Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5322
Gene name Gene Name - the full gene name approved by the HGNC.
Phospholipase A2 group V
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PLA2G5
Synonyms (NCBI Gene) Gene synonyms aliases
FRFB, GV-PLA2, PLA2-10, hVPLA(2)
Disease Acronyms (UniProt) Disease acronyms from UniProt database
FRFB
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p36.13
Summary Summary of gene provided in NCBI Entrez Gene.
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.
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.
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 information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005509 Function Calcium ion binding IBA 21873635
GO:0005543 Function Phospholipid binding IBA 21873635
GO:0005576 Component Extracellular region TAS
GO:0005794 Component Golgi apparatus IEA
GO:0005886 Component Plasma membrane IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601192 9038 ENSG00000127472
Protein
UniProt ID 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 information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Leukemia Leukemia, Myelocytic, Acute rs121909646, rs121913488, rs587776834, rs752746786, rs869312821, rs767454740, rs1554564297 27903959
Unknown
Disease term Disease name Evidence References Source
Benign flecked retina Familial benign flecked retina ClinVar
Retinitis Pigmentosa late-adult onset retinitis pigmentosa GenCC
Benign Flecked Retina familial benign flecked retina GenCC
Crohn Disease Crohn Disease GWAS
Associations from Text Mining
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