GLIS3, GLIS family zinc finger 3, 169792

N. diseases: 105; N. variants: 48
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism
0.500 Biomarker disease BEFREE Deficiency in Krüppel-like zinc finger transcription factor GLI-similar 3 (GLIS3) in humans is associated with the development of congenital hypothyroidism. 29083325 2017
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism
0.500 GeneticVariation disease BEFREE The Glis3 mutant mice have been characterized for their propensity to develop congenital hypothyroidism, polycystic kidney disease, and some types of cancer. 28523428 2017
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE The GLIS3 SNP (rs180867004) associated with T2DM only in men (P = .00006, OR = 1.94 [1.40-2.68]). 27862917 2017
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE Genome-wide association studies revealed that GLIS3 variants are associated with both common type 1 and type 2 diabetes. 27813676 2017
Diabetes Mellitus, Non-Insulin-Dependent
0.500 Biomarker disease BEFREE In addition, GLIS3 is also required for the compensatory β cell proliferation and mass expansion in response to insulin resistance, which if disrupted may predispose to T2D. 27899417 2017
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE GLIS3 rs7034200 and GRK5 rs10886471 were significantly associated with increased T2DM risk (GLIS3 rs7034200 under dominant model: P=0.0307; GRK5 rs10886471 under recessive model: P=0.0092). 26919830 2017
Diabetes Mellitus, Non-Insulin-Dependent
0.500 AlteredExpression disease BEFREE Those with an elevated fasting plasma glucose [impaired fasting glucose or IFG] with or without an elevated HbA1c [non -diabetic hyperglycaemia; NDH] are randomised into three treatment arms: a control arm receiving no trial intervention, an arm receiving an intensive bespoke group-based diet and physical activity intervention, and an arm receiving the same intervention with enhanced support from people with T2DM trained as diabetes prevention mentors [DPM]. 28056894 2017
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASCAT Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. 28869590 2017
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASCAT Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes. 26818947 2016
Diabetes Mellitus, Non-Insulin-Dependent
0.500 Biomarker disease BEFREE GLIS3 is also required for compensatory β-cell proliferation in adults; impairment of this function predisposes to T2D. 27035557 2016
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism
0.500 GeneticVariation disease BEFREE We report the first case of a patient with a compound heterozygous mutation in GLIS3 who did not present with congenital hypothyroidism. 26259131 2015
Diabetes Mellitus, Non-Insulin-Dependent
0.500 Biomarker disease BEFREE Four of eight T1D-specific regions contained known type 2 diabetes (T2D) candidate genes (COBL, GLIS3, RNLS and BCAR1), suggesting a shared cellular etiology. 26053495 2015
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASDB Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. 24509480 2014
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE The GLIS3 gene region has also been identified as a susceptibility risk locus for both type 1 and type 2 diabetes. 23737756 2013
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASDB A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans. 22961080 2013
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASCAT A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans. 22961080 2013
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASDB Genome-wide association study identifies a novel locus contributing to type 2 diabetes susceptibility in Sikhs of Punjabi origin from India. 23300278 2013
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE We analyzed nine single-nucleotide polymorphisms (SNPs), including rs340874 (PROX1), rs4607517 (GCK), rs2191349 (DGKB-TMEM195), rs7034200 (GLIS3), rs10885122 (ADRA2A), rs174550 (FADS1), rs11605924 (CRY2), rs10830963 (MTNR1B) and rs35767 (IGF1). rs340874 (PROX1) and rs174550 (FADS1) were significantly associated with T2D (P=0.0078, OR: 1.12; and P=0.0071, OR: 1.12, respectively). 22992776 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASDB Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. 22885922 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE Glis3 has also been identified as a risk locus for type-1 and type-2 diabetes and additional studies have revealed a role for Glis3 in pancreatic endocrine development, β-cell maintenance, and insulin regulation. 22391303 2012
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASCAT Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes. 22885922 2012
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism
0.500 GeneticVariation disease BEFREE We also report the first case of a recessive GLIS3 mutation causing neonatal diabetes and congenital hypothyroidism in a child from a non-consanguineous pedigree, highlighting the importance of molecular genetic testing in any patient with this phenotype. 21139041 2011
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease BEFREE In conclusion, our results indicate the associations of GLIS3 locus with type 2 diabetes and impaired fasting glucose in Chinese Hans, partially mediated through impaired beta-cell function. 21747906 2011
Diabetes Mellitus, Non-Insulin-Dependent
0.500 GeneticVariation disease GWASCAT The combined analysis identified eight new T2D loci reaching genome-wide significance, which mapped in or near GLIS3, PEPD, FITM2-R3HDML-HNF4A, KCNK16, MAEA, GCC1-PAX4, PSMD6 and ZFAND3. 22158537 2011
Diabetes Mellitus, Non-Insulin-Dependent
0.500 Biomarker disease CTD_human The combined analysis identified eight new T2D loci reaching genome-wide significance, which mapped in or near GLIS3, PEPD, FITM2-R3HDML-HNF4A, KCNK16, MAEA, GCC1-PAX4, PSMD6 and ZFAND3. 22158537 2011