Cellosaurus GM23824 (CVCL_BX12)
| Cell line name | GM23824 | |
|---|---|---|
| Accession | CVCL_BX12 | |
| Resource Identification Initiative | To cite this cell line use: GM23824 (RRID:CVCL_BX12) | |
| Comments | Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. | |
| Sequence variations |
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| Disease | Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type A, 2 (NCIt: C126742) Walker-Warburg syndrome (ORDO: Orphanet_899) | |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | |
| Hierarchy | Children:
| |
| Sex of cell | Female | |
| Age at sampling | Age unspecified | |
| Category | Finite cell line | |
| Cross-references | ||
| Cell line collections (Providers) | Coriell; GM23824 | |
| Encyclopedic resources | Wikidata; Q54853350 | |
| Entry history | ||
| Entry creation | 13-Jul-2016 | |
| Last entry update | 19-Dec-2024 | |
| Version number | 12 | |