Cellosaurus CRICKi021-A (CVCL_D1G0)
| Cell line name | CRICKi021-A |
|---|---|
| Synonyms | iFCI007 |
| Accession | CVCL_D1G0 |
| Resource Identification Initiative | To cite this cell line use: CRICKi021-A (RRID:CVCL_D1G0) |
| Comments | From: The Francis Crick Institute Limited; London; United Kingdom. Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Ullrich congenital muscular dystrophy (NCIt: C123438) Congenital muscular dystrophy, Ullrich type (ORDO: Orphanet_75840) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Male |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line databases/resources | hPSCreg; CRICKi021-A |
| Biological sample resources | BioSamples; SAMEA114466772 |
| Entry history | |
| Entry creation | 30-Jan-2024 |
| Last entry update | 30-Jan-2024 |
| Version number | 1 |