MAGEL2 Products

Antibodies
MAGEL2 Antibody
MAGEL2 Antibody
NBP1-02509
Species: Hu
Applications: ELISA, IHC, IHC-P
Host: Rabbit Polyclonal

Description

Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13. 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)

Bioinformatics

Entrez Human
Uniprot Human
Product By Gene ID 54551
Alternate Names
  • protein nM15
  • necdin-like protein 1
  • nM15
  • NDNL1
  • MAGE-like protein 2
  • MAGE-like 2

PTMs for MAGEL2

Learn more about PTMs related to MAGEL2.

Methylation
Demethylation
Deacetylation
Acetylation

Bioinformatics Tool for MAGEL2

Discover related pathways, diseases and genes to MAGEL2. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.
 
Vizit™, under license from BioVista Inc.