ID   EUFA689
AC   CVCL_G074
DR   Wikidata; Q54832940
RX   PubMed=10094191;
RX   PubMed=10468606;
CC   Sequence variation: Mutation; HGNC; HGNC:3582; FANCA; Simple; p.Phe1263del (c.3788_3790delTCT); ClinVar=VCV000041003; Zygosity=Homozygous (PubMed=10468606; PubMed=10094191).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C125702; Fanconi anemia, complementation group A
DI   ORDO; Orphanet_84; Fanconi anemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
CA   Transformed cell line
DT   Created: 11-02-13; Last updated: 19-12-24; Version: 14
//
RX   PubMed=10094191; DOI=10.1038/sj.ejhg.5200248;
RA   Wijker M., Morgan N.V., Herterich S., van Berkel C.G.M., Tipping A.J.,
RA   Gross H.-J., Gille J.J.P., Pals G., Savino M., Altay C., Mohan S.,
RA   Dokal I., Cavenagh J.D., Marsh J., van Weel M., Ortega J.J., Schuler D.,
RA   Samochatova E., Karwacki M.W., Bekassy A.N., Abecasis M., Ebell W.,
RA   Kwee M.L., de Ravel T.J.L., Mathew C.G.;
RT   "Heterogeneous spectrum of mutations in the Fanconi anaemia group A
RT   gene.";
RL   Eur. J. Hum. Genet. 7:52-59(1999).
//
RX   PubMed=10468606; DOI=10.1073/pnas.96.18.10320; PMCID=PMC17886;
RA   Waisfisz Q., de Winter J.P., Kruyt F.A.E., de Groot J., van der Weel L.,
RA   Dijkmans L.M., Zhi Y., Arwert F., Scheper R.J., Youssoufian H.,
RA   Hoatlin M.E., Joenje H.;
RT   "A physical complex of the Fanconi anemia proteins FANCG/XRCC9 and
RT   FANCA.";
RL   Proc. Natl. Acad. Sci. U.S.A. 96:10320-10325(1999).
//