Entity Detail — Knowledge Graph Node
This page aggregates everything SciDEX knows about GBA: its mechanistic relationships (Knowledge Graph edges), hypotheses targeting it, analyses mentioning it, and supporting scientific papers. The interactive graph below shows its immediate neighbors. All content is AI-synthesized from peer-reviewed literature.
GBA is a gene implicated in neurodegeneration research. Key relationships include: interacts with, associated with, activates. Associated with AD, ALI, ALS. Connected to 591 entities in the SciDEX knowledge graph.
| Gene Symbol | GBA |
| Chromosome | 1q22. |
| 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 |
| LRRK2 | Another Parkinson's disease susceptibility gene with lysosomal dysfunction mechanisms |
| SNCA | Encodes α-synuclein; GBA mutations promote its aggregation |
| SMPD1 | Acid sphingomyelinase; related lysosomal lipid hydrolase |
| Gaucher Disease | GBA mutation disease with primary manifestation |
| Associated Diseases | AD, ALI, ALS, Aging, Alzheimer |
| Interactions | FUNDC1, AMBRA1, PINK1, BCL2L13, NLRP3, ABCD3 |
| KG Connections | 1489 knowledge graph edges |
| Databases | GeneCardsUniProtNCBI GeneHPASTRING |
Knowledge base pages for this entity
graph TD
GBA["GBA"] -->|"causes"| mitochondrial_dysfunction["mitochondrial dysfunction"]
GBA["GBA"] -.->|"inhibits"| autophagy["autophagy"]
GBA["GBA"] -.->|"inhibits"| mitophagy["mitophagy"]
GBA["GBA"] -->|"contributes to"| Parkinson_disease["Parkinson disease"]
GBA["GBA"] -->|"contributes to"| Parkinson_s_disease["Parkinson's disease"]
GBA["GBA"] -->|"activates"| Parkinson["Parkinson"]
Parkinson_1["Parkinson"] -->|"interacts"| GBA["GBA"]
CAT["CAT"] -->|"interacts"| GBA["GBA"]
OPTN["OPTN"] -->|"interacts"| GBA["GBA"]
DNM1L["DNM1L"] -->|"interacts"| GBA["GBA"]
style GBA fill:#4a1a6b,stroke:#4fc3f7,stroke-width:2px,color:#e0e0e0| Target | Relation | Type | Str |
|---|---|---|---|
| Lewy body pathology | associated_with | phenotype | 0.98 |
| right pars triangularis volume | causes | brain_region | 0.98 |
| Parkinson Disease | risk_factor_for | disease | 0.95 |
| GLUCOSYLCERAMIDASE | encodes | enzyme | 0.95 |
| GCASE | encodes | enzyme | 0.95 |
| Glucocerebrosidase | encodes | enzyme | 0.95 |
| Gaucher Disease | causes | disease | 0.95 |
| Gaucher's disease | causes | disease | 0.95 |
| Parkinson's Disease | risk_factor_for | disease | 0.95 |
| Parkinson'S Disease | risk_factor_for | disease | 0.95 |
| Glucosylceramide Accumulation | causes | phenotype | 0.93 |
| autophagy | inhibits | pathway | 0.90 |
| Parkinson disease | contributes_to | disease | 0.90 |
| Glucocerebrosides | associated_with | chemical | 0.90 |
| Glucocerebrosidase | associated_with | enzyme | 0.90 |
| gut-brain axis | participates_in | pathway | 0.90 |
| Gaucher disease | causes | disease | 0.90 |
| mitochondrial dysfunction | causes | phenotype | 0.90 |
| mitophagy | inhibits | pathway | 0.90 |
| Parkinson's disease | contributes_to | disease | 0.90 |
| LYSOSOMAL DYSFUNCTION | regulates | entity | 0.90 |
| oxidative stress response | participates_in | pathway | 0.90 |
| Parkinson's disease | risk_factor | disease | 0.90 |
| Autophagy-Lysosomal Pathway | regulates | pathway | 0.88 |
| Glucosylceramidase Beta 1 | activates | protein | 0.85 |
| Alpha-Synuclein Neurotoxicity | modulates | phenotype | 0.85 |
| α-synuclein neurotoxicity | modulates | phenotype | 0.85 |
| lysosomal degradation | involved_in | process | 0.85 |
| Als | associated_with | disease | 0.85 |
| Parkinson'S Disease | involved_in | disease | 0.85 |
| Autophagy | involved_in | process | 0.85 |
| putamen volume | regulates | brain_region | 0.82 |
