Catharus ustulatus isolate bCatUst1 chromosome 16, 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\nCM020351.1.\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.
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC117003668, 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 19 samples with support for all annotated introns
uncharacterized LOC117003668, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein rogdi homolog
glyoxylate reductase 1 homolog, transcript variant X2
glyoxylate reductase 1 homolog, transcript variant X1
putative oxidoreductase GLYR1 isoform X2
putative oxidoreductase GLYR1 isoform X1
mitochondrial ribosomal protein S34, transcript variant X1
mitochondrial ribosomal protein S34, transcript variant X2
28S ribosomal protein S34, mitochondrial isoform X1
28S ribosomal protein S34, mitochondrial isoform X2
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X29
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X27
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X25
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X17
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X15
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X11
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X28
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X26
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X24
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X20
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X14
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X9
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X22
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X8
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X3
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X21
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X19
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X13
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X4
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X18
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X6
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X5
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X16
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X12
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X10
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X7
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X2
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X1
mitogen-activated protein kinase 8 interacting protein 3, transcript variant X23
C-Jun-amino-terminal kinase-interacting protein 3 isoform X29
C-Jun-amino-terminal kinase-interacting protein 3 isoform X27
C-Jun-amino-terminal kinase-interacting protein 3 isoform X25
C-Jun-amino-terminal kinase-interacting protein 3 isoform X17
C-Jun-amino-terminal kinase-interacting protein 3 isoform X15
C-Jun-amino-terminal kinase-interacting protein 3 isoform X11
C-Jun-amino-terminal kinase-interacting protein 3 isoform X28
C-Jun-amino-terminal kinase-interacting protein 3 isoform X26
C-Jun-amino-terminal kinase-interacting protein 3 isoform X24
C-Jun-amino-terminal kinase-interacting protein 3 isoform X20
C-Jun-amino-terminal kinase-interacting protein 3 isoform X14
C-Jun-amino-terminal kinase-interacting protein 3 isoform X9
C-Jun-amino-terminal kinase-interacting protein 3 isoform X22
C-Jun-amino-terminal kinase-interacting protein 3 isoform X8
C-Jun-amino-terminal kinase-interacting protein 3 isoform X3
C-Jun-amino-terminal kinase-interacting protein 3 isoform X23
C-Jun-amino-terminal kinase-interacting protein 3 isoform X21
C-Jun-amino-terminal kinase-interacting protein 3 isoform X19
C-Jun-amino-terminal kinase-interacting protein 3 isoform X13
C-Jun-amino-terminal kinase-interacting protein 3 isoform X4
C-Jun-amino-terminal kinase-interacting protein 3 isoform X18
C-Jun-amino-terminal kinase-interacting protein 3 isoform X6
C-Jun-amino-terminal kinase-interacting protein 3 isoform X5
C-Jun-amino-terminal kinase-interacting protein 3 isoform X16
C-Jun-amino-terminal kinase-interacting protein 3 isoform X12
C-Jun-amino-terminal kinase-interacting protein 3 isoform X10
C-Jun-amino-terminal kinase-interacting protein 3 isoform X7
C-Jun-amino-terminal kinase-interacting protein 3 isoform X2
C-Jun-amino-terminal kinase-interacting protein 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
Jupiter microtubule associated homolog 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: jupiter microtubule associated homolog 2
cramped chromatin regulator homolog 1, transcript variant X3
cramped chromatin regulator homolog 1, transcript variant X2
cramped chromatin regulator homolog 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68% coverage of the annotated genomic feature by RNAseq alignments
intraflagellar transport 140, transcript variant X3
intraflagellar transport 140, transcript variant X4
intraflagellar transport 140, transcript variant X2
intraflagellar transport 140, transcript variant X1
intraflagellar transport protein 140 homolog isoform X3
intraflagellar transport protein 140 homolog isoform X2
intraflagellar transport protein 140 homolog isoform X1
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 19 samples with support for all annotated introns
telomere maintenance 2, transcript variant X2
telomere maintenance 2, transcript variant X1
telomere length regulation protein TEL2 homolog isoform X2
telomere length regulation protein TEL2 homolog isoform X1
RNA binding protein with serine rich domain 1, transcript variant X1
RNA binding protein with serine rich domain 1, transcript variant X2
RNA-binding protein with serine-rich domain 1 isoform X1
RNA-binding protein with serine-rich domain 1 isoform X2
uncharacterized LOC117003883, transcript variant X3
uncharacterized LOC117003883, transcript variant X1
uncharacterized LOC117003883, transcript variant X2
UPF0488 protein C8orf33 homolog, transcript variant X2
UPF0488 protein C8orf33 homolog, transcript variant X1
UPF0488 protein C8orf33 homolog, transcript variant X5
UPF0488 protein C8orf33 homolog, transcript variant X4
UPF0488 protein C8orf33 homolog, transcript variant X3
uncharacterized protein LOC117003882 isoform X2
uncharacterized protein LOC117003882 isoform X1
UPF0488 protein C8orf33 homolog isoform X4
uncharacterized protein LOC117003882 isoform X3
UPF0488 protein C8orf33 homolog isoform X5
amidohydrolase domain containing 2, transcript variant X1
N-acetylglucosamine-6-phosphate deacetylase isoform X1
amidohydrolase domain containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
amidohydrolase domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
N-acetylglucosamine-6-phosphate deacetylase isoform X2
V-type proton ATPase 16 kDa proteolipid subunit
TBC1 domain family member 24, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
TBC1 domain family member 24, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TBC1 domain family member 24, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TBC1 domain family member 24, transcript variant X4
TBC1 domain family member 24, transcript variant X1
TBC1 domain family member 24, transcript variant X7
TBC1 domain family member 24, transcript variant X6
uncharacterized LOC117004105, transcript variant X1
uncharacterized LOC117004105, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 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: 2 mRNAs, 11 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X2
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X3
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X1
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X4
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X8
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X9
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X6
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X5
ankyrin repeat and fibronectin type-III domain-containing protein 1-like, transcript variant X7
ankyrin repeat and fibronectin type-III domain-containing protein 1-like isoform X2
ankyrin repeat and fibronectin type-III domain-containing protein 1-like isoform X3
ankyrin repeat and fibronectin type-III domain-containing protein 1-like isoform X1
ankyrin repeat and fibronectin type-III domain-containing protein 1-like isoform X4
ankyrin repeat and fibronectin type-III domain-containing protein 1-like isoform X6
ankyrin repeat and fibronectin type-III domain-containing protein 1-like isoform X5
ankyrin repeat and fibronectin type-III domain-containing protein 1-like isoform X7
tubulin epsilon and delta complex protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
inactive serine/threonine-protein kinase VRK3
ATP binding cassette subfamily A member 3
MAPK regulated corepressor interacting protein 2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon CCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
methyltransferase like 26, transcript variant X1
methyltransferase like 26, transcript variant X5
