2.3.1.254	Carcinogenesis	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33219302&form=6&db=m	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	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33219302&form=6&db=m	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	Influenza, Human	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30044982&form=6&db=m	N-Terminal Acetylation by NatB Is Required for the Shutoff Activity of Influenza A Virus PA-X.	unassigned	-	
2.3.1.254	Intellectual Disability	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34230638&form=6&db=m	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	Ischemic Stroke	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30656483&form=6&db=m	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	Microcephaly	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=34230638&form=6&db=m	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	Neoplasms	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=33219302&form=6&db=m	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	Stroke	http://www.ncbi.nlm.nih.gov/htbin-post/Entrez/query?uid=30656483&form=6&db=m	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