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    IMPA1 inositol monophosphatase 1 [ Homo sapiens (human) ]

    Gene ID: 3612, updated on 10-Dec-2024

    Summary

    Official Symbol
    IMPA1provided by HGNC
    Official Full Name
    inositol monophosphatase 1provided by HGNC
    Primary source
    HGNC:HGNC:6050
    See related
    Ensembl:ENSG00000133731 MIM:602064; AllianceGenome:HGNC:6050
    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
    IMP; IMPA; MRT59
    Summary
    This gene encodes an enzyme that dephosphorylates myo-inositol monophosphate to generate free myo-inositol, a precursor of phosphatidylinositol, and is therefore an important modulator of intracellular signal transduction via the production of the second messengers myoinositol 1,4,5-trisphosphate and diacylglycerol. This enzyme can also use myo-inositol-1,3-diphosphate, myo-inositol-1,4-diphosphate, scyllo-inositol-phosphate, glucose-1-phosphate, glucose-6-phosphate, fructose-1-phosphate, beta-glycerophosphate, and 2'-AMP as substrates. This enzyme shows magnesium-dependent phosphatase activity and is inhibited by therapeutic concentrations of lithium. Inhibition of inositol monophosphate hydroylosis and subsequent depletion of inositol for phosphatidylinositol synthesis may explain the anti-manic and anti-depressive effects of lithium administered to treat bipolar disorder. Alternative splicing results in multiple transcript variants encoding distinct isoforms. A pseudogene of this gene is also present on chromosome 8q21.13. [provided by RefSeq, Dec 2014]
    Expression
    Ubiquitous expression in testis (RPKM 15.5), thyroid (RPKM 10.4) and 24 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See IMPA1 in Genome Data Viewer
    Location:
    8q21.13
    Exon count:
    10
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 8 NC_000008.11 (81656914..81686325, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 8 NC_060932.1 (82088505..82118041, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 8 NC_000008.10 (82569149..82598560, complement)

    Chromosome 8 - NC_000008.11Genomic Context describing neighboring genes Neighboring gene inositol monophosphatase 1 pseudogene 1 Neighboring gene Sharpr-MPRA regulatory region 11945 Neighboring gene ribosomal protein S26 pseudogene 34 Neighboring gene SLC10A5 pseudogene 1 Neighboring gene H3K27ac hESC enhancer GRCh37_chr8:82598306-82598806 Neighboring gene solute carrier family 10 member 5 Neighboring gene zinc finger AN1-type containing 1 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr8:82632569-82633513

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Phenotypes

    Associated conditions

    Description Tests
    Intellectual disability, autosomal recessive 59
    MedGen: C4310619 OMIM: 617323 GeneReviews: Not available
    not available

    Copy number response

    Description
    Copy number response
    Haploinsufficency

    No evidence available (Last evaluated 2012-02-08)

    ClinGen Genome Curation Page
    Triplosensitivity

    No evidence available (Last evaluated 2012-02-08)

    ClinGen Genome Curation Page

    EBI GWAS Catalog

    Description
    GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer.
    EBI GWAS Catalog

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Process Evidence Code Pubs
    involved_in inositol biosynthetic process IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in inositol metabolic process IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in phosphate-containing compound metabolic process IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in phosphatidylinositol biosynthetic process IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    involved_in phosphatidylinositol phosphate biosynthetic process IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in signal transduction IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in signal transduction IMP
    Inferred from Mutant Phenotype
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in cytoplasm IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in cytosol TAS
    Traceable Author Statement
    more info
     

    General protein information

    Preferred Names
    inositol monophosphatase 1
    Names
    D-galactose 1-phosphate phosphatase
    IMP 1
    IMPase 1
    inositol(myo)-1(or 4)-monophosphatase 1
    inositol-1(or 4)-monophosphatase 1
    lithium-sensitive myo-inositol monophosphatase A1
    myo-inositol monophosphatase 1
    testicular tissue protein Li 94
    NP_001138350.1
    NP_001138351.1
    NP_005527.1

    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.

    Genomic

    1. NG_015829.1 RefSeqGene

      Range
      5030..34441
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001144878.2NP_001138350.1  inositol monophosphatase 1 isoform 2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) contains an additional in-frame coding exon compared to transcript variant 1, resulting in an isoform (2) with a longer and a novel N-terminus compared to isoform 1.
      Source sequence(s)
      AC090255, AF042729, AI921211, AK300750, BC008381, BP270804, DB299262, DC375686
      Consensus CDS
      CCDS47883.1
      UniProtKB/TrEMBL
      A0A140VJL8
      Related
      ENSP00000408526.2, ENST00000449740.6
      Conserved Domains (1) summary
      cd01639
      Location:67313
      IMPase; IMPase, inositol monophosphatase and related domains. A family of Mg++ dependent phosphatases, inhibited by lithium, many of which may act on inositol monophosphate substrate. They dephosphorylate inositol phosphate to generate inositol, which may be ...
    2. NM_001144879.2NP_001138351.1  inositol monophosphatase 1 isoform 3

      See identical proteins and their annotated locations for NP_001138351.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) is missing an internal coding exon compared to transcript variant 1. This results in a frame-shift and a shorter isoform (3) with a novel C-terminus compared to isoform 1.
      Source sequence(s)
      AC090255, AF042729, AI921211, AK297078, BC008381, DB299262, DC375686
      Consensus CDS
      CCDS47884.1
      UniProtKB/Swiss-Prot
      P29218
      Related
      ENSP00000311803.4, ENST00000311489.8
      Conserved Domains (1) summary
      cd01639
      Location:8164
      IMPase; IMPase, inositol monophosphatase and related domains. A family of Mg++ dependent phosphatases, inhibited by lithium, many of which may act on inositol monophosphate substrate. They dephosphorylate inositol phosphate to generate inositol, which may be ...
    3. NM_005536.4NP_005527.1  inositol monophosphatase 1 isoform 1

      See identical proteins and their annotated locations for NP_005527.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the predominant transcript and encodes isoform 1.
      Source sequence(s)
      AC090255, AF042729, AI921211, BC008381, DB299262, DC375686
      Consensus CDS
      CCDS6231.1
      UniProtKB/Swiss-Prot
      B2R733, B4DLN3, B7Z6Q4, J3KQT7, P29218, Q9UK71
      UniProtKB/TrEMBL
      H0YBL1
      Related
      ENSP00000256108.5, ENST00000256108.10
      Conserved Domains (1) summary
      cd01639
      Location:8254
      IMPase; inositol monophosphatase and related domains. A family of Mg++ dependent phosphatases, inhibited by lithium, many of which may act on inositol monophosphate substrate. They dephosphorylate inositol phosphate to generate inositol, which may be recycled ...

    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_000008.11 Reference GRCh38.p14 Primary Assembly

      Range
      81656914..81686325 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060932.1 Alternate T2T-CHM13v2.0

      Range
      82088505..82118041 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)