TBX21, T-box transcription factor 21, 30009

N. diseases: 124; N. variants: 12
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.050 GeneticVariation disease BEFREE The purpose of this study was to test the hypothesis that genetic variants of TBX21 (T cell specific T-box transcription factor) were associated with the outcomes of HCV infection and F protein generation. 25759111 2015
CUI: C0019196
Disease: Hepatitis C
Hepatitis C
0.050 GeneticVariation disease BEFREE Results showed that TBX21 rs4794067 variant genotypes significantly correlated with increased risk of HCV chronic infection (dominant model: OR = 5.690, 95% CI = 2.024-16.000) and susceptibility (dominant model: OR = 5.658, 95% CI = 2.514-12.735). 29399747 2018
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.040 GeneticVariation phenotype BEFREE TBX21 -1993 polymorphism might contribute to the risk of gastric cancer, especially to the distant metastasis. 22416188 2012
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.040 GeneticVariation phenotype BEFREE TBX21 gene -1514 and -1993 polymorphisms might be counted as the influential factors for lymph node and distant metastasis to ESCC. 25577251 2015
CUI: C0002874
Disease: Aplastic Anemia
Aplastic Anemia
0.030 GeneticVariation disease BEFREE Our results indicated that single nucleotide polymorphisms in TBX21 and STAT4 might contribute to susceptibility to AA in the Chinese population. 22133489 2012
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic
0.030 GeneticVariation disease BEFREE TBX21 SNP rs11079788 carriers developed less symptoms of atopic dermatitis at 3 years of age (p = 0.03). 22303482 2012
Diabetes Mellitus, Insulin-Dependent
0.030 GeneticVariation disease BEFREE Our study suggests the first evidence of an association between type 1 diabetes and polymorphisms in the T-bet gene, and that variation in T-bet transcriptional activity may play a role in the development of type 1 diabetes, possibly through the effect on IFN-gamma production in Th1 cells. 15241679 2004
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.030 GeneticVariation group BEFREE PSMA tumor volumes (PSMA-TV) and tumor lesion PSMA expressions (TL-PSMA) were calculated with a semi-automatic program on Ga-68 PSMA I&T PET/CT images that were obtained before and after Lu-177 PSMA I&T therapies with 19 patients. 31214958 2019
CUI: C0079774
Disease: Peripheral T-Cell Lymphoma
Peripheral T-Cell Lymphoma
0.030 GeneticVariation disease BEFREE Additionally, the 2 IHC-defined subtypes were significantly associated with distinct morphological features (P < .001), and there was a significant enrichment of an activated CD8+ cytotoxic phenotype in the PTCL-TBX21 subtype (P = .03). 31562134 2019
CUI: C0079774
Disease: Peripheral T-Cell Lymphoma
Peripheral T-Cell Lymphoma
0.030 GeneticVariation disease BEFREE The PTCL-TBX21 subgroup had fewer CNAs, primarily targeting cytotoxic effector genes, and was enriched in mutations of genes regulating DNA methylation. 30782609 2019
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.020 GeneticVariation disease BEFREE These results suggest that the polymorphisms of the TBX21 gene might be associated with the susceptibility to male RA patients. 19287198 2009
CUI: C0013595
Disease: Eczema
Eczema
0.020 GeneticVariation disease BEFREE TBX21 SNP rs11079788 carriers developed less symptoms of atopic dermatitis at 3 years of age (p = 0.03). 22303482 2012
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases
0.020 GeneticVariation group BEFREE Eight functional SNPs were associated with anti-TNF response either among patients with CD (TLR5 (rs5744174) and IFNGR2 (rs8126756)), UC (IL12B (rs3212217), IL18 (rs1946518), IFNGR1 (rs2234711), TBX21 (rs17250932) and JAK2 (rs12343867)) or in the combined cohort of patient with CD and UC (IBD) (NLRP3 (rs10754558), IL12B (rs3212217) and IFNGR1 (rs2234711)) (P<0.05). 28139755 2018
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.020 GeneticVariation disease BEFREE T-bet gene mutations may be associated with Th2-dominated condition in gastric cancers. 20193034 2010
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.020 GeneticVariation disease BEFREE TBX21 -1993 polymorphism might contribute to the risk of gastric cancer, especially to the distant metastasis. 22416188 2012
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.020 GeneticVariation disease BEFREE Multiple SNPs in TBX21 and STAT4 were found to be associated with SSc. 19950257 2009
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
0.020 GeneticVariation disease BEFREE Furthermore, gene-gene interaction studies suggest that IRF5, STAT4, and BANK1 as well as TBX21 and STAT4 interact with regard to scleroderma susceptibility. 20090527 2010
CUI: C0038013
Disease: Ankylosing spondylitis
Ankylosing spondylitis
0.020 GeneticVariation disease BEFREE TBX21 encodes T-bet, a transcription factor, lying within a locus with genome-wide significant association with AS. 27125523 2017
CUI: C0155877
Disease: Allergic asthma
Allergic asthma
0.020 GeneticVariation disease BEFREE Polymorphisms rs4794067 and rs16947078 of TBX21 were found to be associated with acetylsalicylic acid-induced and allergic asthma, respectively. 25056814 2014
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
Autoimmune Chronic Hepatitis
0.020 GeneticVariation disease BEFREE Association of TBX21 promoter polymorphisms with type 1 autoimmune hepatitis in a Chinese population. 20977921 2011
CUI: C0241910
Disease: Autoimmune Chronic Hepatitis
Autoimmune Chronic Hepatitis
0.020 GeneticVariation disease BEFREE Influence of TBX21 T-1993C variant on autoimmune hepatitis development by Yin-Yang 1 binding. 29358858 2017
CUI: C0524910
Disease: Hepatitis C, Chronic
Hepatitis C, Chronic
0.020 GeneticVariation disease BEFREE Association of IL-28B, TBX21 gene polymorphisms and predictors of virological response for chronic hepatitis C. 29399747 2018
CUI: C4721555
Disease: Autoimmune hepatitis
Autoimmune hepatitis
0.020 GeneticVariation disease BEFREE Influence of TBX21 T-1993C variant on autoimmune hepatitis development by Yin-Yang 1 binding. 29358858 2017
CUI: C4721555
Disease: Autoimmune hepatitis
Autoimmune hepatitis
0.020 GeneticVariation disease BEFREE Association of TBX21 promoter polymorphisms with type 1 autoimmune hepatitis in a Chinese population. 20977921 2011
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 GeneticVariation disease BEFREE Sixty-four patients with probable or possible AD associated with DM were classified using PiB (detects amyloid, A) and PBB3 (detects tau, T) PET studies. 31356213 2019