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Cellosaurus GM27195 (CVCL_ZG17)

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Cell line name GM27195
Accession CVCL_ZG17
Resource Identification Initiative To cite this cell line use: GM27195 (RRID:CVCL_ZG17)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Merosin-deficient congenital muscular dystrophy type 1A (NCIt: C118783)
Laminin subunit alpha 2-related congenital muscular dystrophy (ORDO: Orphanet_258)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 9Y
Category Finite cell line
Cross-references
Cell line collections (Providers) Coriell; GM27195
Encyclopedic resources Wikidata; Q98126384
Entry history
Entry creation02-Jul-2020
Last entry update29-Jun-2023
Version number5