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    PLPP3 phospholipid phosphatase 3 [ Homo sapiens (human) ]

    Gene ID: 8613, updated on 10-Dec-2024

    Summary

    Official Symbol
    PLPP3provided by HGNC
    Official Full Name
    phospholipid phosphatase 3provided by HGNC
    Primary source
    HGNC:HGNC:9229
    See related
    Ensembl:ENSG00000162407 MIM:607125; AllianceGenome:HGNC:9229
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    LPP3; VCIP; Dri42; PAP2B; PPAP2B
    Summary
    The protein encoded by this gene is a member of the phosphatidic acid phosphatase (PAP) family. PAPs convert phosphatidic acid to diacylglycerol, and function in de novo synthesis of glycerolipids as well as in receptor-activated signal transduction mediated by phospholipase D. This protein is a membrane glycoprotein localized at the cell plasma membrane. It has been shown to actively hydrolyze extracellular lysophosphatidic acid and short-chain phosphatidic acid. The expression of this gene is found to be enhanced by epidermal growth factor in Hela cells. [provided by RefSeq, Mar 2010]
    Expression
    Broad expression in thyroid (RPKM 205.6), placenta (RPKM 102.2) and 23 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See PLPP3 in Genome Data Viewer
    Location:
    1p32.2
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (56494761..56579563, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (56373591..56458441, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (56960433..57045236, complement)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC124904185 Neighboring gene long intergenic non-protein coding RNA 1767 Neighboring gene Sharpr-MPRA regulatory region 1049 Neighboring gene uncharacterized LOC124904189 Neighboring gene Sharpr-MPRA regulatory region 6809 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:56917723-56918398 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr1:56918399-56919074 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:56919075-56919750 Neighboring gene Sharpr-MPRA regulatory region 2463 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:56942601-56943374 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:56956069-56956568 Neighboring gene NANOG hESC enhancer GRCh37_chr1:56959749-56960407 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:56975627-56976357 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:56977343-56977844 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:56977845-56978344 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1077 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1078 Neighboring gene NANOG-H3K4me1 hESC enhancer GRCh37_chr1:56996995-56997730 Neighboring gene Sharpr-MPRA regulatory region 2243 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:57001027-57001670 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:57002869-57003370 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:57014771-57015346 Neighboring gene OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr1:57015922-57016496 Neighboring gene ribosomal protein L21 pseudogene 23 Neighboring gene OCT4-NANOG hESC enhancer GRCh37_chr1:57042654-57043221 Neighboring gene ribosomal protein L23a pseudogene 85 Neighboring gene uncharacterized LOC101929935 Neighboring gene protein kinase AMP-activated catalytic subunit alpha 2

    Genomic regions, transcripts, and products

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    EBI GWAS Catalog

    Description
    A genome-wide association study in europeans and South asians identifies 5 new Loci for coronary artery disease.
    EBI GWAS Catalog
    A genome-wide association study in Europeans and South Asians identifies five new loci for coronary artery disease.
    EBI GWAS Catalog
    Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.
    EBI GWAS Catalog
    Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.
    EBI GWAS Catalog
    Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease.
    EBI GWAS Catalog
    Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants.
    EBI GWAS Catalog

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Clone Names

    • MGC15306

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables ceramide-1-phosphate phosphatase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables integrin binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables phosphatidate phosphatase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables phosphatidate phosphatase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables sphingosine-1-phosphate phosphatase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables sphingosine-1-phosphate phosphatase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables sphingosine-1-phosphate phosphatase activity TAS
    Traceable Author Statement
    more info
     
    Process Evidence Code Pubs
    involved_in Bergmann glial cell differentiation IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in blood vessel development IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in cell-cell adhesion IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in cell-cell adhesion mediated by integrin IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in ceramide metabolic process IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in gastrulation with mouth forming second IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in homotypic cell-cell adhesion IDA
    Inferred from Direct Assay
    more info
    PubMed 
    acts_upstream_of integrin-mediated signaling pathway IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in negative regulation of protein phosphorylation IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in phospholipid dephosphorylation IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in phospholipid dephosphorylation IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in phospholipid metabolic process IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in phospholipid metabolic process IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in phospholipid metabolic process IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in positive regulation of DNA-binding transcription factor activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in positive regulation of cell-cell adhesion IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in positive regulation of endothelial cell migration IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in positive regulation of peptidyl-tyrosine phosphorylation IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in protein stabilization IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in regulation of Wnt signaling pathway IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in regulation of sphingolipid mediated signaling pathway IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in signal transduction IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in sphingolipid catabolic process TAS
    Traceable Author Statement
    more info
     
    involved_in sphingosine metabolic process IDA
    Inferred from Direct Assay
    more info
    PubMed 
    involved_in wound healing IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in Golgi apparatus IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in Golgi membrane IEA
    Inferred from Electronic Annotation
    more info
     
    located_in adherens junction TAS
    Traceable Author Statement
    more info
    PubMed 
    located_in basolateral plasma membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in endoplasmic reticulum exit site IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in endoplasmic reticulum membrane IEA
    Inferred from Electronic Annotation
    more info
     
    located_in endoplasmic reticulum-Golgi intermediate compartment membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in membrane raft IDA
    Inferred from Direct Assay
    more info
    PubMed 
    is_active_in plasma membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in plasma membrane TAS
    Traceable Author Statement
    more info
     
    located_in trans-Golgi network IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    phospholipid phosphatase 3
    Names
    PAP2 beta
    lipid phosphate phosphohydrolase 3
    phosphatidate phosphohydrolase type 2b
    phosphatidic acid phosphatase type 2B
    type-2 phosphatidic acid phosphatase-beta
    vascular endothelial growth factor and type I collagen inducible
    NP_003704.3

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    mRNA and Protein(s)

    1. NM_003713.5NP_003704.3  phospholipid phosphatase 3

      See identical proteins and their annotated locations for NP_003704.3

      Status: REVIEWED

      Source sequence(s)
      AC099562, AF043329, BQ027458, DA580891
      Consensus CDS
      CCDS604.1
      UniProtKB/Swiss-Prot
      B2R651, D3DQ52, O14495, Q5U0F7, Q96GW0, Q99782
      Related
      ENSP00000360296.3, ENST00000371250.4
      Conserved Domains (1) summary
      cd03384
      Location:125271
      PAP2_wunen; PAP2, wunen subfamily. Most likely a family of membrane associated phosphatidic acid phosphatases. Wunen is a drosophila protein expressed in the central nervous system, which provides repellent activity towards primordial germ cells (PGCs), controls the ...

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000001.11 Reference GRCh38.p14 Primary Assembly

      Range
      56494761..56579563 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      56373591..56458441 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_177414.1: Suppressed sequence

      Description
      NM_177414.1: This RefSeq was permanently suppressed because currently there is insufficient support for the transcript, which aligns to the reference assembly with non-consensus splice sites for the intron in the 5' UTR.