PLA2R1 - phospholipase A2 receptor 1 Gene

Also Known as PLA2R; PLA2-R; PLA2IR; CLEC13C; PLA2G1R

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 22925

About PLA2R1

Cytogenetic location: 2q24.2 Genomic coordinates (GRCh38): 2:159,923,933-160,062,615 (from NCBI)

This gene has 3 transcripts (splice variants), 194 orthologues and 4 paralogues. Broad expression in thyroid (RPKM 11.6), kidney (RPKM 5.9) and 16 other tissues.

Summary

This gene represents a Phospholipase A2 receptor. The encoded protein likely exists as both a transmembrane form and a soluble form. The transmembrane receptor may play a role in clearance of Phospholipase A2, thereby inhibiting its action. Polymorphisms at this locus have been associated with susceptibility to idiopathic membranous nephropathy. Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq, Sep 2010]

PLA2R1 Products (3)

mRNA Protein Name
NM_001007267.3 NP_001007268.1 secretory phospholipase A2 receptor isoform 2 precursor
NM_001195641.2 NP_001182570.1 secretory phospholipase A2 receptor isoform 3 precursor
NM_007366.5 NP_031392.3 secretory phospholipase A2 receptor isoform 1 precursor
Molecular Function GO Annotation Evidence References Source
enables phospholipase binding IPI
IPI: Inferred from physical interaction
7721806 GOA
enables signaling receptor activity IDA
IDA: Inferred from direct assay
7721806 GOA
Biological Process GO Annotation Evidence References Source
involved in oxidative stress-induced premature senescence IMP
IMP: Inferred from mutant phenotype
19197340 GOA
involved in positive regulation of DNA damage response, signal transduction by p53 class mediator IMP
IMP: Inferred from mutant phenotype
19197340 GOA
involved in positive regulation of cytokine production IMP
IMP: Inferred from mutant phenotype
15611272 GOA
involved in positive regulation of podocyte apoptotic process IMP
IMP: Inferred from mutant phenotype
25335547 GOA
involved in reactive oxygen species metabolic process IDA
IDA: Inferred from direct assay
19197340 GOA
involved in receptor-mediated endocytosis IDA
IDA: Inferred from direct assay
7721806 GOA
involved in replicative senescence IMP
IMP: Inferred from mutant phenotype
19197340 GOA
Cellular Component GO Annotation Evidence References Source
located in cell surface IDA
IDA: Inferred from direct assay
15611272 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
12225974 GOA
part of receptor complex IDA
IDA: Inferred from direct assay
23382219 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

PLA2R1 Protein Structure

fn2

fn2: Fibronectin type II domain (178 - 219)

Lectin_C

Lectin_C: Lectin C-type domain (250 - 356)

Lectin_C

Lectin_C: Lectin C-type domain (396 - 503)

Lectin_C

Lectin_C: Lectin C-type domain (549 - 644)

Lectin_C

Lectin_C: Lectin C-type domain (689 - 797)

Lectin_C

Lectin_C: Lectin C-type domain (833 - 939)

Lectin_C

Lectin_C: Lectin C-type domain (981 - 1098)

Lectin_C

Lectin_C: Lectin C-type domain (1132 - 1233)

Lectin_C

Lectin_C: Lectin C-type domain (1270 - 1379)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1463 a.a.
Protein Preferred Names Protein Names

secretory phospholipase A2 receptor

  • 180 kDa secretory phospholipase A2 receptor

Related Diseases

Diseases Alias
Membranous Nephropathy
  • Membranous Glomerulonephritis

  • Glomerulonephritis, Membranous

  • Idiopathic Membranous Nephropathy

  • Idiopathic Membranous Glomerulonephritis

  • MBNP

  • Membranous Nephropathy, Susceptibility To

  • Extramembranous Glomerulonephritis

  • Mgn

  • Membranous Gn

  • Primary Membranous Glomerulonephritis

  • Primary Membranous Nephropathy

  • Nephropathy Membranous

Igg4-Related Disease
  • Multifocal Fibrosclerosis

  • Igg4-Related Sclerosing Disease

  • Igg4-Related Systemic Disease

  • Immunoglobulin G4-Related Sclerosing Disease

  • Hyper-Igg4 Disease

  • Igg4-Associated Disease

  • Igg4-Positive Multiorgan Lymphoproliferative Syndrome

  • Igg4-Related Autoimmune Disease

  • Igg4-Related Systemic Sclerosing Disease

  • Igg4-Syndrome

  • Multifocal Idiopathic Fibrosclerosis

  • Systemic Igg4-Related Plasmacytic Syndrome

  • Systemic Igg4-Related Sclerosing Syndrome

  • Mediastinal Fibrosis, Familial

  • Retroperitoneal Fibrosis, Familial

  • Igg4-Rd

Nephrotic Syndrome, Type 7
  • Immunoglobulin-Mediated Membranoproliferative Glomerulonephritis

