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: 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 | 29-Jun-2023 | |
Version number | 9 |