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    AOC2 amine oxidase copper containing 2 [ Homo sapiens (human) ]

    Gene ID: 314, updated on 10-Dec-2024

    Summary

    Official Symbol
    AOC2provided by HGNC
    Official Full Name
    amine oxidase copper containing 2provided by HGNC
    Primary source
    HGNC:HGNC:549
    See related
    Ensembl:ENSG00000131480 MIM:602268; AllianceGenome:HGNC:549
    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
    RAO; DAO2; SSAO
    Summary
    Copper amine oxidases catalyze the oxidative conversion of amines to aldehydes and ammonia in the presence of copper and quinone cofactor. This gene shows high sequence similarity to copper amine oxidases from various species ranging from bacteria to mammals. The protein contains several conserved motifs including the active site of amine oxidases and the histidine residues that likely bind copper. It may be a critical modulator of signal transmission in retina, possibly by degrading the biogenic amines dopamine, histamine, and putrescine. This gene may be a candidate gene for hereditary ocular diseases. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jul 2008]
    Expression
    Broad expression in fat (RPKM 4.0), testis (RPKM 2.5) and 14 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See AOC2 in Genome Data Viewer
    Location:
    17q21.31
    Exon count:
    4
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 17 NC_000017.11 (42844580..42850707)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 17 NC_060941.1 (43701719..43707847)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 17 NC_000017.10 (40996597..41002724)

    Chromosome 17 - NC_000017.11Genomic Context describing neighboring genes Neighboring gene beclin 1 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:40975527-40976093 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr17:40976094-40976661 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr17:40976662-40977228 Neighboring gene microRNA 6781 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 12227 Neighboring gene proteasome activator subunit 3 Neighboring gene amine oxidase copper containing 3 Neighboring gene amine oxidase copper containing 4, pseudogene

    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?

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Markers

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables aliphatic amine oxidase activity IEA
    Inferred from Electronic Annotation
    more info
     
    enables copper ion binding IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables electron transfer activity TAS
    Traceable Author Statement
    more info
    PubMed 
    enables primary methylamine oxidase activity IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    enables primary methylamine oxidase activity IDA
    Inferred from Direct Assay
    more info
    PubMed 
    enables primary methylamine oxidase activity TAS
    Traceable Author Statement
    more info
     
    enables protein binding IPI
    Inferred from Physical Interaction
    more info
    PubMed 
    enables quinone binding IEA
    Inferred from Electronic Annotation
    more info
     
    Process Evidence Code Pubs
    involved_in amine metabolic process IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    involved_in catecholamine metabolic process IEA
    Inferred from Electronic Annotation
    more info
     
    involved_in visual perception TAS
    Traceable Author Statement
    more info
    PubMed 
    involved_in xenobiotic metabolic process TAS
    Traceable Author Statement
    more info
     
    Component Evidence Code Pubs
    located_in cytoplasm IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in cytoplasm IEA
    Inferred from Electronic Annotation
    more info
     
    is_active_in plasma membrane IBA
    Inferred from Biological aspect of Ancestor
    more info
     
    is_active_in plasma membrane IDA
    Inferred from Direct Assay
    more info
    PubMed 
    located_in plasma membrane TAS
    Traceable Author Statement
    more info
     

    General protein information

    Preferred Names
    amine oxidase [copper-containing] 2
    Names
    amine oxidase, copper containing 2 (retina-specific)
    retina-specific copper amine oxidase
    semicarbazide-sensitive amine oxidase
    NP_001149.2
    NP_033720.2

    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_001158.5NP_001149.2  amine oxidase [copper-containing] 2 isoform a

      See identical proteins and their annotated locations for NP_001149.2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1) uses an alternate in-frame splice site in the coding region, compared to variant 2. It encodes isoform a which is shorter than isoform b.
      Source sequence(s)
      AC016889, AF081363, CA427935, CN355968, D88213, DQ426861
      Consensus CDS
      CCDS45690.1
      UniProtKB/Swiss-Prot
      O75106
      Related
      ENSP00000406134.1, ENST00000452774.2
      Conserved Domains (4) summary
      PRK11504
      Location:37691
      tynA; tyramine oxidase; Provisional
      pfam01179
      Location:312689
      Cu_amine_oxid; Copper amine oxidase, enzyme domain
      pfam02727
      Location:62148
      Cu_amine_oxidN2; Copper amine oxidase, N2 domain
      pfam02728
      Location:165263
      Cu_amine_oxidN3; Copper amine oxidase, N3 domain
    2. NM_009590.4NP_033720.2  amine oxidase [copper-containing] 2 isoform b

      See identical proteins and their annotated locations for NP_033720.2

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2) represents the longer transcript and encodes the longer isoform (b).
      Source sequence(s)
      AC016889, AF081363, CA427935, CN355968, D88213, DQ426861
      Consensus CDS
      CCDS11443.1
      UniProtKB/Swiss-Prot
      A5PKW2, O00120, O75105, O75106, Q4TTW5, Q9UNY0
      Related
      ENSP00000253799.2, ENST00000253799.8
      Conserved Domains (3) summary
      pfam01179
      Location:308716
      Cu_amine_oxid; Copper amine oxidase, enzyme domain
      pfam02727
      Location:62148
      Cu_amine_oxidN2; Copper amine oxidase, N2 domain
      pfam02728
      Location:165263
      Cu_amine_oxidN3; Copper amine oxidase, N3 domain

    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_000017.11 Reference GRCh38.p14 Primary Assembly

      Range
      42844580..42850707
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060941.1 Alternate T2T-CHM13v2.0

      Range
      43701719..43707847
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)