Home  |  Contact

Cellosaurus CHDIi008-A (CVCL_VC79)

[Text version]

Cell line name CHDIi008-A
Accession CVCL_VC79
Resource Identification Initiative To cite this cell line use: CHDIi008-A (RRID:CVCL_VC79)
Comments From: CHDI Foundation; New York; USA.
Miscellaneous: At sampling donor was not affected with Huntington disease but at significant risk for disease.
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 45-49Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections EBiSC; CHDIi008-A
ECACC; 66541166
Cell line databases/resources hPSCreg; CHDIi008-A
Biological sample resources BioSamples; SAMEA4675633
Other Wikidata; Q54811769
Entry history
Entry creation14-May-2018
Last entry update12-Mar-2020
Version number4