NAT9

NAT9
Identifiers
Aliases	NAT9 , EBSP, hNATL, N-acetyltransferase 9 (putative)
External IDs	MGI: 1913426 HomoloGene: 9231 GeneCards: NAT9
Gene location (Human)
Chr.	Chromosome 17 (human)
End	74,776,367 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	115,187,859 bp
RNA expression pattern
	Top expressed in
	anterior pituitary; ; Right adrenal gland; ; right lobe of thyroid gland; ; left lobe of thyroid gland; ; canal of the cervix; ; left uterine tube; ; tibial nerve; ; ascending aorta; ; stromal cell of endometrium; ; body of stomach;
	Top expressed in
	spermatocyte; ; seminiferous tubule; ; spermatid; ; yolk sac; ; proximal tubule; ; left lobe of liver; ; internal carotid artery; ; duodenum; ; external carotid artery; ; interventricular septum;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	transferase activity ; acyltransferase activity ; protein binding ; acyltransferase activity, transferring groups other than amino-acyl groups ; N-acetyltransferase activity ;
Cellular component	protein-containing complex ;
Biological process	N-terminal protein amino acid acetylation ; protein acetylation ;
	Sources:Amigo / QuickGO
Orthologs
	26151
	66176
	ENSG00000109065
	ENSMUSG00000015542
	Q9BTE0
	Q3UG98
NM_001305077 ; NM_001305078 ; NM_001305079 ; NM_001305080 ; NM_001305081 ;
	NM_001305082 ; NM_001305083 ; NM_001305084 ; NM_001305085 ; NM_001305086 ; NM_001305087 ; NM_001305088 ; NM_015654
	NM_025400
NP_001292006 ; NP_001292007 ; NP_001292008 ; NP_001292009 ; NP_001292010 ;
	NP_001292011 ; NP_001292012 ; NP_001292013 ; NP_001292014 ; NP_001292015 ; NP_001292016 ; NP_001292017 ; NP_056469
	NP_079676 ; NP_001349818 ; NP_001349819 ; NP_001349820 ; NP_001349821
	Wikidata
View/Edit Human	View/Edit Mouse

Last updated October 14, 2022

N-acetyltransferase 9 is an enzyme that in humans is encoded by the NAT9 gene.^[5]^[6]

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References

1 2 3 GRCh38: Ensembl release 89: ENSG00000109065 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000015542 - Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ Helms C, Cao L, Krueger JG, Wijsman EM, Chamian F, Gordon D, Heffernan M, Daw JA, Robarge J, Ott J, Kwok PY, Menter A, Bowcock AM (Dec 2003). "A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis". Nat Genet. 35 (4): 349–56. doi:10.1038/ng1268. PMID 14608357. S2CID 22368199.
↑ "Entrez Gene: NAT9 N-acetyltransferase 9".

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Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
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Wiemann S, Weil B, Wellenreuther R, et al. (2001). "Toward a Catalog of Human Genes and Proteins: Sequencing and Analysis of 500 Novel Complete Protein Coding Human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072 . PMID 11230166.
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Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi: 10.1073/pnas.242603899 . PMC 139241 . PMID 12477932.
Wiemann S, Arlt D, Huber W, et al. (2004). "From ORFeome to Biology: A Functional Genomics Pipeline". Genome Res. 14 (10B): 2136–44. doi:10.1101/gr.2576704. PMC 528930 . PMID 15489336.
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[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000109065 - Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000015542 - Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[pmid14608357-5] Helms C, Cao L, Krueger JG, Wijsman EM, Chamian F, Gordon D, Heffernan M, Daw JA, Robarge J, Ott J, Kwok PY, Menter A, Bowcock AM (Dec 2003). "A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis". Nat Genet. 35 (4): 349–56. doi:10.1038/ng1268. PMID 14608357. S2CID 22368199.

[entrez-6] "Entrez Gene: NAT9 N-acetyltransferase 9".

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NAT9

Related Research Articles

References

Further reading