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Cellosaurus ND42222 (CVCL_Y844)

[Text version]
Cell line name ND42222
Synonyms ND42222*D
Accession CVCL_Y844
Resource Identification Initiative To cite this cell line use: ND42222 (RRID:CVCL_Y844)
Comments Population: Caucasian.
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=ND42222).
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_1N95 ! ND42223
CVCL_Y845 ! ND42224
CVCL_GP60 ! ND50034
CVCL_RH33 ! ND50036
Sex of cell Female
Age at sampling 9Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; ND42222 - Discontinued
NHCDR; ND42222 - Discontinued
Cell line databases/resources SKIP; SKIP001568
Encyclopedic resources Wikidata; Q54930210
Entry history
Entry creation10-Apr-2015
Last entry update19-Dec-2024
Version number14