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Cellosaurus ND41656 (CVCL_Y834)

[Text version]
Cell line name ND41656
Accession CVCL_Y834
Resource Identification Initiative To cite this cell line use: ND41656 (RRID:CVCL_Y834)
Comments Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; HGNC:4851; HTT; Repeat_expansion; p.Gln18[57] (c.52CAG(57)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (NHCDR=ND41656).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_Y897 (ND33392)
Sex of cell Female
Age at sampling 29Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; ND41656 - Discontinued
NHCDR; ND41656
Cell line databases/resources SKIP; SKIP001561
SKIP; SKIP004723
Encyclopedic resources Wikidata; Q54930199
Entry history
Entry creation10-Apr-2015
Last entry update19-Dec-2024
Version number15