| Cell line name | HPS2138 |
|---|---|
| Accession | CVCL_YS41 |
| Resource Identification Initiative | To cite this cell line use: HPS2138 (RRID:CVCL_YS41) |
| Comments | Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178. |
| Disease | Ring chromosome 20 syndrome (NCIt: C169001) Ring chromosome 20 syndrome (ORDO: Orphanet_1444) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_YS42 ! HPS2139 CVCL_YS43 ! HPS2140 CVCL_YS44 ! HPS2141 CVCL_YS45 ! HPS2142 CVCL_YS46 ! HPS2143 |
| Sex of cell | Male |
| Age at sampling | <10Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS2138 |
| Encyclopedic resources | Wikidata; Q94219977 |
| Entry history | |
| Entry creation | 12-Mar-2020 |
| Last entry update | 29-Jun-2023 |
| Version number | 4 |