| Cell line name | ND50081 |
|---|---|
| Accession | CVCL_SA27 |
| Resource Identification Initiative | To cite this cell line use: ND50081 (RRID:CVCL_SA27) |
| Comments | Population: Caucasian. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Sequence variations |
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| Disease | Werdnig-Hoffmann disease (NCIt: C98670) Proximal spinal muscular atrophy type 1 (ORDO: Orphanet_83330) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_Y965 (GM00232) |
| Sex of cell | Male |
| Age at sampling | 7M |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | NHCDR; ND50081 |
| Encyclopedic resources | Wikidata; Q54930309 |
| Entry history | |
| Entry creation | 14-May-2018 |
| Last entry update | 30-Jan-2024 |
| Version number | 10 |