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G(M2) Activator Protein

An essential cofactor for the degradation of G(M2)GANGLIOSIDE by lysosomal BETA-N-ACETYLHEXOSAMINIDASES. Genetic mutations resulting in loss of G(M2) activator protein are one of the causes of TAY-SACHS DISEASE, AB VARIANT.
推出的年份: 2005(1983)
副标题
树号: D08.211.790.249
MeSH 单一 ID: D049289
进入的组:
  • GM2 Activator Protein
  • Activator Protein, GM2
  • Hexosaminidase Activator
  • GM(2) Activating Protein
早前的内容:
  • Proteins (1983-2004)

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