methyltransferase like 26, transcript variant X2
methyltransferase like 26, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
methyltransferase like 26, transcript variant X3
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 13 samples with support for all annotated introns
methyltransferase like 26, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
WAP, Kazal, immunoglobulin, Kunitz and NTR domain-containing protein 1
phosphatidylinositol glycan anchor biosynthesis class Q, transcript variant X2
phosphatidylinositol glycan anchor biosynthesis class Q, transcript variant X3
phosphatidylinositol glycan anchor biosynthesis class Q, transcript variant X1
phosphatidylinositol glycan anchor biosynthesis class Q, transcript variant X4
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q isoform X1
phosphatidylinositol N-acetylglucosaminyltransferase subunit Q isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% 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: 3 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
eukaryotic elongation factor 2 lysine methyltransferase, transcript variant X2
eukaryotic elongation factor 2 lysine methyltransferase, transcript variant X1
protein-lysine N-methyltransferase EEF2KMT isoform X1
protein-lysine N-methyltransferase EEF2KMT isoform X2
NADH:ubiquinone oxidoreductase subunit B6, transcript variant X2
NADH:ubiquinone oxidoreductase subunit B6, transcript variant X1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 6
eukaryotic elongation factor 2 lysine methyltransferase, transcript variant X3
protein-lysine N-methyltransferase EEF2KMT isoform X3
ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase, transcript variant X1
ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase, transcript variant X3
ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase, transcript variant X5
ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase, transcript variant X2
chitobiosyldiphosphodolichol beta-mannosyltransferase isoform X1
chitobiosyldiphosphodolichol beta-mannosyltransferase isoform X2
chitobiosyldiphosphodolichol beta-mannosyltransferase isoform X4
ALG1 chitobiosyldiphosphodolichol beta-mannosyltransferase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
chitobiosyldiphosphodolichol beta-mannosyltransferase isoform X3
N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase
SEC14 like lipid binding 5, transcript variant X1
SEC14 like lipid binding 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
NME/NM23 nucleoside diphosphate kinase 3
uncharacterized LOC117003781, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC117003781, 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 LOC117003781, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
splA/ryanodine receptor domain and SOCS box containing 3, transcript variant X2
splA/ryanodine receptor domain and SOCS box containing 3, transcript variant X1
splA/ryanodine receptor domain and SOCS box containing 3, transcript variant X3
SPRY domain-containing SOCS box protein 3 isoform X2
SPRY domain-containing SOCS box protein 3 isoform X1
SPRY domain-containing SOCS box protein 3 isoform X3
nucleotide binding protein 2, transcript variant X1
nucleotide binding protein 2, transcript variant X2
cytosolic Fe-S cluster assembly factor NUBP2 isoform X1
cytosolic Fe-S cluster assembly factor NUBP2 isoform X2
insulin like growth factor binding protein acid labile subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
insulin-like growth factor-binding protein complex acid labile subunit
coiled-coil domain containing 78, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain containing 78, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
coiled-coil domain containing 78, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
coiled-coil domain containing 78, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
coiled-coil domain-containing protein 78 isoform X3
coiled-coil domain-containing protein 78 isoform X1
coiled-coil domain-containing protein 78 isoform X2
coiled-coil domain-containing protein 78 isoform X4
adenine nucleotide translocase lysine methyltransferase, transcript variant X1
adenine nucleotide translocase lysine methyltransferase, transcript variant X2
adenine nucleotide translocase lysine N-methyltransferase isoform X1
adenine nucleotide translocase lysine N-methyltransferase isoform X2
meteorin, glial cell differentiation regulator, 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 12 samples with support for all annotated introns
meteorin, glial cell differentiation regulator, transcript variant X1
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, including 11 samples with support for all annotated introns
F-box and leucine rich repeat protein 16
jumonji domain containing 8, transcript variant X1
jmjC domain-containing protein 8 isoform X1
jumonji domain containing 8, transcript variant X3
jumonji domain containing 8, transcript variant X2
jmjC domain-containing protein 8 isoform X2
jmjC domain-containing protein 8 isoform X3
STIP1 homology and U-box containing protein 1
mitochondrial Rho GTPase 2, transcript variant X5
mitochondrial Rho GTPase 2, transcript variant X4
mitochondrial Rho GTPase 2, transcript variant X2
mitochondrial Rho GTPase 2, transcript variant X3
WD repeat-containing protein 90 isoform X5
mitochondrial Rho GTPase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
WD repeat-containing protein 90 isoform X1
cilia and flagella associated protein 70, transcript variant X3
cilia and flagella associated protein 70, transcript variant X5
cilia and flagella associated protein 70, transcript variant X2
cilia and flagella associated protein 70, transcript variant X4
cilia and flagella associated protein 70, transcript variant X1
cilia and flagella associated protein 70, transcript variant X6
cilia- and flagella-associated protein 70 isoform X3
cilia- and flagella-associated protein 70 isoform X5
cilia- and flagella-associated protein 70 isoform X2
cilia- and flagella-associated protein 70 isoform X4
cilia- and flagella-associated protein 70 isoform X1
cilia- and flagella-associated protein 70 isoform X6
MSS51 mitochondrial translational activator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
putative protein MSS51 homolog, mitochondrial
cytoplasmic phosphatidylinositol transfer protein 1-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cytoplasmic phosphatidylinositol transfer protein 1-like
myeloid-associated differentiation marker-like
RAB11 family interacting protein 3, transcript variant X1
RAB11 family interacting protein 3, transcript variant X3
RAB11 family interacting protein 3, transcript variant X2
RAB11 family interacting protein 3, transcript variant X4
rab11 family-interacting protein 3 isoform X3
rab11 family-interacting protein 3 isoform X2
rab11 family-interacting protein 3 isoform X1
rab11 family-interacting protein 3 isoform X4
2,4-dienoyl-CoA reductase 2, transcript variant X1
2,4-dienoyl-CoA reductase 2, transcript variant X2
peroxisomal 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing] isoform X1
peroxisomal 2,4-dienoyl-CoA reductase [(3E)-enoyl-CoA-producing] isoform X2
NME/NM23 nucleoside diphosphate kinase 4
nucleoside diphosphate kinase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 ESTs, 1 Protein, 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: 13 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
SH3 domain binding kinase 1, transcript variant X2
serine/threonine-protein kinase SBK1 isoform X2
SH3 domain binding kinase 1, transcript variant X3
SH3 domain binding kinase 1, transcript variant X1
serine/threonine-protein kinase SBK1 isoform X1
serine/threonine-protein kinase SBK1 isoform X3
dynein axonemal assembly factor 8-like, transcript variant X1
dynein axonemal assembly factor 8-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 2 samples with support for all annotated introns
ankyrin repeat and sterile alpha motif domain containing 3, transcript variant X3
ankyrin repeat and sterile alpha motif domain containing 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
ankyrin repeat and sterile alpha motif domain containing 3, transcript variant X2
ankyrin repeat and SAM domain-containing protein 3 isoform X2
ankyrin repeat and SAM domain-containing protein 3 isoform X1
glucagon receptor-like, transcript variant X2
glucagon receptor-like, transcript variant X1
clusterin associated protein 1, transcript variant X1
clusterin associated protein 1, transcript variant X2
clusterin associated protein 1, transcript variant X4
clusterin-associated protein 1 isoform X1
clusterin-associated protein 1 isoform X2
clusterin-associated protein 1 isoform X4
clusterin associated protein 1, transcript variant X3
clusterin-associated protein 1 isoform X3
NLR family CARD domain containing 3, transcript variant X5
NLR family CARD domain containing 3, transcript variant X4
