EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
6.2.1.4 | Anemia, Sideroblastic |
22740690 |
X-linked Sideroblastic Anemia Due to Carboxyl-terminal ALAS2 Mutations That Cause Loss of Binding to the ?-Subunit of Succinyl-CoA Synthetase (SUCLA2). |
causal interaction unassigned |
4 0 |
6.2.1.4 | Brain Diseases |
33484326 |
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome. |
causal interaction unassigned |
4 0 |
6.2.1.4 | Carcinoma |
28709933 |
Identification of novel biomarker and therapeutic target candidates for diagnosis and treatment of follicular carcinoma. |
diagnostic usage therapeutic application unassigned |
3 1 0 |
6.2.1.4 | Cardiomyopathies |
33484326 |
Contribution of nuclear and mitochondrial gene mutations in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome. |
causal interaction unassigned |
4 0 |
6.2.1.4 | Cardiomyopathy, Hypertrophic |
26475597 |
Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients. |
causal interaction diagnostic usage therapeutic application unassigned |
4 1 1 0 |
6.2.1.4 | Colonic Neoplasms |
33053772 |
Effect of Citric Acid Cycle Genetic Variants and Their Interactions with Obesity, Physical Activity and Energy Intake on the Risk of Colorectal Cancer: Results from a Nested Case-Control Study in the UK Biobank. |
causal interaction unassigned |
1 0 |
6.2.1.4 | Diabetes Mellitus, Experimental |
2936621 |
Inhibition by streptozotocin of the activity of succinyl-CoA synthetase in vitro and in vivo. |
causal interaction ongoing research unassigned |
1 1 0 |
6.2.1.4 | Down Syndrome |
28749033 |
Co-occurring Down syndrome and SUCLA2-related mitochondrial depletion syndrome. |
causal interaction unassigned |
4 0 |
6.2.1.4 | Endometriosis |
23284138 |
Changes in eutopic endometrial gene expression during the progression of experimental endometriosis in the baboon, papio anubis. |
causal interaction ongoing research unassigned |
1 2 0 |
6.2.1.4 | Epilepsy |
26475597 |
Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients. |
causal interaction diagnostic usage therapeutic application unassigned |
4 1 1 0 |