript variant X2
collagen type IV alpha 5 chain, transcript variant X3
collagen type IV alpha 5 chain, transcript variant X1
collagen type IV alpha 5 chain, transcript variant X5
collagen type IV alpha 6 chain, transcript variant X1
collagen type IV alpha 6 chain, transcript variant X2
autophagy related 4A cysteine peptidase, transcript variant X3
autophagy related 4A cysteine peptidase, transcript variant X2
autophagy related 4A cysteine peptidase, transcript variant X1
26S proteasome non-ATPase regulatory subunit 10
V-set and immunoglobulin domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
V-set and immunoglobulin domain-containing protein 1
synaptotagmin-like protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
synaptotagmin-like protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
VHL binding protein 1, transcript variant X8
VHL binding protein 1, transcript variant X6
VHL binding protein 1, transcript variant X4
VHL binding protein 1, transcript variant X3
VHL binding protein 1, transcript variant X2
VHL binding protein 1, transcript variant X1
VHL binding protein 1, transcript variant X7
VHL binding protein 1, transcript variant X5
GRB2 associated binding protein 3, transcript variant X2
GRB2 associated binding protein 3, transcript variant X1
GRB2-associated-binding protein 3 isoform X2
GRB2-associated-binding protein 3 isoform X1
probable global transcription activator SNF2L1
uncharacterized LOC117002772, 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 6 samples with support for all annotated introns
uncharacterized LOC117002772, transcript variant X1
teneurin transmembrane protein 1, transcript variant X2
teneurin transmembrane protein 1, transcript variant X1
teneurin transmembrane protein 1, transcript variant X4
teneurin transmembrane protein 1, transcript variant X6
teneurin transmembrane protein 1, transcript variant X5
teneurin transmembrane protein 1, transcript variant X3
SH2 domain containing 1A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SH2 domain-containing protein 1A isoform X2
SH2 domain containing 1A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
SH2 domain-containing protein 1A isoform X1
stromal antigen 2, transcript variant X3
stromal antigen 2, transcript variant X1
stromal antigen 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 10 ESTs, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
X-linked inhibitor of apoptosis, transcript variant X6
X-linked inhibitor of apoptosis, transcript variant X3
X-linked inhibitor of apoptosis, transcript variant X4
X-linked inhibitor of apoptosis, transcript variant X1
X-linked inhibitor of apoptosis, transcript variant X2
E3 ubiquitin-protein ligase XIAP isoform X3
E3 ubiquitin-protein ligase XIAP isoform X1
X-linked inhibitor of apoptosis, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
E3 ubiquitin-protein ligase XIAP isoform X2
glutamate ionotropic receptor AMPA type subunit 3, transcript variant X3
glutamate ionotropic receptor AMPA type subunit 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 ESTs, 74 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
glutamate ionotropic receptor AMPA type subunit 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 ESTs, 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
glutamate ionotropic receptor AMPA type subunit 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
glutamate ionotropic receptor AMPA type subunit 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 ESTs, 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
glutamate ionotropic receptor AMPA type subunit 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
C1GALT1 specific chaperone 1, transcript variant X2
C1GALT1 specific chaperone 1, transcript variant X1
C1GALT1 specific chaperone 1, transcript variant X3
C1GALT1 specific chaperone 1, transcript variant X4
lysosomal associated membrane protein 2, transcript variant X1
lysosome-associated membrane glycoprotein 2 isoform X1
lysosomal associated membrane protein 2, transcript variant X2
lysosome-associated membrane glycoprotein 2 isoform X2
ATPase Na+/K+ transporting family member beta 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 255A, transcript variant X2
transmembrane protein 255A, transcript variant X1
zinc finger and BTB domain containing 33, transcript variant X1
zinc finger and BTB domain containing 33, transcript variant X2
transcriptional regulator Kaiso isoform X1
transcriptional regulator Kaiso isoform X2
NADH:ubiquinone oxidoreductase subunit A1
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 1
UPF3B regulator of nonsense mediated mRNA decay
COORDINATES: nucleotide motif:Rfam:12.0:RF00265
sosondowah ankyrin repeat domain family member D
ankyrin repeat domain-containing protein SOWAHD
progesterone receptor membrane component 1
membrane-associated progesterone receptor component 1
KIAA1210 ortholog, transcript variant X2
acrosomal protein KIAA1210 homolog isoform X2
KIAA1210 ortholog, transcript variant X4
KIAA1210 ortholog, transcript variant X3
KIAA1210 ortholog, transcript variant X1
acrosomal protein KIAA1210 homolog isoform X1
acrosomal protein KIAA1210 homolog isoform X3
acrosomal protein KIAA1210 homolog isoform X4
LON peptidase N-terminal domain and ring finger 3
LON peptidase N-terminal domain and RING finger protein 3
family with sequence similarity 199, X-linked
