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Cellosaurus ND36998 (CVCL_Y807)

[Text version]
Cell line name ND36998
Synonyms ND36998*G; HD 29
Accession CVCL_Y807
Resource Identification Initiative To cite this cell line use: ND36998 (RRID:CVCL_Y807)
Comments Population: Caucasian.
Derived from site: In situ; Skin; UBERON=UBERON_0002097.
Cell type: Fibroblast of skin; CL=CL_0002620.
Sequence variations
  • Mutation; HGNC; 4851; HTT; Repeat_expansion; p.Gln18[60] (c.52CAG(60)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (NHCDR=ND36998).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_F063 (GM03621)
Sex of cell Female
Age at sampling 29Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; ND36998 - Discontinued
NHCDR; ND36998
Cell line databases/resources SKIP; SKIP001088
SKIP; SKIP004700
Encyclopedic resources Wikidata; Q54930007
Entry history
Entry creation10-Apr-2015
Last entry update30-Jan-2024
Version number15