NLR family CARD domain containing 3, transcript variant X3
NLR family CARD domain containing 3, transcript variant X2
NLR family CARD domain containing 3, transcript variant X1
NLR family CARD domain-containing protein 3 isoform X5
NLR family CARD domain-containing protein 3 isoform X4
NLR family CARD domain-containing protein 3 isoform X3
NLR family CARD domain-containing protein 3 isoform X2
NLR family CARD domain-containing protein 3 isoform X1
nmrA-like family domain-containing protein 1, transcript variant X1
nmrA-like family domain-containing protein 1, transcript variant X2
nmrA-like family domain-containing protein 1 isoform X1
nmrA-like family domain-containing protein 1 isoform X2
nmrA-like family domain-containing protein 1
uncharacterized LOC117003653, transcript variant X2
uncharacterized LOC117003653, transcript variant X1
DnaJ heat shock protein family (Hsp40) member A3
dnaJ homolog subfamily A member 3, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 10 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 18 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC117004060, transcript variant X2
uncharacterized LOC117004060, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
adenylate cyclase 9, transcript variant X2
adenylate cyclase 9, transcript variant X3
adenylate cyclase 9, transcript variant X4
adenylate cyclase 9, transcript variant X1
adenylate cyclase 9, transcript variant X5
CREB binding protein, transcript variant X1
CREB binding protein, transcript variant X5
CREB binding protein, transcript variant X2
CREB binding protein, transcript variant X3
CREB binding protein, transcript variant X4
heat shock protein 75 kDa, mitochondrial
SLX4 structure-specific endonuclease subunit, 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 13 samples with support for all annotated introns
SLX4 structure-specific endonuclease subunit, transcript variant X1
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 13 samples with support for all annotated introns
SLX4 structure-specific endonuclease subunit, transcript variant X6
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 15 samples with support for all annotated introns
SLX4 structure-specific endonuclease subunit, transcript variant X7
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 16 samples with support for all annotated introns
SLX4 structure-specific endonuclease subunit, 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 11 samples with support for all annotated introns
SLX4 structure-specific endonuclease subunit, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
SLX4 structure-specific endonuclease subunit, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
SLX4 structure-specific endonuclease subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
SLX4 structure-specific endonuclease subunit, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
structure-specific endonuclease subunit SLX4 isoform X5
structure-specific endonuclease subunit SLX4 isoform X2
structure-specific endonuclease subunit SLX4 isoform X1
structure-specific endonuclease subunit SLX4 isoform X3
structure-specific endonuclease subunit SLX4 isoform X4
structure-specific endonuclease subunit SLX4 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
cell death inducing p53 target 1, transcript variant X3
cell death inducing p53 target 1, transcript variant X1
cell death inducing p53 target 1, transcript variant X2
cell death-inducing p53-target protein 1 isoform X2
cell death-inducing p53-target protein 1 isoform X1
mahogunin ring finger 1, transcript variant X1
mahogunin ring finger 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
mahogunin ring finger 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 ESTs, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
E3 ubiquitin-protein ligase MGRN1 isoform X1
E3 ubiquitin-protein ligase MGRN1 isoform X2
E3 ubiquitin-protein ligase MGRN1 isoform X3
tudor-interacting repair regulator protein
N-alpha-acetyltransferase 60, NatF catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
enoyl-CoA delta isomerase 1, mitochondrial
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
proline and glutamate rich with coiled coil 1, transcript variant X4
proline and glutamate rich with coiled coil 1, transcript variant X3
proline and glutamate rich with coiled coil 1, transcript variant X2
proline and glutamate rich with coiled coil 1, transcript variant X1
putative RNA-binding protein Luc7-like 1 isoform X1
putative RNA-binding protein Luc7-like 1 isoform X2
putative RNA-binding protein Luc7-like 1 isoform X3
family with sequence similarity 234 member A, transcript variant X3
family with sequence similarity 234 member A, transcript variant X2
family with sequence similarity 234 member A, transcript variant X4
family with sequence similarity 234 member A, transcript variant X1
regulator of G protein signaling 11, transcript variant X1
regulator of G protein signaling 11, transcript variant X2
regulator of G protein signaling 11, transcript variant X4
regulator of G protein signaling 11, transcript variant X3
regulator of G protein signaling 11, transcript variant X5
regulator of G protein signaling 11, transcript variant X6
regulator of G-protein signaling 11 isoform X2
regulator of G-protein signaling 11 isoform X1
regulator of G-protein signaling 11 isoform X4
regulator of G-protein signaling 11 isoform X3
regulator of G-protein signaling 11 isoform X5
protein disulfide isomerase family A member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
39S ribosomal protein L28, mitochondrial
post-glycosylphosphatidylinositol attachment to proteins 6
post-GPI attachment to proteins factor 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 15 ESTs, 243 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NPR3 like, GATOR1 complex subunit, transcript variant X1
NPR3 like, GATOR1 complex subunit, transcript variant X2
NPR3 like, GATOR1 complex subunit, transcript variant X5
NPR3 like, GATOR1 complex subunit, transcript variant X3
NPR3 like, GATOR1 complex subunit, transcript variant X4
N-methylpurine DNA glycosylase, transcript variant X3
N-methylpurine DNA glycosylase, transcript variant X2
N-methylpurine DNA glycosylase, transcript variant X6
N-methylpurine DNA glycosylase, transcript variant X5
N-methylpurine DNA glycosylase, transcript variant X1
N-methylpurine DNA glycosylase, transcript variant X4
rhomboid 5 homolog 1, transcript variant X2
rhomboid 5 homolog 1, transcript variant X5
rhomboid 5 homolog 1, transcript variant X3
rhomboid 5 homolog 1, transcript variant X1
rhomboid 5 homolog 1, transcript variant X4
small nuclear ribonucleoprotein U11/U12 subunit 25, transcript variant X1
small nuclear ribonucleoprotein U11/U12 subunit 25, transcript variant X3
small nuclear ribonucleoprotein U11/U12 subunit 25, transcript variant X2
U11/U12 small nuclear ribonucleoprotein 25 kDa protein
DNA-directed RNA polymerase III subunit RPC10
general transcription factor IIIC subunit 1
general transcription factor 3C polypeptide 1
katanin interacting protein, 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 19 samples with support for all annotated introns
katanin interacting protein, transcript variant X3
katanin interacting protein, transcript variant X2
katanin interacting protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
germ cell-specific gene 1-like protein isoform X2
germ cell-specific gene 1-like protein isoform X1
germ cell-specific gene 1-like protein isoform X3
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 19 samples with support for all annotated introns
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 19 samples with support for all annotated introns
germ cell-specific gene 1-like protein isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
RNA binding fox-1 homolog 1, transcript variant X5
RNA binding fox-1 homolog 1, transcript variant X2
RNA binding fox-1 homolog 1, transcript variant X1
RNA binding fox-1 homolog 1, transcript variant X6
RNA binding fox-1 homolog 1, transcript variant X8
RNA binding fox-1 homolog 1, transcript variant X9
RNA binding fox-1 homolog 1, transcript variant X10
RNA binding fox-1 homolog 1, transcript variant X7
RNA binding fox-1 homolog 1, transcript variant X11
RNA binding fox-1 homolog 1, transcript variant X12
RNA binding fox-1 homolog 1, transcript variant X3
RNA binding fox-1 homolog 1, transcript variant X4
RNA binding protein fox-1 homolog 1 isoform X2
RNA binding protein fox-1 homolog 1 isoform X10
RNA binding protein fox-1 homolog 1 isoform X1
RNA binding protein fox-1 homolog 1 isoform X6
RNA binding protein fox-1 homolog 1 isoform X7
RNA binding protein fox-1 homolog 1 isoform X11
RNA binding protein fox-1 homolog 1 isoform X12
RNA binding protein fox-1 homolog 1 isoform X3
RNA binding protein fox-1 homolog 1 isoform X4
RNA binding protein fox-1 homolog 1 isoform X9
RNA binding protein fox-1 homolog 1 isoform X8
