ID   CCD-186Sk
AC   CVCL_2381
SY   CCD-186SK
DR   CLO; CLO_0002308
DR   ATCC; CRL-1563
DR   BioSample; SAMN03471396
DR   Wikidata; Q54808873
CC   Sequence variation: Mutation; HGNC; 1884; CFTR; Simple; p.Phe508del (c.1521_1523delCTT); ClinVar=VCV000007105; Zygosity=Homozygous (ATCC=CRL-1563).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): ATCC
ST   Amelogenin: X,Y
ST   CSF1PO: 11
ST   D13S317: 8,11
ST   D16S539: 11,12
ST   D5S818: 12
ST   D7S820: 7,10
ST   TH01: 7,8
ST   TPOX: 9,11
ST   vWA: 16,17
DI   NCIt; C2975; Cystic fibrosis
DI   ORDO; Orphanet_586; Cystic fibrosis
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   16Y
CA   Finite cell line
DT   Created: 04-04-12; Last updated: 05-10-23; Version: 18
//