Cell line name | HPS2139 |
---|---|
Accession | CVCL_YS42 |
Resource Identification Initiative | To cite this cell line use: HPS2139 (RRID:CVCL_YS42) |
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_YS41 ! HPS2138 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; HPS2139 |
Encyclopedic resources | Wikidata; Q94219982 |
Entry history | |
Entry creation | 12-Mar-2020 |
Last entry update | 29-Jun-2023 |
Version number | 4 |