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NDN (gene)

NDN
Identifiers
Aliases NDN, HsT16328, PWCR, necdin, MAGE family member
External IDs MGI: 97290 HomoloGene: 20559 GeneCards: NDN
RNA expression pattern
PBB GE NDN 209550 at tn.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_002487

NM_010882

RefSeq (protein)

NP_002478

NP_035012.2
NP_035012

Location (UCSC) Chr 15: 23.69 – 23.69 Mb Chr 7: 62.35 – 62.35 Mb
PubMed search

NM_002487

NM_010882

NP_002478

NP_035012.2
NP_035012

Necdin is a protein that in humans is encoded by the NDN gene.

This intronless gene is located in the Prader-Willi syndrome (PWS) deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mice suggest that the protein encoded by this gene may suppress growth in postmitotic neurons.

Necdin is used to stimulate growth regulation,and DNA-dependent transcription regulation.

NDN (gene) has been shown to interact with:



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Wikipedia

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