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Cellosaurus HPS3023 (CVCL_D0XD)

[Text version]
Cell line name HPS3023
Accession CVCL_D0XD
Resource Identification Initiative To cite this cell line use: HPS3023 (RRID:CVCL_D0XD)
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_D0X8 ! HPS3018
CVCL_D0X9 ! HPS3019
CVCL_D0XA ! HPS3020
CVCL_D0XB ! HPS3021
CVCL_D0XC ! HPS3022
Sex of cell Female
Age at sampling <10Y
Category Induced pluripotent stem cell
Cross-references
Cell line collections (Providers) RCB; HPS3023
Encyclopedic resources Wikidata; Q123032485
Entry history
Entry creation05-Oct-2023
Last entry update30-Jan-2024
Version number2