RNA binding protein fox-1 homolog 1 isoform X5
RNA binding fox-1 homolog 1, transcript variant X16
RNA binding protein fox-1 homolog 1 isoform X16
RNA binding fox-1 homolog 1, transcript variant X27
RNA binding fox-1 homolog 1, transcript variant X24
RNA binding fox-1 homolog 1, transcript variant X25
RNA binding fox-1 homolog 1, transcript variant X13
RNA binding protein fox-1 homolog 1 isoform X13
RNA binding fox-1 homolog 1, transcript variant X14
RNA binding protein fox-1 homolog 1 isoform X14
RNA binding fox-1 homolog 1, transcript variant X17
RNA binding fox-1 homolog 1, transcript variant X20
RNA binding protein fox-1 homolog 1 isoform X17
RNA binding protein fox-1 homolog 1 isoform X20
RNA binding fox-1 homolog 1, transcript variant X15
RNA binding fox-1 homolog 1, transcript variant X19
RNA binding protein fox-1 homolog 1 isoform X15
RNA binding protein fox-1 homolog 1 isoform X19
RNA binding protein fox-1 homolog 1 isoform X23
RNA binding fox-1 homolog 1, transcript variant X26
RNA binding protein fox-1 homolog 1 isoform X24
RNA binding fox-1 homolog 1, transcript variant X30
RNA binding fox-1 homolog 1, transcript variant X29
RNA binding fox-1 homolog 1, transcript variant X18
RNA binding fox-1 homolog 1, transcript variant X21
RNA binding fox-1 homolog 1, transcript variant X22
RNA binding protein fox-1 homolog 1 isoform X18
RNA binding fox-1 homolog 1, transcript variant X28
RNA binding protein fox-1 homolog 1 isoform X27
RNA binding protein fox-1 homolog 1 isoform X21
RNA binding protein fox-1 homolog 1 isoform X26
RNA binding fox-1 homolog 1, transcript variant X23
RNA binding protein fox-1 homolog 1 isoform X22
RNA binding protein fox-1 homolog 1 isoform X25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
methyltransferase 22, Kin17 lysine, transcript variant X1
methyltransferase 22, Kin17 lysine, 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 18 samples with support for all annotated introns
methyltransferase-like protein 22 isoform X1
methyltransferase-like protein 22 isoform X2
4-aminobutyrate aminotransferase, transcript variant X3
4-aminobutyrate aminotransferase, transcript variant X2
4-aminobutyrate aminotransferase, transcript variant X1
4-aminobutyrate aminotransferase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
ubiquitin specific peptidase 7, transcript variant X2
ubiquitin specific peptidase 7, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 7 isoform X2
ubiquitin carboxyl-terminal hydrolase 7 isoform X1
glutamate ionotropic receptor NMDA type subunit 2A, transcript variant X4
glutamate ionotropic receptor NMDA type subunit 2A, transcript variant X3
glutamate ionotropic receptor NMDA type subunit 2A, transcript variant X1
glutamate ionotropic receptor NMDA type subunit 2A, transcript variant X2
glutamate receptor ionotropic, NMDA 2A isoform X3
glutamate receptor ionotropic, NMDA 2A isoform X2
glutamate receptor ionotropic, NMDA 2A isoform X1
nucleotide binding protein 1, transcript variant X2
nucleotide binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 4 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytosolic Fe-S cluster assembly factor NUBP1 isoform X2
cytosolic Fe-S cluster assembly factor NUBP1 isoform X1
trans-golgi network vesicle protein 23 homolog A
Golgi apparatus membrane protein TVP23 homolog A
class II major histocompatibility complex transactivator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
C-type lectin domain containing 16A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
C-type lectin domain containing 16A, transcript variant X5
C-type lectin domain containing 16A, 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 18 samples with support for all annotated introns
C-type lectin domain containing 16A, transcript variant X1
C-type lectin domain containing 16A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 11 ESTs, 8 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
recQ-mediated genome instability protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
lipopolysaccharide induced TNF factor, transcript variant X1
lipopolysaccharide induced TNF factor, transcript variant X3
lipopolysaccharide induced TNF factor, transcript variant X2
lipopolysaccharide-induced tumor necrosis factor-alpha factor
thioredoxin domain containing 11, transcript variant X1
thioredoxin domain containing 11, transcript variant X2
thioredoxin domain containing 11, transcript variant X3
thioredoxin domain-containing protein 11 isoform X1
thioredoxin domain-containing protein 11 isoform X2
thioredoxin domain-containing protein 11 isoform X3
zinc finger CCCH-type containing 7A, transcript variant X2
zinc finger CCCH-type containing 7A, transcript variant X1
zinc finger CCCH domain-containing protein 7A
phospholipase A2 group X, transcript variant X1
phospholipase A2 group X, transcript variant X2
phospholipase A2 group X, transcript variant X3
bifunctional apoptosis regulator, transcript variant X2
bifunctional apoptosis regulator, transcript variant X1
poly(A)-specific ribonuclease, transcript variant X1
poly(A)-specific ribonuclease PARN isoform X1
poly(A)-specific ribonuclease, transcript variant X2
poly(A)-specific ribonuclease PARN isoform X2
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
myocardin related transcription factor B, transcript variant X5
myocardin related transcription factor B, transcript variant X6
myocardin related transcription factor B, transcript variant X1
myocardin related transcription factor B, transcript variant X2
myocardin related transcription factor B, transcript variant X3
myocardin related transcription factor B, transcript variant X4
myocardin-related transcription factor B isoform X3
myocardin-related transcription factor B isoform X4
myocardin-related transcription factor B isoform X1
myocardin-related transcription factor B isoform X2
ERCC excision repair 4, endonuclease catalytic subunit
shisa family member 9, transcript variant X4
shisa family member 9, transcript variant X3
shisa family member 9, transcript variant X2
shisa family member 9, transcript variant X1
calcineurin like phosphoesterase domain containing 1
serine/threonine-protein phosphatase CPPED1
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 8 samples with support for all annotated introns
TNF receptor superfamily member 17, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor receptor superfamily member 17
TNF receptor superfamily member 17, transcript variant X2
eukaryotic peptide chain release factor GTP-binding subunit ERF3A
ribosomal L1 domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
RRN3 homolog, RNA polymerase I transcription factor, transcript variant X1
RNA polymerase I-specific transcription initiation factor RRN3 isoform X1
RRN3 homolog, RNA polymerase I transcription factor, transcript variant X2
RNA polymerase I-specific transcription initiation factor RRN3 isoform X2
protein N-terminal asparagine amidohydrolase
pyridoxal dependent decarboxylase domain containing 1
pyridoxal-dependent decarboxylase domain-containing protein 1
MPV17 mitochondrial inner membrane protein like
meiosis regulator and mRNA stability factor 1, transcript variant X1
meiosis regulator and mRNA stability factor 1, transcript variant X2
meiosis regulator and mRNA stability factor 1, transcript variant X3
meiosis regulator and mRNA stability factor 1 isoform X1
meiosis regulator and mRNA stability factor 1 isoform X2
nudE neurodevelopment protein 1, transcript variant X2
nudE neurodevelopment protein 1, transcript variant X1
nudE neurodevelopment protein 1, transcript variant X3
uncharacterized LOC117003982, 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 15 samples with support for all annotated introns
uncharacterized LOC117003982, transcript variant X1
uncharacterized protein LOC117003982 isoform X1
uncharacterized LOC117003982, transcript variant X3
uncharacterized protein LOC117003982 isoform X2
nuclear distribution protein nudE homolog 1
centrosomal protein 20, transcript variant X2
centrosomal protein 20, transcript variant X1
ATP binding cassette subfamily C member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 18 ESTs, 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
multidrug resistance-associated protein 1
ATP binding cassette subfamily C member 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ATP binding cassette subfamily C member 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
multidrug resistance-associated protein 1 isoform X2
ATP-binding cassette sub-family C member 6 isoform X1
xylosyltransferase 1, transcript variant X2
xylosyltransferase 1, transcript variant X4
xylosyltransferase 1, transcript variant X1
xylosyltransferase 1, transcript variant X3
ADP ribosylation factor like GTPase 6 interacting protein 1
ADP-ribosylation factor-like protein 6-interacting protein 1
SMG1 nonsense mediated mRNA decay associated PI3K related kinase
