EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
|---|
    2.7.1.113 | Adenocarcinoma of Lung |
31633874 |
The mitochondrial deoxyguanosine kinase is required for cancer cell stemness in lung adenocarcinoma. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
1
4
0 |
| 2.7.1.113 | Adenocarcinoma of Lung |
33392072 |
Mitochondrial Deoxyguanosine Kinase Regulates NAD+ Biogenesis Independent of Mitochondria Complex I Activity. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
4
3
4
0 |
| 2.7.1.113 | Anemia, Hemolytic, Autoimmune |
28085791 |
Relevance of C5b9 immunostaining in the diagnosis of neonatal hemochromatosis. |
causal interaction
diagnostic usage
unassigned |
1
1
0 |
| 2.7.1.113 | Brain Diseases |
12110944 |
Depletion of the other genome-mitochondrial DNA depletion syndromes in humans. |
diagnostic usage
ongoing research
therapeutic application
unassigned |
1
1
1
0 |
| 2.7.1.113 | 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 |
| 2.7.1.113 | Carcinoma |
2561501 |
Suppression of deoxyguanosine cytotoxicity and deoxyguanosine kinase activity in mouse FM3A mammary carcinoma cell: mutants defective in hypoxanthine phosphoribosyl-transferase. |
ongoing research
therapeutic application
unassigned |
1
1
0 |
| 2.7.1.113 | 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 |
| 2.7.1.113 | Cholestasis |
24321534 |
Clinical and molecular characteristics of mitochondrial DNA depletion syndrome associated with neonatal cholestasis and liver failure. |
causal interaction
diagnostic usage
unassigned |
1
3
0 |
| 2.7.1.113 | Cystic Fibrosis |
28085791 |
Relevance of C5b9 immunostaining in the diagnosis of neonatal hemochromatosis. |
causal interaction
diagnostic usage
unassigned |
1
1
0 |
| 2.7.1.113 | deoxyguanosine kinase deficiency |
15964659 |
Clinical, biochemical and morphological features of hepatocerebral syndrome with mitochondrial DNA depletion due to deoxyguanosine kinase deficiency. |
causal interaction
unassigned |
4
0 |
