HMGA1, high mobility group AT-hook 1, 3159

N. diseases: 206; N. variants: 5
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Diabetes Mellitus, Non-Insulin-Dependent
0.700 Biomarker disease BEFREE Recent studies firmly indicate an association between HMGA1 and type 2 diabetes. 29634420 2018
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE Consistently, lack of HMGA1 causes insulin resistance and diabetes in humans and mice, while variations in the <i>HMGA1</i> gene are associated with the risk of type 2 diabetes and metabolic syndrome, two highly prevalent diseases that share insulin resistance as a common pathogenetic mechanism. 30034366 2018
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE An association of the HMGA1 rs146052672 variant with T2DM has been recently reported. 27839822 2017
Diabetes Mellitus, Non-Insulin-Dependent
0.700 Biomarker disease BEFREE We also briefly discuss studies linking HMGA1 to Alzheimer's disease and type-2 diabetes. 26980699 2016
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE Our results revealed that SNP rs5498 in ICAM-1 gene and IVS5-13insC variant in HMGA1 gene were not associated with the susceptibility of DR in the Chinese T2DM cohort. 26717491 2016
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE For this reason, several studies have been conducted in recent years examining the association of the HMGA1 gene variant rs146052672 (also designated IVS5-13insC) with T2D. 26296198 2015
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE We have previously shown in three populations of white European ancestry that the HMGA1 gene variant rs146052672 (also designated IVS5-13insC) is associated with type 2 diabetes mellitus (T2DM). 24148075 2014
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE Lack of association of the HMGA1 IVS5-13insC variant with type 2 diabetes in an ethnically diverse hypertensive case control cohort. 23302499 2013
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE We and others previously reported a functional HMGA1 gene variant, rs146052672, predisposing to T2D. 23512162 2013
Diabetes Mellitus, Non-Insulin-Dependent
0.700 Biomarker disease CTD_human Association between rs146052672 variant and MetS occurred independently of T2D, indicating that HMGA1 gene defects play a pathogenetic role in MetS and other insulin-resistance-related conditions. 23512162 2013
Diabetes Mellitus, Non-Insulin-Dependent
0.700 Biomarker disease BEFREE In our study, we attempted to confirm that HMGA1 is a novel type 2 diabetes locus in French Caucasians. 22210315 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.700 GeneticVariation disease BEFREE HMGA1 is an important susceptibility locus that confers a high cross-race risk of the development of type 2 diabetes. 22411136 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.700 AlteredExpression disease BEFREE Messenger RNA and protein expression for HMGA1 and INSR were measured in both peripheral lymphomonocytes and cultured Epstein-Barr virus-transformed lymphoblasts from patients with type 2 DM and controls. 21364139 2011
Diabetes Mellitus, Non-Insulin-Dependent
0.700 PosttranslationalModification disease BEFREE Pseudogene-mediated posttranscriptional silencing of HMGA1 can result in insulin resistance and type 2 diabetes. 20975707 2010
Diabetes Mellitus, Non-Insulin-Dependent
0.700 AlteredExpression disease BEFREE Loss of Hmga1 expression, induced in mice by disrupting the Hmga1 gene, considerably decreased insulin receptor expression in the major targets of insulin action, largely impaired insulin signaling and severely reduced insulin secretion, causing a phenotype characteristic of human type 2 diabetes. 15924147 2005
Diabetes Mellitus, Non-Insulin-Dependent
0.700 Biomarker disease MGD Loss of Hmga1 expression, induced in mice by disrupting the Hmga1 gene, considerably decreased insulin receptor expression in the major targets of insulin action, largely impaired insulin signaling and severely reduced insulin secretion, causing a phenotype characteristic of human type 2 diabetes. 15924147 2005
Diabetes Mellitus, Non-Insulin-Dependent
0.700 Biomarker disease HPO
CUI: C0153567
Disease: Uterine Cancer
Uterine Cancer
0.520 Biomarker disease BEFREE Our work also suggests that targeting HMGA1 could be effective adjuvant therapy for more aggressive uterine cancers and provides compelling data for further preclinical studies. 27001612 2016
CUI: C0153567
Disease: Uterine Cancer
Uterine Cancer
0.520 Biomarker disease CTD_human Both drugs block anchorage-independent growth in high-grade human uterine cancer cells that overexpress HMGA1a (MES-SA cells). 18645019 2008
CUI: C0153567
Disease: Uterine Cancer
Uterine Cancer
0.520 Biomarker disease BEFREE Although a larger study is needed to confirm these results, HMGA1a may be a useful marker for aggressive human uterine cancers. 17483309 2007
CUI: C0153567
Disease: Uterine Cancer
Uterine Cancer
0.520 Biomarker disease MGD
CUI: C0042138
Disease: Uterine Neoplasms
Uterine Neoplasms
0.510 Biomarker group CTD_human Cyclooxygenase inhibitors block uterine tumorigenesis in HMGA1a transgenic mice and human xenografts. 18645019 2008
CUI: C0042138
Disease: Uterine Neoplasms
Uterine Neoplasms
0.510 AlteredExpression group BEFREE To determine whether these findings are relevant to human disease, we evaluated primary human uterine neoplasms and found that HMGA1a mRNA and protein levels are increased in most high-grade neoplasms but not in normal uterine tissue, benign tumors, or most low-grade neoplasms. 17483309 2007
CUI: C0042138
Disease: Uterine Neoplasms
Uterine Neoplasms
0.510 Biomarker group MGD
CUI: C0021655
Disease: Insulin Resistance
Insulin Resistance
0.400 Biomarker phenotype CTD_human Association between rs146052672 variant and MetS occurred independently of T2D, indicating that HMGA1 gene defects play a pathogenetic role in MetS and other insulin-resistance-related conditions. 23512162 2013