Homo sapiens Protein: MOGAT2
Summary
InnateDB Protein IDBP-589983.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MOGAT2
Protein Name monoacylglycerol O-acyltransferase 2
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000436537
InnateDB Gene IDBG-64956 (MOGAT2)
Protein Structure
UniProt Annotation
Function Catalyzes the formation of diacylglycerol from 2- monoacylglycerol and fatty acyl-CoA. Has a preference toward monoacylglycerols containing unsaturated fatty acids in an order of C18:3 > C18:2 > C18:1 > C18:0. Plays a central role in absorption of dietary fat in the small intestine by catalyzing the resynthesis of triacylglycerol in enterocytes. May play a role in diet-induced obesity. {ECO:0000269PubMed:12621063}.
Subcellular Localization Endoplasmic reticulum membrane {ECO:0000269PubMed:12621063}; Multi-pass membrane protein {ECO:0000269PubMed:12621063}.
Disease Associations
Tissue Specificity Highly expressed in liver, small intestine, colon, stomach and kidney. {ECO:0000269PubMed:12621063, ECO:0000269PubMed:12824082}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 3 experimentally validated interaction(s) in this database.
Experimentally validated
Total 3 [view]
Protein-Protein 0
Protein-DNA 0
Protein-RNA 0
DNA-DNA 3 [view]
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003846 2-acylglycerol O-acyltransferase activity
GO:0016747 transferase activity, transferring acyl groups other than amino-acyl groups
Biological Process
GO:0006071 glycerol metabolic process
GO:0019432 triglyceride biosynthetic process
Cellular Component
GO:0005783 endoplasmic reticulum
GO:0005789 endoplasmic reticulum membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR007130 Diacylglycerol acyltransferase
PFAM PF03982
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q3SYC2
PhosphoSite PhosphoSite-Q3SYC2
TrEMBL
UniProt Splice Variant
Entrez Gene 80168
UniGene Hs.288568
RefSeq
HUGO HGNC:23248
OMIM 610270
CCDS
HPRD 11367
IMGT
EMBL AK026297 AK128620 AK291998 AY157608 BC103876 BC103877 BC103878 CH471076
GenPept AAI03877 AAI03878 AAI03879 AAO23672 BAB15436 BAC87534 BAF84687 EAW74983