| non-manifesting carriers | expressed_in | cell_type | 0.80 |
| Lewy body dementia | associated_with | disease | 0.80 |
| alpha-synuclein | regulates | protein | 0.80 |
| Parkinson | activates | entity | 0.80 |
| Microglial Autophagy and Phagocytosis | contributes_to | process | 0.75 |
| Parkinson | associated_with | disease | 0.75 |
| Parkinson | therapeutic_target | disease | 0.75 |
| Dementia | associated_with | disease | 0.75 |
| Depression | therapeutic_target | disease | 0.75 |
| Als | activates | disease | 0.75 |
| REM sleep behavior disorder | associated_with | disease | 0.70 |
| glucosylceramidase beta | encodes | protein | 0.70 |
| neurodegeneration | associated_with | disease | 0.70 |
| neurodegeneration | interacts_with | disease | 0.70 |
| neuroinflammation | implicated_in | disease | 0.70 |
| lysosomal degradation | regulates | process | 0.70 |
| Parkinson | regulates | entity | 0.70 |
| Parkinson's disease | associated_with | disease | 0.70 |
| Source | Relation | Type | Str |
|---|---|---|---|
| ALZHEIMER'S DISEASE | associated_with | gene | 1.00 |
| PARKINSON'S DISEASE | associated_with | gene | 1.00 |
| rs75548401 | associated_with | compound | 0.92 |
| NEURODEGENERATION | associated_with | gene | 0.90 |
| LRRK2 | interacts_with | gene | 0.85 |
| AMYLOID | associated_with | gene | 0.74 |
| MICROGLIA | associated_with | cell_type | 0.74 |
| LRRK2 | associated_with | gene | 0.70 |
| SNCA | associated_with | gene | 0.70 |
| Parkinson | interacts_with | entity | 0.70 |
| PARKINSON'S DISEASE | therapeutic_target | gene | 0.70 |
| PARKINSON'S DISEASE | activates | gene | 0.70 |
| ALPHA-SYNUCLEIN | causes | gene | 0.70 |
| PARKINSON | associated_with | gene | 0.70 |
| PARKINSON | therapeutic_target | gene | 0.70 |
| AUTOPHAGY | associated_with | gene | 0.66 |
| APOE | associated_with | gene | 0.65 |
| APOE | co_discussed | gene | 0.65 |
| BIN1 | co_discussed | gene | 0.65 |
| ACHE | protects_against | gene | 0.65 |
| ATP | activates | gene | 0.65 |
| FRONTOTEMPORAL DEMENTIA | causes | disease | 0.65 |
| NEURONS | produces | cell_type | 0.65 |
| LEVODOPA | exacerbates | drug | 0.65 |
| DEPRESSION | increases_risk | disease | 0.65 |
| DEMENTIA | regulates | disease | 0.65 |
| CAT | interacts_with | gene | 0.60 |
| OPTN | interacts_with | gene | 0.60 |
| DNM1L | interacts_with | gene | 0.60 |
| CANX | interacts_with | gene | 0.60 |
| LGALS3 | interacts_with | gene | 0.60 |
| CALCOCO2 | interacts_with | gene | 0.60 |
| G3BP1 | interacts_with | gene | 0.60 |
| PEX3 | interacts_with | gene | 0.60 |
| SQSTM1 | interacts_with | gene | 0.60 |
| BCL2 | interacts_with | gene | 0.60 |
| LMNA | interacts_with | gene | 0.60 |
| STING1 | interacts_with | gene | 0.60 |
| TAX1BP1 | interacts_with | gene | 0.60 |
| ATM | interacts_with | gene | 0.60 |
| SNCAIP | interacts_with | gene | 0.60 |
| RB1CC1 | interacts_with | gene | 0.60 |
| MFN1 | interacts_with | gene | 0.60 |
| ERN1 | interacts_with | gene | 0.60 |
| PARKIN | interacts_with | gene | 0.60 |
| FMR1 | interacts_with | gene | 0.60 |
| SNCA | interacts_with | gene | 0.60 |
| FAM134B | interacts_with | gene | 0.60 |
| LC3 | interacts_with | gene | 0.60 |
| EPAS1 | interacts_with | gene | 0.60 |
Hypotheses where this entity is a therapeutic target
| Hypothesis | Score | Disease | Analysis |
|---|---|---|---|
| No targeting hypotheses | |||
Scientific analyses that reference this entity
molecular biology | 2026-04-11 | 0 hypotheses
neurodegeneration | 2026-04-01 | 0 hypotheses
neurodegeneration | 2026-04-01 | 0 hypotheses
Scientific publications cited in analyses involving this entity
| Title & PMID | Authors | Journal | Year | Citations |
|---|---|---|---|---|
| No papers found | ||||