Home  |  Contact

Cellosaurus FA29(SVT) (CVCL_VH81)

Cell line name FA29(SVT)
Accession CVCL_VH81
Resource Identification Initiative To cite this cell line use: FA29(SVT) (RRID:CVCL_VH81)
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
  • Mutation; HGNC; 3588; FANCG; Simple; c.1761-2A>G (IVS13-2A>G); Zygosity=Homozygous; Note=Splice acceptor mutation (from parent cell line).
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_VH80 (FA29P)
Sex of cell Male
Age at sampling 12Y
Category Transformed cell line
Cross-references
Cell line collections (Providers) JCRB; KURB1478
Encyclopedic resources Wikidata; Q54833199
Entry history
Entry creation14-May-2018
Last entry update05-Oct-2023
Version number11