Arvicola amphibius chromosome 17, mArvAmp1.2, whole genome shotgun sequence.
Arvicola amphibius (Eurasian water vole)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Muroidea; Cricetidae; Arvicolinae; Arvicola.
REFSEQ INFORMATION: The reference sequence is identical to\nLR862397.2.\nOn Jun 14, 2021 this sequence version replaced NC_052063.1.\nAssembly name: mArvAmp1.2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Wellcome Sanger Institute on\n2021/05/15. The original whole-genome shotgun project has the\naccession CAJEUG000000000.2.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Arvicola amphibius 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.
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: olfactory receptor 4C11-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 103 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 Proteins
olfactory receptor 140-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 121 Proteins
olfactory receptor 140-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 127 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 141 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 101 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 142 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 161 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 153 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 118 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 156 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84 Proteins
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: olfactory receptor 4X2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
TIMP metallopeptidase inhibitor 3, transcript variant X1
COORDINATES: polyA evidence [ECO:0006239]
TIMP metallopeptidase inhibitor 3, transcript variant X2
metalloproteinase inhibitor 3 isoform X1
metalloproteinase inhibitor 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
RNA 2',3'-cyclic phosphate and 5'-OH ligase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
achaete-scute family bHLH transcription factor 4
PR domain zinc finger protein 4 isoform X1
PR domain zinc finger protein 4 isoform X2
BTB domain containing 11, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
BTB domain containing 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
BTB domain containing 11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and BTB/POZ domain-containing protein BTBD11 isoform X2
ankyrin repeat and BTB/POZ domain-containing protein BTBD11 isoform X1
ankyrin repeat and BTB/POZ domain-containing protein BTBD11 isoform X3
mitochondrial transcription termination factor 2
transcription termination factor 2, mitochondrial
transmembrane protein 263, transcript variant X1
transmembrane protein 263, transcript variant X2
four and a half LIM domains protein 1-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments
four and a half LIM domains protein 1-like, transcript variant X5
four and a half LIM domains protein 1-like, transcript variant X2
four and a half LIM domains protein 1-like, transcript variant X4
four and a half LIM domains protein 1-like, transcript variant X1
four and a half LIM domains protein 1-like
RIC8 guanine nucleotide exchange factor B, transcript variant X3
RIC8 guanine nucleotide exchange factor B, transcript variant X2
RIC8 guanine nucleotide exchange factor B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
regulatory factor X4, transcript variant X2
regulatory factor X4, transcript variant X1
DNA-directed RNA polymerase III subunit RPC2
t-complex 11 like 2, 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 6 samples with support for all annotated introns
t-complex 11 like 2, 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
T-complex protein 11-like protein 2 isoform X2
T-complex protein 11-like protein 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
overexpressed in colon carcinoma 1 protein
adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 2, transcript variant X3
adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 2, transcript variant X1
adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 2, transcript variant X2
adaptor protein, phosphotyrosine interacting with PH domain and leucine zipper 2, transcript variant X4
DCC-interacting protein 13-beta isoform X3
DCC-interacting protein 13-beta isoform X2
DCC-interacting protein 13-beta isoform X1
WASH complex subunit 4, transcript variant X4
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 3 samples with support for all annotated introns
WASH complex subunit 4, transcript variant X3
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 4 samples with support for all annotated introns
WASH complex subunit 4, transcript variant X8
WASH complex subunit 4, transcript variant X5
WASH complex subunit 4, transcript variant X7
WASH complex subunit 4, transcript variant X6
WASH complex subunit 4, transcript variant X2
WASH complex subunit 4, transcript variant X1
WASH complex subunit 4, transcript variant X10
WASH complex subunit 4, transcript variant X9
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 6 samples with support for all annotated introns
aldehyde dehydrogenase 1 family member L2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial 10-formyltetrahydrofolate dehydrogenase
uncharacterized protein C12orf45 homolog
solute carrier family 41 member 2, transcript variant X1
solute carrier family 41 member 2, transcript variant X2
uncharacterized LOC119803588, transcript variant X5
uncharacterized LOC119803588, transcript variant X2
uncharacterized LOC119803588, transcript variant X3
uncharacterized LOC119803588, transcript variant X4
uncharacterized LOC119803588, transcript variant X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00428
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 2 samples with support for all annotated introns
thioredoxin reductase 1, transcript variant X3
thioredoxin reductase 1, transcript variant X2
thioredoxin reductase 1, transcript variant X1
thioredoxin reductase 1, cytoplasmic isoform X1
thioredoxin reductase 1, cytoplasmic isoform X2
EP300 interacting inhibitor of differentiation 3
EP300-interacting inhibitor of differentiation 3
nuclear transcription factor Y subunit beta, transcript variant X1
nuclear transcription factor Y subunit beta, transcript variant X2
nuclear transcription factor Y subunit beta
host cell factor C2, transcript variant X2
host cell factor C2, transcript variant X1
glycosyltransferase 8 domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
glycosyltransferase 8 domain-containing protein 2
thymine DNA glycosylase, transcript variant X3
thymine DNA glycosylase, transcript variant X2
thymine DNA glycosylase, transcript variant X1
thymine DNA glycosylase, transcript variant X4
G/T mismatch-specific thymine DNA glycosylase isoform X2
G/T mismatch-specific thymine DNA glycosylase isoform X1
G/T mismatch-specific thymine DNA glycosylase isoform X3
heat shock protein 90 beta family member 1
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
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.
