EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
2.3.1.254 | Intellectual Disability |
34230638 |
Missense NAA20 variants impairing the NatB protein N-terminal acetyltransferase cause autosomal recessive developmental delay, intellectual disability, and microcephaly. |
therapeutic application unassigned |
1 0 |
2.3.1.254 | Microcephaly |
34230638 |
Missense NAA20 variants impairing the NatB protein N-terminal acetyltransferase cause autosomal recessive developmental delay, intellectual disability, and microcephaly. |
therapeutic application unassigned |
1 0 |
2.3.1.254 | Influenza, Human |
30044982 |
N-Terminal Acetylation by NatB Is Required for the Shutoff Activity of Influenza A Virus PA-X. |
unassigned |
0 |
2.3.1.254 | Carcinogenesis |
33219302 |
Naa20, the catalytic subunit of NatB complex, contributes to hepatocellular carcinoma by regulating the LKB1-AMPK-mTOR axis. |
causal interaction diagnostic usage therapeutic application unassigned |
3 3 1 0 |
2.3.1.254 | Carcinoma, Hepatocellular |
33219302 |
Naa20, the catalytic subunit of NatB complex, contributes to hepatocellular carcinoma by regulating the LKB1-AMPK-mTOR axis. |
causal interaction diagnostic usage therapeutic application unassigned |
3 3 1 0 |
2.3.1.254 | Neoplasms |
33219302 |
Naa20, the catalytic subunit of NatB complex, contributes to hepatocellular carcinoma by regulating the LKB1-AMPK-mTOR axis. |
causal interaction diagnostic usage therapeutic application unassigned |
3 3 1 0 |
2.3.1.254 | Ischemic Stroke |
30656483 |
The relationship between the prognosis of children with acute arterial stroke and polymorphisms of CDKN2B, HDAC9, NINJ2, NAA25 genes. |
causal interaction diagnostic usage unassigned |
4 3 0 |
2.3.1.254 | Stroke |
30656483 |
The relationship between the prognosis of children with acute arterial stroke and polymorphisms of CDKN2B, HDAC9, NINJ2, NAA25 genes. |
causal interaction diagnostic usage unassigned |
4 3 0 |