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Cellosaurus CHDIi021-A (CVCL_VC92)

[Text version]
Cell line name CHDIi021-A
Synonyms #21C5; #21c5; CHDI-90002169
Accession CVCL_VC92
Resource Identification Initiative To cite this cell line use: CHDIi021-A (RRID:CVCL_VC92)
Comments From: CHDI Foundation; New York; USA.
Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease.
Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; HGNC:4851; HTT; Repeat_expansion; p.Gln18[44] (c.52CAG(44)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (EBiSC=CHDIi021-A).
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 40-44Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) EBiSC; CHDIi021-A
ECACC; 66541156 - Discontinued
Cell line databases/resources hPSCreg; CHDIi021-A
Biological sample resources BioSamples; SAMEA1088053
Encyclopedic resources Wikidata; Q54811787
Entry history
Entry creation14-May-2018
Last entry update19-Dec-2024
Version number12