tetratricopeptide repeat protein 41-like, transcript variant X17
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
tetratricopeptide repeat protein 41-like, transcript variant X16
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
tetratricopeptide repeat protein 41-like, transcript variant X15
tetratricopeptide repeat protein 41-like, transcript variant X20
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
tetratricopeptide repeat protein 41-like, transcript variant X22
tetratricopeptide repeat protein 41-like, transcript variant X19
tetratricopeptide repeat protein 41-like, transcript variant X18
tetratricopeptide repeat protein 41-like, transcript variant X21
tetratricopeptide repeat protein 41-like, transcript variant X23
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
tetratricopeptide repeat protein 41-like, transcript variant X14
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 2 samples with support for all annotated introns
tetratricopeptide repeat protein 41-like, transcript variant X10
tetratricopeptide repeat protein 41-like, transcript variant X13
tetratricopeptide repeat protein 41-like, transcript variant X12
tetratricopeptide repeat protein 41-like, transcript variant X11
tetratricopeptide repeat protein 41-like, transcript variant X9
tetratricopeptide repeat protein 41-like, transcript variant X6
tetratricopeptide repeat protein 41-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tetratricopeptide repeat protein 41-like, transcript variant X4
tetratricopeptide repeat protein 41-like, transcript variant X8
tetratricopeptide repeat protein 41-like, transcript variant X1
tetratricopeptide repeat protein 41-like, transcript variant X2
tetratricopeptide repeat protein 41-like, transcript variant X3
tetratricopeptide repeat protein 41-like, transcript variant X5
tetratricopeptide repeat protein 41-like isoform X1
tetratricopeptide repeat protein 41-like isoform X2
tetratricopeptide repeat protein 41-like isoform X4
tetratricopeptide repeat protein 41-like isoform X3
tetratricopeptide repeat protein 41-like isoform X6
tetratricopeptide repeat protein 41-like isoform X5
tetratricopeptide repeat protein 41-like isoform X9
tetratricopeptide repeat protein 41-like isoform X7
tetratricopeptide repeat protein 41-like isoform X8
tetratricopeptide repeat protein 41-like isoform X10
tetratricopeptide repeat protein 41-like isoform X11
tetratricopeptide repeat protein 41-like isoform X13
tetratricopeptide repeat protein 41-like isoform X12
tetratricopeptide repeat protein 41-like isoform X15
tetratricopeptide repeat protein 41-like isoform X14
tetratricopeptide repeat protein 41-like isoform X17
tetratricopeptide repeat protein 41-like isoform X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
5'-nucleotidase domain-containing protein 3
activity-dependent neuroprotector homeobox protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
uncharacterized protein C12orf42 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
achaete-scute family bHLH transcription factor 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 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: phenylalanine-4-hydroxylase
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
insulin like growth factor 1, transcript variant X1
insulin like growth factor 1, transcript variant X2
insulin like growth factor 1, transcript variant X3
insulin like growth factor 1, transcript variant X4
insulin like growth factor 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
PARP1 binding protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
PARP1 binding protein, transcript variant X3
PARP1 binding protein, transcript variant X5
PARP1 binding protein, transcript variant X4
PARP1 binding protein, transcript variant X1
WASH complex subunit 3, transcript variant X2
WASH complex subunit 3, transcript variant X1
WASH complex subunit 3, 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 6 samples with support for all annotated introns
DNA damage regulated autophagy modulator 1
DNA damage-regulated autophagy modulator protein 1
N-acetylglucosamine-1-phosphate transferase subunits alpha and beta
N-acetylglucosamine-1-phosphotransferase subunits alpha/beta
choline phosphotransferase 1, transcript variant X2
choline phosphotransferase 1, transcript variant X1
choline phosphotransferase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
UTP20 small subunit processome component
small subunit processome component 20 homolog
sodium-coupled monocarboxylate transporter 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
growth arrest specific 2 like 3, transcript variant X2
growth arrest specific 2 like 3, transcript variant X1
growth arrest specific 2 like 3, transcript variant X3
nuclear receptor subfamily 1 group H member 4, transcript variant X3
nuclear receptor subfamily 1 group H member 4, transcript variant X4
nuclear receptor subfamily 1 group H member 4, transcript variant X2
nuclear receptor subfamily 1 group H member 4, transcript variant X1
solute carrier family 17 member 8, 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 1 sample with support for all annotated introns
solute carrier family 17 member 8, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
vesicular glutamate transporter 3 isoform X1
vesicular glutamate transporter 3 isoform X2
SCY1 like pseudokinase 2, transcript variant X3
SCY1 like pseudokinase 2, transcript variant X1
SCY1 like pseudokinase 2, transcript variant X2
uncharacterized LOC119803214, transcript variant X1
uncharacterized LOC119803214, transcript variant X2
actin related protein 6, transcript variant X1
actin related protein 6, transcript variant X2
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; deleted 5 bases in 3 codons
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; deleted 5 bases in 3 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: UHRF1-binding protein 1-like
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X1
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X2
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X5
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X3
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X6
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X1
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X2
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X4
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X5
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X3
