DGAT1

DGAT1
Identifiers
AliasesDGAT1, ARAT, ARGP1, DGAT, DIAR7, diacylglycerol O-acyltransferase 1
External IDsMGI: 1333825 HomoloGene: 7688 GeneCards: DGAT1
EC number2.3.1.76
Gene location (Human)
Chr.Chromosome 8 (human)[1]
Band8q24.3Start144,314,584 bp[1]
End144,326,910 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

8694

13350

Ensembl

ENSG00000185000
ENSG00000285482

ENSMUSG00000022555

UniProt

O75907

Q9Z2A7

RefSeq (mRNA)

NM_012079

NM_010046

RefSeq (protein)

NP_036211

NP_034176

Location (UCSC)Chr 8: 144.31 – 144.33 MbChr 15: 76.5 – 76.51 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Diacylglycerol O-acyltransferase 1 is an enzyme that in humans is encoded by the DGAT1 gene.[5]

Function

This gene encodes an multipass transmembrane protein that functions as a key metabolic enzyme. The encoded protein catalyzes the conversion of diacylglycerol and fatty acyl CoA to triacylglycerol. This enzyme can also transfer acyl CoA to retinol. Activity of this protein may be associated with obesity and other metabolic diseases.[6]

See also

References

  1. 1 2 3 ENSG00000285482 GRCh38: Ensembl release 89: ENSG00000185000, ENSG00000285482 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000022555 - Ensembl, May 2017
  3. "Human PubMed Reference:".
  4. "Mouse PubMed Reference:".
  5. "Entrez Gene: Diacylglycerol O-acyltransferase 1". Retrieved 2016-08-28.
  6. Yen CL, Stone SJ, Koliwad S, Harris C, Farese RV (2008). "Thematic review series: glycerolipids. DGAT enzymes and triacylglycerol biosynthesis". Journal of Lipid Research. 49 (11): 2283–301. doi:10.1194/jlr.R800018-JLR200. PMC 3837458. PMID 18757836.

Further reading

  • Ludwig EH, Mahley RW, Palaoglu E, Ozbayrakçi S, Balestra ME, Borecki IB, Innerarity TL, Farese RV (July 2002). "DGAT1 promoter polymorphism associated with alterations in body mass index, high density lipoprotein levels and blood pressure in Turkish women". Clinical Genetics. 62 (1): 68–73. doi:10.1034/j.1399-0004.2002.620109.x. PMID 12123490.

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

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