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Cellosaurus ICGi018-A (CVCL_YK93)

[Text version]

Cell line name ICGi018-A
Synonyms iHD38Q-3
Accession CVCL_YK93
Resource Identification Initiative To cite this cell line use: ICGi018-A (RRID:CVCL_YK93)
Comments From: The Federal Research Center Institute of Cytology and Genetics; Novosibirsk; Russia.
Derived from sampling site: Peripheral blood.
Sequence variations Heterozygous for HTT p.Gln18[38]; has 38 CAG repeats in one of the 2 alleles (PubMed=32179492).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_YK94 ! ICGi018-B
CVCL_YK95 ! ICGi018-C
Sex of cell Female
Age at sampling 83Y
Category Induced pluripotent stem cell

PubMed=32179492; DOI=10.1016/j.scr.2020.101743
Malakhova A.A., Grigor'eva E.V., Malankhanova T.B., Pavlova S.V., Valetdinova K.R., Abramycheva N.Y., Vetchinova A.S., Illarioshkin S.N., Zakian S.M.
Generation of induced pluripotent stem cell line ICGi018-A from peripheral blood mononuclear cells of a patient with Huntington's disease.
Stem Cell Res. 44:101743-101743(2020)

Cell line databases/resources hPSCreg; ICGi018-A
SKIP; SKIP005696
Biological sample resources BioSamples; SAMEA6438237
Other Wikidata; Q94313465
Entry history
Entry creation19-Dec-2019
Last entry update12-Jan-2021
Version number4