inositol 1,4,5-trisphosphate receptor-interacting protein-like 2
5-demethoxyubiquinone hydroxylase, mitochondrial
transmembrane channel like 5, transcript variant X1
transmembrane channel like 5, transcript variant X2
transmembrane channel like 5, transcript variant X3
transmembrane channel-like protein 5 isoform X1
transmembrane channel-like protein 5 isoform X2
transmembrane channel-like protein 5 isoform X3
glycerophosphodiester phosphodiesterase 1, transcript variant X1
glycerophosphodiester phosphodiesterase 1, transcript variant X2
glycerophosphodiester phosphodiesterase 1 isoform X1
glycerophosphodiester phosphodiesterase 1 isoform X2
centriolar coiled-coil protein 110, transcript variant X2
centriolar coiled-coil protein 110, transcript variant X4
centriolar coiled-coil protein 110, transcript variant X3
centriolar coiled-coil protein 110, transcript variant X6
centriolar coiled-coil protein 110, transcript variant X5
centriolar coiled-coil protein 110, transcript variant X1
centriolar coiled-coil protein of 110 kDa isoform X1
centriolar coiled-coil protein of 110 kDa isoform X2
VPS35 endosomal protein sorting factor like
VPS35 endosomal protein-sorting factor-like
lysine rich nucleolar protein 1, transcript variant X3
lysine rich nucleolar protein 1, transcript variant X4
lysine rich nucleolar protein 1, transcript variant X2
lysine rich nucleolar protein 1, transcript variant X1
lysine-rich nucleolar protein 1 isoform X2
lysine-rich nucleolar protein 1 isoform X4
lysine-rich nucleolar protein 1 isoform X1
lysine-rich nucleolar protein 1 isoform X3
G protein-coupled receptor class C group 5 member B, transcript variant X2
G protein-coupled receptor class C group 5 member B, transcript variant X1
G-protein coupled receptor family C group 5 member B
protein disulfide isomerase like, testis expressed
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein disulfide-isomerase-like protein of the testis
acyl-coenzyme A synthetase ACSM4, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
acyl-coenzyme A synthetase ACSM4, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acyl-coenzyme A synthetase ACSM4, mitochondrial-like isoform X1
acyl-coenzyme A synthetase ACSM3, mitochondrial-like isoform X2
acyl-coenzyme A synthetase ACSM3, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acyl-coenzyme A synthetase ACSM3, mitochondrial-like, transcript variant X2
acyl-coenzyme A synthetase ACSM3, mitochondrial-like isoform X1
acyl-coenzyme A synthetase ACSM4, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 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: 4 ESTs, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
RNA exonuclease 5, transcript variant X1
RNA exonuclease 5, transcript variant X3
RNA exonuclease 5, transcript variant X2
defective in cullin neddylation 1 domain containing 3
LYR motif containing 1, transcript variant X2
LYR motif containing 1, transcript variant X3
LYR motif containing 1, transcript variant X4
LYR motif containing 1, transcript variant X1
LYR motif-containing protein 1 isoform X4
LYR motif-containing protein 1 isoform X3
LYR motif-containing protein 1 isoform X1
LYR motif-containing protein 1 isoform X2
dynein axonemal heavy chain 3, transcript variant X2
dynein axonemal heavy chain 3, transcript variant X3
dynein axonemal heavy chain 3, transcript variant X1
dynein axonemal heavy chain 3, transcript variant X4
dynein axonemal heavy chain 3 isoform X2
dynein axonemal heavy chain 3 isoform X1
dynein axonemal heavy chain 3 isoform X3
lipid droplet assembly factor 1, transcript variant X1
lipid droplet assembly factor 1, transcript variant X2
lipid droplet assembly factor 1, transcript variant X3
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
ankyrin repeat and sterile alpha motif domain containing 4B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
ankyrin repeat and SAM domain-containing protein 4B
cytochrome b-c1 complex subunit 2, mitochondrial
modulator of smoothened, transcript variant X1
modulator of smoothened, transcript variant X2
modulator of smoothened protein isoform X1
modulator of smoothened protein isoform X2
modulator of smoothened, transcript variant X3
modulator of smoothened protein isoform X3
von Willebrand factor A domain containing 3A, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
von Willebrand factor A domain containing 3A, transcript variant X9
von Willebrand factor A domain containing 3A, transcript variant X7
von Willebrand factor A domain containing 3A, transcript variant X8
von Willebrand factor A domain containing 3A, transcript variant X10
von Willebrand factor A domain containing 3A, transcript variant X2
von Willebrand factor A domain containing 3A, transcript variant X1
von Willebrand factor A domain containing 3A, transcript variant X5
von Willebrand factor A domain containing 3A, transcript variant X6
von Willebrand factor A domain containing 3A, transcript variant X3
von Willebrand factor A domain containing 3A, transcript variant X4
von Willebrand factor A domain containing 3A, transcript variant X11
von Willebrand factor A domain-containing protein 3A isoform X1
von Willebrand factor A domain-containing protein 3A isoform X2
von Willebrand factor A domain-containing protein 3A isoform X3
von Willebrand factor A domain-containing protein 3A isoform X5
von Willebrand factor A domain-containing protein 3A isoform X4
putative short-chain dehydrogenase/reductase family 42E member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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 7% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: putative short-chain dehydrogenase/reductase family 42E member 2
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
eukaryotic elongation factor 2 kinase, transcript variant X1
eukaryotic elongation factor 2 kinase, transcript variant X5
eukaryotic elongation factor 2 kinase, transcript variant X4
eukaryotic elongation factor 2 kinase, transcript variant X3
eukaryotic elongation factor 2 kinase, transcript variant X2
eukaryotic elongation factor 2 kinase isoform X1
eukaryotic elongation factor 2 kinase isoform X3
eukaryotic elongation factor 2 kinase isoform X2
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
DNA-directed RNA polymerase III subunit RPC5
cerebellar degeneration related protein 2
cerebellar degeneration-related protein 2
transmembrane protein 180-like, transcript variant X1
transmembrane protein 180-like, transcript variant X4
transmembrane protein 180-like, transcript variant X2
transmembrane protein 180-like, transcript variant X3
transmembrane protein 180-like isoform X1
transmembrane protein 180-like isoform X2
methyltransferase like 9, transcript variant X1
methyltransferase like 9, transcript variant X2
protein-L-histidine N-pros-methyltransferase isoform X1
protein-L-histidine N-pros-methyltransferase isoform X2
immunoglobulin superfamily member 6, 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
immunoglobulin superfamily member 6 isoform X2
immunoglobulin superfamily member 6, 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
immunoglobulin superfamily member 6 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
KDEL endoplasmic reticulum protein retention receptor 2
ras-related C3 botulinum toxin substrate 1
small integral membrane protein 10-like protein 2A
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, including 19 samples with support for all annotated introns
ubiquitin specific peptidase 42, transcript variant X5
ubiquitin specific peptidase 42, transcript variant X1
ubiquitin specific peptidase 42, transcript variant X4
ubiquitin specific peptidase 42, transcript variant X3
ubiquitin specific peptidase 42, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 42 isoform X1
ubiquitin specific peptidase 42, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 42 isoform X2
eukaryotic translation initiation factor 2 alpha kinase 1
eukaryotic translation initiation factor 2-alpha kinase 1
aminoacyl tRNA synthetase complex interacting multifunctional protein 2
aminoacyl tRNA synthase complex-interacting multifunctional protein 2
PMS1 homolog 2, mismatch repair system component
radial spoke head 10 homolog B2-like, transcript variant X5
radial spoke head 10 homolog B2-like, transcript variant X3
radial spoke head 10 homolog B2-like, transcript variant X6
radial spoke head 10 homolog B2-like, transcript variant X1
radial spoke head 10 homolog B2-like, transcript variant X8
radial spoke head 10 homolog B2-like, transcript variant X7
radial spoke head 10 homolog B2-like, transcript variant X2
radial spoke head 10 homolog B2-like, transcript variant X4
radial spoke head 10 homolog B2-like isoform X1
radial spoke head 10 homolog B2-like isoform X3
radial spoke head 10 homolog B2-like isoform X2
CCZ1 homolog, vacuolar protein trafficking and biogenesis associated
