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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.
AI528698; HsT16328; Ndn; NECD; Necdin; necdin homolog; necdin, MAGE family member; necdin, melanoma antigen (MAGE) family member; necdin-like protein; Peg6; Prader-Willi syndrome chromosome region; PWCR
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