  • Hemolytic Uremic Syndrome, Atypical, Susceptibility To, 7

  • NPHS7

  • Nephrotic Syndrome Type 7

  • Ig-Mediated Membranoproliferative Glomerulonephritis

  • Ig-Mediated Mpgn

  • Immunoglobulin-Mediated Mpgn

  • Nephrotic Syndrome, Type 7, With Membranoproliferative Glomerulonephritis

  • Hemolytic Uremic Syndrome, Atypical 7

  • Nephrotic Syndrome Type 7 With Membranoptoliferative Glomerulonephritis

  • Hemolytic Uremic Syndrome With Dgke Deficiency

  • Hus With Dgke Deficiency

  • Hemolytic Uremic Syndrome Atypical 7

  • AHUS7

  • Nephrotic Syndrome 7

  • Nephrotic Syndrome Type 7 With Membranoproliferative Glomerulonephritis

Glomerulonephritis
  • Bright'S Disease

Goodpasture Syndrome
  • Anti-Glomerular Basement Membrane Disease

  • Anti-Gbm Disease

  • Pulmonary Renal Syndrome

  • Anti-Glomerular Basement Membrane Antibody Disease

  • Glomerulonephritis - Pulmonary Hemorrhage

  • Rapidly Progressive Glomerulonephritis With Pulmonary Hemorrhage

  • Anti-Gbm Syndrome

  • Goodpasture'S Syndrome

  • Anti-Basement Membrane Glomerulonephritis

Autoimmune Disease Of Urogenital Tract
Kimura Disease
  • Kimura'S Disease

  • Eosinophilic Lymphogranuloma

  • Eosinophilic Granuloma Of Soft Tissue

  • Eosinophilic Hyperplastic Lymphogranuloma

  • Eosinophilic Lymphofollicular Granuloma

  • Eosinophilic Lymphofolliculosis

Immunoglobulin Heavy Chain Amyloidosis
  • Ah Amyloidosis

  • Heavy Chain Amyloidosis

  • Amyloidosis Derived From Immunoglobulin Heavy Chain

  • Ig Heavy-Chain-Associated Amyloidosis

Crescentic Glomerulonephritis
  • Idiopathic Crescentic Glomerulonephritis

Acute Proliferative Glomerulonephritis
  • Acute Glomerulonephritis With Lesion Of Proliferative Glomerulonephritis

  • Acute Post-Streptococcal Glomerulonephritis

Bronchiectasis 3
Lipoid Nephrosis
  • Minimal Change Disease

  • Minimal Change Glomerulonephritis

  • Nephrotic Syndrome With Lesion Of Minimal Change Glomerulonephritis

  • Nephrotic Syndrome With Lesion Of Minimal Change Nephrotic Syndrome

  • Idiopathic Minimal Change Nephrotic Syndrome

  • Mcns

  • Minimal Change Glomerulopathy

  • Minimal Change Nephrotic Syndrome

  • Nephrotic Syndrome Minimal Change

  • Nephrosis, Lipoid

  • Glomerulonephritis, Minimal Change

  • Nephrotic Syndrome, Minimal Change

Rapidly Progressive Glomerulonephritis
  • Glomerulonephritis Rapidly Progressive

  • Idiopathic Crescentic Glomerulonephritis

Acute Diffuse Nephritis
  • Acute Diffuse Glomerulonephritis

Membranoproliferative Glomerulonephritis
  • Mesangiocapillary Glomerulonephritis

  • Dense Deposit Disease

  • Membranoproliferative Glomerulonephritis Type 2

  • Primary Membranoproliferative Glomerulonephritis

  • Mesangiocapillary Glomerulonephritis, Type Ii

  • Glomerulonephritis, Membranoproliferative

  • Chronic Glomerulonephritis, Lobular

  • Lobular Glomerulonephritis

  • Ddd

  • Glomerulonephritis Membranoproliferative Type 2

  • Mpgn 2

  • Membranoproliferative Glomerulonephritis Type Ii

  • Mesangiocapillary Glomerulonephritis Type 2

  • Mpgn

  • Primary Mpgn

  • Glomerulonephritis Membranoproliferative

  • Membranoproliferative Glomerulonephritis, Type Ii

Proliferative Glomerulonephritis
Anti-Basement Membrane Glomerulonephritis
  • Anti-Gbm Glomerulonephritis

Interstitial Nephritis
  • Nephritis, Interstitial

  • Renal Tubulo-Interstitial Disease

  • Nephritis Interstitial

  • Nephritis, Tubulointerstitial

Immune-Complex Glomerulonephritis
  • Immune Complex Glomerulonephritis

Mesangial Proliferative Glomerulonephritis
  • Glomerulonephritis - Mesangial Proliferative

  • Mesangial Proliferative Gn

  • Mesangioproliferative Glomerulonephritis

  • Glomerulonephritis Mesangial Proliferative

Iga Glomerulonephritis
  • Iga Nephropathy

  • Glomerulonephritis, Iga

  • Berger'S Iga Or Igg Nephropathy

  • Focal Glomerulonephritis

  • Primary Iga Nephropathy

  • Segmental Glomerulonephritis

  • Berger Disease

  • Berger'S Disease

  • Igan

  • Nephritis, Iga Type

  • Nephropathy Iga

  • Glomerulonephritis Focal

  • Iga Nephropathy, Susceptibility To

  • Primary Immunoglobulin A Nephropathy

Focal Segmental Glomerulosclerosis
  • Familial Idiopathic Steroid-Resistant Nephrotic Syndrome

  • Focal Glomerulosclerosis

  • Fsgs

  • Segmental Glomerulosclerosis

  • Glomerulosclerosis, Focal Segmental

  • Fgs

  • Focal Glomerular Sclerosis

  • Familial Idiopathic Nephrotic Syndrome

  • Focal Sclerosis With Hyalinosis

  • Glomerulosclerosis, Focal

  • Glomerulosclerosis Focal

  • Glomerulosclerosis, Segmental, Focal

  • Focal Segmental Glomerulosclerosis, Not Otherwise Specified

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta PLA2R1 VGNC VGNC:104550
Mus musculus PLA2R1 MGD MGI:102468
Rattus norvegicus PLA2R1 RGD RGD:1309777
Felis catus PLA2R1 VGNC VGNC:80306
Bos taurus PLA2R1 VGNC VGNC:32966
Canis familiaris PLA2R1 VGNC VGNC:44633
Others PLA2R1 NCBI