Cellosaurus GM21890 (CVCL_U543)
| Cell line name | GM21890 |
|---|---|
| Accession | CVCL_U543 |
| Resource Identification Initiative | To cite this cell line use: GM21890 (RRID:CVCL_U543) |
| Comments | Omics: Variations; CNV analysis. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Prader-Willi syndrome (NCIt: C75463) Prader-Willi syndrome (ORDO: Orphanet_739) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Originate from same individual | CVCL_U544 ! GM21891 |
| Sex of cell | Male |
| Age at sampling | 19Y |
| Category | Finite cell line |
| Publications | PubMed=23665875; DOI=10.1534/g3.113.006577; PMCID=PMC3704242 |
| Cross-references | |
| Cell line collections (Providers) | Coriell; GM21890 |
| Encyclopedic resources | Wikidata; Q54852211 |
| Entry history | |
| Entry creation | 16-Apr-2014 |
| Last entry update | 10-Apr-2025 |
| Version number | 11 |