Cellosaurus GM03767 (CVCL_X111)
| Cell line name | GM03767 |
|---|---|
| Synonyms | GM 3767 |
| Accession | CVCL_X111 |
| Resource Identification Initiative | To cite this cell line use: GM03767 (RRID:CVCL_X111) |
| Comments | Population: Caucasian. Karyotypic information: 46,XY,del(18)(qter->p11) (Coriell=GM03767). Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Deletion 18p syndrome (NCIt: C84521) Monosomy 18p (ORDO: Orphanet_1598) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Sex of cell | Male |
| Age at sampling | 3Y |
| Category | Finite cell line |
| Publications | PubMed=6617268; DOI=10.1159/000131883 PubMed=6661932; DOI=10.1159/000131990 CLPUB00447 |
| Cross-references | |
| Cell line collections (Providers) | Coriell; GM03767 |
| Cell line databases/resources | CLO; CLO_0015491 |
| Biological sample resources | BioSample; SAMN00808521 |
| Encyclopedic resources | Wikidata; Q54838222 |
| Entry history | |
| Entry creation | 17-Jul-2014 |
| Last entry update | 29-Jun-2023 |
| Version number | 10 |