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Cellosaurus HPS3256 (CVCL_D1BF)

Cell line name HPS3256
Accession CVCL_D1BF
Resource Identification Initiative To cite this cell line use: HPS3256 (RRID:CVCL_D1BF)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Glycogen storage disease type V (NCIt: C84738)
Glycogen storage disease due to muscle glycogen phosphorylase deficiency (ORDO: Orphanet_368)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_D1BD ! HPS3254
CVCL_D1BE ! HPS3255
CVCL_D1BG ! HPS3257
CVCL_D1BH ! HPS3258
CVCL_D1BI ! HPS3259
Sex of cell Male
Age at sampling 70-79Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS3256
Encyclopedic resources Wikidata; Q123032580
Entry history
Entry creation05-Oct-2023
Last entry update30-Jan-2024
Version number2