Cellosaurus GM10382 (CVCL_0I28)
| Cell line name | GM10382 |
|---|---|
| Synonyms | GM10382A |
| Accession | CVCL_0I28 |
| Resource Identification Initiative | To cite this cell line use: GM10382 (RRID:CVCL_0I28) |
| Comments | Population: Caucasian. Omics: Variations; CNV analysis. Cell type: Fibroblast; CL=CL_0000057. |
| Disease | 22q11.2 deletion syndrome (NCIt: C2989) 22q11.2 deletion syndrome (ORDO: Orphanet_567) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Male |
| Age at sampling | Children |
| Category | Finite cell line |
| Publications | CLPUB00447 PubMed=23665875; DOI=10.1534/g3.113.006577; PMCID=PMC3704242 |
| Cross-references | |
| Cell line collections (Providers) | Coriell; GM10382 |
| Cell line databases/resources | CLO; CLO_0028575 |
| Biological sample resources | BioSample; SAMN00799971 |
| Encyclopedic resources | Wikidata; Q54844424 |
| Entry history | |
| Entry creation | 10-Apr-2015 |
| Last entry update | 10-Apr-2025 |
| Version number | 12 |