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Cellosaurus ICGi033-B (CVCL_C0PM)

[Text version]
Cell line name ICGi033-B
Synonyms 77Q-9
Accession CVCL_C0PM
Resource Identification Initiative To cite this cell line use: ICGi033-B (RRID:CVCL_C0PM)
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; 4851; HTT; Repeat_expansion; p.Gln18[77] (c.52CAG(46)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (from autologous cell line ICGi033-A).
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_B3RX ! ICGi033-A
CVCL_C0PN ! ICGi033-C
Sex of cell Male
Age at sampling 19Y
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; ICGi033-B
Biological sample resources BioSamples; SAMEA20004557
Encyclopedic resources Wikidata; Q112929834
Entry history
Entry creation23-Jun-2022
Last entry update29-Jun-2023
Version number5