Cellosaurus GM21889 (CVCL_U542)
Cell line name | GM21889 | ||
---|---|---|---|
Accession | CVCL_U542 | ||
Resource Identification Initiative | To cite this cell line use: GM21889 (RRID:CVCL_U542) | ||
Comments | Population: African American. 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) | ||
Hierarchy | Children:
| ||
Sex of cell | Male | ||
Age at sampling | 8Y | ||
Category | Finite cell line | ||
Publications | PubMed=23665875; DOI=10.1534/g3.113.006577; PMCID=PMC3704242 PubMed=24816254; DOI=10.1038/ng.2968 | ||
Cross-references | |||
Cell line collections (Providers) | Coriell; GM21889 | ||
Encyclopedic resources | Wikidata; Q54852210 | ||
Entry history | |||
Entry creation | 16-Apr-2014 | ||
Last entry update | 10-Apr-2025 | ||
Version number | 11 |