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X6
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X8
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X9
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X10
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X11
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X12
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X13
ankyrin repeat and sterile alpha motif domain containing 1B, transcript variant X14
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X8
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X9
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X10
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X11
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X12
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X13
ankyrin repeat and sterile alpha motif domain-containing protein 1B isoform X14
IKBKB interacting protein, transcript variant X1
IKBKB interacting protein, transcript variant X2
inhibitor of nuclear factor kappa-B kinase-interacting protein isoform X2
inhibitor of nuclear factor kappa-B kinase-interacting protein isoform X1
solute carrier family 25 member 3, transcript variant X2
solute carrier family 25 member 3, transcript variant X1
phosphate carrier protein, mitochondrial
COORDINATES: nucleotide motif:Rfam:12.0:RF00563
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA tryptophan (anticodon CCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
NEDD1 gamma-tubulin ring complex targeting factor
COORDINATES: nucleotide motif:Rfam:12.0:RF00600
cilia and flagella associated protein 54
cilia- and flagella-associated protein 54
cyclin dependent kinase 17, transcript variant X1
cyclin dependent kinase 17, transcript variant X2
ETS transcription factor ELK3, transcript variant X2
ETS transcription factor ELK3, transcript variant X1
leukotriene A4 hydrolase, transcript variant X2
leukotriene A4 hydrolase, transcript variant X1
coiled-coil domain-containing protein 38
small nuclear ribonucleoprotein polypeptide F
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
ubiquitin carboxyl-terminal hydrolase 44
methionyl aminopeptidase 2, transcript variant X2
methionyl aminopeptidase 2, transcript variant X1
vezatin, adherens junctions transmembrane protein, transcript variant X2
vezatin, adherens junctions transmembrane protein, transcript variant X1
vezatin, adherens junctions transmembrane protein, transcript variant X3
FYVE, RhoGEF and PH domain-containing protein 6
nuclear receptor subfamily 2 group C member 1, transcript variant X1
nuclear receptor subfamily 2 group C member 1, transcript variant X2
nuclear receptor subfamily 2 group C member 1
NADH:ubiquinone oxidoreductase subunit A12, transcript variant X2
NADH:ubiquinone oxidoreductase subunit A12, transcript variant X1
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 12
transmembrane and coiled-coil domain family 3, transcript variant X2
transmembrane and coiled-coil domain protein 3 isoform X2
transmembrane and coiled-coil domain family 3, transcript variant X1
transmembrane and coiled-coil domain protein 3 isoform X1
transmembrane and coiled-coil domain family 3, transcript variant X3
transmembrane and coiled-coil domain protein 3 isoform X3
centrosomal protein 83, transcript variant X5
centrosomal protein 83, transcript variant X4
centrosomal protein 83, transcript variant X6
centrosomal protein 83, transcript variant X2
centrosomal protein 83, transcript variant X1
centrosomal protein 83, transcript variant X3
centrosomal protein 83, transcript variant X7
centrosomal protein of 83 kDa isoform X1
centrosomal protein of 83 kDa isoform X3
centrosomal protein of 83 kDa isoform X2
uncharacterized LOC119803300, transcript variant X2
uncharacterized LOC119803300, transcript variant X1
CASP2 and RIPK1 domain containing adaptor with death domain, transcript variant X2
CASP2 and RIPK1 domain containing adaptor with death domain, transcript variant X1
CASP2 and RIPK1 domain containing adaptor with death domain, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: suppressor of cytokine signaling 2
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
39S ribosomal protein L42, mitochondrial
nudix hydrolase 4, transcript variant X3
nudix hydrolase 4, transcript variant X2
nudix hydrolase 4, transcript variant X1
diphosphoinositol polyphosphate phosphohydrolase 2 isoform X2
diphosphoinositol polyphosphate phosphohydrolase 2 isoform X1
uncharacterized LOC119803550, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC119803550, transcript variant X3
uncharacterized LOC119803550, 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 5 samples with support for all annotated introns
early endosome antigen 1, transcript variant X1
early endosome antigen 1, transcript variant X2
early endosome antigen 1, transcript variant X4
early endosome antigen 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain-containing glutamate-rich protein 1
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
ATPase plasma membrane Ca2+ transporting 1, transcript variant X3
ATPase plasma membrane Ca2+ transporting 1, transcript variant X1
ATPase plasma membrane Ca2+ transporting 1, transcript variant X2
plasma membrane calcium-transporting ATPase 1 isoform X2
plasma membrane calcium-transporting ATPase 1 isoform X1
POC1 centriolar protein B, transcript variant X2
POC1 centriolar protein B, transcript variant X1
POC1 centriolar protein homolog B isoform X1
POC1 centriolar protein homolog B isoform X2
polypeptide N-acetylgalactosaminyltransferase 4-like
uncharacterized LOC119803738, transcript variant X2
uncharacterized LOC119803738, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane O-mannosyltransferase targeting cadherins 3, transcript variant X1
transmembrane O-mannosyltransferase targeting cadherins 3, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 9 bases in 6 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% 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 2 bases in 2 codons; deleted 9 bases in 6 codons; substituted 7 bases at 7 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: centrosomal protein of 290 kDa
uncharacterized protein C12orf29 homolog
chromosome 17 C12orf50 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 11% coverage of the annotated genomic feature by RNAseq alignments
chromosome 17 C12orf50 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 13% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C12orf50 homolog isoform X1
