EC Number   |
Disease |
PubMed ID |
Title of Publication  |
Category |
Confidence Level |
|---|
    2.8.3.5 | Ovarian Neoplasms |
29434981 |
3-Oxoacid CoA transferase 1 as a therapeutic target gene for cisplatin-resistant ovarian cancer. |
diagnostic usage
therapeutic application
unassigned |
1
3
0 |
| 2.8.3.5 | Breast Neoplasms |
33281976 |
?-hydroxybutyrate does not alter the effects of glucose deprivation on breast cancer cells. |
causal interaction
diagnostic usage
unassigned |
4
3
0 |
| 2.8.3.5 | Genetic Diseases, Inborn |
16765626 |
A 6-bp deletion at the splice donor site of the first intron resulted in aberrant splicing using a cryptic splice site within exon 1 in a patient with succinyl-CoA: 3-Ketoacid CoA transferase (SCOT) deficiency. |
causal interaction
unassigned |
3
0 |
| 2.8.3.5 | 3-oxoacid coa-transferase deficiency |
31073471 |
A Case of Succinyl-CoA:3-Oxoacid CoA Transferase Deficiency Presenting with Severe Acidosis in a 14-Month-Old Female: Evidence for Pathogenicity of a Point Mutation in the OXCT1 Gene. |
causal interaction
unassigned |
4
0 |
| 2.8.3.5 | Acidosis |
31073471 |
A Case of Succinyl-CoA:3-Oxoacid CoA Transferase Deficiency Presenting with Severe Acidosis in a 14-Month-Old Female: Evidence for Pathogenicity of a Point Mutation in the OXCT1 Gene. |
causal interaction
unassigned |
4
0 |
| 2.8.3.5 | 3-oxoacid coa-transferase deficiency |
7474899 |
A new Japanese case of succinyl-CoA: 3-ketoacid CoA-transferase deficiency. |
causal interaction
unassigned |
4
0 |
| 2.8.3.5 | 3-oxoacid coa-transferase deficiency |
30799594 |
A Rare Cause of Life-Threatening Ketoacidosis: Novel Compound Heterozygous OXCT1 Mutations Causing Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. |
causal interaction
unassigned |
4
0 |
| 2.8.3.5 | Ketosis |
30799594 |
A Rare Cause of Life-Threatening Ketoacidosis: Novel Compound Heterozygous OXCT1 Mutations Causing Succinyl-CoA:3-Ketoacid CoA Transferase Deficiency. |
causal interaction
unassigned |
4
0 |
| 2.8.3.5 | Ketosis |
23420214 |
A structural mapping of mutations causing succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency. |
unassigned |
0 |
| 2.8.3.5 | Carcinoma, Hepatocellular |
167950 |
Acetoacetate coenzyme A transferase activity in rat hepatomas. |
causal interaction
ongoing research
unassigned |
3
2
0 |
