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GBA1 gene

glucosylceramidase beta 1

Key facts

Official symbol
GBA1
Full name
GBA1
Chromosome
1
Map location
1q22
Organism
Homo sapiens
NCBI Gene ID
2629
Also known as
GBA, GCB, GLUC

Function summary

This gene encodes a lysosomal membrane protein that cleaves the beta-glucosidic linkage of glycosylceramide, an intermediate in glycolipid metabolism. Mutations in this gene cause Gaucher disease, a lysosomal storage disease characterized by an accumulation of glucocerebrosides. A related pseudogene is approximately 12 kb downstream of this gene on chromosome 1. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2010].

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Data source: NCBI Gene · alsesAI Gene Library