Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.140 GeneticVariation disease BEFREE Variants originally associated with juvenile idiopathic arthritis (VTCN1 gene), sarcoidosis (ANXA11 gene), primary biliary cirrhosis (IL12RB2 gene) and celiac disease (LPP gene) were not associated with type 1 diabetes in our dataset. 23152861 2012
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.140 Biomarker disease BEFREE CONCLUSION: Our data show an increased sensitivity of PBC and pSS Treg cells to low dose IL-12 stimulation, providing ongoing support for the importance of the IL12-IL-12Rβ2-STAT4 pathway on Treg cells in disease pathogenesis and potentially treatment. 30119881 2018
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.140 GeneticVariation disease BEFREE Polymorphisms of IL12RB2 May Affect the Natural History of Primary Biliary Cholangitis: A Single Centre Study. 28299343 2017
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis
0.140 GeneticVariation disease BEFREE Our data show significant associations between primary biliary cirrhosis and common genetic variants at the HLA class II, IL12A, and IL12RB2 loci and suggest that the interleukin-12 immunoregulatory signaling axis is relevant to the pathophysiology of primary biliary cirrhosis. 19458352 2009
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.110 AlteredExpression disease BEFREE IL-35R subunits, gp130 and IL-27Rα, but not IL-12Rβ2, were expressed in B cells extracted from the synovium and periphery of patients with RA/OA. 29247146 2018
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic
0.110 Biomarker disease BEFREE The results supported the theory that IL12RB2 is associated with SLE in the Chinese population. 25720506 2015
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.110 GeneticVariation disease BEFREE Aiming to reveal the possible implication of the IL12RB2 gene in SSc, we conducted a follow-up study of this locus in different Caucasian cohorts. 22076442 2012
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE Our findings not only confirmed the association of IL10/rs1800871 and IL23R-IL12RB2/rs924080 with BD but also identified 2 susceptibility single nucleotide polymorphisms in IL10 and IL23R-IL12RB2 (rs3024490 and rs12141431) with BD in Han Chinese. 27464962 2017
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE We tested 14 single-nucleotide polymorphisms (SNPs) in 13 genomic loci (excluding the major histocompatibility complex [MHC], IL10, and IL23R-IL12RB2, which have already been associated with BD in Iranians) for allelic and genotypic associations with BD in 973 patients and 828 controls from Iran and performed meta-analyses of the significantly associated markers. 26097239 2015
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE SNPs (rs924080 and rs11209032) of the IL23R-IL12RB2 region were found to be associated with BD in a Northern Chinese Han population. 27660093 2016
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE An IL23R-IL12RB2 intergenic SNP rs1495965 was significantly associated with BD risk (OR (95% CI) = 1.5 (1.3, 1.7), P = 2.5 × 10<sup>-7</sup>) in the pooled meta-analysis of the discovery (1.4 (1.2, 1.7), P = 4.9 × 10<sup>-7</sup>) and replication (1.9 (1.3, 2.6), P = 6.0 × 10<sup>-4</sup>) phases. 29017598 2017
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE Six SNPs in IL23R-IL12RB2 were found to be associated with BD after Bonferroni correction for multiple testing, the most significant of which were rs17375018 (OR for G allele 1.51, 95% CI 1.27-1.78, P(unadj) = 1.93 × 10(-6) ), rs7517847 (OR for T allele 1.48, 95% CI 1.26-1.74, P(unadj) = 1.23 × 10(-6) ), and rs924080 (OR for T allele 1.29, 95% CI 1.20-1.39, P = 1.78 × 10(-5) ). 22378604 2012
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 GeneticVariation disease BEFREE Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease. 20622878 2010
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE Although we were not able to formally replicate the association with IL10 and IL23R-IL12RB2, we do report that BD in Iran is strongly associated with HLA-B*51, MICA-A6, and the three HLA-linked SNPs (odds ratio (OR) = 3.38, P = 6.21 × 10(-14); OR = 2.08, P = 1.58 × 10(-13); and OR = 1.67-4.05, P = 1.45 × 10(-04) to 4.79 × 10(-34), respectively). 25940109 2015
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE Genetic variations of IL-12B, IL-12Rβ1, IL-12Rβ2 in Behcet's disease and VKH syndrome. 24859272 2014
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE Two recent large genome-wide association study (GWAS) conducted in Turkey and Japan reported association between single nucleotide polymorphism (SNP) of interleukin (IL)-10 and IL-23R/IL-12RB2 genes and BD. 22197900 2012
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
0.100 Biomarker disease BEFREE Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci. 20622879 2010
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.030 AlteredExpression disease BEFREE Compared with in benign pulmonary tissues, the expression levels of IL‑12Rβ2 and p38MAPK were not demonstrated to be significantly different in I+II pathological tumor‑node‑metastasis (pTNM) stage NSCLC tissues; however, reduced expression was detected in III+IV pTNM stage NSCLC tissues. 29956791 2018
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.030 Biomarker disease BEFREE In order to perform in vivo studies, the Calu6 NSCLC cell line was transfected with the IL-12RB2 containing plasmid (Calu6/beta2). 19582164 2009
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma
0.030 AlteredExpression disease BEFREE In contrast to benign pulmonary, ERβ2 and IL-12Rβ2 were over-expressed in NSCLC (p = 0.000). 23677568 2013
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 Biomarker group BEFREE Interestingly, p40 was involved in the arrest of IL-12 receptor (IL-12R) IL-12Rβ1, but not IL-12Rβ2, in the membrane, and that p40 neutralization induced the internalization of IL-12Rβ1 via caveolin and caused cancer cell death via the IL-12-IFN-γ pathway. 29073075 2017
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 Biomarker group BEFREE These studies, together with others performed in Il12rb2 knockout mice, have established the concept that the IL-12Rbeta2 gene is a gatekeeper from cancer. 19720917 2009
CUI: C0007107
Disease: Malignant neoplasm of larynx
Malignant neoplasm of larynx
0.020 AlteredExpression disease BEFREE The significant correlations between IL-12Rβ2 and IL-23R expression and TIL ratios were identified in LC tissues, particularly in well-differentiated LC. 30355949 2018
CUI: C0007107
Disease: Malignant neoplasm of larynx
Malignant neoplasm of larynx
0.020 AlteredExpression disease BEFREE Tumor cell differentiation is associated with TILs' expression of IL-12Rβ2, and an IL-12Rβ2<sup>+</sup> TIL ratio ≥35%) indicates favorable prognosis in LC. 29103744 2017
CUI: C0023343
Disease: Leprosy
Leprosy
0.020 GeneticVariation disease BEFREE Our data suggest that polymorphisms present in the promoter region of IL12RB2 may not be associated with susceptibility to leprosy or its clinical forms. 24486579 2014