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Cellosaurus ICGi018-B (CVCL_YK94)

[Text version]
Cell line name ICGi018-B
Synonyms iHD38Q-2
Accession CVCL_YK94
Resource Identification Initiative To cite this cell line use: ICGi018-B (RRID:CVCL_YK94)
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[38] (c.52CAG(38)) (c.52CAG[(36_39)]); ClinVar=VCV000031916; Zygosity=Heterozygous (from autologous cell line ICGi018-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_YK93 ! ICGi018-A
CVCL_YK95 ! ICGi018-C
Sex of cell Female
Age at sampling 83Y
Category Induced pluripotent stem cell
Cross-references
Cell line databases/resources hPSCreg; ICGi018-B
Biological sample resources BioSamples; SAMEA6438550
Encyclopedic resources Wikidata; Q94313469
Entry history
Entry creation19-Dec-2019
Last entry update19-Dec-2024
Version number9