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Cellosaurus CHDIi026-A (CVCL_VC97)

[Text version]

Cell line name CHDIi026-A
Synonyms #26C3; #26c3; CHDI-90002174
Accession CVCL_VC97
Resource Identification Initiative To cite this cell line use: CHDIi026-A (RRID:CVCL_VC97)
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: Cell type=Fibroblast.
Sequence variations
  • Mutation; HGNC; 4851; HTT; Repeat_expansion; p.Gln18[47] (c.52CAG(47)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (EBiSC).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Sex of cell Female
Age at sampling 30-34Y
Category Induced pluripotent stem cell
Cell line collections EBiSC; CHDIi026-A
ECACC; 66541158
Cell line databases/resources hPSCreg; CHDIi026-A
Biological sample resources BioSamples; SAMEA1088047
Encyclopedic resources Wikidata; Q54811793
Entry history
Entry creation14-May-2018
Last entry update16-Dec-2021
Version number7