IPW imprinted in Prader-Willi syndrome
Information
- Symbol
- IPW
- Type
- ncRNA
- Description
- imprinted in Prader-Willi syndrome
- Entrez Gene ID
- 3653
- MIM
- 601491 OMIM
- HGNC
- HGNC:6109 HGNC
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
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Ranking
| ClinVar | |
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Frequency
[No Data.]
Disease area statistics
[No Data.]
Locus Zoom
[No Data.]
Variants
Search Word
| Target data | : |
MGeND data only
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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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| 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
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| 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 | |||||||||||||||
| Descrption | Source | Links |
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Genome browser
[No Data.]