Cellosaurus GM25378 (CVCL_5K92)
| Cell line name | GM25378 | |
|---|---|---|
| Accession | CVCL_5K92 | |
| Resource Identification Initiative | To cite this cell line use: GM25378 (RRID:CVCL_5K92) | |
| Comments | Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. | |
| Disease | Smith-Magenis syndrome (NCIt: C75469) Smith-Magenis syndrome (ORDO: Orphanet_819) | |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | |
| Hierarchy | Children:
| |
| Originate from same individual | CVCL_5K91 ! GM25377 | |
| Sex of cell | Female | |
| Age at sampling | 21Y | |
| Category | Finite cell line | |
| Cross-references | ||
| Cell line collections (Providers) | Coriell; GM25378 | |
| Encyclopedic resources | Wikidata; Q54853910 | |
| Entry history | ||
| Entry creation | 14-Dec-2015 | |
| Last entry update | 29-Jun-2023 | |
| Version number | 8 | |