Cellosaurus GM16549 (CVCL_X436)
| Cell line name | GM16549 |
|---|---|
| Accession | CVCL_X436 |
| Resource Identification Initiative | To cite this cell line use: GM16549 (RRID:CVCL_X436) |
| Comments | Derived from site: In situ; Placenta; UBERON=UBERON_0001987. Cell type: Fibroblast; CL=CL_0000057. |
| Disease | Smith-Lemli-Opitz syndrome (NCIt: C85071) Smith-Lemli-Opitz syndrome (ORDO: Orphanet_818) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Male |
| Age at sampling | 1D |
| Category | Finite cell line |
| Cross-references | |
| Cell line collections (Providers) | Coriell; GM16549 |
| Encyclopedic resources | Wikidata; Q54848637 |
| Entry history | |
| Entry creation | 05-Sep-2014 |
| Last entry update | 29-Jun-2023 |
| Version number | 7 |