EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    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 |
| 6.2.1.4 | Acidosis, Lactic |
21639866 |
Neonatal lactic acidosis with methylmalonic aciduria by novel mutations in the SUCLG1 gene. |
causal interaction
unassigned |
4
0 |
| 6.2.1.4 | Adenocarcinoma, Mucinous |
34174878 |
Multi-omics analyses of human colorectal cancer revealed three mitochondrial genes potentially associated with poor outcomes of patients. |
unassigned |
0 |
| 6.2.1.4 | Adenoma |
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 | Adenoma |
34174878 |
Multi-omics analyses of human colorectal cancer revealed three mitochondrial genes potentially associated with poor outcomes of patients. |
unassigned |
0 |
| 6.2.1.4 | Alzheimer Disease |
25027320 |
SUCLG2 identified as both a determinator of CSF A?1-42 levels and an attenuator of cognitive decline in Alzheimer's disease. |
causal interaction
unassigned |
2
0 |
| 6.2.1.4 | Anemia, Sideroblastic |
10727444 |
Interaction between succinyl CoA synthetase and the heme-biosynthetic enzyme ALAS-E is disrupted in sideroblastic anemia. |
causal interaction
unassigned |
2
0 |
