ID   FA29(SVT)
AC   CVCL_VH81
DR   JCRB; KURB1478
DR   Wikidata; Q54833199
CC   Population: Japanese.
CC   Sequence variation: Mutation; HGNC; HGNC:3588; FANCG; Simple; c.1761-2A>G (IVS13-2A>G); Zygosity=Homozygous; Note=Splice acceptor mutation (from parent cell line).
CC   Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40) (Note=pSVori-).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C125708; Fanconi anemia, complementation group G
DI   ORDO; Orphanet_84; Fanconi anemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_VH80 ! FA29P
SX   Male
AG   12Y
CA   Transformed cell line
DT   Created: 14-05-18; Last updated: 19-12-24; Version: 13
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