The human XRCC9 gene corrects chromosomal instability and mutagen sensitivities in CHO UV40 cells.Liu N., Lamerdin J.E., Tucker J.D., Zhou Z.-Q., Walter C.A., Albala J.S., Busch D.B., Thompson L.H.View abstractCited forNUCLEOTIDE SEQUENCE [MRNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCProc. Natl. Acad. Sci. U.S.A. 94:9232-9237 (1997)Cited in1
The Fanconi anaemia group G gene FANCG is identical with XRCC9.De Winter J.P., Waisfisz Q., Rooimans M.A., Van Berkel C.G.M., Bosnoyan-Collins L., Alon N., Carreau M., Bender O., Demuth I.[...], Joenje H.View abstractCited forNUCLEOTIDE SEQUENCE [GENOMIC DNA / MRNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Genet. 20:281-283 (1998)Cited in1
No title available.NIEHS SNPs programCited forNUCLEOTIDE SEQUENCE [GENOMIC DNA], VARIANTS GLU-294; ILE-297; SER-330; LEU-378; GLU-430; GLN-513 AND PHE-603CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)Submission Submitted to EMBL/GenBank/DDBJ databases (OCT-2004)Cited in25
DNA sequence and analysis of human chromosome 9.Humphray S.J., Oliver K., Hunt A.R., Plumb R.W., Loveland J.E., Howe K.L., Andrews T.D., Searle S., Hunt S.E.[...], Dunham I.View abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNature 429:369-374 (2004)Cited in99+99+
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).The MGC Project TeamView abstractCited forNUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]TissueKidney, UterusCategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCGenome Res. 14:2121-2127 (2004)Cited in99+99+
Fanconi anemia proteins FANCA, FANCC, and FANCG/XRCC9 interact in a functional nuclear complex.Garcia-Higuera I., Kuang Y., Naf D., Wasik J., D'Andrea A.D.View abstractCited forCHARACTERIZATIONSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCMol. Cell. Biol. 19:4866-4873 (1999)Cited in1Mapped to1
A multiprotein nuclear complex connects Fanconi anemia and Bloom syndrome.Meetei A.R., Sechi S., Wallisch M., Yang D., Young M.K., Joenje H., Hoatlin M.E., Wang W.View abstractCited forIDENTIFICATION IN A COMPLEX WITH FANCA; FANCC; FANCE; FANCF AND FANCLCategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCMol. Cell. Biol. 23:3417-3426 (2003)Cited in6
The Fanconi anemia proteins functionally interact with the protein kinase regulated by RNA (PKR).Zhang X., Li J., Sejas D.P., Rathbun K.R., Bagby G.C., Pang Q.View abstractCited forIDENTIFICATION IN A COMPLEX WITH EIF2AK2; FANCA; FANCC AND HSP70CategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCJ. Biol. Chem. 279:43910-43919 (2004)Cited in4Mapped to23
X-linked inheritance of Fanconi anemia complementation group B.Meetei A.R., Levitus M., Xue Y., Medhurst A.L., Zwaan M., Ling C., Rooimans M.A., Bier P., Hoatlin M.[...], Joenje H.View abstractCited forIDENTIFICATION IN A COMPLEX WITH FANCA; FANCB; FANCC; FANCE; FANCF AND FANCLCategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Genet. 36:1219-1224 (2004)Cited in8Mapped to1
A human ortholog of archaeal DNA repair protein Hef is defective in Fanconi anemia complementation group M.Meetei A.R., Medhurst A.L., Ling C., Xue Y., Singh T.R., Bier P., Steltenpool J., Stone S., Dokal I.[...], Wang W.View abstractCited forIDENTIFICATION IN A COMPLEX WITH FANCA; FANCB; FANCC; FANCE; FANCF; FANCL AND FANCMCategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Genet. 37:958-963 (2005)Cited in9Mapped to1
FANCG promotes formation of a newly identified protein complex containing BRCA2, FANCD2 and XRCC3.Wilson J.B., Yamamoto K., Marriott A.S., Hussain S., Sung P., Hoatlin M.E., Mathew C.G., Takata M., Thompson L.H.[...], Jones N.J.View abstractCited forINTERACTION WITH BRCA2; FANCD2 AND XRCC3, PHOSPHORYLATION AT SER-7, MUTAGENESIS OF SER-7; SER-383 AND SER-387CategoriesPTM / Processing, Disease & Variants, InteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCOncogene 27:3641-3652 (2008)Cited in3Mapped to99+
FAAP20: a novel ubiquitin-binding FA nuclear core-complex protein required for functional integrity of the FA-BRCA DNA repair pathway.Ali A.M., Pradhan A., Singh T.R., Du C., Li J., Wahengbam K., Grassman E., Auerbach A.D., Pang Q., Meetei A.R.View abstractCited forIDENTIFICATION IN THE FA COMPLEXCategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBlood 119:3285-3294 (2012)Cited in4Mapped to3
A ubiquitin-binding protein, FAAP20, links RNF8-mediated ubiquitination to the Fanconi anemia DNA repair network.Yan Z., Guo R., Paramasivam M., Shen W., Ling C., Fox D. III, Wang Y., Oostra A.B., Kuehl J.[...], Wang W.View abstractCited forIDENTIFICATION IN THE FA COMPLEXCategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCMol. Cell 47:61-75 (2012)Cited in5Mapped to4
