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.
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Protein Aliases: Necdin; necdin homolog; necdin, melanoma antigen (MAGE) family member; necdin-like protein; Prader-Willi syndrome chromosome region
Gene Aliases: HsT16328; NDN; PWCR
UniProt ID: (Human) Q99608
Entrez Gene ID: (Human) 4692
Molecular Function: scaffold/adaptor protein