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Cellosaurus ND50036 (CVCL_RH33)

[Text version]
Cell line name ND50036
Accession CVCL_RH33
Resource Identification Initiative To cite this cell line use: ND50036 (RRID:CVCL_RH33)
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 (from autologous cell lines ND42222; ND42223; ND42224).
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_Y844 ! ND42222
CVCL_1N95 ! ND42223
CVCL_Y845 ! ND42224
CVCL_GP60 ! ND50034
Sex of cell Female
Age at sampling 9Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) NHCDR; ND50036
Cell line databases/resources SKIP; SKIP001570
Encyclopedic resources Wikidata; Q54930255
Entry history
Entry creation05-Mar-2018
Last entry update19-Dec-2024
Version number11