Pages
Products

MAGEL2


Official Full Name
MAGE family member L2
Organism
Homo sapiens
Gene ID
54551
Background
Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS. [provided by RefSeq, Oct 2010]
Synonyms
PWLS; nM15; NDNL1; SHFYNG

Cat.No. Product Name Price
SHH336995 shRNA set against Human MAGEL2 (NM_019066.4) Inquiry
SHH336999 shRNA set against Mouse MAGEL2 (NM_013779.2) Inquiry
Cat.No. Product Name Price
CDFG002241 Human MAGEL2 cDNA Clone(NM_019066.4) Inquiry
CDFL007303 Mouse Magel2 cDNA Clone(NM_013779.2) Inquiry
MiUTR3H-07540 MAGEL2 miRNA 3'UTR clone Inquiry
CDCB191720 Rabbit MAGEL2 ORF clone (XM_008269769.1) Inquiry
CDCL129867 Mouse Magel2 ORF clone (NM_013779.2) Inquiry
CDCR304526 Human MAGEL2 ORF Clone(NM_019066.4) Inquiry
Quick Inquiry