Entity Details
| Primary name |
CCN6_HUMAN |
| Entity type |
UniProt |
| Source |
Source Link |
Details
| Accession | O95389 |
| EntryName | CCN6_HUMAN |
| FullName | Cellular communication network factor 6 |
| TaxID | 9606 |
| Evidence | evidence at transcript level |
| Length | 354 |
| SequenceStatus | complete |
| DateCreated | 2003-08-15 |
| DateModified | 2021-06-02 |
Subcellular Location
Show/Hide Table
| Subcellular Location |
| Mitochondrion |
| Secreted |
Domains
Show/Hide Table
| Domain | Name | Category | Type |
| IPR000867 | Insulin-like growth factor-binding protein, IGFBP | Domain | Domain |
| IPR000884 | Thrombospondin type-1 (TSP1) repeat | Repeat | Repeat |
| IPR006207 | Cystine knot, C-terminal | Domain | Domain |
| IPR006208 | Glycoprotein hormone subunit beta | Domain | Domain |
| IPR009030 | Growth factor receptor cysteine-rich domain superfamily | Family | Homologous superfamily |
| IPR012395 | IGFBP-related, CNN | Family | Family |
| IPR017891 | Insulin-like growth factor binding protein, N-terminal, Cys-rich conserved site | Site | Conserved site |
| IPR036383 | Thrombospondin type-1 (TSP1) repeat superfamily | Family | Homologous superfamily |
| IPR043973 | CCN, TSP1 domain | Domain | Domain |
Diseases
Show/Hide Table
| Disease ID | Source | Name | Description |
| 208230 | OMIM | Progressive pseudorheumatoid arthropathy of childhood (PPAC) | Autosomal recessive disorder characterized by stiffness and swelling of joints, motor weakness and joint contractures. Signs and symptoms of the disease develop typically between three and eight years of age. This progressive disease is a primary disorder of articular cartilage with continued cartilage loss and destructive bone changes with aging. The disease is caused by variants affecting the gene represented in this entry. |
Interactions
0 interactions
| Interactor | Partner | Sources | Publications | Link |