Cellosaurus GM23824 (CVCL_BX12)
Cell line name | GM23824 |
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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) |
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 |