Full Name: Necdin, MAGE Family Member
BACKGROUND: 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.
Synonyms: HsT16328; PWCR
Research Areas: Cancer
Pathways: Cancer Pathway
Amerigo scientific offers a comprehensive range of antibodies targeting NDN. Use the filter to find the NDN antibody that best fits your needs.
