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Cellosaurus ICGi033-A (CVCL_B3RX)

[Text version]
Cell line name ICGi033-A
Synonyms 77Q-17
Accession CVCL_B3RX
Resource Identification Initiative To cite this cell line use: ICGi033-A (RRID:CVCL_B3RX)
Comments From: The Federal Research Center Institute of Cytology and Genetics; Novosibirsk; Russia.
Population: Caucasian.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:4851; HTT; Repeat_expansion; p.Gln18[77] (c.52CAG(46)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (PubMed=35872525).
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_C0PM ! ICGi033-B
CVCL_C0PN ! ICGi033-C
Sex of cell Male
Age at sampling 19Y
Category Induced pluripotent stem cell
Publications

PubMed=35872525; DOI=10.1016/j.scr.2022.102868
Grigor'eva E.V., Malakhova A.A., Sorogina D.A., Pavlova S.V., Malankhanova T.B., Abramycheva N.Y., Klyushnikov S.A., Illarioshkin S.N., Zakian S.M.
Generation of induced pluripotent stem cell line, ICGi033-A, by reprogramming peripheral blood mononuclear cells from a patient with Huntington's disease.
Stem Cell Res. 63:102868-102868(2022)

Cross-references
Cell line databases/resources hPSCreg; ICGi033-A
Biological sample resources BioSamples; SAMEA10329920
Encyclopedic resources Wikidata; Q110432906
Entry history
Entry creation16-Dec-2021
Last entry update19-Dec-2024
Version number7