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Cellosaurus ND41113 (CVCL_Y809)

[Text version]
Cell line name ND41113
Synonyms ND41113*D
Accession CVCL_Y809
Resource Identification Initiative To cite this cell line use: ND41113 (RRID:CVCL_Y809)
Comments Population: Caucasian.
Donor information: At sampling donor was not affected with Huntington disease but at significant risk for disease.
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[33] (c.52CAG(33)) (c.52CAG[(27_35)]); ClinVar=VCV000031915; Zygosity=Heterozygous (NHCDR=ND41113).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_W557 (GM02183)
Sex of cell Female
Age at sampling 21Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; ND41113 - Discontinued
NHCDR; ND41113
Cell line databases/resources SKIP; SKIP001555
SKIP; SKIP004720
Encyclopedic resources Wikidata; Q54930193
Entry history
Entry creation10-Apr-2015
Last entry update19-Dec-2024
Version number16