RFX6, regulatory factor X6, 222546

N. diseases: 39; N. variants: 13
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2748662
Disease: Mitchell-Riley Syndrome
Mitchell-Riley Syndrome
0.750 GeneticVariation disease BEFREE This is the first reported case of a classical Mitchell-Riley syndrome in the Arab peninsula along with additional features and novel mutations in the RFX6 gene. 26761945 2016
CUI: C2748662
Disease: Mitchell-Riley Syndrome
Mitchell-Riley Syndrome
0.750 GeneticVariation disease UNIPROT Rfx6 directs islet formation and insulin production in mice and humans. 20148032 2010
CUI: C2748662
Disease: Mitchell-Riley Syndrome
Mitchell-Riley Syndrome
0.750 GeneticVariation disease BEFREE Mutations in rfx6 were recently associated with Mitchell-Riley syndrome, which involves neonatal diabetes, and other digestive system defects. 21215266 2011
CUI: C2748662
Disease: Mitchell-Riley Syndrome
Mitchell-Riley Syndrome
0.750 GeneticVariation disease BEFREE We describe Mitchell-Riley syndrome in two sisters with two novel compound heterozygous variants in the RFX6 gene: c.1154G > A, p.(Arg385Gln), and c.1316_1319delTCTA, p.(Ile439Thrfs*13). 27523286 2016
CUI: C2748662
Disease: Mitchell-Riley Syndrome
Mitchell-Riley Syndrome
0.750 GeneticVariation disease UNIPROT RFX6 regulates insulin secretion by modulating Ca2+ homeostasis in human β cells. 25497100 2014
CUI: C2748662
Disease: Mitchell-Riley Syndrome
Mitchell-Riley Syndrome
0.750 GeneticVariation disease CLINVAR
CUI: C2748662
Disease: Mitchell-Riley Syndrome
Mitchell-Riley Syndrome
0.750 GeneticVariation disease BEFREE After other gene testing was negative, the clinical diagnosis of Mitchell-Riley syndrome was ultimately considered and further genetic analysis revealed a novel missense homozygous variant in RFX6: c.983A>T (p.asp328Val). 31275908 2019
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.460 GeneticVariation disease GWASDB Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population. 20676098 2010
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.460 GeneticVariation disease BEFREE Association of THADA, FOXP4, GPRC6A/RFX6 genes and 8q24 risk alleles with prostate cancer in Northern Chinese men. 26537068 2016
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.460 GeneticVariation disease BEFREE In addition, we report here five new loci for prostate cancer susceptibility, at 5p15 (lambda-corrected probability P(GC) = 3.9 x 10(-18)), GPRC6A/RFX6 (P(GC) = 1.6 x 10(-12)), 13q22 (P(GC) = 2.8 x 10(-9)), C2orf43 (P(GC) = 7.5 x 10(-8)) and FOXP4 (P(GC) = 7.6 x 10(-8)). 20676098 2010
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.460 GeneticVariation disease BEFREE Case-control analysis of allelic frequency of PCa associated with PCa showed that one of the 6 candidate risk loci, rs339331 in the RFX6 gene, was associated with reduced risk of prostate cancer (odds ratio (OR) = 0.73, 95% confidence interval (CI) =0.57-0.94, P = 0.013) in northern Chinese men. 23803082 2013
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.460 GeneticVariation disease BEFREE We successfully replicated the association of rs13385191 (located in the C2orf43 gene, P = 8.60×10(-5)), rs12653946 (P = 1.33×10(-6)), rs1983891 (FOXP4, P = 6.22×10(-5)), and rs339331 (GPRC6A/RFX6, P = 1.42×10(-5)) with prostate cancer. 22662242 2012
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.460 GeneticVariation disease BEFREE Together, our results suggest that rs339331 affects prostate cancer risk by altering RFX6 expression through a functional interaction with the prostate cancer susceptibility gene HOXB13. 24390282 2014
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus
0.340 GeneticVariation disease BEFREE The phenotype of neonatal diabetes with intestinal atresia and biliary agenesis clearly pointed to RFX6 as the causative gene; indeed, whole exome sequencing revealed a novel homozygous RFX6 mutation c.779A>C; p.Lys260Thr (K260T). 23914949 2014
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus
0.340 GeneticVariation disease BEFREE Mutations in the RFX6 gene were recently described to underlie a distinct autosomal recessive syndrome of neonatal diabetes comprising intestinal atresia and hepatobiliary abnormalities. 21965172 2011
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus
0.340 GeneticVariation disease BEFREE When the particular phenotype of MFS includes a mutation on the RFX6 gene and neonatal diabetes, it has been called Mitchell-Riley syndrome. 25421130 2014
CUI: C0158981
Disease: Neonatal diabetes mellitus
Neonatal diabetes mellitus
0.340 GeneticVariation disease BEFREE Genetic testing for RFX6 mutations should be considered in patients presenting with intestinal atresias in the absence of neonatal diabetes. 26264437 2015
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms
0.310 GeneticVariation group BEFREE Finally, we observe a significant association between the risk-associated T allele at rs339331 and increased RFX6 mRNA levels in human prostate tumors. 24390282 2014
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.160 GeneticVariation disease GWASCAT A large multiethnic genome-wide association study of prostate cancer identifies novel risk variants and substantial ethnic differences. 26034056 2015
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.160 GeneticVariation disease BEFREE Association of THADA, FOXP4, GPRC6A/RFX6 genes and 8q24 risk alleles with prostate cancer in Northern Chinese men. 26537068 2016
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.160 GeneticVariation disease BEFREE In addition, we report here five new loci for prostate cancer susceptibility, at 5p15 (lambda-corrected probability P(GC) = 3.9 x 10(-18)), GPRC6A/RFX6 (P(GC) = 1.6 x 10(-12)), 13q22 (P(GC) = 2.8 x 10(-9)), C2orf43 (P(GC) = 7.5 x 10(-8)) and FOXP4 (P(GC) = 7.6 x 10(-8)). 20676098 2010
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.160 GeneticVariation disease GWASCAT 12 new susceptibility loci for prostate cancer identified by genome-wide association study in Japanese population. 31562322 2019
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.160 GeneticVariation disease BEFREE Case-control analysis of allelic frequency of PCa associated with PCa showed that one of the 6 candidate risk loci, rs339331 in the RFX6 gene, was associated with reduced risk of prostate cancer (odds ratio (OR) = 0.73, 95% confidence interval (CI) =0.57-0.94, P = 0.013) in northern Chinese men. 23803082 2013
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.160 GeneticVariation disease GWASCAT Large-scale association analysis in Asians identifies new susceptibility loci for prostate cancer. 26443449 2015
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma
0.160 GeneticVariation disease BEFREE Together, our results suggest that rs339331 affects prostate cancer risk by altering RFX6 expression through a functional interaction with the prostate cancer susceptibility gene HOXB13. 24390282 2014