Uncharacterized protein C1orf122 (C1orf122)
Homo sapiens — UniProt Q6ZSJ8
Data last refreshed: (UniProt release unknown)
Key facts
Uncharacterized protein C1orf122 (C1orf122) is a protein from Homo sapiens identified by UniProt accession Q6ZSJ8, 110 residues long. MolForge cross-references it against 0 known binders and 24 disease associations.
- UniProt accession: Q6ZSJ8; gene symbol C1orf122.
- Organism: Homo sapiens.
- Length: 110 amino acids.
- Top disease associations (Open Targets): neurodegenerative disease, Galloway-Mowat syndrome 10 and lysosomal storage disease.
- 3D structure: AlphaFold model available.
Target properties
| Protein name | Uncharacterized protein C1orf122 |
|---|---|
| UniProt accession | Q6ZSJ8 |
| Gene | C1orf122 |
| Organism | Homo sapiens |
| Length | 110 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 (24)
Diseases linked to this target (Open Targets).
- neurodegenerative disease · score 0.35
- Galloway-Mowat syndrome 10 · score 0.33
- lysosomal storage disease · score 0.18
- mathematical ability · score 0.12
- pulse pressure measurement · score 0.11
- systemic lupus erythematosus · score 0.08
- vital capacity · score 0.07
- hypothyroidism · score 0.05
- platelet component distribution width · score 0.05
- blood protein measurement · score 0.04
3D Structure (1)
Experimental (PDB) and predicted (AlphaFold) structures for this protein.
| Structure | Source | Method | Mean pLDDT | Resolution (Å) |
|---|---|---|---|---|
| AF-Q6ZSJ8-F1 | alphafold | PREDICTED | 67.04 | — |
Experimental structures are not indexed in MolForge yet — search RCSB PDB for Q6ZSJ8.
Amino-acid sequence (110 residues)
Frequently asked questions
Answers are generated from the structured data on this page, not written by hand.
Which diseases are associated with C1orf122?
The strongest Open Targets associations for C1orf122 are neurodegenerative disease, Galloway-Mowat syndrome 10, lysosomal storage disease, mathematical ability and pulse pressure measurement.
How long is the C1orf122 protein?
The Homo sapiens C1orf122 protein (UniProt Q6ZSJ8) is 110 amino acids long.
Browse: Targets: C · all protein targets A–Z · drugs A–Z.
Sources
- UniProtKB Q6ZSJ8 — name, gene, function, sequence, keywords (CC BY 4.0)
- AlphaFold DB Q6ZSJ8 — predicted 3D structure (CC BY 4.0)
- Open Targets Platform — disease associations and tractability (CC0)
How this page is built: methodology · editorial policy & corrections.
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