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Cellosaurus HPS3059 (CVCL_D0XJ)

[Text version]
Cell line name HPS3059
Accession CVCL_D0XJ
Resource Identification Initiative To cite this cell line use: HPS3059 (RRID:CVCL_D0XJ)
Comments Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
Disease Congenital disorder of deglycosylation (NCIt: C126746)
Alacrimia-choreoathetosis-liver dysfunction syndrome (ORDO: Orphanet_404454)
Species of origin Homo sapiens (Human) (NCBI Taxonomy: 9606)
Originate from same individual CVCL_D0XE ! HPS3054
CVCL_D0XF ! HPS3055
CVCL_D0XG ! HPS3056
CVCL_D0XH ! HPS3057
CVCL_D0XI ! HPS3058
Sex of cell Male
Age at sampling 10-19Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS3059
Encyclopedic resources Wikidata; Q123032492
Entry history
Entry creation05-Oct-2023
Last entry update30-Jan-2024
Version number2