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Cellosaurus HPS1067 (CVCL_UP78)

[Text version]
Cell line name HPS1067
Accession CVCL_UP78
Resource Identification Initiative To cite this cell line use: HPS1067 (RRID:CVCL_UP78)
Comments Population: Japanese.
Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Congenital myasthenic syndrome (NCIt: C84647)
Congenital myasthenic syndrome (ORDO: Orphanet_590)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_UN57 ! HPS1066
CVCL_UP79 ! HPS1068
CVCL_UP80 ! HPS1069
CVCL_UP81 ! HPS1070
Sex of cell Male
Age at sampling 10-19Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS1067
Encyclopedic resources Wikidata; Q94219466
Entry history
Entry creation25-Feb-2019
Last entry update29-Jun-2023
Version number5