ID   BHD-F59RSVT
AC   CVCL_IR12
DR   cancercelllines; CVCL_IR12
DR   Wikidata; Q54796341
RX   PubMed=27991910;
CC   Population: Japanese.
CC   Sequence variation: Mutation; HGNC; HGNC:27310; FLCN; Simple; p.Glu510del (c.1525GAG[1]) (c.1528_1530delGAG); ClinVar=VCV000253256; Zygosity=Unspecified (PubMed=27991910).
CC   Genetic integration: Method=Transduction; Gene=UniProtKB; P13249; S.alboniger pac (PuroR).
CC   Genetic integration: Method=Transduction; Gene=UniProtKB; P03070; SV40 large T antigen.
CC   Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40) (Note=SV40gp6).
CC   Derived from site: In situ; Kidney; UBERON=UBERON_0002113.
DI   NCIt; C28244; Birt-Hogg-Dube syndrome
DI   ORDO; Orphanet_122; Birt-Hogg-Dube syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   Adult
CA   Transformed cell line
DT   Created: 03-03-17; Last updated: 10-04-25; Version: 13
//
RX   PubMed=27991910; DOI=10.1038/labinvest.2016.137;
RA   Furuya M., Hasumi H., Baba M., Tanaka R., Iribe Y., Onishi T.,
RA   Nagashima Y., Nakatani Y., Isono Y., Yao M.;
RT   "Establishment and characterization of BHD-F59RSVT, an immortalized
RT   cell line derived from a renal cell carcinoma in a patient with
RT   Birt-Hogg-Dube syndrome.";
RL   Lab. Invest. 97:343-351(2017).
//