- 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.
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"g(m2) activator protein." Rhymes.net. STANDS4 LLC, 2016. Web. 3 May 2016. <http://www.rhymes.net/rhyme/g%28m2%29%20activator%20protein>.