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Cellosaurus ND42235 (CVCL_Y848)

[Text version]
Cell line name ND42235
Accession CVCL_Y848
Resource Identification Initiative To cite this cell line use: ND42235 (RRID:CVCL_Y848)
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[49-50] (c.52CAG(49-50)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (from parent cell line).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_Y861 (GM04687)
Sex of cell Female
Age at sampling 37Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; ND42235 - Discontinued
NHCDR; ND42235
Cell line databases/resources SKIP; SKIP001574
Encyclopedic resources Wikidata; Q54930217
Entry history
Entry creation10-Apr-2015
Last entry update19-Dec-2024
Version number12