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Cellosaurus ND38552 (CVCL_Y820)

[Text version]
Cell line name ND38552
Accession CVCL_Y820
Resource Identification Initiative To cite this cell line use: ND38552 (RRID:CVCL_Y820)
Comments 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[49-50] (c.52CAG(49-50)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (NHCDR=ND38552).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_Y861 (GM04687)
Sex of cell Female
Age at sampling 37Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; ND38552 - Discontinued
NHCDR; ND38552
Cell line databases/resources SKIP; SKIP001094
SKIP; SKIP004709
Encyclopedic resources Wikidata; Q54930073
Entry history
Entry creation10-Apr-2015
Last entry update19-Dec-2024
Version number15