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Cellosaurus CHDIi028-A (CVCL_VC99)

[Text version]

Cell line name CHDIi028-A
Synonyms #28c3
Accession CVCL_VC99
Resource Identification Initiative To cite this cell line use: CHDIi028-A (RRID:CVCL_VC99)
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[46]; has 46 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 30-34Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections ECACC; 66541162
Cell line databases/resources hPSCreg; CHDIi028-A
Biological sample resources BioSamples; SAMEA4675324
Other Wikidata; Q54811795
Entry history
Entry creation14-May-2018
Last entry update12-Mar-2020
Version number4