NAT8: Difference between revisions

Jump to navigation Jump to search
m (Bot: HTTP→HTTPS (v475))
 
imported>OAbot
m (Open access bot: add pmc identifier to citation with #oabot.)
 
Line 4: Line 4:


==Clinical relevance==
==Clinical relevance==
Mutations in the NAT8 gene have been associated with chronic kidney disease.<ref name="pmid21886157">{{cite journal |vauthors=Suhre K, Shin SY, Petersen AK, Mohney RP, Meredith D, Wägele B, Altmaier E, Deloukas P, Erdmann J, Grundberg E, Hammond CJ, de Angelis MH, Kastenmüller G, Köttgen A, Kronenberg F, Mangino M, Meisinger C, Meitinger T, Mewes HW, Milburn MV, Prehn C, Raffler J, Ried JS, Römisch-Margl W, Samani NJ, Small KS, Wichmann HE, Zhai G, Illig T, Spector TD, Adamski J, Soranzo N, Gieger C | title = Human metabolic individuality in biomedical and pharmaceutical research | journal = Nature |  volume = 477 | issue = 7362 | pages = 54–60 |date=September 2011 | pmid = 21886157 | doi = 10.1038/nature10354 }}</ref>
Mutations in the NAT8 gene have been associated with chronic kidney disease.<ref name="pmid21886157">{{cite journal |vauthors=Suhre K, Shin SY, Petersen AK, Mohney RP, Meredith D, Wägele B, Altmaier E, Deloukas P, Erdmann J, Grundberg E, Hammond CJ, de Angelis MH, Kastenmüller G, Köttgen A, Kronenberg F, Mangino M, Meisinger C, Meitinger T, Mewes HW, Milburn MV, Prehn C, Raffler J, Ried JS, Römisch-Margl W, Samani NJ, Small KS, Wichmann HE, Zhai G, Illig T, Spector TD, Adamski J, Soranzo N, Gieger C | title = Human metabolic individuality in biomedical and pharmaceutical research | journal = Nature |  volume = 477 | issue = 7362 | pages = 54–60 |date=September 2011 | pmid = 21886157 | doi = 10.1038/nature10354 |pmc = 3832838 }}</ref>


==References==
==References==
Line 20: Line 20:
*{{cite journal  |vauthors=Veréb J, Démant F, Pavkovceková O, Tischler V |title=[Agenesis and aplasia of the kidney in children in the x-ray diagnostic picture]. |journal=Cesk Pediatr |volume=30 |issue= 3 |pages= 94–7 |year= 1975 |pmid= 1139715 |doi=  }}
*{{cite journal  |vauthors=Veréb J, Démant F, Pavkovceková O, Tischler V |title=[Agenesis and aplasia of the kidney in children in the x-ray diagnostic picture]. |journal=Cesk Pediatr |volume=30 |issue= 3 |pages= 94–7 |year= 1975 |pmid= 1139715 |doi=  }}
*{{cite journal  |vauthors=Köttgen A, Pattaro C, Böger CA, etal |title=New loci associated with kidney function and chronic kidney disease. |journal=Nat. Genet. |volume=42 |issue= 5 |pages= 376–84 |year= 2010 |pmid= 20383146 |doi= 10.1038/ng.568 |pmc=2997674}}
*{{cite journal  |vauthors=Köttgen A, Pattaro C, Böger CA, etal |title=New loci associated with kidney function and chronic kidney disease. |journal=Nat. Genet. |volume=42 |issue= 5 |pages= 376–84 |year= 2010 |pmid= 20383146 |doi= 10.1038/ng.568 |pmc=2997674}}
*{{cite journal  |vauthors=Chambers JC, Zhang W, Lord GM, etal |title=Genetic loci influencing kidney function and chronic kidney disease. |journal=Nat. Genet. |volume=42 |issue= 5 |pages= 373–5 |year= 2010 |pmid= 20383145 |doi= 10.1038/ng.566 }}
*{{cite journal  |vauthors=Chambers JC, Zhang W, Lord GM, etal |title=Genetic loci influencing kidney function and chronic kidney disease. |journal=Nat. Genet. |volume=42 |issue= 5 |pages= 373–5 |year= 2010 |pmid= 20383145 |doi= 10.1038/ng.566 |pmc=3748585 }}
{{refend}}
{{refend}}



Latest revision as of 05:18, 23 May 2018

VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

N-acetyltransferase 8 is a protein that in humans is encoded by the NAT8 gene.[1]

Clinical relevance

Mutations in the NAT8 gene have been associated with chronic kidney disease.[2]

References

  1. "Entrez Gene: N-acetyltransferase 8 (GCN5-related".
  2. Suhre K, Shin SY, Petersen AK, Mohney RP, Meredith D, Wägele B, Altmaier E, Deloukas P, Erdmann J, Grundberg E, Hammond CJ, de Angelis MH, Kastenmüller G, Köttgen A, Kronenberg F, Mangino M, Meisinger C, Meitinger T, Mewes HW, Milburn MV, Prehn C, Raffler J, Ried JS, Römisch-Margl W, Samani NJ, Small KS, Wichmann HE, Zhai G, Illig T, Spector TD, Adamski J, Soranzo N, Gieger C (September 2011). "Human metabolic individuality in biomedical and pharmaceutical research". Nature. 477 (7362): 54–60. doi:10.1038/nature10354. PMC 3832838. PMID 21886157.

Further reading