ID   CF-KM4
AC   CVCL_IN80
DR   Wikidata; Q54811352
RX   PubMed=10101000;
RX   PubMed=15463957;
CC   Sequence variation: Mutation; HGNC; HGNC:1884; CFTR; Simple; p.Phe508del (c.1521_1523delCTT); ClinVar=VCV000007105; Zygosity=Homozygous (PubMed=10101000).
CC   Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40).
CC   Derived from site: In situ; Trachea gland; UBERON=UBERON_0005203.
CC   Cell type: Serous cell of epithelium of trachea; CL=CL_1000330.
DI   NCIt; C2975; Cystic fibrosis
DI   ORDO; Orphanet_586; Cystic fibrosis
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex unspecified
AG   Adult
CA   Transformed cell line
DT   Created: 01-12-16; Last updated: 19-12-24; Version: 12
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RX   PubMed=10101000; DOI=10.1165/ajrcmb.20.4.3341;
RA   Kammouni W., Moreau B., Becq F., Saleh A., Pavirani A., Figarella C.,
RA   Merten M.D.;
RT   "A cystic fibrosis tracheal gland cell line, CF-KM4. Correction by
RT   adenovirus-mediated CFTR gene transfer.";
RL   Am. J. Respir. Cell Mol. Biol. 20:684-691(1999).
//
RX   PubMed=15463957; DOI=10.1016/j.jcf.2004.05.040;
RA   Gruenert D.C., Willems M., Cassiman J.-J., Frizzell R.A.;
RT   "Established cell lines used in cystic fibrosis research.";
RL   J. Cyst. Fibros. 3:191-196(2004).
//