EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
2.3.1.22 | 2-acylglycerol o-acyltransferase deficiency |
19419693 |
MGAT2 deficiency (CDG-IIa): The Life of J. |
causal interaction unassigned |
3 0 |
2.3.1.22 | 2-acylglycerol o-acyltransferase deficiency |
21734185 |
Deficiency of MGAT2 increases energy expenditure without high-fat feeding and protects genetically obese mice from excessive weight gain. |
causal interaction ongoing research therapeutic application unassigned |
3 4 3 0 |
2.3.1.22 | 2-acylglycerol o-acyltransferase deficiency |
22698140 |
MGAT2 deficiency ameliorates high-fat diet-induced obesity and insulin resistance by inhibiting intestinal fat absorption in mice. |
causal interaction unassigned |
3 0 |
2.3.1.22 | 2-acylglycerol o-acyltransferase deficiency |
25315695 |
MGAT2 deficiency and vertical sleeve gastrectomy have independent metabolic effects in the mouse. |
causal interaction therapeutic application unassigned |
4 4 0 |
2.3.1.22 | 2-acylglycerol o-acyltransferase deficiency |
25535286 |
Adult-onset deficiency of acyl CoA:monoacylglycerol acyltransferase 2 protects mice from diet-induced obesity and glucose intolerance. |
causal interaction ongoing research therapeutic application unassigned |
4 4 1 0 |
2.3.1.22 | 2-acylglycerol o-acyltransferase deficiency |
30831319 |
Defective Phosphatidylglycerol Remodeling Causes Hepatopathy, Linking Mitochondrial Dysfunction to Hepatosteatosis. |
causal interaction ongoing research therapeutic application unassigned |
3 3 1 0 |
2.3.1.22 | Alzheimer Disease |
21368380 |
MGAT3 mRNA: A Biomarker for Prognosis and Therapy of Alzheimer's Disease by Vitamin D and Curcuminoids. |
causal interaction diagnostic usage therapeutic application unassigned |
3 3 3 0 |
2.3.1.22 | Alzheimer Disease |
22003913 |
Delineating Alzheimer's disease progression with MGAT3, a biomarker for improved prognosis and personalized therapy. |
causal interaction diagnostic usage therapeutic application unassigned |
3 2 4 0 |
2.3.1.22 | Bardet-Biedl Syndrome |
32789750 |
Novel variants in women with premature ovarian function decline identified via whole-exome sequencing. |
diagnostic usage unassigned |
2 0 |
2.3.1.22 | beta-1,4-mannosyl-glycoprotein 4-beta-n-acetylglucosaminyltransferase deficiency |
26467158 |
Bisecting GlcNAc modification stabilizes BACE1 protein under oxidative stress conditions. |
causal interaction unassigned |
4 0 |