WIPI2 WD repeat domain, phosphoinositide interacting 2
Information
- Symbol
- WIPI2
- Type
- protein-coding
- Description
- WD repeat domain, phosphoinositide interacting 2
- Entrez Gene ID
- 26100
- Genome
- hg19
- Position
- chr7:5,229,864-5,273,471
- Genome
- hg38
- Position
- chr7:5,190,233-5,233,840
- MIM
- 609225 OMIM
- HGNC
- HGNC:32225 HGNC
- Ensembl
- ENSG00000157954 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Pathogenic | 0 | 4 |
| Benign | 0 | 26 |
| Likely benign | 0 | 18 |
| Uncertain significance | 0 | 30 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
14 |
 |
56 |
 |
6 |
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | ATG18B |
| SYNONYM | Atg21 |
| SYNONYM | CGI-50 |
| SYNONYM | IDDSSA |
| SYNONYM | WIPI-2 |
| MIM | 609225 OMIM |
| HGNC | HGNC:32225 HGNC |
| Ensembl | ENSG00000157954 Ensembl |
| AllianceGenome | HGNC:32225 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000288828.9 | hg38 | chr7 | 5,190,233 | 5,233,840 | 43,608 |
| ENST00000484262.1 | hg38 | chr7 | 5,214,269 | 5,231,064 | 16,796 |
| ENST00000401525.7 | hg38 | chr7 | 5,190,196 | 5,231,524 | 41,329 |
| ENST00000382384.6 | hg38 | chr7 | 5,190,273 | 5,231,470 | 41,198 |
| ENST00000404704.7 | hg38 | chr7 | 5,190,246 | 5,231,104 | 40,859 |
| ENST00000401525.7 | hg19 | chr7 | 5,229,827 | 5,271,155 | 41,329 |
| ENST00000288828.9 | hg19 | chr7 | 5,229,864 | 5,273,471 | 43,608 |
| ENST00000404704.7 | hg19 | chr7 | 5,229,877 | 5,270,735 | 40,859 |
| ENST00000382384.6 | hg19 | chr7 | 5,229,904 | 5,271,101 | 41,198 |
| ENST00000484262.1 | hg19 | chr7 | 5,253,900 | 5,270,695 | 16,796 |
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