EC Number   |
Disease |
PubMed ID |
Title of Publication |
Category  |
Confidence Level |
|---|
   2.3.1.255 | Breast Neoplasms |
10464641 |
Evaluation of genotype data in clinical risk assessment: methods and application to BRCA1, BRCA2, and N-acetyl transferase-2 genotypes in breast cancer. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
3
3
3
0 |
| 2.3.1.255 | Carcinogenesis |
20592467 |
hNaa10p contributes to tumorigenesis by facilitating DNMT1-mediated tumor suppressor gene silencing. |
causal interaction
diagnostic usage
ongoing research
therapeutic application |
1
1
2
1 |
| 2.3.1.255 | Atherosclerosis |
27755984 |
miRNA-27b modulates endothelial cell angiogenesis by directly targeting Naa15 in atherogenesis. |
unassigned |
0 |
| 2.3.1.255 | Carcinogenesis |
18794801 |
Implication of human N-alpha-acetyltransferase 5 in cellular proliferation and carcinogenesis. |
causal interaction
ongoing research
unassigned |
2
2
0 |
| 2.3.1.255 | Carcinoma, Hepatocellular |
20419844 |
LOH analysis of genes around D4S2964 identifies ARD1B as a prognostic predictor of hepatocellular carcinoma. |
causal interaction
diagnostic usage
therapeutic application
unassigned |
3
4
2
0 |
| 2.3.1.255 | Carcinoma, Hepatocellular |
23258102 |
Clinical implications of arrest-defective protein 1 expression in hepatocellular carcinoma: a novel predictor of microvascular invasion. |
causal interaction
diagnostic usage
ongoing research
unassigned |
4
3
2
0 |
| 2.3.1.255 | Cardiomyopathy, Hypertrophic |
33103328 |
Variants in NAA15 cause pediatric hypertrophic cardiomyopathy. |
causal interaction
diagnostic usage
unassigned |
3
1
0 |
| 2.3.1.255 | Cleft Lip |
33103328 |
Variants in NAA15 cause pediatric hypertrophic cardiomyopathy. |
causal interaction
diagnostic usage
unassigned |
3
1
0 |
| 2.3.1.255 | Colonic Neoplasms |
22261620 |
Combined Phenotype of 4 Markers Improves Prognostic Value of Patients With Colon Cancer. |
diagnostic usage
ongoing research
unassigned |
1
3
0 |
| 2.3.1.255 | Heart Defects, Congenital |
29621621 |
Phenotypic consequences of gene disruption by a balanced de novo translocation involving SLC6A1 and NAA15. |
causal interaction
unassigned |
4
0 |
