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Cellosaurus GM29742 (CVCL_F1A2)

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Cell line name GM29742
Accession CVCL_F1A2
Resource Identification Initiative To cite this cell line use: GM29742 (RRID:CVCL_F1A2)
Comments Population: Caucasian.
Donor information: At sampling donor was not affected with frontotemporal dementia but at risk for disease.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:6893; MAPT; Simple; p.Arg798Trp (c.2392C>T) (p.Arg406Trp, c.1216C>T or p.Arg723Trp, c.2167C>T); ClinVar=VCV000014247; Zygosity=Heterozygous (Coriell=GM29742).
Disease Frontotemporal dementia (NCIt: C84719)
Behavioral variant of frontotemporal dementia (ORDO: Orphanet_275864)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 34Y
Category Finite cell line
Cross-references
Cell line collections (Providers) Coriell; GM29742
Entry history
Entry creation27-Nov-2025
Last entry update27-Nov-2025
Version number1