Cellosaurus GM06938 (CVCL_5N52)
| Cell line name | GM06938 | |
|---|---|---|
| Synonyms | GM6938; GM06938B; 6938 | |
| Accession | CVCL_5N52 | |
| Resource Identification Initiative | To cite this cell line use: GM06938 (RRID:CVCL_5N52) | |
| Comments | Population: Caucasian. Omics: Variations; CNV analysis. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. | |
| Disease | Wilms tumor-aniridia-genitourinary anomalies-mental retardation syndrome (NCIt: C3718) WAGR syndrome (ORDO: Orphanet_893) | |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) | |
| Hierarchy | Children:
| |
| Originate from same individual | CVCL_5N68 ! GM07736 | |
| Sex of cell | Male | |
| Age at sampling | 3W | |
| Category | Finite cell line | |
| Publications | PubMed=2559742; DOI=10.1002/mc.2940020606 CLPUB00447 PubMed=23665875; DOI=10.1534/g3.113.006577; PMCID=PMC3704242 | |
| Cross-references | ||
| Cell line collections (Providers) | Coriell; GM06938 | |
| Cell line databases/resources | CLO; CLO_0036455 | |
| Encyclopedic resources | Wikidata; Q54842399 | |
| Entry history | ||
| Entry creation | 23-Feb-2016 | |
| Last entry update | 10-Apr-2025 | |
| Version number | 10 | |