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Cellosaurus ND39258 (CVCL_ZC78)

[Text version]
Cell line name ND39258
Accession CVCL_ZC78
Resource Identification Initiative To cite this cell line use: ND39258 (RRID:CVCL_ZC78)
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[109] (c.52CAG(109)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (Coriell=ND39258).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Children:
CVCL_ZC79 (CS09iHD109-n1)CVCL_ZC80 (CS09iHD109-n4)CVCL_ZC81 (CS09iHD109-n5)
CVCL_W579 (HD109i.1)
Sex of cell Female
Age at sampling 9Y
Category Finite cell line
Cross-references
Cell line collections (Providers) Coriell; ND39258 - Discontinued
Encyclopedic resources Wikidata; Q98127479
Entry history
Entry creation02-Jul-2020
Last entry update19-Dec-2024
Version number8