| Cell line name | FA17P(SVT) |
|---|---|
| Accession | CVCL_VH75 |
| Resource Identification Initiative | To cite this cell line use: FA17P(SVT) (RRID:CVCL_VH75) |
| Comments | Population: Japanese. Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40) [Note=pSVori-]. Derived from site: In situ; Skin; UBERON=UBERON_0002097. Cell type: Fibroblast of skin; CL=CL_0002620. |
| Sequence variations |
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| Disease | Fanconi anemia, complementation group G (NCIt: C125708) Fanconi anemia (ORDO: Orphanet_84) |
| Species of origin | Homo sapiens (Human) (NCBI Taxonomy: 9606) |
| Hierarchy | Parent: CVCL_VH74 (FA17P) |
| Sex of cell | Male |
| Age at sampling | 11Y |
| Category | Transformed cell line |
| Cross-references | |
| Cell line collections (Providers) | JCRB; KURB1469 |
| Encyclopedic resources | Wikidata; Q54833173 |
| Entry history | |
| Entry creation | 14-May-2018 |
| Last entry update | 05-Oct-2023 |
| Version number | 10 |