Regulation of Rev1 by the Fanconi anemia core complex.Kim H., Yang K., Dejsuphong D., D'Andrea A.D.View abstractCited forIDENTIFICATION IN THE FA COMPLEXCategoriesInteractionSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCNat. Struct. Mol. Biol. 19:164-170 (2012)Cited in6Mapped to9
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9.Demuth I., Wlodarski M., Tipping A.J., Morgan N.V., de Winter J.P., Thiel M., Grasl S., Schindler D., D'Andrea A.D.[...], Digweed M.View abstractCited forVARIANT FANCG PRO-71CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCEur. J. Hum. Genet. 8:861-868 (2000)Cited in2
The consensus coding sequences of human breast and colorectal cancers.Sjoeblom T., Jones S., Wood L.D., Parsons D.W., Lin J., Barber T.D., Mandelker D., Leary R.J., Ptak J.[...], Velculescu V.E.View abstractCited forVARIANT [LARGE SCALE ANALYSIS] THR-607CategoriesSequencesSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCScience 314:268-274 (2006)Cited in99+Mapped to3
HES1 is a novel interactor of the Fanconi anemia core complex.Tremblay C.S., Huang F.F., Habi O., Huard C.C., Godin C., Levesque G., Carreau M.View abstractCited forVARIANT FANCG PRO-71, INTERACTION WITH HES1, SUBCELLULAR LOCATION, MUTAGENESIS OF GLY-546CategoriesSequences, Disease & Variants, Interaction, Subcellular LocationSourceUniProtKB reviewed (Swiss-Prot)PubMedEurope PMCBlood 112:2062-2070 (2008)Cited in5Mapped to3
Double-stranded (ds) RNA binding and not dimerization correlates with the activation of the dsRNA-dependent protein kinase (PKR).Wu S., Kaufman R.J.View abstractAnnotationPathwayCategoriesFunctionSourceReactome: R-HSA-420788PubMedEurope PMCJ Biol Chem 271:1756-1763 (1996)Mapped to30
The interferon-inducible double-stranded RNA-activated protein kinase self-associates in vitro and in vivo.Patel R.C., Stanton P., McMillan N.M., Williams B.R., Sen G.C.View abstractAnnotationPathwayCategoriesFunctionSourceReactome: R-HSA-420788PubMedEurope PMCProc Natl Acad Sci U S A 92:8283-8287 (1995)Mapped to30
In silico study of missense variants of FANCA, FANCC and FANCG genes reveals high risk deleterious alleles predisposing to Fanconi anemia pathogenesis.Shahid M., Azfaralariff A., Zubair M., Abdulkareem Najm A., Khalili N., Law D., Firasat S., Fazry S.View abstractAnnotationIn silico study of missense variants of FANCA FANCC and FANCG genes reveals high risk deleterious alleles predisposing to Fanconi anemia pathogenesis.SourceGeneRif: 2189PubMedEurope PMCGene 812:146104-146104 (2022)Mapped to23
Frequent internuclear bridging in a Fanconi anemia patient with FANCG mutation.Cochran T., Li W.AnnotationFrequent internuclear bridging in a Fanconi anemia patient with FANCG mutation.CategoriesFunctionSourceGeneRif: 2189PubMedEurope PMCBlood 138:738-738 (2021)Mapped to8
Structure of the FA core ubiquitin ligase closing the ID clamp on DNA.Wang S., Wang R., Peralta C., Yaseen A., Pavletich N.P.View abstractCategoriesStructureSourcePDB: 7KZP, PDB: 7KZQ, PDB: 7KZR, PDB: 7KZS, PDB: 7KZT, PDB: 7KZVPubMedEurope PMCNat Struct Mol Biol 28:300-309 (2021)Cited in1Mapped to10
Severe telomere shortening in Fanconi anemia complementation group L.Shah A., George M., Dhangar S., Rajendran A., Mohan S., Vundinti B.R.View abstractAnnotationSevere telomere shortening in Fanconi anemia complementation group L.CategoriesFunctionSourceGeneRif: 2189PubMedEurope PMCMol Biol Rep 48:585-593 (2021)Mapped to21
Loss of Mitochondrial Localization of Human FANCG Causes Defective FANCJ Helicase.K J.C.B., Kapoor B.S., Mandal K., Ghosh S., Mokhamatam R.B., Manna S.K., Mukhopadhyay S.S.View abstractAnnotationLoss of Mitochondrial Localization of Human FANCG Causes Defective FANCJ Helicase.CategoriesSequences, Disease & VariantsSourceGeneRif: 2189PubMedEurope PMCMol Cell Biol 40:e00306-20 (2020)Mapped to8
Clinical and Genetic Features of Patients With Fanconi Anemia in Lebanon and Report on Novel Mutations in the FANCA and FANCG Genes.Farah R.A., Nair P., Koueik J., Yammine T., Khalifeh H., Korban R., Collet A., Khayat C., Dubois-Denghien C.[...], Megarbane A.View abstractAnnotationClinical and Genetic Features of Patients With Fanconi Anemia in Lebanon and Report on Novel Mutations in the FANCA and FANCG Genes.CategoriesSequencesSourceGeneRif: 2189PubMedEurope PMCJ Pediatr Hematol Oncol 43:e727-e735 (2021)Mapped to18