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Cellosaurus ND36999 (CVCL_W577)

[Text version]
Cell line name ND36999
Synonyms ND36999*F; HD 6
Accession CVCL_W577
Resource Identification Initiative To cite this cell line use: ND36999 (RRID:CVCL_W577)
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[179] (c.52CAG(179)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (NHCDR=ND36999).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_W576 (GM09197)
Children:
CVCL_B6HM (NH50329)CVCL_B6HN (NH50359)
Sex of cell Male
Age at sampling 6Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; ND36999 - Discontinued
NHCDR; ND36999
Cell line databases/resources SKIP; SKIP001089
SKIP; SKIP004701
Encyclopedic resources Wikidata; Q54930008
Entry history
Entry creation16-Apr-2014
Last entry update19-Dec-2024
Version number18