Cellosaurus GM16632 (CVCL_AK41)
| Cell line name | GM16632 |
|---|---|
| Synonyms | PD720.F RV:FANCA; 720-Retro |
| Accession | CVCL_AK41 |
| Resource Identification Initiative | To cite this cell line use: GM16632 (RRID:CVCL_AK41) |
| Comments | Transfected with: HGNC; 3582; FANCA. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Disease | Fanconi anemia, complementation group A (NCIt: C125702) Fanconi anemia (ORDO: Orphanet_84) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_AK40 (GM16631) |
| Sex of cell | Female |
| Age at sampling | 13Y |
| Category | Finite cell line |
| Publications | PubMed=12361951; DOI=10.1074/jbc.M207937200 |
| Cross-references | |
| Cell line collections (Providers) | Coriell; GM16632 |
| Cell line databases/resources | CLO; CLO_0017356 |
| Encyclopedic resources | Wikidata; Q54848675 |
| Entry history | |
| Entry creation | 02-May-2016 |
| Last entry update | 29-Jun-2023 |
| Version number | 7 |