interleukin 1 receptor accessory protein like 2, transcript variant X6
interleukin 1 receptor accessory protein like 2, transcript variant X1
interleukin 1 receptor accessory protein like 2, transcript variant X4
interleukin 1 receptor accessory protein like 2, transcript variant X2
interleukin 1 receptor accessory protein like 2, transcript variant X5
interleukin 1 receptor accessory protein like 2, transcript variant X3
X-linked interleukin-1 receptor accessory protein-like 2 isoform X1
X-linked interleukin-1 receptor accessory protein-like 2 isoform X2
interleukin 1 receptor accessory protein like 2, transcript variant X7
X-linked interleukin-1 receptor accessory protein-like 2 isoform X3
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X1
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X2
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X3
mitogen-activated protein kinase kinase kinase kinase 4-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X1
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X2
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X3
mitogen-activated protein kinase kinase kinase kinase 4-like isoform X4
RPA1 related single stranded DNA binding protein, X-linked
dedicator of cytokinesis 11, transcript variant X2
dedicator of cytokinesis 11, transcript variant X1
dedicator of cytokinesis 11, transcript variant X4
dedicator of cytokinesis protein 11 isoform X2
dedicator of cytokinesis protein 11 isoform X1
dedicator of cytokinesis protein 11 isoform X4
dedicator of cytokinesis 11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
dedicator of cytokinesis protein 11 isoform X3
kelch like family member 13, transcript variant X5
kelch like family member 13, transcript variant X8
kelch like family member 13, transcript variant X3
kelch like family member 13, transcript variant X7
kelch like family member 13, transcript variant X6
kelch like family member 13, transcript variant X4
kelch like family member 13, transcript variant X2
kelch like family member 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins
FERM domain containing 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
FERM domain containing 7, transcript variant X1
FERM domain-containing protein 7 isoform X2
FERM domain-containing protein 7 isoform X1
muscleblind like splicing regulator 3, transcript variant X5
muscleblind like splicing regulator 3, transcript variant X3
muscleblind like splicing regulator 3, transcript variant X6
muscleblind like splicing regulator 3, transcript variant X7
muscleblind like splicing regulator 3, transcript variant X1
muscleblind like splicing regulator 3, transcript variant X4
muscleblind like splicing regulator 3, transcript variant X2
muscleblind like splicing regulator 3, transcript variant X8
PHD finger protein 6, transcript variant X1
PHD finger protein 6, transcript variant X2
hypoxanthine phosphoribosyltransferase 1
hypoxanthine-guanine phosphoribosyltransferase
COORDINATES: nucleotide motif:Rfam:12.0:RF01233
P2R1A-PPP2R2A-interacting phosphatase regulator 1, transcript variant X2
P2R1A-PPP2R2A-interacting phosphatase regulator 1, transcript variant X1
P2R1A-PPP2R2A-interacting phosphatase regulator 1 isoform X1
P2R1A-PPP2R2A-interacting phosphatase regulator 1 isoform X2
motile sperm domain-containing protein 1
integrator complex subunit 6-like, transcript variant X1
integrator complex subunit 6-like, transcript variant X2
integrator complex subunit 6-like, transcript variant X3
integrator complex subunit 6-like, transcript variant X4
integrator complex subunit 6-like, transcript variant X5
integrator complex subunit 6-like, transcript variant X6
integrator complex subunit 6-like isoform X1
integrator complex subunit 6-like isoform X2
integrator complex subunit 6-like isoform X3
integrator complex subunit 6-like isoform X4
four and a half LIM domains 1, transcript variant X1
four and a half LIM domains protein 1 isoform X1
four and a half LIM domains 1, transcript variant X2
four and a half LIM domains protein 1 isoform X2
zinc finger C4H2-type containing, transcript variant X3
zinc finger C4H2-type containing, transcript variant X1
zinc finger C4H2-type containing, transcript variant X2
zinc finger C4H2 domain-containing protein isoform X1
zinc finger C4H2 domain-containing protein isoform X2
zinc finger C4H2 domain-containing protein isoform X3
zinc finger CCCH-type containing 12B, transcript variant X1
zinc finger CCCH-type containing 12B, transcript variant X3
zinc finger CCCH-type containing 12B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments
V-set and immunoglobulin domain-containing protein 4-like, transcript variant X2
V-set and immunoglobulin domain-containing protein 4-like, transcript variant X5
V-set and immunoglobulin domain-containing protein 4-like, transcript variant X4
V-set and immunoglobulin domain-containing protein 4-like, transcript variant X1
V-set and immunoglobulin domain-containing protein 4-like, transcript variant X6
V-set and immunoglobulin domain-containing protein 4-like, transcript variant X3
V-set and immunoglobulin domain-containing protein 4-like isoform X2
V-set and immunoglobulin domain-containing protein 4-like isoform X6
V-set and immunoglobulin domain-containing protein 4-like isoform X5
V-set and immunoglobulin domain-containing protein 4-like isoform X4
V-set and immunoglobulin domain-containing protein 4-like isoform X1
