MIA3, MIA SH3 domain ER export factor 3, 375056

N. diseases: 27; N. variants: 7
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.010 Biomarker group BEFREE We digitised tissue sections of both diagnostic and surgical samples of breast tumours from 768 patients enrolled in the Neo-tAnGo randomized controlled trial. 26882907 2016
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.440 GeneticVariation disease BEFREE We conclude that SNP rs17465637 in MIA3 is indeed a genetic risk factor for CAD across different ethnic populations. 24125424 2013
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.030 AlteredExpression group BEFREE Thus, functional relevant loss of TANGO expression may contribute to general tumor development and progression, and may provide a new target for therapeutic strategies. 17786351 2007
CUI: C0013080
Disease: Down Syndrome
Down Syndrome
0.010 Biomarker disease BEFREE The proposal relies on stimulating the cognitive visual-motor skills of individuals with Down Syndrome (DS) using exercises with a gestural interaction platform based on the KINECT sensor named TANGO:H, the goal being to improve them. 31540138 2019
CUI: C4521042
Disease: Complete Trisomy 21 Syndrome
Complete Trisomy 21 Syndrome
0.010 Biomarker disease BEFREE The proposal relies on stimulating the cognitive visual-motor skills of individuals with Down Syndrome (DS) using exercises with a gestural interaction platform based on the KINECT sensor named TANGO:H, the goal being to improve them. 31540138 2019
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.150 GeneticVariation disease BEFREE The Ch9p21 SNPs rs1333049 (OR 1.17; 95% confidence limits 1.11-1.24) and rs10757274 (OR 1.17; 1.09-1.26), MIA3 rs17465637 (OR 1.10; 1.04-1.15), Ch2q36 rs2943634 (OR 1.08; 1.03-1.14), APC rs383830 (OR 1.10; 1.02, 1.18), MTHFD1L rs6922269 (OR 1.10; 1.03, 1.16), CXCL12 rs501120 (OR 1.12; 1.04, 1.20), and SMAD3 rs17228212 (OR 1.11; 1.05, 1.17) were all associated with CHD risk, but not with the CHD biomarkers and risk factors measured. 21804106 2012
CUI: C0028734
Disease: Nocturia
Nocturia
0.010 Biomarker disease BEFREE The acronym TANGO stands for Targeting the individual's Aetiology of Nocturia to Guide Outcomes. 28075514 2017
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 GeneticVariation group BEFREE The MIA3 mutant allele showed predominant mRNA expression in normal, cancer and precancerous tissues. 28742792 2017
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.010 GeneticVariation group BEFREE The MIA3 mutant allele showed predominant mRNA expression in normal, cancer and precancerous tissues. 28742792 2017
CUI: C0025202
Disease: melanoma
melanoma
0.040 Biomarker disease BEFREE Recently, we identified TANGO as a tumor suppressor in malignant melanoma. 17786351 2007
CUI: C0178874
Disease: Tumor Progression
Tumor Progression
0.020 AlteredExpression phenotype BEFREE Our studies, therefore, indicate that reduction of TANGO expression contributes to tumor progression. 17044017 2006
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 AlteredExpression disease LHGDN Our studies present for the first time the down-regulation of TANGO in colon and hepatocellular carcinoma and provide the first indications for a tumor suppressor role of the TANGO gene in human colon and hepatocellular carcinoma. 17786351 2007
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.010 Biomarker disease BEFREE Our studies present for the first time the down-regulation of TANGO in colon and hepatocellular carcinoma and provide the first indications for a tumor suppressor role of the TANGO gene in human colon and hepatocellular carcinoma. 17786351 2007
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 Biomarker group BEFREE Our results suggest that MIA, MIA2, and TANGO may be useful diagnostic and therapeutic molecular targets in human malignancies. 27145272 2016
CUI: C0027051
Disease: Myocardial Infarction
Myocardial Infarction
0.430 GeneticVariation disease BEFREE Our results establish two SNPs, rs17465637 in MIA3 and rs599839 near SORT1 as significant risk factors for MI in the American Genebank Caucasian population. 21463265 2011
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.010 Biomarker disease BEFREE MicroRNA-222 influences migration and invasion through MIA3 in colorectal cancer. 28855850 2017
Malignant neoplasm of colon and/or rectum
0.010 Biomarker disease BEFREE MicroRNA-222 influences migration and invasion through MIA3 in colorectal cancer. 28855850 2017
CUI: C0025202
Disease: melanoma
melanoma
0.040 AlteredExpression disease BEFREE MIA has a pivotal role in the progression and metastasis of melanoma; MIA2 and TANGO have been suggested to possess tumor-suppressive functions; and OTOR is uniquely expressed in cochlea of the inner ear. 29655307 2018
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.020 Biomarker phenotype BEFREE MIA has a pivotal role in the progression and metastasis of melanoma; MIA2 and TANGO have been suggested to possess tumor-suppressive functions; and OTOR is uniquely expressed in cochlea of the inner ear. 29655307 2018
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.330 GeneticVariation disease BEFREE Meta-analysis identifies robust association between SNP rs17465637 in MIA3 on chromosome 1q41 and coronary artery disease. 24125424 2013
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.150 GeneticVariation disease BEFREE Meta-analysis identifies robust association between SNP rs17465637 in MIA3 on chromosome 1q41 and coronary artery disease. 24125424 2013
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.030 Biomarker group BEFREE Melanoma inhibitor protein 3 (MIA3) is required for the export of collagen VlI (COL7A1) from the endoplasmic reticulum and it appears to be a tumor suppressor of malignant melanoma. 22577832 2012
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.150 GeneticVariation disease GWASDB Large-scale gene-centric analysis identifies novel variants for coronary artery disease. 21966275 2011
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.440 Biomarker disease CTD_human Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. 21378990 2011
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.330 Biomarker disease CTD_human Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. 21378990 2011