| Cell line name | HPS3055 |
|---|---|
| Accession | CVCL_D0XF |
| Resource Identification Initiative | To cite this cell line use: HPS3055 (RRID:CVCL_D0XF) |
| 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_D0XG ! HPS3056 CVCL_D0XH ! HPS3057 CVCL_D0XI ! HPS3058 CVCL_D0XJ ! HPS3059 |
| Sex of cell | Male |
| Age at sampling | 10-19Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS3055 |
| Encyclopedic resources | Wikidata; Q123032487 |
| Entry history | |
| Entry creation | 05-Oct-2023 |
| Last entry update | 30-Jan-2024 |
| Version number | 2 |