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    PAOX polyamine oxidase [ Homo sapiens (human) ]

    Gene ID: 196743, updated on 10-Dec-2024

    Summary

    Official Symbol
    PAOXprovided by HGNC
    Official Full Name
    polyamine oxidaseprovided by HGNC
    Primary source
    HGNC:HGNC:20837
    See related
    Ensembl:ENSG00000148832 MIM:615853; AllianceGenome:HGNC:20837
    Gene type
    protein coding
    RefSeq status
    VALIDATED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    PAO
    Summary
    Enables polyamine oxidase activity. Involved in polyamine catabolic process; positive regulation of spermidine biosynthetic process; and putrescine biosynthetic process. Predicted to be located in cytosol and peroxisomal matrix. Implicated in lung non-small cell carcinoma. [provided by Alliance of Genome Resources, Dec 2024]
    Expression
    Broad expression in testis (RPKM 17.7), spleen (RPKM 4.1) and 20 other tissues See more
    Orthologs
    NEW
    Try the new Gene table
    Try the new Transcript table

    Genomic context

    See PAOX in Genome Data Viewer
    Location:
    10q26.3
    Exon count:
    8
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 10 NC_000010.11 (133379262..133391694)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 10 NC_060934.1 (134334280..134346667)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 10 NC_000010.10 (135192766..135205198)

    Chromosome 10 - NC_000010.11Genomic Context describing neighboring genes Neighboring gene enoyl-CoA hydratase, short chain 1 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2977 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4248 Neighboring gene uncharacterized LOC124902563 Neighboring gene microRNA 3944 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr10:135191859-135192358 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2978 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2979 Neighboring gene ReSE screen-validated silencer GRCh37_chr10:135202015-135202172 Neighboring gene Sharpr-MPRA regulatory region 11835 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2980 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2981 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 2982 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:135208387-135209341 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4250 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 4251 Neighboring gene mitochondrial ribosome associated GTPase 1 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:135236507-135237126 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr10:135237945-135238452 Neighboring gene uncharacterized LOC124902564 Neighboring gene shadow of prion protein

    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

    EBI GWAS Catalog

    Description
    An atlas of genetic influences on human blood metabolites.
    EBI GWAS Catalog

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Potential readthrough

    Included gene: MTG1

    Clone Names

    • MGC45464, DKFZp434J245

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables N(1)-acetylpolyamine oxidase (3-acetamidopropanal-forming) activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables polyamine oxidase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables polyamine oxidase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    Component Evidence Code Pubs
    is_active_in cytoplasm IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    located_in cytosol TAS
    Traceable Author Statement
    more info
     
    located_in peroxisomal matrix TAS
    Traceable Author Statement
    more info
     

    General protein information

    Preferred Names
    peroxisomal N(1)-acetyl-spermine/spermidine oxidase
    Names
    peroxisomal N1-acetyl-spermine/spermidine oxidase
    polyamine oxidase (exo-N4-amino)
    NP_690875.1
    NP_997010.1
    NP_997011.1

    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.

    mRNA and Protein(s)

    1. NM_152911.4NP_690875.1  peroxisomal N(1)-acetyl-spermine/spermidine oxidase isoform 1

      See identical proteins and their annotated locations for NP_690875.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (1) represents the longest transcript and encodes the longest isoform (1).
      Source sequence(s)
      AF312698, BE646315
      Consensus CDS
      CCDS7683.1
      UniProtKB/Swiss-Prot
      D3DXI6, Q5VWY0, Q6QHF5, Q6QHF6, Q6QHF7, Q6QHF8, Q6QHF9, Q6QHG0, Q6QHG1, Q6QHG2, Q6QHG3, Q6QHG4, Q6QHG5, Q6QHG6, Q86WP9, Q8N555, Q8NCX3
      Related
      ENSP00000278060.5, ENST00000278060.10
      Conserved Domains (1) summary
      PLN02568
      Location:14497
      PLN02568; polyamine oxidase
    2. NM_207127.3NP_997010.1  peroxisomal N(1)-acetyl-spermine/spermidine oxidase isoform 2

      See identical proteins and their annotated locations for NP_997010.1

      Status: VALIDATED

      Description
      Transcript Variant: This variant (4) lacks two exons in the 3' coding region, resulting in a frameshift and an early stop codon, compared to variant 1. It encodes isoform 2, which is shorter and has a distinct C-terminus, compared to isoform 1.
      Source sequence(s)
      AA280165, AF312698, AY541514, AY541519
      Consensus CDS
      CCDS7684.1
      UniProtKB/Swiss-Prot
      Q6QHF9
      Related
      ENSP00000435514.1, ENST00000480071.2
      Conserved Domains (2) summary
      PLN02568
      Location:14297
      PLN02568; polyamine oxidase
      pfam13450
      Location:4387
      NAD_binding_8; NAD(P)-binding Rossmann-like domain
    3. NM_207128.3NP_997011.1  peroxisomal N(1)-acetyl-spermine/spermidine oxidase isoform 4

      Status: VALIDATED

      Description
      Transcript Variant: This variant (5) lacks an alternate exon in the 3' coding region, resulting in a frameshift, compared to variant 1. It encodes isoform 4, which is shorter and has a distinct C-terminus, compared to isoform 1.
      Source sequence(s)
      AF312698, BE646315
      Consensus CDS
      CCDS7682.1
      UniProtKB/Swiss-Prot
      Q6QHF9
      Related
      ENSP00000349847.3, ENST00000357296.7
      Conserved Domains (2) summary
      PLN02568
      Location:14400
      PLN02568; polyamine oxidase
      pfam13450
      Location:4387
      NAD_binding_8; NAD(P)-binding Rossmann-like domain

    RNA

    1. NR_109763.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (6) lacks an alternate exon in the 3' region, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AA280165, AF312698, AY541513, AY541519
    2. NR_109764.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (7) includes an alternate exon in the 5' coding region compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AA280165, AF312698, AY541518, AY541519
      Related
      ENST00000476834.6
    3. NR_109765.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (8) lacks two alternate internal exons compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AA280165, AF312698, AY541517
      Related
      ENST00000483211.6
    4. NR_109766.2 RNA Sequence

      Status: VALIDATED

      Description
      Transcript Variant: This variant (9) lacks three internal exons, compared to variant 1. This variant is represented as non-coding because the use of the 5'-most expected translational start codon, as used in variant 1, renders the transcript a candidate for nonsense-mediated mRNA decay (NMD).
      Source sequence(s)
      AA280165, AF312698, AY541514, AY541519
      Related
      ENST00000529585.5

    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_000010.11 Reference GRCh38.p14 Primary Assembly

      Range
      133379262..133391694
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060934.1 Alternate T2T-CHM13v2.0

      Range
      134334280..134346667
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Suppressed Reference Sequence(s)

    The following Reference Sequences have been suppressed. Explain

    1. NM_207125.1: Suppressed sequence

      Description
      NM_207125.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.
    2. NM_207126.1: Suppressed sequence

      Description
      NM_207126.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.
    3. NM_207129.1: Suppressed sequence

      Description
      NM_207129.1: This RefSeq was permanently suppressed because it is a nonsense-mediated mRNA decay (NMD) candidate.