Home  |  Contact

Cellosaurus HPS2380 (CVCL_A3RD)

Cell line name HPS2380
Accession CVCL_A3RD
Resource Identification Initiative To cite this cell line use: HPS2380 (RRID:CVCL_A3RD)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; 4851; HTT; Unexplicit; Not described; Zygosity=Unspecified (RCB=HPS2380).
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_UP11 ! HPS2377
CVCL_A3RB ! HPS2378
CVCL_A3RC ! HPS2379
CVCL_A3RE ! HPS2381
CVCL_A3RF ! HPS2382
Sex of cell Male
Age at sampling 70-79Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS2380
Encyclopedic resources Wikidata; Q105508656
Entry history
Entry creation12-Jan-2021
Last entry update05-Oct-2023
Version number5