uncharacterized protein C12orf50 homolog isoform X2
alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ras association domain-containing protein 9
leucine rich repeats and IQ motif containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat and IQ domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
sodium-dependent neutral amino acid transporter B(0)AT2
NADH dehydrogenase [ubiquinone] iron-sulfur protein 5-like
transmembrane O-mannosyltransferase targeting cadherins 2
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 3 samples with support for all annotated introns
methyltransferase like 25, transcript variant X1
methyltransferase like 25, transcript variant X8
methyltransferase like 25, transcript variant X7
methyltransferase like 25, transcript variant X6
methyltransferase-like protein 25 isoform X1
methyltransferase-like protein 25 isoform X5
methyltransferase like 25, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
methyltransferase-like protein 25 isoform X2
methyltransferase like 25, transcript variant X5
methyltransferase like 25, 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 2 samples with support for all annotated introns
methyltransferase-like protein 25 isoform X4
methyltransferase like 25, transcript variant X3
methyltransferase-like protein 25 isoform X3
thyroid transcription factor 1-associated protein 26
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% 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 2 bases in 2 codons; deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
acyl-CoA synthetase short chain family member 3
acyl-CoA synthetase short-chain family member 3, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins
lin-7 homolog A, crumbs cell polarity complex component, transcript variant X1
lin-7 homolog A, crumbs cell polarity complex component, transcript variant X2
lin-7 homolog A, crumbs cell polarity complex component, transcript variant X3
lin-7 homolog A, crumbs cell polarity complex component, transcript variant X4
lin-7 homolog A, crumbs cell polarity complex component, transcript variant X6
lin-7 homolog A, crumbs cell polarity complex component, transcript variant X5
protein tyrosine phosphatase receptor type Q
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
LOW QUALITY PROTEIN: phosphatidylinositol phosphatase PTPRQ
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 5% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
protein phosphatase 1 regulatory subunit 12A, transcript variant X1
protein phosphatase 1 regulatory subunit 12A, transcript variant X4
protein phosphatase 1 regulatory subunit 12A, transcript variant X2
protein phosphatase 1 regulatory subunit 12A, transcript variant X3
protein phosphatase 1 regulatory subunit 12A isoform X1
protein phosphatase 1 regulatory subunit 12A isoform X4
protein phosphatase 1 regulatory subunit 12A isoform X2
protein phosphatase 1 regulatory subunit 12A isoform X3
LOW QUALITY PROTEIN: PRKC apoptosis WT1 regulator protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% 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 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
zinc finger DHHC-type palmitoyltransferase 17, transcript variant X1
zinc finger DHHC-type palmitoyltransferase 17, transcript variant X2
oxysterol binding protein like 8, transcript variant X2
oxysterol binding protein like 8, transcript variant X1
oxysterol binding protein like 8, transcript variant X3
oxysterol binding protein like 8, transcript variant X4
oxysterol binding protein like 8, transcript variant X7
oxysterol binding protein like 8, transcript variant X6
oxysterol binding protein like 8, transcript variant X8
oxysterol-binding protein-related protein 8 isoform X1
oxysterol-binding protein-related protein 8 isoform X2
oxysterol-binding protein-related protein 8 isoform X3
oxysterol binding protein like 8, transcript variant X9
oxysterol binding protein like 8, transcript variant X5
oxysterol-binding protein-related protein 8 isoform X5
oxysterol-binding protein-related protein 8 isoform X4
nucleosome assembly protein 1 like 1, transcript variant X1
nucleosome assembly protein 1 like 1, transcript variant X2
nucleosome assembly protein 1 like 1, transcript variant X4
nucleosome assembly protein 1 like 1, transcript variant X3
nucleosome assembly protein 1-like 1 isoform X1
nucleosome assembly protein 1-like 1 isoform X3
nucleosome assembly protein 1-like 1 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00554
pleckstrin homology like domain family A member 1
pleckstrin homology-like domain family A member 1
KRR1 small subunit processome component homolog
GLI pathogenesis related 1, transcript variant X2
GLI pathogenesis related 1, transcript variant X1
glioma pathogenesis-related protein 1 isoform X2
glioma pathogenesis-related protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily C member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 72% 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: 6 Proteins, and 89% 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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: 40S ribosomal protein S16-like
thyrotropin releasing hormone degrading enzyme
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
LOW QUALITY PROTEIN: thyrotropin-releasing hormone-degrading ectoenzyme
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
tryptophan hydroxylase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
tryptophan hydroxylase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
TBC1 domain family member 15, transcript variant X2
TBC1 domain family member 15, transcript variant X1
transmembrane protein 19, transcript variant X8
transmembrane protein 19, transcript variant X7
transmembrane protein 19, transcript variant X6
transmembrane protein 19, transcript variant X3
transmembrane protein 19, transcript variant X4
transmembrane protein 19, transcript variant X9
transmembrane protein 19, transcript variant X5
transmembrane protein 19, transcript variant X1
transmembrane protein 19, transcript variant X2
zinc finger C3H1-type containing, transcript variant X1
zinc finger C3H1-type containing, transcript variant X2
zinc finger C3H1 domain-containing protein isoform X1
zinc finger C3H1 domain-containing protein isoform X2
leucine rich repeat containing G protein-coupled receptor 5, transcript variant X2
