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GBA2 gene

Known as: GLUCOSYLCERAMIDASE, NONLYSOSOMAL, DKFZp762K054, BETA-GLUCOSIDASE, BILE ACID 
This gene plays a role in bile acid hydrolysis.
National Institutes of Health

Related topics

Related topics

3 relations
GBA3 geneHydrolysisNon-Lysosomal Glucosylceramidase

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2017
2017
Glucosylceramide metabolism: from 3D structure to the development of selective chemical probes
Gaucher's disease, the most prevalent of the lysosomal storage disorders, is caused by insufficient lysosomal glucocerebrosidase… 
2016
2016
Characterization of the Zebrafish Homolog of β-Glucosidase 2: A Target of the Drug Miglustat
Abstract The small-molecular compound miglustat (N-butyldeoxynojirimycin, Zavesca®) has been approved for clinical use in type 1… 
2016
2016
The role of Glucocerebrosidase GBA2 in cystic fibrosis lung inflammation: from molecular mechanism to therapeutic strategies
Background. Several studies indicate that sphingolipids (SL) play a regulatory role in airway inflammation, the most critical… 
Review
2015
Review
2015
Current and Novel Aspects on the Non-lysosomal β-Glucosylceramidase GBA2
The non-lysosomal β-glucosylceramidase GBA2 (EC3.2.1.45, GH116) is ubiquitously expressed in various mammal tissues and cell… 
2008
2008
Beta-glucosidase 2 (GBA2) deficiency leads to zonal glucosylceramide accumulation in the liver
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