Annotation Detail

Information
Associated Genes
GBA1
Associated Variants
GBA1 MUTATION
GBA1 MUTATION
Associated Disease
Lysosomal Storage Diseases
Source Database
DisGeNET
Description
Mutations in the gene that encodes the lysosomal enzyme acid β-glucosidase lead to reduced cellular activity and accumulation of glycosphingolipid substrates, biochemical hallmarks of the lysosomal storage disorder Gaucher disease (GD).
Pubmed
24894562
Section of the abstract supporting the evidence
ALL_TEXT_1/3
Number of the section of the abstract supporting the evidence
1
Number of the sentence supporting the evidence
1
Original source reporting the Gene Disease association
BeFree
DisGENET score for the Gene Disease association
0.00732893054616819
Drugs