Cellosaurus GM29132 (CVCL_D6WS)
| Cell line name | GM29132 |
|---|---|
| Synonyms | GM29132*B |
| Accession | CVCL_D6WS |
| Resource Identification Initiative | To cite this cell line use: GM29132 (RRID:CVCL_D6WS) |
| Comments | Population: Indian. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Sequence variations |
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| Disease | Leigh disease (NCIt: C84814) Mitochondrial complex IV deficiency, nuclear type 1 (NCIt: C176895) Leigh syndrome (ORDO: Orphanet_506) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_B3SE (GM28063) |
| Sex of cell | Male |
| Age at sampling | 33Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | Coriell; GM29132 |
| Entry history | |
| Entry creation | 10-Sep-2024 |
| Last entry update | 19-Dec-2024 |
| Version number | 2 |