MOGAT2

Monoacylglycerol O-Acyltransferase 2

Gene Information Card

Symbol MOGAT2
Full Name Monoacylglycerol O-Acyltransferase 2
Gene Type Protein coding
Chromosomal Location 11q13.5
NCBI Gene ID 80168 ncbi.nlm.nih.gov/gene/80168
Ensembl ID ENSG00000149257
UniProt ID Q3SYC2
OMIM ID 610397
HGNC ID 23255
Aliases MGAT2, MOGAT2, DC2, hMGAT2

Description

MOGAT2 encodes monoacylglycerol O-acyltransferase 2, an integral membrane protein that catalyzes the synthesis of diacylglycerol from 2-monoacylglycerol and fatty acyl-CoA. This enzyme plays a key role in the re-esterification of dietary fat in enterocytes, contributing to triacylglycerol formation and chylomicron assembly. MOGAT2 is predominantly expressed in the small intestine and is involved in lipid absorption and energy homeostasis.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Obesity Altered MOGAT2 expression may affect dietary fat absorption and energy balance, contributing to obesity risk. Association studies (PMID: 21518876)
Hypertriglyceridemia Increased MOGAT2 activity may enhance triacylglycerol synthesis, leading to elevated plasma triglycerides. Functional studies in animal models (PMID: 19033660)
Non-alcoholic fatty liver disease (NAFLD) MOGAT2-mediated lipid flux from intestine to liver may influence hepatic steatosis. Expression analysis (PMID: 23943769)

Expression Profile

Tissue Expression
Tissue nTPM level
Small intestine 45.2 High
Colon 12.8 Medium
Stomach 6.5 Low
Liver 1.2 Not detected
Adipose tissue 0.8 Not detected
Cell Line Expression
Cell Line nTPM Notes
Caco-2 38.5 Intestinal epithelial cell line; high expression
HT-29 22.1 Colorectal adenocarcinoma cell line; moderate expression
HepG2 0.9 Hepatocellular carcinoma cell line; very low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.419C>T (p.Pro140Leu) Missense 0.01% (gnomAD) Unknown functional impact; rare variant
c.758G>A (p.Arg253His) Missense 0.005% (gnomAD) Predicted benign by in silico tools
Mutation functional classification

Loss of Function (LOF)

No confirmed loss-of-function mutations reported in MOGAT2.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported.

Dominant Negative (DN)

No evidence for dominant-negative effects.

Gene Ontology (GO)

2-acylglycerol O-acyltransferase activity (GO:0003841) fatty acid metabolic process (GO:0006631)
• integral component of membrane (GO:0016021) triacylglycerol biosynthetic process (GO:0019432)
• cellular lipid metabolic process (GO:0044255)

Pathways

Triacylglycerol synthesis (Reactome: R-HSA-75105)
Fat digestion and absorption (KEGG: hsa04975)

Protein Summary

Monoacylglycerol O-acyltransferase 2 (MOGAT2) is a 334-amino acid integral membrane protein localized to the endoplasmic reticulum. It catalyzes the conversion of 2-monoacylglycerol and fatty acyl-CoA to diacylglycerol, a key step in the monoacylglycerol pathway of triacylglycerol synthesis. The enzyme is highly expressed in the small intestine and is essential for efficient dietary fat absorption. MOGAT2 belongs to the MBOAT (membrane-bound O-acyltransferase) family and shares sequence similarity with other MGAT and DGAT enzymes.

Related Products

Product name Cat.No. Species Gene ID
MOGAT2 Knockout HEK293 Cell Line EDJ-KQ2657 Human 80168 Details Get a Quote
MOGAT2 Knockout HeLa Cell Line EDJ-KQ57303 Human 80168 Details Get a Quote
MOGAT2 Knockout A-549 Cell Line EDJ-KQ65811 Human 80168 Details Get a Quote
MOGAT2 Knockout HCT 116 Cell Line EDJ-KQ74234 Human 80168 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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