ID   PD20 RV:D2
AC   CVCL_AK49
SY   PD.20hygro:RV; PD20-wtD2
DR   Wikidata; Q54946782
RX   PubMed=12361951;
WW   http://www.ohsu.edu/research/fanconi-anemia/celllines.cfm
CC   Characteristics: Transfection of wildtype FANCD2 restores the full activity of the protein which is mutated in the parent cell line.
CC   Genetic integration: Method=Transfection/transduction; Gene=HGNC; HGNC:3585; FANCD2.
CC   Genetic integration: Method=Transfection/transduction; Gene=UniProtKB; P00557; Escherichia coli hygromycin-B 4-O-kinase (hph) (HygR).
CC   Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C125706; Fanconi anemia, complementation group D2
DI   ORDO; Orphanet_84; Fanconi anemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_G042 ! GM16633
SX   Male
AG   7Y
CA   Transformed cell line
DT   Created: 02-05-16; Last updated: 19-12-24; Version: 14
//
RX   PubMed=12361951; DOI=10.1074/jbc.M207937200;
RA   Donahue S.L., Campbell C.;
RT   "A DNA double strand break repair defect in Fanconi anemia
RT   fibroblasts.";
RL   J. Biol. Chem. 277:46243-46247(2002).
//