Cellosaurus HPS3058 (CVCL_D0XI)
Cell line name | HPS3058 |
---|---|
Accession | CVCL_D0XI |
Resource Identification Initiative | To cite this cell line use: HPS3058 (RRID:CVCL_D0XI) |
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_D0XJ ! HPS3059 |
Sex of cell | Male |
Age at sampling | 10-19Y |
Category | Induced pluripotent stem cell |
Cross-references | |
Cell line collections (Providers) | RCB; HPS3058 |
Encyclopedic resources | Wikidata; Q123032491 |
Entry history | |
Entry creation | 05-Oct-2023 |
Last entry update | 30-Jan-2024 |
Version number | 2 |