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 96% 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 2 bases in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 39 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
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: parvalbumin, thymic-like
basic helix-loop-helix family member a15, 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 5 samples with support for all annotated introns
basic helix-loop-helix family member a15, transcript variant X1
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 8 samples with support for all annotated introns
class A basic helix-loop-helix protein 15
tectonin beta-propeller repeat containing 1
tectonin beta-propeller repeat-containing protein 1
BAR/IMD domain containing adaptor protein 2 like 1
brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 1
transformation/transcription domain associated protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
transformation/transcription domain associated protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
transformation/transcription domain associated protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transformation/transcription domain-associated protein
FAM20C golgi associated secretory pathway kinase
extracellular serine/threonine protein kinase FAM20C
platelet derived growth factor subunit A, transcript variant X3
platelet derived growth factor subunit A, transcript variant X2
platelet derived growth factor subunit A, transcript variant X1
platelet-derived growth factor subunit A isoform X1
platelet derived growth factor subunit A, transcript variant X6
platelet derived growth factor subunit A, transcript variant X7
platelet derived growth factor subunit A, transcript variant X5
platelet derived growth factor subunit A, transcript variant X4
platelet-derived growth factor subunit A isoform X3
platelet-derived growth factor subunit A isoform X2
protein kinase cAMP-dependent type I regulatory subunit beta, transcript variant X1
protein kinase cAMP-dependent type I regulatory subunit beta, transcript variant X2
cAMP-dependent protein kinase type I-beta regulatory subunit
Sad1 and UNC84 domain containing 1, transcript variant X3
Sad1 and UNC84 domain containing 1, transcript variant X1
Sad1 and UNC84 domain containing 1, transcript variant X5
Sad1 and UNC84 domain containing 1, transcript variant X6
Sad1 and UNC84 domain containing 1, transcript variant X4
Sad1 and UNC84 domain containing 1, transcript variant X2
SUN domain-containing protein 1 isoform X1
SUN domain-containing protein 1 isoform X2
SUN domain-containing protein 1 isoform X3
guided entry of tail-anchored proteins factor 4
arf-GAP with dual PH domain-containing protein 1
cytochrome c oxidase assembly protein COX19, transcript variant X1
cytochrome c oxidase assembly protein COX19, transcript variant X2
cytochrome c oxidase assembly protein COX19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 69 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
G protein-coupled receptor 146, transcript variant X1
G protein-coupled receptor 146, transcript variant X3
G protein-coupled receptor 146, transcript variant X4
G protein-coupled receptor 146, 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 9 samples with support for all annotated introns
zinc finger AN1-type containing 2A, transcript variant X2
AN1-type zinc finger protein 2A isoform X2
zinc finger AN1-type containing 2A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
AN1-type zinc finger protein 2A isoform X1
zinc finger AN1-type containing 2A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
AN1-type zinc finger protein 2A isoform X3
zinc finger AN1-type containing 2A, transcript variant X4
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 19 samples with support for all annotated introns
AN1-type zinc finger protein 2A isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
integrator complex subunit 1, transcript variant X2
integrator complex subunit 1, transcript variant X1
lysosomal alpha-glucosidase-like, transcript variant X2
lysosomal alpha-glucosidase-like, transcript variant X3
lysosomal alpha-glucosidase-like, transcript variant X1
lysosomal alpha-glucosidase-like isoform X1
lysosomal alpha-glucosidase-like isoform X2
MAF bZIP transcription factor K, transcript variant X1
MAF bZIP transcription factor K, transcript variant X3
MAF bZIP transcription factor K, transcript variant X4
MAF bZIP transcription factor K, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
proteasome assembly chaperone 3, transcript variant X1
proteasome assembly chaperone 3, transcript variant X2
proteasome assembly chaperone 3, transcript variant X3
proteasome assembly chaperone 3, transcript variant X4
proteasome assembly chaperone 3 isoform X1
proteasome assembly chaperone 3 isoform X2
proteasome assembly chaperone 3 isoform X3
extracellular leucine rich repeat and fibronectin type III domain containing 1, transcript variant X2
extracellular leucine rich repeat and fibronectin type III domain containing 1, transcript variant X1
extracellular leucine rich repeat and fibronectin type III domain containing 1, transcript variant X3
mitotic spindle assembly checkpoint protein MAD1
eukaryotic translation initiation factor 3 subunit B
carbohydrate sulfotransferase 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 ESTs, 23 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
carbohydrate sulfotransferase 12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 ESTs, 21 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
beta-1,3-N-acetylglucosaminyltransferase lunatic fringe
IQ motif containing E, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 ESTs, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
IQ motif containing E, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
IQ domain-containing protein E isoform X2
IQ domain-containing protein E isoform X1
IQ motif containing E, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
IQ domain-containing protein E isoform X3
BRCA1 associated ATM activator 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
BRCA1 associated ATM activator 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
BRCA1-associated ATM activator 1 isoform X1
BRCA1-associated ATM activator 1 isoform X2
guanine nucleotide-binding protein subunit alpha-12
caspase recruitment domain family member 11, transcript variant X2
caspase recruitment domain family member 11, transcript variant X1
caspase recruitment domain family member 11, transcript variant X3
caspase recruitment domain-containing protein 11 isoform X1
caspase recruitment domain-containing protein 11 isoform X2
sidekick cell adhesion molecule 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sidekick cell adhesion molecule 1, transcript variant X4
sidekick cell adhesion molecule 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sidekick cell adhesion molecule 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
adaptor related protein complex 5 subunit zeta 1, transcript variant X1
adaptor related protein complex 5 subunit zeta 1, transcript variant X2
ras-associating and dilute domain-containing protein
monocyte to macrophage differentiation associated 2
monocyte to macrophage differentiation factor 2
WD repeat domain, phosphoinositide interacting 2, transcript variant X1
WD repeat domain, phosphoinositide interacting 2, transcript variant X2
WD repeat domain phosphoinositide-interacting protein 2 isoform X1
WD repeat domain phosphoinositide-interacting protein 2 isoform X2
solute carrier family 29 member 4, transcript variant X1
solute carrier family 29 member 4, transcript variant X2
trinucleotide repeat containing 18, transcript variant X2
trinucleotide repeat containing 18, transcript variant X3
trinucleotide repeat containing 18, transcript variant X1
trinucleotide repeat-containing gene 18 protein isoform X2
trinucleotide repeat-containing gene 18 protein isoform X3
trinucleotide repeat-containing gene 18 protein isoform X1
F-box and leucine rich repeat protein 18, transcript variant X2
F-box and leucine rich repeat protein 18, transcript variant X1
ring finger protein 216, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ring finger protein 216, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
ring finger protein 216, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ring finger protein 216, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ring finger protein 216, transcript variant X5
SMAD specific E3 ubiquitin protein ligase 1, transcript variant X4
SMAD specific E3 ubiquitin protein ligase 1, transcript variant X3
SMAD specific E3 ubiquitin protein ligase 1, transcript variant X2
SMAD specific E3 ubiquitin protein ligase 1, transcript variant X1
E3 ubiquitin-protein ligase SMURF1 isoform X4
E3 ubiquitin-protein ligase SMURF1 isoform X3
E3 ubiquitin-protein ligase SMURF1 isoform X2
E3 ubiquitin-protein ligase SMURF1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
actin related protein 2/3 complex subunit 1A, transcript variant X2
actin related protein 2/3 complex subunit 1A, transcript variant X1
actin-related protein 2/3 complex subunit 1A
actin related protein 2/3 complex subunit 1B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 13 ESTs, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
actin related protein 2/3 complex subunit 1B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 14 ESTs, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
actin-related protein 2/3 complex subunit 1B
28 kDa heat- and acid-stable phosphoprotein
pentatricopeptide repeat-containing protein 1, mitochondrial
cleavage and polyadenylation specific factor 4
cleavage and polyadenylation specificity factor subunit 4
ATP-sensitive inward rectifier potassium channel 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
mitogen-activated protein kinase kinase 3, transcript variant X2
mitogen-activated protein kinase kinase 3, transcript variant X1
dual specificity mitogen-activated protein kinase kinase 3 isoform X2
dual specificity mitogen-activated protein kinase kinase 3 isoform X1
dehydrogenase/reductase SDR family member 7B
ubiquitin specific peptidase 22, transcript variant X2
ubiquitin specific peptidase 22, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 22 isoform X1
ubiquitin carboxyl-terminal hydrolase 22 isoform X2
TNF receptor superfamily member 13B, transcript variant X2
TNF receptor superfamily member 13B, transcript variant X3
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
TNF receptor superfamily member 13B, 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 3 samples with support for all annotated introns
tumor necrosis factor receptor superfamily member 13B
myosin phosphatase Rho interacting protein, transcript variant X1
myosin phosphatase Rho interacting protein, transcript variant X3
myosin phosphatase Rho interacting protein, transcript variant X2
myosin phosphatase Rho interacting protein, transcript variant X6
myosin phosphatase Rho interacting protein, transcript variant X5
myosin phosphatase Rho interacting protein, transcript variant X4
myosin phosphatase Rho interacting protein, transcript variant X8
myosin phosphatase Rho interacting protein, transcript variant X7
myosin phosphatase Rho-interacting protein isoform X1
myosin phosphatase Rho-interacting protein isoform X2
myosin phosphatase Rho-interacting protein isoform X5
myosin phosphatase Rho-interacting protein isoform X4
myosin phosphatase Rho-interacting protein isoform X6
myosin phosphatase Rho-interacting protein isoform X3
myosin phosphatase Rho-interacting protein isoform X7
5'(3')-deoxyribonucleotidase, mitochondrial
mediator of RNA polymerase II transcription subunit 9
dexamethasone-induced Ras-related protein 1
phosphatidylethanolamine N-methyltransferase
retinoic acid induced 1, transcript variant X4
retinoic acid induced 1, transcript variant X6
retinoic acid induced 1, transcript variant X3
retinoic acid induced 1, transcript variant X7
retinoic acid induced 1, transcript variant X5
retinoic acid induced 1, transcript variant X1
retinoic acid induced 1, transcript variant X2
retinoic acid induced 1, transcript variant X8
sterol regulatory element binding transcription factor 1, transcript variant X5
sterol regulatory element-binding protein 1 isoform X5
sterol regulatory element binding transcription factor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
sterol regulatory element binding transcription factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
sterol regulatory element binding transcription factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
sterol regulatory element binding transcription factor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
sterol regulatory element-binding protein 1 isoform X3
sterol regulatory element-binding protein 1 isoform X1
sterol regulatory element-binding protein 1 isoform X2
sterol regulatory element-binding protein 1 isoform X4
target of myb1 like 2 membrane trafficking protein, transcript variant X3
target of myb1 like 2 membrane trafficking protein, transcript variant X2
target of myb1 like 2 membrane trafficking protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
ATP synthase mitochondrial F1 complex assembly factor 2
glucose-induced degradation protein 4 homolog
developmentally regulated GTP binding protein 2
developmentally-regulated GTP-binding protein 2
LLGL scribble cell polarity complex component 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
LLGL scribble cell polarity complex component 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
lethal(2) giant larvae protein homolog 1 isoform X1
lethal(2) giant larvae protein homolog 1 isoform X2
mitochondrial elongation factor 2, transcript variant X1
mitochondrial elongation factor 2, transcript variant X2
mitochondrial elongation factor 2, transcript variant X3
DNA topoisomerase III alpha, transcript variant X2
DNA topoisomerase III alpha, transcript variant X1
DNA topoisomerase III alpha, transcript variant X3
guanine nucleotide exchange protein SMCR8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
serine hydroxymethyltransferase, cytosolic
phosphoribosyl pyrophosphate synthetase associated protein 2, transcript variant X1
phosphoribosyl pyrophosphate synthetase associated protein 2, transcript variant X2
phosphoribosyl pyrophosphate synthase-associated protein 2
family with sequence similarity 83 member G
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 80% 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, 3 ESTs, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
calcium voltage-gated channel subunit alpha1 H, transcript variant X1
calcium voltage-gated channel subunit alpha1 H, transcript variant X2
voltage-dependent T-type calcium channel subunit alpha-1H isoform X1
voltage-dependent T-type calcium channel subunit alpha-1H isoform X2
somatostatin receptor 5, transcript variant X2
somatostatin receptor 5, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 13% 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 3 bases in 2 codons; substituted 4 bases at 4 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: complement C1q tumor necrosis factor-related protein 8
lipase maturation factor 1, transcript variant X1
lipase maturation factor 1, transcript variant X2
lipase maturation factor 1, transcript variant X3
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-13
chromosome transmission fidelity factor 18, transcript variant X1
chromosome transmission fidelity factor 18, transcript variant X2
chromosome transmission fidelity factor 18, transcript variant X4
chromosome transmission fidelity protein 18 homolog isoform X1
chromosome transmission fidelity protein 18 homolog isoform X4
chromosome transmission fidelity protein 18 homolog isoform X2
chromosome transmission fidelity factor 18, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
chromosome transmission fidelity protein 18 homolog isoform X3
RNA pseudouridine synthase domain containing 1, transcript variant X2
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 16 samples with support for all annotated introns
RNA pseudouridine synthase domain containing 1, transcript variant X1
RNA pseudouridylate synthase domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytosolic iron-sulfur assembly component 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
hydroxyacylglutathione hydrolase-like protein, 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 19 samples with support for all annotated introns
hydroxyacylglutathione hydrolase-like protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
hydroxyacylglutathione hydrolase-like protein isoform X2
hydroxyacylglutathione hydrolase-like protein isoform X1
hydroxyacylglutathione hydrolase, mitochondrial, transcript variant X3
hydroxyacylglutathione hydrolase, mitochondrial, transcript variant X2
hydroxyacylglutathione hydrolase, mitochondrial, transcript variant X1
hydroxyacylglutathione hydrolase, mitochondrial, transcript variant X4
hydroxyacylglutathione hydrolase, mitochondrial isoform X1
hydroxyacylglutathione hydrolase, mitochondrial isoform X2
fumarylacetoacetate hydrolase domain containing 1
meiosis-specific with OB domain-containing protein
heparan sulfate-glucosamine 3-sulfotransferase 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
heparan sulfate glucosamine 3-O-sulfotransferase 6
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 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 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: testis-expressed protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 13 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase subunit B10
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 10
Derived by automated computational analysis using gene prediction method: cmsearch.
