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GeneE
10 sources retrieved Β· Most recent: April 2026 Β· Index updated 14 days ago
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PLA1A
phospholipase A1 member A
Chromosome 3 Β· 3q13.33
NCBI Gene: 51365Ensembl: ENSG00000144837.10HGNC: HGNC:17661UniProt: G5E9W0
37PubMed Papers
20Diseases
0Drugs
1Pathogenic Variants
DATA QUALITY
βœ“ Experimental GO Evidenceβœ“ Swiss-Prot Reviewed
glycerophospholipid phospholipase A1 activitylipid catabolic processGO:0005615phosphatidylserine acyl-chain remodelingmale reproductive organ cancermelanomahepatocellular carcinomatransient myeloproliferative syndrome
✦AI Summary

PLA1A (phospholipase A1 member A) is a phosphatidylserine-specific enzyme that hydrolyzes sn-1 fatty acids from phosphatidylserine (PS) to produce lysophosphatidylserine (lysoPS) 1. The enzyme belongs to the pancreatic lipase family and is expressed in various human tissues including liver, lung, prostate, and immune cells 1. PLA1A functions through the autotaxin-lysophosphatidic acid receptor axis, where generated lysoPS is converted to lysophosphatidic acid (LPA) by autotaxin, subsequently activating downstream signaling pathways 2. The enzyme plays critical roles in multiple disease processes. In viral infection, PLA1A serves as an essential host factor for hepatitis C virus assembly by facilitating NS2-E2 and NS2-NS5A protein complex formation and bridging viral replication and assembly machinery 34. Clinically, elevated PLA1A levels are associated with autoimmune disorders including rheumatoid arthritis, systemic lupus erythematosus, and early-diagnosed arthritis 2. High expression correlates with metastatic melanomas and contributes to cardiometabolic disorders through cholesterol transportation 1. PLA1A also regulates immune cell functions including T cells, dendritic cells, macrophages, and mast cells through lysoPS signaling via receptors GPR34, GPR174, and P2Y10 1. In kidney transplant rejection, PLA1A expression strongly correlates with active molecular rejection processes 5.

Sources cited
1
PLA1A specifically hydrolyzes sn-1 fatty acids from PS to produce lysoPS, belongs to pancreatic lipase family, expressed in multiple tissues, and associated with autoimmune disorders and cancer metastasis
PMID: 34166709
2
PLA1A activates fibroblast-like synoviocytes through autotaxin-LPA receptor axis and elevated levels found in rheumatoid arthritis and lupus patients
PMID: 34884486
3
PLA1A is essential for HCV assembly through NS2 complex formation and bridging replication and assembly machinery
PMID: 25505071
4
PLA1A serves as critical bridge for HCV assembly through interaction with E2, NS2, and NS5A proteins
PMID: 31161554
5
PLA1A expression strongly correlates with active molecular rejection in kidney transplant biopsies
PMID: 35058354
Disease Associationsβ“˜20
male reproductive organ cancerOpen Targets
0.27Weak
melanomaOpen Targets
0.09Suggestive
hepatocellular carcinomaOpen Targets
0.08Suggestive
transient myeloproliferative syndromeOpen Targets
0.05Suggestive
esophageal adenocarcinomaOpen Targets
0.05Suggestive
neoplasmOpen Targets
0.04Suggestive
X-linked lymphoproliferative diseaseOpen Targets
0.04Suggestive
Chronic mucocutaneous candidosisOpen Targets
0.04Suggestive
immunodeficiency 51Open Targets
0.04Suggestive
acne inversa, familial, 3Open Targets
0.04Suggestive
gamma chain deficiencyOpen Targets
0.04Suggestive
Pyogenic arthritis - pyoderma gangrenosum - acneOpen Targets
0.04Suggestive
pyogenic arthritis-pyoderma gangrenosum-acne syndromeOpen Targets
0.04Suggestive
systemic lupus erythematosusOpen Targets
0.04Suggestive
immunodeficiency 15aOpen Targets
0.04Suggestive
pulmonary fibrosis and/or bone marrow failure syndrome, telomere-related, 9Open Targets
0.04Suggestive
Miyoshi myopathyOpen Targets
0.04Suggestive
combined immunodeficiency due to ZAP70 deficiencyOpen Targets
0.04Suggestive
immunodeficiency 105Open Targets
0.04Suggestive
hyper-IgE recurrent infection syndrome 5, autosomal recessiveOpen Targets
0.04Suggestive
Pathogenic Variants1
NM_015900.4(PLA1A):c.1361C>G (p.Ala454Gly)Pathogenic
Familial hypercholesterolemia
β˜†β˜†β˜†β˜†2022β†’ Residue 454
View on ClinVar β†—
Related Genes
LPCAT4Protein interaction96%MBOAT2Protein interaction93%LPAR3Protein interaction92%POU2F3Protein interaction92%MBOAT1Protein interaction92%PTDSS1Protein interaction92%
Tissue Expression6 tissues
Liver
100%
Lung
55%
Heart
11%
Brain
8%
Ovary
3%
Bone Marrow
2%
Gene Interaction Network
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PLA1ALPCAT4MBOAT2LPAR3POU2F3MBOAT1PTDSS1
PROTEIN STRUCTURE
Preparing viewer…
AlphaFoldAI-predicted Β· UniProt Q53H76
View on AlphaFold β†—
Constraintβ“˜
LOEUFβ“˜
1.14LoF Tolerant
pLIβ“˜
0.00Tolerant
Observed/Expected LoF0.80 [0.57–1.14]
RankingsWhere PLA1A stands among ~20K protein-coding genes
  • #10,671of 20,598
    Most Researched37
  • #5,198of 5,498
    Most Pathogenic Variants1
  • #11,752of 17,882
    Most Constrained (LOEUF)1.14
Genes detectedPLA1A
Sources retrieved10 papers
Response timeβ€”
πŸ“„ Sources
10β–Ό
1
Phosphatidylserine-specific phospholipase A1: A friend or the devil in disguise.
PMID: 34166709
Prog Lipid Res Β· 2021
1.00
2
The Trifecta Study: Comparing Plasma Levels of Donor-derived Cell-Free DNA with the Molecular Phenotype of Kidney Transplant Biopsies.
PMID: 35058354
J Am Soc Nephrol Β· 2022
0.90
3
Tumor and Peritoneum-Associated Macrophage Gene Signature as a Novel Molecular Biomarker in Gastric Cancer.
PMID: 38612926
Int J Mol Sci Β· 2024
0.80
4
A defective lysophosphatidic acid-autophagy axis increases miscarriage risk by restricting decidual macrophage residence.
PMID: 35220880
Autophagy Β· 2022
0.70
5
M2 Macrophage-Derived Migrasomes Mediate Ischaemia-Induced Retinal Neovascularization by Targeting TREM2.
PMID: 41170761
J Extracell Vesicles Β· 2025
0.60