MAGEL2
MAGE-like 2
别名:
NDNL1, nM15
物种:
UniProtKB ID:
基因ID:
- Human(54551) Summary: 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]
- Mouse(27385) melanoma antigen, family L, 2
- Rat(679875) MAGE-like 2
- cow(538665) MAGE-like 2
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Antibodies
货号
说明
物种反应性
应用
Anti-MAGEL2 antibody produced in rabbit, affinity isolated antibody,
物种反应性
human
应用
western blot