leucine rich repeat containing G protein-coupled receptor 5, transcript variant X3
leucine rich repeat containing G protein-coupled receptor 5, transcript variant X1
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 6 samples with support for all annotated introns
leucine-rich repeat-containing G-protein coupled receptor 5 isoform X2
leucine-rich repeat-containing G-protein coupled receptor 5 isoform X3
leucine-rich repeat-containing G-protein coupled receptor 5 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119803539, transcript variant X2
uncharacterized LOC119803539, transcript variant X1
protein tyrosine phosphatase receptor type R
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
receptor-type tyrosine-protein phosphatase R
transcription initiation factor TFIID subunit 7-like
protein tyrosine phosphatase receptor type B, transcript variant X1
receptor-type tyrosine-protein phosphatase beta isoform X1
protein tyrosine phosphatase receptor type B, transcript variant X2
receptor-type tyrosine-protein phosphatase beta isoform X2
uncharacterized LOC119803560, transcript variant X1
uncharacterized LOC119803560, transcript variant X2
potassium calcium-activated channel subfamily M regulatory beta subunit 4
calcium-activated potassium channel subunit beta-4
CCR4-NOT transcription complex subunit 2, transcript variant X5
CCR4-NOT transcription complex subunit 2, transcript variant X2
CCR4-NOT transcription complex subunit 2, transcript variant X4
CCR4-NOT transcription complex subunit 2, transcript variant X1
CCR4-NOT transcription complex subunit 2, transcript variant X3
CCR4-NOT transcription complex subunit 2, transcript variant X6
CCR4-NOT transcription complex subunit 2, transcript variant X7
CCR4-NOT transcription complex subunit 2 isoform X4
CCR4-NOT transcription complex subunit 2 isoform X1
CCR4-NOT transcription complex subunit 2 isoform X5
CCR4-NOT transcription complex subunit 2 isoform X2
CCR4-NOT transcription complex subunit 2 isoform X3
CCR4-NOT transcription complex subunit 2 isoform X6
CCR4-NOT transcription complex subunit 2 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
RAB3A interacting protein, transcript variant X3
RAB3A interacting protein, transcript variant X1
RAB3A interacting protein, transcript variant X2
RAB3A interacting protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
leucine-rich repeat-containing protein 10
fibroblast growth factor receptor substrate 2
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: 16 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LOW QUALITY PROTEIN: fibroblast growth factor receptor substrate 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins
thymocyte expressed, positive selection associated 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% 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: 17 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 108 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 132 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 107 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 129 Proteins
olfactory receptor 6C76, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 124 Proteins
olfactory receptor 6C76, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 139 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 133 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 114 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 134 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 120 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 131 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 136 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 109 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 113 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins
LOW QUALITY PROTEIN: olfactory receptor 6C2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82 Proteins
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
integrin subunit alpha 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
integrin subunit alpha 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
biogenesis of lysosomal organelles complex 1 subunit 1
biogenesis of lysosome-related organelles complex 1 subunit 1
retinol dehydrogenase 5, transcript variant X2
retinol dehydrogenase 5, transcript variant X1
retinol dehydrogenase 5, transcript variant X4
retinol dehydrogenase 5, transcript variant X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00066
ORMDL sphingolipid biosynthesis regulator 2, transcript variant X1
ORMDL sphingolipid biosynthesis regulator 2, transcript variant X2
DnaJ heat shock protein family (Hsp40) member C14, transcript variant X2
DnaJ heat shock protein family (Hsp40) member C14, transcript variant X3
dnaJ homolog subfamily C member 14 isoform X2
DnaJ heat shock protein family (Hsp40) member C14, transcript variant X1
dnaJ homolog subfamily C member 14 isoform X1
transmembrane protein 198-like, transcript variant X1
transmembrane protein 198-like, transcript variant X2
matrix metallopeptidase 19, transcript variant X3
matrix metallopeptidase 19, transcript variant X1
matrix metallopeptidase 19, transcript variant X2
diacylglycerol kinase alpha, transcript variant X3
diacylglycerol kinase alpha, transcript variant X1
diacylglycerol kinase alpha, transcript variant X4
diacylglycerol kinase alpha, transcript variant X2
uncharacterized LOC119803309, transcript variant X2
uncharacterized LOC119803309, 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
cyclin dependent kinase 2, transcript variant X1
cyclin dependent kinase 2, transcript variant X2
RAB5B, member RAS oncogene family, transcript variant X2
RAB5B, member RAS oncogene family, transcript variant X1
sulfite oxidase, mitochondrial isoform X1
sulfite oxidase, mitochondrial isoform X2
IKAROS family zinc finger 4, transcript variant X1
IKAROS family zinc finger 4, transcript variant X9
IKAROS family zinc finger 4, transcript variant X14
IKAROS family zinc finger 4, transcript variant X11
IKAROS family zinc finger 4, transcript variant X10
IKAROS family zinc finger 4, transcript variant X4
IKAROS family zinc finger 4, transcript variant X2
IKAROS family zinc finger 4, transcript variant X5
IKAROS family zinc finger 4, transcript variant X6
IKAROS family zinc finger 4, transcript variant X3
IKAROS family zinc finger 4, transcript variant X13
IKAROS family zinc finger 4, transcript variant X8
IKAROS family zinc finger 4, transcript variant X12
