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    PMVK phosphomevalonate kinase [ Homo sapiens (human) ]

    Gene ID: 10654, updated on 10-Dec-2024

    Summary

    Official Symbol
    PMVKprovided by HGNC
    Official Full Name
    phosphomevalonate kinaseprovided by HGNC
    Primary source
    HGNC:HGNC:9141
    See related
    Ensembl:ENSG00000163344 MIM:607622; AllianceGenome:HGNC:9141
    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
    PMK; PMKA; PMKASE; POROK1; HUMPMKI
    Summary
    This gene encodes a peroxisomal enzyme that is a member of the galactokinase, homoserine kinase, mevalonate kinase, and phosphomevalonate kinase (GHMP) family of ATP-dependent enzymes. The encoded protein catalyzes the conversion of mevalonate 5-phosphate to mevalonate 5-diphosphate, which is the fifth step in the mevalonate pathway of isoprenoid biosynthesis. Mutations in this gene are linked to certain types of porokeratosis including disseminated superficial porokeratosis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2017]
    Expression
    Ubiquitous expression in kidney (RPKM 26.9), liver (RPKM 17.8) and 25 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See PMVK in Genome Data Viewer
    Location:
    1q21.3
    Exon count:
    6
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 1 NC_000001.11 (154924740..154942658, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 1 NC_060925.1 (154064101..154082019, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 1 NC_000001.10 (154897216..154915134, complement)

    Chromosome 1 - NC_000001.11Genomic Context describing neighboring genes Neighboring gene potassium calcium-activated channel subfamily N member 3 Neighboring gene uncharacterized LOC124904429 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:154702946-154703755 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:154703756-154704564 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154708005-154708564 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr1:154708837-154710036 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154714090-154714590 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1782 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1365 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154721874-154722377 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1366 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1783 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:154785391-154786050 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:154786051-154786708 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154812853-154813354 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1784 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1785 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1786 Neighboring gene H3K27ac hESC enhancer GRCh37_chr1:154831699-154832199 Neighboring gene Sharpr-MPRA regulatory region 4766 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:154834547-154835222 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:154835223-154835896 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1788 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154836963-154837852 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1789 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154840581-154841100 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154842508-154843464 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154849802-154850387 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154850973-154851557 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154883471-154883971 Neighboring gene uncharacterized LOC105371449 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:154908701-154909643 Neighboring gene NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:154909644-154910585 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 1368 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154914379-154915254 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1795 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154917055-154917556 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 1796 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154924461-154924960 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr1:154931761-154932260 Neighboring gene H3K27ac hESC enhancers GRCh37_chr1:154933865-154934605 and GRCh37_chr1:154934606-154935345 Neighboring gene PBX homeobox interacting protein 1 Neighboring gene PYGO2 and SHC1 antisense RNA 1 Neighboring gene pygopus family PHD finger 2

    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
    Porokeratosis 1, Mibelli type
    MedGen: CN297066 OMIM: 175800 GeneReviews: Not available
    Compare labs

    EBI GWAS Catalog

    Description
    Discovery and refinement of loci associated with lipid levels.
    EBI GWAS Catalog
    Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array.
    EBI GWAS Catalog
    Meta-analysis identifies six new susceptibility loci for atrial fibrillation.
    EBI GWAS Catalog

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Potential readthrough

    Included gene: PBXIP1

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables ATP binding IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables phosphomevalonate kinase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables phosphomevalonate kinase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables phosphomevalonate kinase activity TAS
    Traceable Author Statement
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    Component Evidence Code Pubs
    located_in cytosol IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in cytosol TAS
    Traceable Author Statement
    more info
     
    located_in extracellular exosome HDA PubMed 
    located_in membrane HDA PubMed 
    NOT located_in peroxisome IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in peroxisome IDA
    Inferred from Direct Assay
    more info
    PubMed 

    General protein information

    Preferred Names
    phosphomevalonate kinase
    Names
    testis tissue sperm-binding protein Li 95mP
    NP_001309940.1
    NP_001309941.1
    NP_001335625.1
    NP_006547.1

    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_053028.1 RefSeqGene

      Range
      10932..22911
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001323011.3NP_001309940.1  phosphomevalonate kinase isoform 2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) differs in the 5' UTR and initiates translation at an alternate start codon, compared to variant 1. The encoded isoform (2) is shorter and has a distinct N-terminus, compared to isoform 1.
      Source sequence(s)
      AL451085, CN344384, HM005718
      UniProtKB/TrEMBL
      Q6FGV9
      Conserved Domains (1) summary
      pfam04275
      Location:16109
      P-mevalo_kinase; Phosphomevalonate kinase
    2. NM_001323012.3NP_001309941.1  phosphomevalonate kinase isoform 3

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3) contains an alternate exon in the 5' UTR and initiates translation at a downstream start codon, compared to variant 1. The encoded isoform (3) has a shorter N-terminus, compared to isoform 1.
      Source sequence(s)
      AL451085, BQ057770, HM005718
      UniProtKB/TrEMBL
      Q6FGV9
      Conserved Domains (1) summary
      cl04466
      Location:1111
      P-mevalo_kinase; Phosphomevalonate kinase
    3. NM_001348696.2NP_001335625.1  phosphomevalonate kinase isoform 4

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4) uses an alternate splice site in the coding region and initiates translation at an alternate start codon compared to variant 1. The encoded isoform (4) has a shorter and distinct N-terminus, compared to isoform 1.
      Source sequence(s)
      BM793483, BQ057770, HM005718
      UniProtKB/TrEMBL
      Q6FGV9
      Conserved Domains (1) summary
      cl04466
      Location:18111
      P-mevalo_kinase; Phosphomevalonate kinase
    4. NM_006556.4NP_006547.1  phosphomevalonate kinase isoform 1

      See identical proteins and their annotated locations for NP_006547.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1).
      Source sequence(s)
      BC007694
      Consensus CDS
      CCDS1073.1
      UniProtKB/Swiss-Prot
      Q15126, Q5TZW9
      UniProtKB/TrEMBL
      D3DV77, Q6FGV9
      Related
      ENSP00000357452.3, ENST00000368467.4
      Conserved Domains (1) summary
      pfam04275
      Location:14123
      P-mevalo_kinase; Phosphomevalonate kinase

    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
      154924740..154942658 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060925.1 Alternate T2T-CHM13v2.0

      Range
      154064101..154082019 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)