XB-GENEPAGE-6054130
???displayGene.symbol???:
gaa
???displayGene.name???:
alpha glucosidase
???displayGene.synonyms???
lyag
(
Nomenclature history )
AI Protein Function
:
gaa encodes a lysosomal acid‑alpha‑glucosidase that hydrolyzes glycogen to glucose, functioning as a glycosidase involved in glycogen catabolism; the protein localizes to lysosomes and is expressed in ...[+]
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Diseases:
Disease Ontology:
glycogen storage disease II
MIM:
POMPE DISEASE
External Links:
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| ???displayGene.expression??? | Development Stages Embryonic Tissues Adult Tissues | |||||||||||
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