IKAROS family zinc finger 4, transcript variant X7
ribosomal protein S26, transcript variant X2
ribosomal protein S26, transcript variant X1
zinc finger CCCH-type containing 10, transcript variant X4
zinc finger CCCH-type containing 10, transcript variant X3
zinc finger CCCH-type containing 10, transcript variant X2
zinc finger CCCH-type containing 10, transcript variant X1
zinc finger CCCH domain-containing protein 10
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 6 samples with support for all annotated introns
myosin light chain 6, transcript variant X3
myosin light chain 6, transcript variant X2
myosin light chain 6, transcript variant X1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X8
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X11
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X7
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X4
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X10
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X3
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X6
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X5
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X9
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 2, transcript variant X1
SWI/SNF complex subunit SMARCC2 isoform X8
SWI/SNF complex subunit SMARCC2 isoform X11
SWI/SNF complex subunit SMARCC2 isoform X7
SWI/SNF complex subunit SMARCC2 isoform X4
SWI/SNF complex subunit SMARCC2 isoform X10
SWI/SNF complex subunit SMARCC2 isoform X3
SWI/SNF complex subunit SMARCC2 isoform X6
SWI/SNF complex subunit SMARCC2 isoform X5
SWI/SNF complex subunit SMARCC2 isoform X2
SWI/SNF complex subunit SMARCC2 isoform X9
SWI/SNF complex subunit SMARCC2 isoform X1
transfer RNA serine (anticodon CGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ring finger protein 41, transcript variant X4
ring finger protein 41, transcript variant X3
ring finger protein 41, transcript variant X2
ring finger protein 41, transcript variant X1
E3 ubiquitin-protein ligase NRDP1 isoform X3
E3 ubiquitin-protein ligase NRDP1 isoform X2
E3 ubiquitin-protein ligase NRDP1 isoform X1
uncharacterized LOC119803351, transcript variant X2
uncharacterized LOC119803351, transcript variant X1
nucleic acid binding protein 2, transcript variant X1
nucleic acid binding protein 2, transcript variant X3
nucleic acid binding protein 2, transcript variant X2
nucleic acid binding protein 2, transcript variant X4
solute carrier family 39 member 5, transcript variant X1
solute carrier family 39 member 5, 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 3 samples with support for all annotated introns
solute carrier family 39 member 5, transcript variant X4
solute carrier family 39 member 5, transcript variant X2
solute carrier family 39 member 5, transcript variant X5
solute carrier family 39 member 5, transcript variant X3
ankyrin repeat domain 52, transcript variant X2
ankyrin repeat domain 52, transcript variant X1
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C isoform X2
serine/threonine-protein phosphatase 6 regulatory ankyrin repeat subunit C isoform X1
coenzyme Q-binding protein COQ10 homolog A, mitochondrial isoform X2
coenzyme Q-binding protein COQ10 homolog A, mitochondrial isoform X1
canopy FGF signaling regulator 2, transcript variant X2
canopy FGF signaling regulator 2, transcript variant X1
poly(A) specific ribonuclease subunit PAN2, transcript variant X5
poly(A) specific ribonuclease subunit PAN2, transcript variant X3
poly(A) specific ribonuclease subunit PAN2, transcript variant X4
poly(A) specific ribonuclease subunit PAN2, transcript variant X1
poly(A) specific ribonuclease subunit PAN2, transcript variant X2
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X4
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X2
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X3
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X1
poly(A) specific ribonuclease subunit PAN2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
poly(A) specific ribonuclease subunit PAN2, 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 6 samples with support for all annotated introns
poly(A) specific ribonuclease subunit PAN2, transcript variant X6
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X7
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X6
PAN2-PAN3 deadenylation complex catalytic subunit PAN2 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
signal transducer and activator of transcription 2
apolipoprotein F-like, transcript variant X2
apolipoprotein F-like, transcript variant X1
uncharacterized protein LOC119803483 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LOW QUALITY PROTEIN: protein timeless homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: lens fiber major intrinsic protein
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; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 6 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 3 bases in 2 codons; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: glutaminase liver isoform, mitochondrial
RNA binding motif single stranded interacting protein 2, transcript variant X2
RNA binding motif single stranded interacting protein 2, transcript variant X3
RNA binding motif single stranded interacting protein 2, transcript variant X1
RNA-binding motif, single-stranded-interacting protein 2 isoform X1
RNA-binding motif, single-stranded-interacting protein 2 isoform X2
bromodomain adjacent to zinc finger domain 2A, transcript variant X2
bromodomain adjacent to zinc finger domain 2A, transcript variant X1
bromodomain adjacent to zinc finger domain 2A, transcript variant X3
bromodomain adjacent to zinc finger domain 2A, transcript variant X4
bromodomain adjacent to zinc finger domain 2A, transcript variant X5
bromodomain adjacent to zinc finger domain 2A, transcript variant X6
bromodomain adjacent to zinc finger domain protein 2A isoform X2
bromodomain adjacent to zinc finger domain protein 2A isoform X1
bromodomain adjacent to zinc finger domain protein 2A isoform X3
ATP synthase subunit beta, mitochondrial
COORDINATES: nucleotide motif:Rfam:12.0:RF00273
nascent polypeptide associated complex subunit alpha, transcript variant X3
nascent polypeptide associated complex subunit alpha, transcript variant X1
nascent polypeptide associated complex subunit alpha, transcript variant X2
nascent polypeptide-associated complex subunit alpha isoform X2
nascent polypeptide-associated complex subunit alpha isoform X1