V-set and immunoglobulin domain-containing protein 4-like isoform X3
V-set and immunoglobulin domain-containing protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
probable G-protein coupled receptor 83, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
probable G-protein coupled receptor 83, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
ectodysplasin A2 receptor, transcript variant X2
ectodysplasin A2 receptor, transcript variant X1
tumor necrosis factor receptor superfamily member 27
StAR related lipid transfer domain containing 8, transcript variant X2
stAR-related lipid transfer protein 8 isoform X2
StAR related lipid transfer domain containing 8, transcript variant X4
StAR related lipid transfer domain containing 8, transcript variant X3
stAR-related lipid transfer protein 8 isoform X3
StAR related lipid transfer domain containing 8, transcript variant X1
stAR-related lipid transfer protein 8 isoform X1
stAR-related lipid transfer protein 8 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 18 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
transforming growth factor beta activator LRRC32-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
transforming growth factor beta activator LRRC32-like isoform X2
transforming growth factor beta activator LRRC32-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transforming growth factor beta activator LRRC32-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transforming growth factor beta activator LRRC32-like isoform X1
protein Wnt-11b-2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein Wnt-11b-2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
immunoglobulin binding protein 1, transcript variant X1
immunoglobulin binding protein 1, transcript variant X2
immunoglobulin-binding protein 1 isoform X1
immunoglobulin-binding protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 24 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 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 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: PDZ domain-containing protein 11
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 ESTs, 7 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: chromosome-associated kinesin KIF4A
TATA-box binding protein associated factor 9b
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
transcription initiation factor TFIID subunit 9B
fibronectin type-III domain-containing protein 3a-like, transcript variant X1
fibronectin type-III domain-containing protein 3a-like, transcript variant X2
fibronectin type-III domain-containing protein 3a-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
lysophosphatidic acid receptor 4, transcript variant X1
lysophosphatidic acid receptor 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
bromodomain and WD repeat domain containing 3
bromodomain and WD repeat-containing protein 3
high mobility group nucleosome binding domain 5, transcript variant X2
high mobility group nucleosome binding domain 5, transcript variant X4
high mobility group nucleosome binding domain 5, transcript variant X3
high mobility group nucleosome binding domain 5, transcript variant X1
high mobility group nucleosome-binding domain-containing protein 5 isoform X2
high mobility group nucleosome-binding domain-containing protein 5 isoform X1
SH3 domain binding glutamate rich protein like
SH3 domain-binding glutamic acid-rich-like protein
TLR adapter interacting with SLC15A4 on the lysosome-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC117002791, transcript variant X3
uncharacterized LOC117002791, transcript variant X9
uncharacterized LOC117002791, transcript variant X10
uncharacterized LOC117002791, transcript variant X6
uncharacterized LOC117002791, transcript variant X1
uncharacterized LOC117002791, transcript variant X4
uncharacterized LOC117002791, transcript variant X8
uncharacterized LOC117002791, transcript variant X2
uncharacterized LOC117002791, transcript variant X5
uncharacterized LOC117002791, transcript variant X11
uncharacterized LOC117002791, transcript variant X12
uncharacterized LOC117002791, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 28 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
POU domain, class 3, transcription factor 4
ribosomal protein S6 kinase A6, transcript variant X2
ribosomal protein S6 kinase A6, transcript variant X1
ribosomal protein S6 kinase A6, transcript variant X3
ribosomal protein S6 kinase alpha-6 isoform X2
ribosomal protein S6 kinase alpha-6 isoform X1
ribosomal protein S6 kinase alpha-6 isoform X3
highly divergent homeobox, transcript variant X2
highly divergent homeobox, transcript variant X1
connector enhancer of kinase suppressor of ras 2-like, transcript variant X1
connector enhancer of kinase suppressor of ras 2-like, transcript variant X2
connector enhancer of kinase suppressor of ras 2-like isoform X1
connector enhancer of kinase suppressor of ras 2-like isoform X2
zinc finger protein 711, transcript variant X1
zinc finger protein 711, transcript variant X2
POF1B actin binding protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
POF1B actin binding protein, transcript variant X1
rab proteins geranylgeranyltransferase component A 1
dachshund family transcription factor 2, transcript variant X1
dachshund family transcription factor 2, transcript variant X2
kelch like family member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