small nucleolar RNA SNORA64/SNORA10 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00264
COORDINATES: nucleotide motif:Rfam:12.0:RF01225
growth factor, augmenter of liver regeneration
zinc finger protein 598, E3 ubiquitin ligase, transcript variant X2
zinc finger protein 598, E3 ubiquitin ligase, transcript variant X1
E3 ubiquitin-protein ligase ZNF598 isoform X2
E3 ubiquitin-protein ligase ZNF598 isoform X1
SLC9A3 regulator 2, transcript variant X1
SLC9A3 regulator 2, transcript variant X2
Na(+)/H(+) exchange regulatory cofactor NHE-RF2 isoform X1
Na(+)/H(+) exchange regulatory cofactor NHE-RF2 isoform X2
nth like DNA glycosylase 1, transcript variant X1
nth like DNA glycosylase 1, transcript variant X2
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 11 samples with support for all annotated introns
TSC complex subunit 2, transcript variant X1
TSC complex subunit 2, transcript variant X2
TSC complex subunit 2, transcript variant X3
TSC complex subunit 2, transcript variant X4
polycystin 1, transient receptor potential channel interacting
TNF receptor associated factor 7, transcript variant X1
E3 ubiquitin-protein ligase TRAF7 isoform X1
TNF receptor associated factor 7, transcript variant X2
E3 ubiquitin-protein ligase TRAF7 isoform X2
CASK interacting protein 1, transcript variant X2
CASK interacting protein 1, transcript variant X1
hexosaminidase D-like, transcript variant X2
hexosaminidase D-like, transcript variant X3
hexosaminidase D-like, transcript variant X1
hexosaminidase D-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
target of rapamycin complex subunit LST8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 76% coverage of the annotated genomic feature by RNAseq alignments
zinc finger DHHC-type palmitoyltransferase 4, transcript variant X3
zinc finger DHHC-type palmitoyltransferase 4, transcript variant X1
zinc finger DHHC-type palmitoyltransferase 4, transcript variant X2
Grid2 interacting protein, transcript variant X3
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 14 samples with support for all annotated introns
Grid2 interacting protein, transcript variant X7
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 14 samples with support for all annotated introns
Grid2 interacting protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Grid2 interacting protein, transcript variant X5
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 17 samples with support for all annotated introns
Grid2 interacting protein, 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 17 samples with support for all annotated introns
Grid2 interacting protein, transcript variant X2
Grid2 interacting protein, transcript variant X6
Rho GTPase activating protein 17, transcript variant X7
Rho GTPase activating protein 17, transcript variant X2
Rho GTPase activating protein 17, transcript variant X1
Rho GTPase activating protein 17, transcript variant X8
rho GTPase-activating protein 17 isoform X6
rho GTPase-activating protein 17 isoform X2
rho GTPase-activating protein 17 isoform X1
rho GTPase-activating protein 17 isoform X7
Rho GTPase activating protein 17, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Rho GTPase activating protein 17, transcript variant X6
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 15 samples with support for all annotated introns
Rho GTPase activating protein 17, transcript variant X5
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 6 samples with support for all annotated introns
Rho GTPase activating protein 17, transcript variant X4
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 16 samples with support for all annotated introns
rho GTPase-activating protein 17 isoform X3
rho GTPase-activating protein 17 isoform X5
rho GTPase-activating protein 17 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
protein kinase C beta, transcript variant X2
protein kinase C beta, transcript variant X1
calcium voltage-gated channel auxiliary subunit gamma 3
voltage-dependent calcium channel gamma-3 subunit
E3 ubiquitin-protein ligase RBBP6-like, transcript variant X1
E3 ubiquitin-protein ligase RBBP6-like, transcript variant X2
E3 ubiquitin-protein ligase RBBP6-like isoform X1
E3 ubiquitin-protein ligase RBBP6-like isoform X2
E3 ubiquitin-protein ligase RBBP6, transcript variant X2
E3 ubiquitin-protein ligase RBBP6, transcript variant X1
E3 ubiquitin-protein ligase RBBP6 isoform X1
E3 ubiquitin-protein ligase RBBP6 isoform X2
SH3 domain-containing protein C23A1.17-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87% coverage of the annotated genomic feature by RNAseq alignments
trinucleotide repeat containing adaptor 6A, transcript variant X1
trinucleotide repeat containing adaptor 6A, transcript variant X2
trinucleotide repeat containing adaptor 6A, transcript variant X5
trinucleotide repeat containing adaptor 6A, transcript variant X6
trinucleotide repeat containing adaptor 6A, transcript variant X8
trinucleotide repeat containing adaptor 6A, transcript variant X3
trinucleotide repeat containing adaptor 6A, transcript variant X7
trinucleotide repeat containing adaptor 6A, transcript variant X9
trinucleotide repeat containing adaptor 6A, transcript variant X10
trinucleotide repeat-containing gene 6A protein isoform X1
trinucleotide repeat-containing gene 6A protein isoform X2
trinucleotide repeat-containing gene 6A protein isoform X5
trinucleotide repeat-containing gene 6A protein isoform X6
trinucleotide repeat-containing gene 6A protein isoform X8
trinucleotide repeat-containing gene 6A protein isoform X3
trinucleotide repeat-containing gene 6A protein isoform X7
trinucleotide repeat-containing gene 6A protein isoform X9
trinucleotide repeat-containing gene 6A protein isoform X10
trinucleotide repeat containing adaptor 6A, transcript variant X4
trinucleotide repeat-containing gene 6A protein isoform X4
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
NADH:ubiquinone oxidoreductase subunit AB1
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 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 11 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
endoplasmic reticulum to nucleus signaling 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 13 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase/endoribonuclease IRE2
ubiquitin domain-containing protein UBFD1
glutamyl-tRNA synthetase 2, mitochondrial
probable glutamate--tRNA ligase, mitochondrial
golgi associated, gamma adaptin ear containing, ARF binding protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
golgi associated, gamma adaptin ear containing, ARF binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ADP-ribosylation factor-binding protein GGA2 isoform X2
ADP-ribosylation factor-binding protein GGA2 isoform X1
conserved oligomeric Golgi complex subunit 7
sodium channel epithelial 1 subunit beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
sodium channel epithelial 1 subunit beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
amiloride-sensitive sodium channel subunit beta
sodium channel epithelial 1 subunit gamma
amiloride-sensitive sodium channel subunit gamma
ubiquitin specific peptidase 31, transcript variant X3
ubiquitin specific peptidase 31, transcript variant X4
ubiquitin specific peptidase 31, transcript variant X5
ubiquitin specific peptidase 31, transcript variant X7
ubiquitin specific peptidase 31, transcript variant X8
ubiquitin specific peptidase 31, transcript variant X9
ubiquitin specific peptidase 31, transcript variant X1
ubiquitin specific peptidase 31, transcript variant X2
ubiquitin specific peptidase 31, transcript variant X6
ubiquitin carboxyl-terminal hydrolase 31
heparan sulfate-glucosamine 3-sulfotransferase 2
heparan sulfate glucosamine 3-O-sulfotransferase 2
heparan sulfate glucosamine 3-O-sulfotransferase 4
bifunctional peptidase and arginyl-hydroxylase JMJD5
NSE1 homolog, SMC5-SMC6 complex component, transcript variant X3
NSE1 homolog, SMC5-SMC6 complex component, transcript variant X1
NSE1 homolog, SMC5-SMC6 complex component, transcript variant X6
NSE1 homolog, SMC5-SMC6 complex component, transcript variant X5
NSE1 homolog, SMC5-SMC6 complex component, transcript variant X7
NSE1 homolog, SMC5-SMC6 complex component, transcript variant X2
NSE1 homolog, SMC5-SMC6 complex component, transcript variant X4
non-structural maintenance of chromosomes element 1 homolog
interleukin 4 receptor, transcript variant X1
interleukin 4 receptor, transcript variant X3
interleukin 4 receptor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 81% 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 42% coverage of the annotated genomic feature by RNAseq alignments
3-phosphoinositide dependent protein kinase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
3-phosphoinositide dependent protein kinase 1, transcript variant X1
3-phosphoinositide-dependent protein kinase 1 isoform X1
3-phosphoinositide dependent protein kinase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
3-phosphoinositide-dependent protein kinase 1 isoform X2
potassium channel tetramerization domain containing 5, transcript variant X1
potassium channel tetramerization domain containing 5, transcript variant X2
potassium channel tetramerization domain containing 5, transcript variant X3
BTB/POZ domain-containing protein KCTD5 isoform X2
BTB/POZ domain-containing protein KCTD5 isoform X1
BTB/POZ domain-containing protein KCTD5 isoform X3
ubiquitin conjugating enzyme E2 I, transcript variant X2
ubiquitin conjugating enzyme E2 I, transcript variant X3
ubiquitin conjugating enzyme E2 I, transcript variant X1
N-acetylglucosamine-1-phosphate transferase subunit gamma, transcript variant X2
N-acetylglucosamine-1-phosphotransferase subunit gamma isoform X2
N-acetylglucosamine-1-phosphate transferase subunit gamma, transcript variant X1
N-acetylglucosamine-1-phosphotransferase subunit gamma isoform X1
protein sidekick-2-like, transcript variant X11
protein sidekick-2-like, transcript variant X13
protein sidekick-2-like, transcript variant X5
protein sidekick-2-like, transcript variant X3
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like isoform X5
protein sidekick-2-like, transcript variant X15
protein sidekick-2-like, transcript variant X12
protein sidekick-2-like, transcript variant X17
protein sidekick-2-like, transcript variant X19
protein sidekick-2-like, transcript variant X1
protein sidekick-2-like, transcript variant X2
protein sidekick-2-like, transcript variant X10
protein sidekick-2-like, transcript variant X8
uncharacterized protein LOC117004010 isoform X2
protein sidekick-2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
protein sidekick-2-like, transcript variant X16
protein sidekick-2-like, transcript variant X14
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like isoform X4
protein sidekick-2-like, transcript variant X7
protein sidekick-2-like, transcript variant X6
protein sidekick-2-like, transcript variant X9
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like isoform X3
protein sidekick-2-like, transcript variant X18
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