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Cellosaurus GM25456 (CVCL_BA17)

[Text version]
Cell line name GM25456
Accession CVCL_BA17
Resource Identification Initiative To cite this cell line use: GM25456 (RRID:CVCL_BA17)
Comments Population: Jewish; Ashkenazi.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:6990; MECP2; Simple; c.62+1delGT; Zygosity=Unspecified; Note=De novo mutation (Coriell=GM25456).
Disease Rett syndrome (NCIt: C75488)
Rett syndrome (ORDO: Orphanet_778)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_BA16 ! GM25455
Sex of cell Female
Age at sampling 18Y
Category Finite cell line
Cross-references
Cell line collections (Providers) Coriell; GM25456
Encyclopedic resources Wikidata; Q54853980
Entry history
Entry creation02-May-2016
Last entry update19-Dec-2024
Version number13