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Cellosaurus CHDIi011-A (CVCL_VC82)

[Text version]

Cell line name CHDIi011-A
Synonyms #11c2; CHDI-90002159
Accession CVCL_VC82
Resource Identification Initiative To cite this cell line use: CHDIi011-A (RRID:CVCL_VC82)
Comments From: CHDI Foundation; New York; USA.
Miscellaneous: At sampling donor was not affected with Huntington disease but at significant risk for disease.
Derived from sampling site: Fibroblast.
Sequence variations Heterozygous for HTT p.Gln18[43]; has 43 CAG repeats in one of the 2 alleles (hPSCreg).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Male
Age at sampling 50-54Y
Category Induced pluripotent stem cell
Cell line collections EBiSC; CHDIi011-A
ECACC; 66541169
Cell line databases/resources hPSCreg; CHDIi011-A
Biological sample resources BioSamples; SAMEA4675639
Other Wikidata; Q54811772
Entry history
Entry creation14-May-2018
Last entry update29-Oct-2020
Version number5