Rab3 GTPase-activating protein non-catalytic subunit (RAB3GAP2)
Homo sapiens — UniProt Q9H2M9
Data last refreshed: (UniProt release unknown)
Key facts
Rab3 GTPase-activating protein non-catalytic subunit (RAB3GAP2) is a protein from Homo sapiens identified by UniProt accession Q9H2M9, 1393 residues long. MolForge cross-references it against 0 known binders and 60 disease associations.
- UniProt accession: Q9H2M9; gene symbol RAB3GAP2.
- Organism: Homo sapiens.
- Length: 1393 amino acids.
- Top disease associations (Open Targets): Micro syndrome, Cataract - intellectual disability - hypogonadism and Martsolf syndrome.
- 3D structure: AlphaFold model available.
Target properties
| Protein name | Rab3 GTPase-activating protein non-catalytic subunit |
|---|---|
| UniProt accession | Q9H2M9 |
| Gene | RAB3GAP2 |
| Organism | Homo sapiens |
| Length | 1393 residues |
| Molecular weight | — |
| EC numbers | — |
| Target class | — |
| Subcellular location | — |
| Keywords | — |
Druggability
Target tractability assessment (Open Targets + pocket analysis). No approved drug
| Druggability tier | MEDIUM |
|---|---|
| Druggability score | — |
| Pocket score | — |
| Max clinical phase | — |
Disease associations (60)
Diseases linked to this target (Open Targets).
- Micro syndrome · score 0.77
- Cataract - intellectual disability - hypogonadism · score 0.77
- Martsolf syndrome · score 0.73
- neurodegenerative disease · score 0.51
- Warburg micro syndrome · score 0.42
- genetic disorder · score 0.41
- autosomal recessive spastic paraplegia type 69 · score 0.37
- Neurodevelopmental delay · score 0.27
- Tracheoesophageal fistula · score 0.26
- brain measurement · score 0.20
3D Structure (1)
Experimental (PDB) and predicted (AlphaFold) structures for this protein.
| Structure | Source | Method | Mean pLDDT | Resolution (Å) |
|---|---|---|---|---|
| AF-Q9H2M9-F1 | alphafold | PREDICTED | 79.60 | — |
Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q9H2M9.
Amino-acid sequence (1393 residues)
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
Which diseases are associated with RAB3GAP2?
The strongest Open Targets associations for RAB3GAP2 are Micro syndrome, Cataract - intellectual disability - hypogonadism, Martsolf syndrome, neurodegenerative disease and Warburg micro syndrome.
How long is the RAB3GAP2 protein?
The Homo sapiens RAB3GAP2 protein (UniProt Q9H2M9) is 1393 amino acids long.
Browse: Targets: R · all protein targets A–Z · drugs A–Z.
Sources
- UniProtKB Q9H2M9 — name, gene, function, sequence, keywords (CC BY 4.0)
- AlphaFold DB Q9H2M9 — predicted 3D structure (CC BY 4.0)
- Open Targets Platform — disease associations and tractability (CC0)
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