| Cell line name | HPS3022 |
|---|---|
| Accession | CVCL_D0XC |
| Resource Identification Initiative | To cite this cell line use: HPS3022 (RRID:CVCL_D0XC) |
| 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_D0XD ! HPS3023 |
| Sex of cell | Female |
| Age at sampling | <10Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS3022 |
| Encyclopedic resources | Wikidata; Q123032484 |
| Entry history | |
| Entry creation | 05-Oct-2023 |
| Last entry update | 30-Jan-2024 |
| Version number | 2 |