PLAAT3 Gene (Phospholipase A and Acyltransferase 3)

Gene encoding a phospholipid-metabolizing enzyme with roles in adipogenesis, ferroptosis, and cancer

Gene Information Card

Symbol PLAAT3
Full Name Phospholipase A and Acyltransferase 3
Gene Type Protein coding
Chromosomal Location 11q12.3
NCBI Gene ID 11145 ncbi.nlm.nih.gov/gene/11145
Ensembl ID ENSG00000149257
UniProt ID Q9UNK4
OMIM ID 607123
HGNC ID 17826
Aliases HRASLS3, H-REV107-1, PLA2G16, AdPLA, HREV107-1

Description

PLAAT3 (Phospholipase A and Acyltransferase 3) is a protein-coding gene located on chromosome 11q12.3. The encoded enzyme exhibits both phospholipase A1/A2 and acyltransferase activities, playing a key role in phospholipid metabolism. It is involved in adipogenesis, ferroptosis regulation, and has been implicated in several cancers. The gene is also known as HRASLS3, H-REV107-1, PLA2G16, and AdPLA.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Breast cancer Overexpression of PLAAT3 promotes tumor growth and metastasis through modulation of lipid signaling and ferroptosis resistance. PMID: 30936463; COSMIC
Colorectal cancer PLAAT3 upregulation correlates with poor prognosis and enhanced cell proliferation via phospholipid remodeling. PMID: 31525674; COSMIC
Obesity / Adipose tissue dysfunction PLAAT3 (AdPLA) is the major phospholipase A2 in adipose tissue; its deficiency reduces adipogenesis and protects against diet-induced obesity. PMID: 19136964; OMIM 607123
Ferroptosis-related disorders PLAAT3 suppresses ferroptosis by reducing cellular phospholipid hydroperoxides, linking to neurodegenerative and ischemic conditions. PMID: 33542149; ClinVar

Expression Profile

Tissue Expression
Tissue nTPM level
Adipose tissue 45.2 High
Liver 12.8 Medium
Lung 8.5 Medium
Breast 6.3 Low
Colon 5.1 Low
Cell Line Expression
Cell Line nTPM Notes
MCF7 (breast cancer) 18.4 Overexpressed compared to normal breast
HCT116 (colorectal cancer) 14.7 Moderate expression
HepG2 (liver cancer) 9.2 Basal expression
3T3-L1 (adipocyte) 52.1 High during differentiation
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.215C>T (p.Pro72Leu) Missense <0.01% Unknown; rare population variant (gnomAD)
c.346G>A (p.Gly116Arg) Missense <0.01% Predicted damaging (SIFT, PolyPhen); not validated in disease
c.1A>G (p.Met1?) Start loss <0.01% Likely loss of function; rare
Mutation functional classification

Loss of Function (LOF)

Start loss mutations (e.g., c.1A>G) and truncating variants are predicted to abolish enzyme activity, potentially impairing adipogenesis and ferroptosis suppression.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported in PLAAT3; overexpression in cancer may mimic gain-of-function effects.

Dominant Negative (DN)

No dominant-negative mutations described for PLAAT3.

Pathways

• Ferroptosis (Reactome: R-HSA-9648895)
• Phospholipid metabolism (Reactome: R-HSA-1483206)
• Adipogenesis (WikiPathways: WP236)

Protein Summary

The PLAAT3 protein (UniProt Q9UNK4) is a 184-amino acid membrane-associated enzyme with dual phospholipase A1/A2 and acyltransferase activities. It localizes to the endoplasmic reticulum and plasma membrane. In adipose tissue, it functions as the major phospholipase A2 (AdPLA), regulating prostaglandin production and adipocyte differentiation. In cancer cells, PLAAT3 overexpression promotes resistance to ferroptosis by reducing phospholipid hydroperoxide levels, thereby supporting tumor growth. The protein contains a conserved HxxxD motif essential for catalytic activity.

Related Products

Product name Cat.No. Species Gene ID
PLAAT3 Knockout HEK293 Cell Line EDJ-KQ1272 Human 11145 Details Get a Quote
PLAAT3 Knockout A-549 Cell Line EDJ-KQ20650 Human 11145 Details Get a Quote
PLAAT3 Knockout HCT 116 Cell Line EDJ-KQ20651 Human 11145 Details Get a Quote
PLAAT3 Knockout HeLa Cell Line EDJ-KQ20652 Human 11145 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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