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Cellosaurus H236 C6 GC (CVCL_A4GA)

[Text version]
Cell line name H236 C6 GC
Synonyms H236 clone 6 GC
Accession CVCL_A4GA
Resource Identification Initiative To cite this cell line use: H236 C6 GC (RRID:CVCL_A4GA)
Comments From: Bioneer A/S; Horsholm; Denmark.
Donor information: At sampling donor was pre-symptomatic for frontotemporal dementia.
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_corrected; p.Arg406Trp (c.1216C>T); ClinVar=VCV000014247; Zygosity=Heterozygous; Note=By CRISPR/Cas9 (PubMed=27934590).
Disease Frontotemporal dementia (NCIt: C84719)
Behavioral variant of frontotemporal dementia (ORDO: Orphanet_275864)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_DQ58 (H236 C6)
Sex of cell Female
Age at sampling 28Y
Category Induced pluripotent stem cell
Publications

PubMed=27934590; DOI=10.1016/j.scr.2016.09.024
Nimsanor N., Poulsen U.B., Rasmussen M.A., Clausen C., Mau-Holzmann U.A., Nielsen J.E., Nielsen T.T., Hyttel P., Holst B., Schmid B.
Generation of an isogenic, gene-corrected iPSC line from a pre-symptomatic 28-year-old woman with an R406W mutation in the microtubule associated protein Tau (MAPT) gene.
Stem Cell Res. 17:600-602(2016)

Cross-references
Cell line databases/resources SKIP; SKIP003203
Encyclopedic resources Wikidata; Q105507530
Entry history
Entry creation12-Jan-2021
Last entry update19-Dec-2024
Version number7