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Cellosaurus ND42228 (CVCL_1N96)

[Text version]
Cell line name ND42228
Synonyms ND42228*E
Accession CVCL_1N96
Resource Identification Initiative To cite this cell line use: ND42228 (RRID:CVCL_1N96)
Comments 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[71] (c.52CAG(71)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (from parent cell line).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Hierarchy Parent: CVCL_8519 (GM04281)
Sex of cell Female
Age at sampling 20Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) Coriell; ND42228 - Discontinued
NHCDR; ND42228 - Discontinued
Encyclopedic resources Wikidata; Q54930213
Entry history
Entry creation08-Jul-2015
Last entry update29-Jun-2023
Version number11