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Cellosaurus FA17P(SVT) (CVCL_VH75)

[Text version]
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
  • Mutation; HGNC; 3588; FANCG; Simple; c.307+1G>C (IVS3+1G>C); ClinVar=VCV000006714; Zygosity=Homozygous; Note=Splice donor 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_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 creation14-May-2018
Last entry update10-Sep-2024
Version number11