Ubiquitin carboxyl-terminal hydrolase 17-like protein 12 (USP17L12)
Homo sapiens — UniProt C9JPN9
Data last refreshed: (UniProt release unknown)
Key facts
Ubiquitin carboxyl-terminal hydrolase 17-like protein 12 (USP17L12) is a protein from Homo sapiens identified by UniProt accession C9JPN9, 530 residues long. MolForge cross-references it against 0 known binders and 21 disease associations.
- UniProt accession: C9JPN9; gene symbol USP17L12.
- Organism: Homo sapiens.
- Length: 530 amino acids.
- Top disease associations (Open Targets): immunodeficiency 19, urate measurement and combined immunodeficiency with skin granulomas.
- 3D structure: AlphaFold model available.
Target properties
| Protein name | Ubiquitin carboxyl-terminal hydrolase 17-like protein 12 |
|---|---|
| UniProt accession | C9JPN9 |
| Gene | USP17L12 |
| Organism | Homo sapiens |
| Length | 530 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 (21)
Diseases linked to this target (Open Targets).
- immunodeficiency 19 · score 0.04
- urate measurement · score 0.04
- combined immunodeficiency with skin granulomas · score 0.03
- immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia · score 0.03
- severe combined immunodeficiency due to IKK2 deficiency · score 0.03
- ring chromosome Y · score 0.03
- X-Linked Combined Immunodeficiency Diseases · score 0.03
- severe combined immunodeficiency due to LAT deficiency · score 0.03
- obesity due to congenital leptin deficiency · score 0.03
- immunodeficiency 99 with hypogammaglobulinemia and autoimmune cytopenias · score 0.03
3D Structure (1)
Experimental (PDB) and predicted (AlphaFold) structures for this protein.
| Structure | Source | Method | Mean pLDDT | Resolution (Å) |
|---|---|---|---|---|
| AF-C9JPN9-F1 | alphafold | PREDICTED | 67.89 | — |
Experimental structures are not indexed in MolForge yet — search RCSB PDB for C9JPN9.
Amino-acid sequence (530 residues)
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
Which diseases are associated with USP17L12?
The strongest Open Targets associations for USP17L12 are immunodeficiency 19, urate measurement, combined immunodeficiency with skin granulomas, immunodeficiency 73c with defective neutrophil chemotaxis and hypogammaglobulinemia and severe combined immunodeficiency due to IKK2 deficiency.
How long is the USP17L12 protein?
The Homo sapiens USP17L12 protein (UniProt C9JPN9) is 530 amino acids long.
Browse: Targets: U · all protein targets A–Z · drugs A–Z.
Sources
- UniProtKB C9JPN9 — name, gene, function, sequence, keywords (CC BY 4.0)
- AlphaFold DB C9JPN9 — predicted 3D structure (CC BY 4.0)
- Open Targets Platform — disease associations and tractability (CC0)
How this page is built: methodology · editorial policy & corrections.
For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.