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Cellosaurus GM11269 (CVCL_4F12)

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Cell line name GM11269
Accession CVCL_4F12
Resource Identification Initiative To cite this cell line use: GM11269 (RRID:CVCL_4F12)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Disease Rett syndrome (NCIt: C75488)
Rett syndrome (ORDO: Orphanet_778)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 13Y
Category Finite cell line
Publications

PubMed=11738860; DOI=10.1016/S0387-7604(01)00339-4
Stephen Sung Jae Lee, Mi-Mi Wan, Uta Francke;
Spectrum of MECP2 mutations in Rett syndrome.
Brain Dev. 23 Suppl. 1:S138-S143(2001)

Cross-references
Cell line collections (Providers) Coriell; GM11269
Cell line databases/resources CLO; CLO_0025966
Encyclopedic resources Wikidata; Q54844949
Entry history
Entry creation22-Sep-2015
Last entry update29-Jun-2023
Version number7