kelch like family member 4, transcript variant X1
protocadherin 11 X-linked, transcript variant X1
protocadherin 11 X-linked, transcript variant X2
protocadherin 11 X-linked, transcript variant X3
diaphanous related formin 2, transcript variant X1
diaphanous related formin 2, transcript variant X2
diaphanous related formin 2, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; deleted 3 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
sushi repeat containing protein X-linked 2
tRNA methyltransferase 12 homolog, transcript variant X2
tRNA methyltransferase 12 homolog, transcript variant X1
tRNA wybutosine-synthesizing protein 2 homolog isoform X1
tRNA wybutosine-synthesizing protein 2 homolog isoform X2
cleavage stimulation factor subunit 2, transcript variant X1
cleavage stimulation factor subunit 2, transcript variant X2
cleavage stimulation factor subunit 2, transcript variant X4
cleavage stimulation factor subunit 2, transcript variant X3
cleavage stimulation factor subunit 2, transcript variant X5
cleavage stimulation factor subunit 2 isoform X1
cleavage stimulation factor subunit 2 isoform X2
cleavage stimulation factor subunit 2 isoform X4
cleavage stimulation factor subunit 2 isoform X3
cleavage stimulation factor subunit 2 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 66% coverage of the annotated genomic feature by RNAseq alignments
ADP-ribosylation factor-like protein 13A
MCF.2 cell line derived transforming sequence, transcript variant X4
MCF.2 cell line derived transforming sequence, transcript variant X5
MCF.2 cell line derived transforming sequence, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
MCF.2 cell line derived transforming sequence, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
MCF.2 cell line derived transforming sequence, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
MCF.2 cell line derived transforming sequence, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
fibroblast growth factor 13, transcript variant X2
fibroblast growth factor 13, transcript variant X4
fibroblast growth factor 13, transcript variant X1
fibroblast growth factor 13, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
uncharacterized LOC117002722, transcript variant X2
uncharacterized LOC117002722, transcript variant X1
uncharacterized LOC117002907, transcript variant X3
uncharacterized LOC117002907, transcript variant X1
uncharacterized LOC117002907, transcript variant X2
transmembrane 9 superfamily member 2-like
RNA binding motif protein X-linked, transcript variant X2
RNA binding motif protein X-linked, transcript variant X4
RNA binding motif protein X-linked, transcript variant X1
RNA binding motif protein X-linked, transcript variant X3
RNA-binding motif protein, X chromosome isoform X1
RNA-binding motif protein, X chromosome isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00270
Rac/Cdc42 guanine nucleotide exchange factor 6, transcript variant X1
Rac/Cdc42 guanine nucleotide exchange factor 6, transcript variant X2
rho guanine nucleotide exchange factor 6 isoform X1
rho guanine nucleotide exchange factor 6 isoform X2
Rac/Cdc42 guanine nucleotide exchange factor 6, transcript variant X3
rho guanine nucleotide exchange factor 6 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
vestigial like family member 1, transcript variant X3
vestigial like family member 1, transcript variant X2
vestigial like family member 1, transcript variant X1
transcription cofactor vestigial-like protein 1 isoform X3
transcription cofactor vestigial-like protein 1 isoform X2
transcription cofactor vestigial-like protein 1 isoform X1
adhesion G-protein coupled receptor G2-like, transcript variant X2
adhesion G-protein coupled receptor G2-like isoform X2
adhesion G-protein coupled receptor G2-like, transcript variant X1
adhesion G-protein coupled receptor G2-like isoform X1
uncharacterized LOC117002758, transcript variant X5
uncharacterized LOC117002758, transcript variant X4
uncharacterized LOC117002758, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
uncharacterized LOC117002758, transcript variant X6
uncharacterized LOC117002758, transcript variant X2
uncharacterized LOC117002758, transcript variant X7
uncharacterized LOC117002758, transcript variant X23
uncharacterized LOC117002758, transcript variant X21
uncharacterized LOC117002758, transcript variant X22
uncharacterized LOC117002758, transcript variant X3
uncharacterized LOC117002758, transcript variant X13
uncharacterized LOC117002758, transcript variant X20
uncharacterized LOC117002758, transcript variant X1
uncharacterized LOC117002758, transcript variant X8
uncharacterized LOC117002759, transcript variant X2
uncharacterized LOC117002759, transcript variant X3
uncharacterized LOC117002759, transcript variant X1
uncharacterized LOC117002758, transcript variant X12
uncharacterized LOC117002758, transcript variant X18
uncharacterized LOC117002758, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC117002758, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized LOC117002758, transcript variant X14
uncharacterized LOC117002758, transcript variant X11
uncharacterized LOC117002758, transcript variant X16
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 18 samples with support for all annotated introns
uncharacterized LOC117002758, transcript variant X17
uncharacterized LOC117002758, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns