Gene Gene information from NCBI Gene database.
Entrez ID 5322
Gene name Phospholipase A2 group V
Gene symbol PLA2G5
Synonyms (NCBI Gene)
FRFBGV-PLA2PLA2-10hVPLA(2)
Chromosome 1
Chromosome location 1p36.13
Summary This gene is a member of the secretory phospholipase A2 family. It is located in a tightly-linked cluster of secretory phospholipase A2 genes on chromosome 1. The encoded enzyme catalyzes the hydrolysis of membrane phospholipids to generate lysophospholip
SNPs SNP information provided by dbSNP.
6
SNP ID Visualize variation Clinical significance Consequence
rs200954922 C>T Affects Coding sequence variant, stop gained
rs387906795 G>A,T Affects Coding sequence variant, missense variant
rs387906796 G>A Affects Coding sequence variant, missense variant
rs746408116 G>A Affects Stop gained, coding sequence variant
rs766454085 A>- Affects 3 prime UTR variant, frameshift variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
101
miRTarBase ID miRNA Experiments Reference
MIRT021933 hsa-miR-128-3p Microarray 17612493
MIRT441766 hsa-miR-3125 PAR-CLIP 22100165
MIRT441767 hsa-miR-3916 PAR-CLIP 22100165
MIRT441765 hsa-miR-6859-5p PAR-CLIP 22100165
MIRT441764 hsa-miR-6847-5p PAR-CLIP 22100165
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
44
GO ID Ontology Definition Evidence Reference
GO:0004623 Function Phospholipase A2 activity IEA
GO:0005509 Function Calcium ion binding IBA
GO:0005509 Function Calcium ion binding IEA
GO:0005543 Function Phospholipid binding IBA
GO:0005576 Component Extracellular region IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601192 9038 ENSG00000127472
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P39877
Protein name Phospholipase A2 group V (EC 3.1.1.4) (PLA2-10) (Phosphatidylcholine 2-acylhydrolase 5)
Protein function Secretory calcium-dependent phospholipase A2 that primarily targets extracellular phospholipids (PubMed:8300559). Hydrolyzes the ester bond of the fatty acyl group attached at sn-2 position of phospholipids (phospholipase A2 activity), preferent
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00068 Phospholip_A2_1 22 130 Phospholipase A2 Domain
Tissue specificity TISSUE SPECIFICITY: Heart, placenta and less abundantly, in lung. Detected in the outer and inner plexiform layers of the retina (at protein level) (PubMed:22137173). Expressed in monocytes and macrophages (PubMed:25725101). {ECO:0000269|PubMed:22137173,
Sequence
Sequence length 138
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Glycerophospholipid metabolism
Ether lipid metabolism
Arachidonic acid metabolism
Linoleic acid metabolism
alpha-Linolenic acid metabolism
Metabolic pathways
Ras signaling pathway
Vascular smooth muscle contraction
Pancreatic secretion
Fat digestion and absorption
  Acyl chain remodelling of PC
Acyl chain remodelling of PS
Acyl chain remodelling of PE
Acyl chain remodelling of PI
Acyl chain remodelling of PG
Synthesis of PA
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
7
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Late-onset retinal degeneration Pathogenic rs1569848362 RCV001003122
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Familial benign flecked retina Uncertain significance; Affects; Conflicting classifications of pathogenicity rs387906795, rs746408116, rs387906796, rs200954922, rs766454085, rs149833360 RCV000023076
RCV000023077
RCV000023078
RCV000023079
RCV000023080
RCV000625306
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma Inhibit 18212756
Breast Neoplasms Inhibit 26715269
Carcinoma Pancreatic Ductal Associate 36102738
Coronary Artery Disease Associate 24959594, 37239897
Down Syndrome Associate 27293319
Fleck Retina Familial Benign Associate 22137173
Hypertension Associate 24959594
Neoplasms Associate 26715269
Pancreatic Neoplasms Associate 36102738
Prostatic Neoplasms Associate 26715269