ID   2CFSMEo-
AC   CVCL_IN60
DR   Wikidata; Q54584432
RX   PubMed=1375758;
WW   Info; Dartmouth; -; https://web.archive.org/web/20190126194809/http://www.dartmouth.edu/~cysfib/cell-lines.html
CC   Sequence variation: Mutation; HGNC; HGNC:1884; CFTR; Simple; p.Gln2Ter (c.4C>T); ClinVar=VCV000053980; Zygosity=Heterozygous (from autologous cell lines 6CFSMEo-; CFSMEo-).
CC   Sequence variation: Mutation; HGNC; HGNC:1884; CFTR; Simple; p.Phe508del (c.1521_1523delCTT); ClinVar=VCV000007105; Zygosity=Heterozygous (from autologous cell lines 6CFSMEo-; CFSMEo-).
CC   Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40) (Note=pSVori-).
CC   Derived from site: In situ; Lung, bronchus, submucosal gland; UBERON=UBERON_8410043.
CC   Cell type: Epithelial cell of bronchus; CL=CL_0002328.
DI   NCIt; C2975; Cystic fibrosis
DI   ORDO; Orphanet_586; Cystic fibrosis
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
OI   CVCL_VP33 ! CFSMEo-
OI   CVCL_IN58 ! 3ACFSMEo-
OI   CVCL_IN62 ! 6CFSMEo-
SX   Sex unspecified
AG   Age unspecified
CA   Transformed cell line
DT   Created: 01-12-16; Last updated: 10-04-25; Version: 18
//
RX   PubMed=1375758; DOI=10.1073/pnas.89.11.5171; PMCID=PMC49251;
RA   Cozens A.L., Yezzi M.J., Chin L., Simon E.M., Finkbeiner W.E.,
RA   Wagner J.A., Gruenert D.C.;
RT   "Characterization of immortal cystic fibrosis tracheobronchial gland
RT   epithelial cells.";
RL   Proc. Natl. Acad. Sci. U.S.A. 89:5171-5175(1992).
//