| Cell line name | HPS1132 |
|---|---|
| Accession | CVCL_UN23 |
| Resource Identification Initiative | To cite this cell line use: HPS1132 (RRID:CVCL_UN23) |
| Comments | Population: Japanese. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Congenital pure red cell aplasia (NCIt: C61236) Blackfan-Diamond anemia (ORDO: Orphanet_124) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_UN20 ! HPS1126 CVCL_UN21 ! HPS1127 CVCL_UN22 ! HPS1128 CVCL_UN24 ! HPS1133 CVCL_UN25 ! HPS1134 |
| Sex of cell | Male |
| Age at sampling | 10-19Y |
| Category | Induced pluripotent stem cell |
| Cross-references | |
| Cell line collections (Providers) | RCB; HPS1132 |
| Encyclopedic resources | Wikidata; Q94219527 |
| Entry history | |
| Entry creation | 25-Feb-2019 |
| Last entry update | 29-Jun-2023 |
| Version number | 7 |