| Gene Symbol | GBA |
| Full Name | N370S Heterozygous Neurons |
| Function | is a critical gene in the intersection of lysosomal storage disorders and neurodegenerative diseases. |
| Molecular Weight | 60 kDa |
| Amino Acids | 536 aa |
| Pathways | Amyloid, Autophagy, Autophagy-Lysosomal Pathway, Chaperone, Epigenetic |
| Ensembl ID | ENSG00000177628 |
| GeneCards | GBA |
| Human Protein Atlas | GBA |
| Glucosidase Beta (GBA) | the mutated gene encoding glucocerebrosidase |
| Parkinson's Disease | primary neurodegeneration associated with GBA mutations |
| Gaucher Disease | lysosomal storage disorder caused by homozygous GBA mutations |
| Lysosomal-Autophagy Pathway | cellular system compromise |
| Associated Diseases | AD, Aging, ALI, Als, Alzheimer |
| Known Drugs/Compounds | AAV.GMU01_SS3-GBA1, glucosylceramide, NCGC00188758 |
| Interactions | ABCD3, ACHE, Actin, AD, AGING, ALPHA-SYNUCLEIN |
| SciDEX Hypotheses | Glucosylceramide accumulation nucleates alpha-synu |
| KG Connections | 1588 knowledge graph edges |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
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