IPW (imprinted in Prader-Willi syndrome)
| Gene | |
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Entrez ID
Entrez Gene ID - the GENE ID in NCBI Gene database.
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3653 |
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Gene name
Gene Name - the full gene name approved by the HGNC.
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Imprinted in Prader-Willi syndrome |
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Gene symbol
Gene Symbol - the official gene symbol approved by the HGNC.
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IPW |
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Synonyms (NCBI Gene)
Gene synonyms aliases
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NCRNA00002 |
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Chromosome
Chromosome number
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15 |
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Chromosome location
Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
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15q11.2 |
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Summary
Summary of gene provided in NCBI Entrez Gene.
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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 ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
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