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Mammalian protein found in Homo sapiens
GM2 ganglioside activator also known as GM2A is a protein which in humans is encoded by the GM2A gene. The protein encoded by this gene is a small glycolipid
GM2A
Concept in gravitational orbital mechanics
12va2=GM2a−rara(2a)=GM(1ra−12a)=GMra−GM2a Substituting this into our original expression for specific orbital energy, ε=v22−GMr=vp22−GMrp=va22−GMra=−GM2a Thus
Vis-viva_equation
Medical condition
in the GM2A gene cause GM2-gangliosidosis, AB variant. This condition is inherited in an autosomal recessive pattern.[citation needed] The GM2A gene provides
GM2-gangliosidosis, AB variant
GM2-gangliosidosis,_AB_variant
Rare, severe disease of lysosomal storage
third is a small glycolipid transport protein, the GM2 activator protein (GM2A), which acts as a substrate-specific cofactor for the enzyme. Deficiency
Tay–Sachs_disease
Medical condition
nerve cells in the brain and spinal cord. Mutations in the GM2A gene cause AB variant. The GM2A gene provides instructions for making a protein called the
GM2_gangliosidoses
Human chromosome
(acidic fibroblast growth factor) FGFR4: fibroblast growth factor receptor 4 GM2A: GM2 ganglioside activator GNPDA1: Glucosamine-6-phosphate isomerase 1 GPBP1:
Chromosome_5
Protein-coding gene in the species Homo sapiens
specific for this particular glycoprotein and it not understood completely. GM2A (GM2 ganglioside activator) has been viewed as a member of the SAP family
Prosaposin
Q5SZD4 6331 GLYCTK HGNC:24247; Q8IVS8 6332 GLYR1 HGNC:24434; Q49A26 6333 GM2A HGNC:4367; P17900 6334 GMCL1 HGNC:23843; Q96IK5 6335 GMCL2 HGNC:19717; Q8NEA9
List of human protein-coding genes 3
List_of_human_protein-coding_genes_3
GM1-gangliosidosis, type III; 230650; GLB1 GM2-gangliosidosis, AB variant; 272750; GM2A GM2-gangliosidosis, several forms; 272800; HEXA Gnathodiaphyseal dysplasia;
List_of_OMIM_disorder_codes
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