DNA primase subunit 1, transcript variant X1
DNA primase subunit 1, transcript variant X2
17-beta-hydroxysteroid dehydrogenase type 6-like
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: 5 Proteins
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: 17-beta-hydroxysteroid dehydrogenase type 6-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00156
short chain dehydrogenase/reductase family 9C member 7, transcript variant X2
short chain dehydrogenase/reductase family 9C member 7, transcript variant X1
short-chain dehydrogenase/reductase family 9C member 7
retinol dehydrogenase 16, transcript variant X2
retinol dehydrogenase 16, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
retinol dehydrogenase 16-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
retinol dehydrogenase 16-like, transcript variant X3
retinol dehydrogenase 16-like, transcript variant X1
retinol dehydrogenase 16-like isoform X1
retinol dehydrogenase 16-like isoform X2
G protein-coupled receptor 182, transcript variant X2
G protein-coupled receptor 182, transcript variant X1
zinc finger and BTB domain containing 39, transcript variant X2
zinc finger and BTB domain containing 39, transcript variant X1
zinc finger and BTB domain containing 39, transcript variant X3
zinc finger and BTB domain-containing protein 39
nuclear envelope integral membrane protein 1, transcript variant X1
nuclear envelope integral membrane protein 1
nuclear envelope integral membrane protein 1, 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 5 samples with support for all annotated introns
NGFI-A binding protein 2, transcript variant X5
NGFI-A binding protein 2, transcript variant X3
NGFI-A binding protein 2, transcript variant 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 6 samples with support for all annotated introns
NGFI-A binding protein 2, transcript variant X2
NGFI-A binding protein 2, transcript variant X6
NGFI-A binding protein 2, transcript variant X4
signal transducer and activator of transcription 6, transcript variant X1
signal transducer and activator of transcription 6, transcript variant X2
signal transducer and activator of transcription 6, transcript variant X3
signal transducer and activator of transcription 6 isoform X1
signal transducer and activator of transcription 6 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 11 bases in 8 codons; deleted 12 bases in 7 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 11 bases in 8 codons; deleted 12 bases in 7 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: prolow-density lipoprotein receptor-related protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments
serine hydroxymethyltransferase, mitochondrial
NDUFA4 mitochondrial complex associated like 2
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 4-like 2
SH3 and cysteine-rich domain-containing protein 3
R3H domain containing 2, transcript variant X18
R3H domain containing 2, transcript variant X15
R3H domain containing 2, transcript variant X17
R3H domain containing 2, transcript variant X12
R3H domain containing 2, transcript variant X11
R3H domain containing 2, transcript variant X10
R3H domain containing 2, transcript variant X8
R3H domain containing 2, transcript variant X7
R3H domain containing 2, transcript variant X16
R3H domain containing 2, transcript variant X9
R3H domain containing 2, transcript variant X14
R3H domain containing 2, transcript variant X5
R3H domain containing 2, transcript variant X19
R3H domain containing 2, transcript variant X13
R3H domain containing 2, transcript variant X6
R3H domain containing 2, transcript variant X1
R3H domain containing 2, transcript variant X4
R3H domain containing 2, transcript variant X2
R3H domain containing 2, transcript variant X3
R3H domain-containing protein 2 isoform X15
R3H domain-containing protein 2 isoform X12
R3H domain-containing protein 2 isoform X14
R3H domain-containing protein 2 isoform X9
R3H domain-containing protein 2 isoform X8
R3H domain-containing protein 2 isoform X7
R3H domain-containing protein 2 isoform X5
R3H domain-containing protein 2 isoform X4
R3H domain-containing protein 2 isoform X13
R3H domain-containing protein 2 isoform X6
R3H domain-containing protein 2 isoform X11
R3H domain-containing protein 2 isoform X2
R3H domain-containing protein 2 isoform X16
R3H domain-containing protein 2 isoform X10
R3H domain-containing protein 2 isoform X3
R3H domain-containing protein 2 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
LOW QUALITY PROTEIN: inhibin beta C chain
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 5 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 17% 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 5 bases in 3 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein GLI1
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: rho GTPase-activating protein 9
DNA damage-inducible transcript 3 protein
LOW QUALITY PROTEIN: methyl-CpG-binding domain protein 6
dynactin subunit 2, transcript variant X1
dynactin subunit 2, transcript variant X2
kinesin family member 5A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
kinesin family member 5A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol-5-phosphate 4-kinase type 2 gamma
phosphatidylinositol 5-phosphate 4-kinase type-2 gamma
deltex E3 ubiquitin ligase 3, transcript variant X1
deltex E3 ubiquitin ligase 3, transcript variant X2
deltex E3 ubiquitin ligase 3, transcript variant X3
deltex E3 ubiquitin ligase 3, transcript variant X4
probable E3 ubiquitin-protein ligase DTX3 isoform X3
probable E3 ubiquitin-protein ligase DTX3 isoform X1
probable E3 ubiquitin-protein ligase DTX3 isoform X4
probable E3 ubiquitin-protein ligase DTX3 isoform X2
Rho guanine nucleotide exchange factor 25, transcript variant X1
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
Rho guanine nucleotide exchange factor 25, transcript variant X2
Rho guanine nucleotide exchange factor 25, transcript variant X3
rho guanine nucleotide exchange factor 25 isoform X1
rho guanine nucleotide exchange factor 25 isoform X3
rho guanine nucleotide exchange factor 25 isoform X2
Rho guanine nucleotide exchange factor 25, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
rho guanine nucleotide exchange factor 25 isoform X4
beta-1,4-N-acetyl-galactosaminyltransferase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
beta-1,4 N-acetylgalactosaminyltransferase 1
