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Cellosaurus CHDIi018-A (CVCL_VC89)

[Text version]

Cell line name CHDIi018-A
Synonyms #18c1; CHDI-90002166
Accession CVCL_VC89
Resource Identification Initiative To cite this cell line use: CHDIi018-A (RRID:CVCL_VC89)
Comments From: CHDI Foundation; New York; USA.
Derived from sampling site: Cell type=Fibroblast.
Sequence variations Mutation; HGNC; 4851; HTT; Repeat_expansion; p.Gln18[43] (c.52CAG(43)) (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 Male
Age at sampling 40-44Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections EBiSC; CHDIi018-A
ECACC; 66541173
Cell line databases/resources hPSCreg; CHDIi018-A
Biological sample resources BioSamples; SAMEA4675647
Encyclopedic resources Wikidata; Q54811780
Entry history
Entry creation14-May-2018
Last entry update16-Dec-2021
Version number7