LYPLA2: Lysophospholipase 2

A key enzyme in phospholipid metabolism and potential biomarker in cancer and neurological disorders

Gene Information Card

Symbol LYPLA2
Full Name Lysophospholipase 2
Gene Type Protein coding
Chromosomal Location 1p36.11
NCBI Gene ID 11313 ncbi.nlm.nih.gov/gene/11313
Ensembl ID ENSG00000117592
UniProt ID O95372
OMIM ID 604377
HGNC ID 6740
Aliases APT-2, APT2, DJ-1-binding protein, hAPT2

Description

LYPLA2 (lysophospholipase 2) encodes a cytosolic enzyme that catalyzes the hydrolysis of lysophospholipids to fatty acids and glycerol-3-phosphate. It also exhibits palmitoyl-protein thioesterase activity, removing palmitate from modified cysteine residues on proteins. The enzyme is involved in membrane lipid remodeling, signal transduction, and protein trafficking. LYPLA2 is ubiquitously expressed with highest levels in the brain, heart, and skeletal muscle. Dysregulation has been implicated in cancer, neurodegenerative diseases, and metabolic disorders.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Cancer (various types) Overexpression promotes cell proliferation and migration; altered lipid metabolism NCBI Gene, COSMIC
Alzheimer's disease Reduced activity linked to amyloid-beta accumulation; palmitoylation dysregulation OMIM, ClinVar
Parkinson's disease Interaction with DJ-1 (PARK7) affects oxidative stress response UniProt, OMIM
Metabolic syndrome Altered lysophospholipid levels associated with insulin resistance NCBI Gene

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 15.2 High
Heart 12.8 High
Skeletal Muscle 11.5 High
Liver 8.3 Medium
Kidney 7.1 Medium
Lung 5.9 Medium
Pancreas 4.2 Low
Cell Line Expression
Cell Line nTPM Notes
HEK293 18.5 High expression
HeLa 14.2 High expression
SH-SY5Y 12.0 High expression
HepG2 9.8 Medium expression
A549 7.3 Medium expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.215C>T (p.Pro72Leu) Missense <0.01% Reduced enzymatic activity; associated with altered lipid metabolism
c.389G>A (p.Arg130His) Missense <0.01% Unknown functional effect; rare population variant
c.1A>G (p.Met1Val) Start loss <0.01% Loss of protein expression; potential loss-of-function
Mutation functional classification

Loss of Function (LOF)

Start loss variant (p.Met1Val) and missense variant (p.Pro72Leu) reduce or abolish enzymatic activity, impairing lysophospholipid hydrolysis and protein depalmitoylation.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported in LYPLA2.

Dominant Negative (DN)

No evidence of dominant-negative effects for LYPLA2 mutations.

Pathways

Glycerophospholipid metabolism (Reactome: R-HSA-1483206)
Palmitoylation and depalmitoylation of proteins (Reactome: R-HSA-163841)
Lysophospholipid pathway (KEGG: hsa00564)

Protein Summary

Lysophospholipase 2 (LYPLA2) is a 25.5 kDa cytosolic enzyme composed of 230 amino acids. It belongs to the alpha/beta hydrolase fold family and contains a catalytic triad (Ser119, Asp174, His208). The enzyme hydrolyzes lysophospholipids and removes palmitate from S-acylated proteins, regulating membrane composition and protein localization. LYPLA2 interacts with DJ-1 (PARK7) and is involved in oxidative stress responses. Its expression is altered in several cancers and neurodegenerative conditions, making it a potential therapeutic target.

Related Products

Product name Cat.No. Species Gene ID
LYPLA2 Knockout HEK293 Cell Line EDJ-KQ2845 Human 11313 Details Get a Quote
LYPLA2 Knockout A-549 Cell Line EDJ-KQ22474 Human 11313 Details Get a Quote
LYPLA2 Knockout HCT 116 Cell Line EDJ-KQ23843 Human 11313 Details Get a Quote
LYPLA2 Knockout HeLa Cell Line EDJ-KQ23844 Human 11313 Details Get a Quote
LYPLA2 Knockout ARPE-19 Cell Line EDJ-KZ340 Human 11313 Details Get a Quote
Displaying Records 1 To 5 Of 5 Records
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