EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category  |
Confidence Level |
|---|
    6.2.1.4 | Heart Failure |
31836543 |
Defining decreased protein succinylation of failing human cardiac myofibrils in ischemic cardiomyopathy. |
causal interaction
unassigned |
1
0 |
| 6.2.1.4 | Mitochondrial Encephalomyopathies |
29217198 |
Clinical, Molecular, and Computational Analysis in two cases with mitochondrial encephalomyopathy associated with SUCLG1 mutation in a consanguineous family. |
causal interaction
diagnostic usage
unassigned |
4
4
0 |
| 6.2.1.4 | Seizures |
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 | Prostatic Neoplasms |
32963351 |
EGFR-upregulated LIFR promotes SUCLG2-dependent castration resistance and neuroendocrine differentiation of prostate cancer. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
3
4
0 |
| 6.2.1.4 | Neoplasms |
32963351 |
EGFR-upregulated LIFR promotes SUCLG2-dependent castration resistance and neuroendocrine differentiation of prostate cancer. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
3
4
0 |
| 6.2.1.4 | Neoplasms |
34415331 |
Germline SUCLG2 Variants in Patients with Pheochromocytoma and Paraganglioma. |
causal interaction
diagnostic usage
ongoing research
unassigned |
1
3
4
0 |
| 6.2.1.4 | Acidosis |
18392745 |
Disorders caused by deficiency of succinate-CoA ligase. |
causal interaction
unassigned |
4
0 |
| 6.2.1.4 | Acidosis |
20227526 |
Marked mitochondrial DNA depletion associated with a novel SUCLG1 gene mutation resulting in lethal neonatal acidosis, multi-organ failure, and interrupted aortic arch. |
causal interaction
unassigned |
4
0 |
| 6.2.1.4 | Acidosis, Lactic |
19526370 |
A novel missense mutation in SUCLG1 associated with mitochondrial DNA depletion, encephalomyopathic form, with methylmalonic aciduria. |
causal interaction
unassigned |
3
0 |
| 6.2.1.4 | Acidosis, Lactic |
21093335 |
Fatal infantile lactic acidosis and a novel homozygous mutation in the SUCLG1 gene: a mitochondrial DNA depletion disorder. |
causal interaction
ongoing research
unassigned |
4
2
0 |
