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Cellosaurus HPS2377 (CVCL_UP11)

[Text version]
Cell line name HPS2377
Accession CVCL_UP11
Resource Identification Initiative To cite this cell line use: HPS2377 (RRID:CVCL_UP11)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Sequence variations
  • Mutation; HGNC; HGNC:4851; HTT; Unexplicit; Not described; Zygosity=Unspecified (RCB=HPS2377).
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_A3RB ! HPS2378
CVCL_A3RC ! HPS2379
CVCL_A3RD ! HPS2380
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; HPS2377
Encyclopedic resources Wikidata; Q94220107
Entry history
Entry creation25-Feb-2019
Last entry update19-Dec-2024
Version number8