IRF7, interferon regulatory factor 7, 3665

N. diseases: 121; N. variants: 11
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4225358
Disease: IMMUNODEFICIENCY 39
IMMUNODEFICIENCY 39
0.700 GeneticVariation disease UNIPROT Infectious disease. Life-threatening influenza and impaired interferon amplification in human IRF7 deficiency. 25814066 2015
CUI: C4225358
Disease: IMMUNODEFICIENCY 39
IMMUNODEFICIENCY 39
0.700 Biomarker disease GENOMICS_ENGLAND IRF-7, a new interferon regulatory factor associated with Epstein-Barr virus latency. 9315633 1997
CUI: C4225358
Disease: IMMUNODEFICIENCY 39
IMMUNODEFICIENCY 39
0.700 CausalMutation disease CLINVAR
CUI: C4225358
Disease: IMMUNODEFICIENCY 39
IMMUNODEFICIENCY 39
0.700 Biomarker disease CTD_human
CUI: C0021400
Disease: Influenza
Influenza
0.370 GeneticVariation disease BEFREE Defective interferon priming and impaired antiviral responses in a patient with an IRF7 variant and severe influenza. 31172279 2019
CUI: C0021400
Disease: Influenza
Influenza
0.370 GeneticVariation disease BEFREE These diseases encompass herpes simplex encephalitis (HSE) and severe influenza in IRF3- and IRF7/IRF9 deficiency, respectively. 30671054 2018
CUI: C0021400
Disease: Influenza
Influenza
0.370 Biomarker disease BEFREE These findings suggest that chicken IRF7 could modulate a wide range of cellular processes in the host innate immune response thus meticulous control of IRF7 expression is crucial to the host in response to AIV infection. 30356848 2018
CUI: C0021400
Disease: Influenza
Influenza
0.370 Biomarker disease BEFREE Recently however, human IRF7 was shown to be essential for IFN-α/β- and IFN-λ-dependent protective immunity against primary influenza in vivo, as inferred from a patient with life-threatening influenza revealed to be IRF7-deficient by whole exome sequencing. 26761402 2016
CUI: C0021400
Disease: Influenza
Influenza
0.370 Biomarker disease BEFREE These findings suggest that IRF7-dependent amplification of type I and III IFNs is required for protection against primary infection by influenza virus in humans. 25814066 2015
CUI: C0021400
Disease: Influenza
Influenza
0.370 GeneticVariation disease BEFREE We also identified a common variant in IRF7 that is associated in trans with type I IFN induction in response to influenza infection. 24604203 2014
CUI: C0021400
Disease: Influenza
Influenza
0.370 Biomarker disease CTD_human A host transcriptional signature for presymptomatic detection of infection in humans exposed to influenza H1N1 or H3N2. 23326326 2013
CUI: C0021400
Disease: Influenza
Influenza
0.370 AlteredExpression disease BEFREE These data demonstrate that infection with influenza results in the reduced expression of transcription factor IRF7 in NECs from smokers, and that these effects may be mediated by an epigenetic modification of the IRF7 gene, thus providing a potential mechanism rendering smokers more susceptible to respiratory virus infections. 19880818 2010
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.310 Biomarker disease PSYGENET We found these results to be concordant with our observation of decreased expression of IRF7 in the prefrontal cortex of MDDs with negative toxicological evidence for antidepressant treatment at the time of death. 22832429 2011
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.310 AlteredExpression disease BEFREE We found these results to be concordant with our observation of decreased expression of IRF7 in the prefrontal cortex of MDDs with negative toxicological evidence for antidepressant treatment at the time of death. 22832429 2011
CUI: C0041696
Disease: Unipolar Depression
Unipolar Depression
0.300 Biomarker disease PSYGENET Gene expression biomarkers of response to citalopram treatment in major depressive disorder. 22832429 2011
CUI: C0021368
Disease: Inflammation
Inflammation
0.300 Biomarker phenotype CTD_human Type I interferon signaling contributes to chronic inflammation in a murine model of silicosis. 20513754 2010
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.200 GeneticVariation disease GWASCAT Transancestral mapping and genetic load in systemic lupus erythematosus. 28714469 2017
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.200 AlteredExpression disease BEFREE Furthermore, inhibition of Pin1 using either validated Pin1 shRNA or ATRA blocked TLR-7-induced activation of IRAK-1 and IRF-7 in SLE patient-derived immune cells. 27159270 2016
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.200 GeneticVariation disease GWASCAT Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus. 27399966 2016
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.200 Biomarker disease BEFREE The type-I interferon master regulator gene IRF7 is only hypomethylated in lupus patients with renal involvement. 26005050 2015
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.200 Biomarker disease BEFREE IRF7, a functional factor associates with systemic lupus erythematosus. 22455868 2012
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.200 Biomarker disease BEFREE These results confirmed recently reported association of PHRF1 rs4963128T with anti-Sm antibody positive SLE in African-American populations, and supported the role of PHRF1-IRF7 region in the genetics of SLE. 22433914 2012
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.200 Biomarker disease BEFREE Recent studies have reported an association between IRF7 and SLE which confers a risk to autoantibody production. 21926187 2012
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.200 Biomarker disease BEFREE This result provides direct genetic evidence that IRF7 may be a risk gene for human SLE. 21360504 2011
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.200 GeneticVariation disease BEFREE We decided to investigate the association of single-nucleotide polymorphisms (SNPs) in the IRF7/KIAA1542 region (rs4963128, rs2246614, and rs702966) and in STAT4 (rs7574865 and rs7582694) with SLE disease in a Northern Han Chinese population of 748 patients and 750 healthy controls. 21167895 2011