WDSUB1 WD repeat, sterile alpha motif and U-box domain containing 1
Information
- Symbol
- WDSUB1
- Type
- protein-coding
- Description
- WD repeat, sterile alpha motif and U-box domain containing 1
- Entrez Gene ID
- 151525
- Genome
- hg19
- Position
- chr2:160,092,312-160,143,103
- Genome
- hg38
- Position
- chr2:159,235,801-159,286,592
- MIM
- 620802 OMIM
- HGNC
- HGNC:26697 HGNC
- Ensembl
- ENSG00000196151 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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50 |
![]() |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | UBOX6 |
SYNONYM | WDSAM1 |
MIM | 620802 OMIM |
HGNC | HGNC:26697 HGNC |
Ensembl | ENSG00000196151 Ensembl |
AllianceGenome | HGNC:26697 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000359774.9 | hg38 | chr2 | 159,235,798 | 159,286,703 | 50,906 |
ENST00000392796.7 | hg38 | chr2 | 159,235,801 | 159,286,552 | 50,752 |
ENST00000358147.8 | hg38 | chr2 | 159,235,798 | 159,286,703 | 50,906 |
ENST00000409124.1 | hg38 | chr2 | 159,235,834 | 159,286,669 | 50,836 |
ENST00000409990.7 | hg38 | chr2 | 159,235,801 | 159,286,592 | 50,792 |
ENST00000359774.9 | hg19 | chr2 | 160,092,309 | 160,143,214 | 50,906 |
ENST00000358147.8 | hg19 | chr2 | 160,092,309 | 160,143,214 | 50,906 |
ENST00000392796.7 | hg19 | chr2 | 160,092,312 | 160,143,063 | 50,752 |
ENST00000409990.7 | hg19 | chr2 | 160,092,312 | 160,143,103 | 50,792 |
ENST00000409124.1 | hg19 | chr2 | 160,092,345 | 160,143,180 | 50,836 |
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