IPW (imprinted in Prader-Willi syndrome)
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Gene
Gene information from NCBI Gene database.
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| Entrez ID | 3653 |
| Gene name | Imprinted in Prader-Willi syndrome |
| Gene symbol | IPW |
| Synonyms (NCBI Gene) |
NCRNA00002
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| Chromosome | 15 |
| Chromosome location | 15q11.2 |
| Summary | This gene is non-protein coding, is expressed exclusively from the paternal allele, and may play a role in the imprinting process. Mutations in this gene are associated with Prader-Willi syndrome. [provided by RefSeq, May 2010] |
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Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
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Related Genes
Genes most often co-reported with IPW across shared curated disease and pathway associations.
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Diseases Linked via Similar Genes
Diseases curated for genes most similar to IPW (see Related Genes above), that are NOT already directly curated for IPW itself -- a lead worth checking, not a confirmed association.
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