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Cellosaurus IIMCBi006-A (CVCL_C1Q6)

[Text version]
Cell line name IIMCBi006-A
Synonyms M-T1
Accession CVCL_C1Q6
Resource Identification Initiative To cite this cell line use: IIMCBi006-A (RRID:CVCL_C1Q6)
Comments From: International Institute of Molecular and Cell Biology; Warsaw; Poland.
Population: Caucasian.
Derived from site: In situ; Skin, dermis; UBERON=UBERON_0002067.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 4851; HTT; Repeat_expansion; p.Gln18[47] (c.52CAG(47)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (PubMed=36228511).
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_C9D5 ! IIMCBi006-B
Sex of cell Female
Age at sampling 43Y
Category Induced pluripotent stem cell

PubMed=36228511; DOI=10.1016/j.scr.2022.102931
Latoszek E., Piechota M., Liszewska E., Hansikova H., Klempir J., Muhlback A., Landwehrmeyer G.B., Kuznicki J., Czeredys M.
Generation of three human iPSC lines from patients with Huntington's disease with different CAG lengths and human control iPSC line from a healthy donor.
Stem Cell Res. 64:102931-102931(2022)

Cell line databases/resources hPSCreg; IIMCBi006-A
Biological sample resources BioSamples; SAMEA111377770
Encyclopedic resources Wikidata; Q114311721
Entry history
Entry creation22-Sep-2022
Last entry update05-Oct-2023
Version number5