OS9 endoplasmic reticulum lectin, transcript variant X2
OS9 endoplasmic reticulum lectin, transcript variant X1
ArfGAP with GTPase domain, ankyrin repeat and PH domain 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ArfGAP with GTPase domain, ankyrin repeat and PH domain 2, transcript variant X2
ArfGAP with GTPase domain, ankyrin repeat and PH domain 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 2 isoform X3
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 2 isoform X2
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 2 isoform X1
membrane associated ring-CH-type finger 9
25-hydroxyvitamin D-1 alpha hydroxylase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
methyltransferase 1, tRNA methylguanosine
Ts translation elongation factor, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
carboxy-terminal domain RNA polymerase II polypeptide A small phosphatase 2
ATP23 metallopeptidase and ATP synthase assembly factor homolog, transcript variant X1
ATP23 metallopeptidase and ATP synthase assembly factor homolog, transcript variant X2
mitochondrial inner membrane protease ATP23 homolog isoform X1
mitochondrial inner membrane protease ATP23 homolog isoform X2
leucine rich repeats and immunoglobulin like domains 3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: leucine-rich repeats and immunoglobulin-like domains protein 3
uncharacterized LOC121677007, transcript variant X3
uncharacterized LOC121677007, transcript variant X1
uncharacterized LOC121677007, transcript variant X2
peptidyl-prolyl cis-trans isomerase NIMA-interacting 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119803304, transcript variant X4
uncharacterized LOC119803304, transcript variant X3
uncharacterized LOC119803304, transcript variant X2
uncharacterized LOC119803304, transcript variant X1
uncharacterized LOC119803306, transcript variant X1
uncharacterized LOC119803306, transcript variant X2
uncharacterized LOC119803304, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin specific peptidase 15, transcript variant X1
ubiquitin specific peptidase 15, transcript variant X2
ubiquitin specific peptidase 15, 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 3 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 15 isoform X1
ubiquitin carboxyl-terminal hydrolase 15 isoform X2
ubiquitin carboxyl-terminal hydrolase 15 isoform X4
ubiquitin specific peptidase 15, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 15 isoform X3
MON2 homolog, regulator of endosome-to-Golgi trafficking, transcript variant X1
MON2 homolog, regulator of endosome-to-Golgi trafficking, transcript variant X2
protein phosphatase, Mg2+/Mn2+ dependent 1H
HIG1 hypoxia inducible domain family member 1C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ribitol xylosyltransferase 1, transcript variant X1
ribitol-5-phosphate xylosyltransferase 1 isoform X1
ribitol xylosyltransferase 1, transcript variant X2
ribitol-5-phosphate xylosyltransferase 1 isoform X2
SLIT-ROBO Rho GTPase activating protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
SLIT-ROBO Rho GTPase activating protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
SLIT-ROBO Rho GTPase-activating protein 1 isoform X1
SLIT-ROBO Rho GTPase-activating protein 1 isoform X2
KICSTOR subunit 2, transcript variant X1
KICSTOR subunit 2, transcript variant X2
KICSTOR complex protein C12orf66 homolog isoform X1
KICSTOR complex protein C12orf66 homolog isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00564
uncharacterized protein C12orf56 homolog
ATP synthase subunit ATP5MJ, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
Ras association domain family member 3, transcript variant X2
ras association domain-containing protein 3 isoform X2
Ras association domain family member 3, transcript variant X1
ras association domain-containing protein 3 isoform X1
TBC1 domain family member 30, transcript variant X1
TBC1 domain family member 30, transcript variant X2
TBC1 domain family member 30, transcript variant X3
TBC1 domain family member 30, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
methionine sulfoxide reductase B3, transcript variant X4
methionine sulfoxide reductase B3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
methionine sulfoxide reductase B3, transcript variant X2
methionine sulfoxide reductase B3, transcript variant X1
methionine-R-sulfoxide reductase B3 isoform X1
methionine-R-sulfoxide reductase B3 isoform X2
methionine sulfoxide reductase B3, transcript variant X5
methionine-R-sulfoxide reductase B3 isoform X3
LLP homolog, long-term synaptic facilitation factor
transmembrane BAX inhibitor motif containing 4
interleukin 1 receptor associated kinase 3, transcript variant X1
interleukin 1 receptor associated kinase 3, transcript variant X2
interleukin-1 receptor-associated kinase 3 isoform X1
interleukin-1 receptor-associated kinase 3 isoform X2
glutamate receptor interacting protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: glutamate receptor-interacting protein 1
COORDINATES: nucleotide motif:Rfam:12.0:RF00429
cullin associated and neddylation dissociated 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 7 bases in 6 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 7 bases in 6 codons; substituted 4 bases at 4 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cullin-associated NEDD8-dissociated protein 1
dual specificity tyrosine phosphorylation regulated kinase 2, transcript variant X1
dual specificity tyrosine-phosphorylation-regulated kinase 2 isoform X1
dual specificity tyrosine phosphorylation regulated kinase 2, transcript variant X3
dual specificity tyrosine phosphorylation regulated kinase 2, transcript variant X2
dual specificity tyrosine-phosphorylation-regulated kinase 2 isoform X2
Mdm1 nuclear protein, transcript variant X2
Mdm1 nuclear protein, transcript variant X1
solute carrier family 35 member E3, transcript variant X2
solute carrier family 35 member E3, transcript variant X1
MDM2 proto-oncogene, transcript variant X3
MDM2 proto-oncogene, transcript variant X1
MDM2 proto-oncogene, transcript variant X2
cleavage and polyadenylation specific factor 6
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 12 bases in 9 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 23% 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 2 bases in 2 codons; deleted 12 bases in 9 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cleavage and polyadenylation specificity factor subunit 6