Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 3565
Gene Symbol: IL4
IL4
0.030 AlteredExpression disease BEFREE Human pulmonary fibroblasts exhibit altered interleukin-4 and interleukin-13 receptor subunit expression in idiopathic interstitial pneumonia. 15161635 2004
Entrez Id: 3566
Gene Symbol: IL4R
IL4R
0.010 AlteredExpression disease BEFREE Human pulmonary fibroblasts exhibit altered interleukin-4 and interleukin-13 receptor subunit expression in idiopathic interstitial pneumonia. 15161635 2004
Entrez Id: 3663
Gene Symbol: IRF5
IRF5
0.020 GeneticVariation disease BEFREE In a multivariate analysis model including the diffuse cutaneous subtype of SSc and positivity for anti-topoisomerase I antibodies, the IRF5 rs2004640 TT genotype remained associated with fibrosing alveolitis (P=0.029, OR 1.92, 95% CI 1.07-3.44). 19116937 2009
Entrez Id: 6440
Gene Symbol: SFTPC
SFTPC
0.320 GeneticVariation disease BEFREE In conclusion, mutations in the gene encoding surfactant protein C are not common in sporadic cases of idiopathic pulmonary fibrosis and nonspecific interstitial pneumonia, suggesting that the mutated gene does not play an important role in the pathogenesis of these forms of idiopathic interstitial pneumonia. 17005585 2007
Entrez Id: 3569
Gene Symbol: IL6
IL6
0.200 Biomarker disease RGD Increased levels of interleukin-6 are associated with lymphocytosis in bronchoalveolar lavage fluids of idiopathic nonspecific interstitial pneumonia. 10988147 2000
Entrez Id: 7124
Gene Symbol: TNF
TNF
0.010 GeneticVariation disease BEFREE Increased risk of fibrosing alveolitis associated with interleukin-1 receptor antagonist and tumor necrosis factor-alpha gene polymorphisms. 10934117 2000
Entrez Id: 107075310
Gene Symbol: MTCO2P12
MTCO2P12
0.010 AlteredExpression disease BEFREE Interestingly, atypical alveolar epithelium, which associates with asbestosis and idiopathic fibrosing alveolitis and is considered to be a precursor lesion for lung cancer, expressed the Cox-2 protein. 9823297 1998
Entrez Id: 4513
Gene Symbol: COX2
COX2
0.010 AlteredExpression disease BEFREE Interestingly, atypical alveolar epithelium, which associates with asbestosis and idiopathic fibrosing alveolitis and is considered to be a precursor lesion for lung cancer, expressed the Cox-2 protein. 9823297 1998
Entrez Id: 5743
Gene Symbol: PTGS2
PTGS2
0.010 AlteredExpression disease BEFREE Interestingly, atypical alveolar epithelium, which associates with asbestosis and idiopathic fibrosing alveolitis and is considered to be a precursor lesion for lung cancer, expressed the Cox-2 protein. 9823297 1998
Entrez Id: 22861
Gene Symbol: NLRP1
NLRP1
0.010 GeneticVariation disease BEFREE Logistic regression analysis showed an additive effect of IRF5 rs2004640, STAT4 rs7574865 and NLRP1 rs8182352 risk alleles on SSc-related FA. 21149496 2011
Entrez Id: 21
Gene Symbol: ABCA3
ABCA3
0.400 GeneticVariation disease CLINVAR Polymorphism analysis of the ABCA3 gene: association with neonatal respiratory distress syndrome in preterm infants. 22800827 2012
Entrez Id: 21
Gene Symbol: ABCA3
ABCA3
0.400 GeneticVariation disease CLINVAR Population and disease-based prevalence of the common mutations associated with surfactant deficiency. 18317237 2008
Entrez Id: 21
Gene Symbol: ABCA3
ABCA3
0.400 GeneticVariation disease ORPHANET Sequencing of idiopathic pulmonary fibrosis-related genes reveals independent single gene associations. 25553246 2014
Entrez Id: 21
Gene Symbol: ABCA3
ABCA3
0.400 GeneticVariation disease CLINVAR Sequencing of idiopathic pulmonary fibrosis-related genes reveals independent single gene associations. 25553246 2014
Entrez Id: 6385
Gene Symbol: SDC4
SDC4
0.010 AlteredExpression disease BEFREE Serum syndecan-4 levels were significantly lower in patients with acute exacerbation of idiopathic interstitial pneumonia than in patients in the clinically stable phase. 28467516 2017
Entrez Id: 7012
Gene Symbol: TERC
TERC
0.310 SusceptibilityMutation disease ORPHANET Short telomeres are a risk factor for idiopathic pulmonary fibrosis. 18753630 2008
Entrez Id: 21
Gene Symbol: ABCA3
ABCA3
0.400 GeneticVariation disease CLINVAR Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome. 23166334 2012
Entrez Id: 21
Gene Symbol: ABCA3
ABCA3
0.400 GeneticVariation disease CLINVAR Single mutations in ABCA3 increase the risk for neonatal respiratory distress syndrome in late preterm infants (gestational age 34-36 weeks). 25073622 2014
Entrez Id: 3663
Gene Symbol: IRF5
IRF5
0.020 Biomarker disease BEFREE STAT4 and IRF5 act with additive effects in terms of susceptibility to both SSc and SSc-related fibrosing alveolitis. 19644887 2009
Entrez Id: 21
Gene Symbol: ABCA3
ABCA3
0.400 GeneticVariation disease CLINVAR Structural and dynamic aspects of Ca2+ and Mg2+ binding of the regulatory domains of the Na+/Ca2+ exchanger. 22435821 2012
Entrez Id: 653509
Gene Symbol: SFTPA1
SFTPA1
0.310 SusceptibilityMutation disease ORPHANET Surfactant protein A and B genetic variants predispose to idiopathic pulmonary fibrosis. 13680361 2003
Entrez Id: 7012
Gene Symbol: TERC
TERC
0.310 SusceptibilityMutation disease ORPHANET Telomerase mutations in families with idiopathic pulmonary fibrosis. 17392301 2007
Entrez Id: 3172
Gene Symbol: HNF4A
HNF4A
0.010 AlteredExpression disease BEFREE The purposes of the present study are to report the frequency and distribution of HNF4α-expressing cells at the different airway levels, and to investigate the potential significance of the expression of HNF4α in the histogenesis of non-TRU LADC with a special reference to the relationship to bronchiolar metaplasia in idiopathic interstitial pneumonia. 30848476 2019
Entrez Id: 3557
Gene Symbol: IL1RN
IL1RN
0.010 GeneticVariation disease BEFREE These data suggest IL-1RN (+2018) allele 2 and TNF-A (-308) allele 2 confer increased risk of developing FA and, therefore, that unopposed IL-1beta and/or excessive TNF-alpha may play a pathophysiologic role in this condition. 10934117 2000
Entrez Id: 7392
Gene Symbol: USF2
USF2
0.010 Biomarker disease BEFREE These findings suggest that FIP may be caused by an interaction between a specific environmental exposure and a gene (or genes) that predisposes to the development of several subtypes of idiopathic interstitial pneumonia. 16109978 2005