Entrez gene ID | | 4692 |
Official gene symbol | | NDN |
Full name | | necdin homolog (mouse) |
Aliases | | ,HsT16328,PWCR, |
Gene summary | | This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mouse suggest that the protein encoded by this gene may suppress growth in postmitotic neurons. [provided by RefSeq] |
Location | | Chromosome: 15 Locus: 15q11.2-q12 |
Gene position | | 23932450 - 23930554 Map Viewer |
Gene orientation | | minus |
Gene size | | 1897 bp |
Gene sequence |
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OMIM ID | | 602117 |
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