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Cellosaurus GM21757 (CVCL_1J85)

[Text version]
Cell line name GM21757
Accession CVCL_1J85
Resource Identification Initiative To cite this cell line use: GM21757 (RRID:CVCL_1J85)
Comments Cell type: Fibroblast; CL=CL_0000057.
Sequence variations
  • Mutation; HGNC; 4851; HTT; Repeat_expansion; p.Gln18[66] (c.52CAG(66)) (c.52CAG[(40_?)]); ClinVar=VCV000000409; Zygosity=Heterozygous (from autologous cell line GM13515).
Disease Huntington's disease (NCIt: C82342)
Huntington disease (ORDO: Orphanet_399)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_1J82 ! GM13515
Sex of cell Male
Age at sampling Age unspecified
Category Finite cell line
Cross-references
Cell line collections (Providers) Coriell; GM21757
Cell line databases/resources CLO; CLO_0014924
Encyclopedic resources Wikidata; Q54852125
Entry history
Entry creation08-Jul-2015
Last entry update29-Jun-2023
Version number11