| Image |
No pdb structure |
| GO Annotations |
Cellular Component |
|
| Molecular Function |
|
| Biological Process |
|
| Pathways |
|
| Drugs |
|
| Diseases |
|
| GWAS |
- Copper levels ( 26025379)
- Limited cutaneous systemic scleroderma ( 29293537)
- Neonatal cytokine/chemokine levels (fetal genetic effect) ( 30134952)
- Obesity-related traits ( 23251661)
- Spherical equivalent or myopia (age of diagnosis) ( 29808027)
|
| Interacting Genes |
1 interacting genes:
PCM1
|
| Entrez ID |
123016 |
| HPRD ID |
10484 |
| Ensembl ID |
ENSG00000165533
|
| Uniprot IDs |
A0A0C4DFT4
A0A0C4DGH8
A0A0C4DGX9
A0A0C4DGY3
B3KSL8
Q86U25
Q8TAM2
|
| PDB IDs |
|
| Enriched GO Terms of Interacting Partners? |
|
| Tagcloud ? |
|