FMR1, FMRP translational regulator 1, 2332

N. diseases: 346; N. variants: 10
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.040 Biomarker group BEFREE Deficits in immune responses in female premutation carriers may lead to increased susceptibility to autoimmunity and further research is warranted to determine the link between FMR1 CGG repeat lengths and onset of autoinflammatory conditions. 24718368 2014
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.040 GeneticVariation group BEFREE Autoimmune disease in mothers with the FMR1 premutation is associated with seizures in their children with fragile X syndrome. 20809278 2010
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.040 Biomarker group BEFREE FMR1 sub-genotype het-norm/low is strongly associated with autoimmunity and decreased pregnancy chances in IVF, reaffirming the importance of the distal long arm of the X chromosome (FMR1 maps at Xq27.3) for autoimmunity, ovarian function and, likely, pregnancy chance with IVF. 21179569 2010
CUI: C0004364
Disease: Autoimmune Diseases
Autoimmune Diseases
0.040 Biomarker group BEFREE Co-occurrent autoimmune disease and fragile X syndrome has been reported in the literature and we have therefore studied the expansion of Cytosine-Guanine-Guanine (CGG) repeat in FMR1 gene in a series of females with autoimmune diseases such as systemic lupus erythematosus and Sjögren's syndrome, with PCR and Southern blot methods. 10941804 2000