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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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Necdin; necdin homolog; necdin, melanoma antigen (MAGE) family member; necdin-like protein; Prader-Willi syndrome chromosome region
基因别名: HsT16328; NDN; PWCR
UniProt ID: (Human) Q99608
Entrez Gene ID: (Human) 4692