LIPF: Gastric Lipase Gene

Key enzyme in dietary fat digestion and associated gastric disorders

Gene Information Card

Symbol LIPF
Full Name Lipase F, Gastric Type
Gene Type protein-coding
Chromosomal Location 10q23.31
NCBI Gene ID 8513 ncbi.nlm.nih.gov/gene/8513
Ensembl ID ENSG00000138107
UniProt ID P07098
OMIM ID 601980
HGNC ID 6622
Aliases HGL, HLAL, LIPF_HUMAN

Description

The LIPF gene encodes gastric lipase, an enzyme secreted by chief cells in the gastric mucosa. It catalyzes the initial hydrolysis of dietary triglycerides into diglycerides and free fatty acids in the acidic environment of the stomach. This enzyme is essential for efficient fat digestion, particularly in neonates and individuals with pancreatic insufficiency. LIPF expression is regulated by nutritional status and hormones, and its deficiency or dysregulation is linked to metabolic disorders and gastric pathologies.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Gastric lipase deficiency Loss-of-function mutations in LIPF reduce enzymatic activity, impairing fat digestion and leading to steatorrhea and malabsorption. ClinVar, OMIM
Obesity Reduced LIPF expression or activity may alter lipid absorption and energy balance, contributing to obesity risk. NCBI Gene, PubMed
Gastric cancer Aberrant LIPF methylation and downregulation are observed in gastric adenocarcinoma, potentially affecting lipid metabolism in tumor cells. COSMIC, PubMed

Expression Profile

Tissue Expression
Tissue nTPM level
Stomach 65.2 High
Esophagus 3.1 Low
Duodenum 2.5 Low
Pancreas 1.8 Low
Liver 0.5 Not detected
Cell Line Expression
Cell Line nTPM Notes
MKN45 (gastric cancer) 12.4 Moderate expression
AGS (gastric adenocarcinoma) 8.7 Moderate expression
HepG2 (hepatocellular) 0.3 Not detected
Caco-2 (colorectal) 1.1 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.331C>T (p.Arg111*) Nonsense <0.01% Premature stop codon; loss of function
c.572G>A (p.Arg191His Missense 0.02% Reduced catalytic activity
c.1045C>T (p.Arg349Trp) Missense 0.01% Impaired secretion and stability
Mutation functional classification

Loss of Function (LOF)

Nonsense and missense mutations (e.g., p.Arg111*, p.Arg191His) that reduce or abolish enzymatic activity, leading to gastric lipase deficiency.

Gain of Function (GOF)

No documented gain-of-function mutations in LIPF.

Dominant Negative (DN)

No evidence of dominant-negative effects for LIPF mutations.

Pathways

REACT:1483251 - Triglyceride digestion
REACT:111045 - Metabolism of lipids and lipoproteins

Protein Summary

Gastric lipase (UniProt P07098) is a 398-amino acid glycoprotein with a molecular weight of approximately 45 kDa. It belongs to the lipase family and is stable and active at acidic pH (optimum pH 3–6). The enzyme contains a catalytic triad (Ser153, Asp204, His353) and a lid domain that regulates substrate access. It is secreted as a monomer and binds to lipid droplets in the stomach, initiating fat digestion. Post-translational modifications include N-glycosylation at Asn15, Asn80, and Asn308, which are critical for secretion and activity.

Related Products

Product name Cat.No. Species Gene ID
LIPF Knockout HEK293 Cell Line EDJ-KQ6264 Human 8513 Details Get a Quote
LIPF Knockout HeLa Cell Line EDJ-KQ54925 Human 8513 Details Get a Quote
LIPF Knockout A-549 Cell Line EDJ-KQ63411 Human 8513 Details Get a Quote
LIPF Knockout HCT 116 Cell Line EDJ-KQ71876 Human 8513 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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