ID   JME/CF 12
AC   CVCL_IN69
SY   JME/CF12
DR   Wikidata; Q54899006
RX   PubMed=1701980;
CC   Sequence variation: Mutation; HGNC; HGNC:1884; CFTR; Simple; p.Phe508del (c.1521_1523delCTT); ClinVar=VCV000007105; Zygosity=Heterozygous (PubMed=1701980).
CC   Genetic integration: Method=Transduction; Gene=UniProtKB; P03070; SV40 large T antigen.
CC   Genetic integration: Method=Transduction; Gene=UniProtKB; P00552; Transposon Tn5 neo.
CC   Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40).
CC   Derived from site: In situ; Nose, nasal cavity, epithelium; UBERON=UBERON_0005384.
DI   NCIt; C2975; Cystic fibrosis
DI   ORDO; Orphanet_586; Cystic fibrosis
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex unspecified
AG   Age unspecified
CA   Transformed cell line
DT   Created: 01-12-16; Last updated: 19-12-24; Version: 16
//
RX   PubMed=1701980; DOI=10.1152/ajplung.1990.259.6.L496;
RA   Jefferson D.M., Valentich J.D., Marini F.C., Grubman S.A.,
RA   Iannuzzi M.C., Dorkin H.L., Li M., Klinger K.W., Welsh M.J.;
RT   "Expression of normal and cystic fibrosis phenotypes by continuous
RT   airway epithelial cell lines.";
RL   Am. J. Physiol. 259:L496-L505(1990).
//