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. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| NDN-20-RE | 20 (40 μL) | 200 μL |  |
Request Pricing |
| NDN-20-OR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| NDN-20-GO | 20 (40 μL) | 200 μL |  |
Request Pricing |
| NDN-20-GR | 20 (40 μL) | 200 μL |  |
Request Pricing |
| NDN-20-AQ | 20 (40 μL) | 200 μL |  |
Request Pricing |
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. [provided by RefSeq, Jul 2008]
Gene Symbol : NDN
Gene Name : Necdin, MAGE family member
Chromosome : CHR 15: 236,873,02-236,854,06
Locus : 15q11.2
Alt. Genes : WASF2
Lorem Ipsum is simply dummy text of the printing and typesetting industry.
Lorem Ipsum is simply dummy text of the printing and typesetting industry.