ENSMUSG00000029811


Mus musculus

Features
Gene ID: ENSMUSG00000029811
  
Biological name :Aoc1
  
Synonyms : Aoc1
  
Possible biological names infered from orthology : amine oxidase, copper containing 1 / P19801
  
Species: Mus musculus
  
Chr. number: 6
Strand: 1
Band: B2.3
Gene start: 48872896
Gene end: 48909188
  
Corresponding Affymetrix probe sets: 10538163 (MoGene1.0st)   1424600_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000128816
Ensembl peptide - ENSMUSP00000144764
Ensembl peptide - ENSMUSP00000031835
Ensembl peptide - ENSMUSP00000124085
NCBI entrez gene - 76507     See in Manteia.
MGI - MGI:1923757
RefSeq - NM_001161622
RefSeq - NM_029638
RefSeq - NM_001161621
RefSeq Peptide - NP_083914
RefSeq Peptide - NP_001155093
RefSeq Peptide - NP_001155094
swissprot - A0A0N4SUP5
swissprot - E9PYN9
Ensembl - ENSMUSG00000029811
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 aoc1ENSDARG00000061355Danio rerio
 ENSGALG00000036190Gallus gallus
 AOC1ENSG00000002726Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Doxl2 / AOC1* / P19801* / amine oxidase, copper containing 1*ENSMUSG0000006853658
Svs1 / seminal vesicle secretory protein 1 / AOC1* / P19801* / amine oxidase, copper containing 1*ENSMUSG0000003921557
1600015I10Rik / RIKEN cDNA 1600015I10 gene / AOC1* / P19801* / amine oxidase, copper containing 1*ENSMUSG0000002981354
Aoc3 / O70423 / Membrane primary amine oxidase / Q16853* / amine oxidase, copper containing 3*ENSMUSG0000001932639
Aoc2 / Q812C9 / Retina-specific copper amine oxidase / O75106* / amine oxidase, copper containing 2*ENSMUSG0000007865138


Protein motifs (from Interpro)
Interpro ID Name
 IPR000269  Copper amine oxidase
 IPR015798  Copper amine oxidase, catalytic domain
 IPR015800  Copper amine oxidase, N2-terminal
 IPR015802  Copper amine oxidase, N3-terminal
 IPR016182  Copper amine oxidase, N-terminal
 IPR036460  Copper amine oxidase, catalytic domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0009308 amine metabolic process IEA
 biological_processGO:0055114 oxidation-reduction process IEA
 molecular_functionGO:0005507 copper ion binding IEA
 molecular_functionGO:0008131 primary amine oxidase activity IEA
 molecular_functionGO:0016491 oxidoreductase activity IEA
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:0048038 quinone binding IEA


Pathways (from Reactome)
Pathway description
Phase I - Functionalization of compounds
Neutrophil degranulation


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0001303 abnormal lens morphology "malformed transparent structure of the eye responsible for focusing light rays" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:40203]
Show

Allelic Composition: Anks6tm1b(KOMP)Wtsi/Anks6tm1b(KOMP)Wtsi
Genetic Background: C57BL/6N-Anks6tm1b(KOMP)Wtsi/Wtsi

 MP:0001325 abnormal retina morphology "structural or developmental anomaly of the thin layer of neural tissue lining the back of the eyeball which contains visual receptors " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Anks6tm1b(KOMP)Wtsi/Anks6tm1b(KOMP)Wtsi
Genetic Background: C57BL/6N-Anks6tm1b(KOMP)Wtsi/Wtsi

 MP:0001488 increased startle reflex "reduced threshold or more severe reflex response to variable stimuli, often auditory; usually measured by amplitude of whole body flinch" [What s Wrong With My Mouse?:ISBN 0-471-31639-3, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Anks6tm1b(KOMP)Wtsi/Anks6tm1b(KOMP)Wtsi
Genetic Background: C57BL/6N-Anks6tm1b(KOMP)Wtsi/Wtsi

 MP:0002079 increased circulating insulin level "greater than normal levels of insulin in blood" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Anks6tm1b(KOMP)Wtsi/Anks6tm1b(KOMP)Wtsi
Genetic Background: C57BL/6N-Anks6tm1b(KOMP)Wtsi/Wtsi

 MP:0002792 abnormal retinal vascularization "malformation or disorganization of the blood vessels supplying the retina" [cml:Cathleen M. Lutz , Mouse Genome Informatics Curator]
Show

Allelic Composition: Anks6tm1b(KOMP)Wtsi/Anks6tm1b(KOMP)Wtsi
Genetic Background: C57BL/6N-Anks6tm1b(KOMP)Wtsi/Wtsi

 MP:0010067 increased red blood cell distribution width "higher than normal coefficient of variance (reference range) of the red blood cell volume for an organism" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator", NCI:C64800 "NCI Thesaurus (Code C64800)"]
Show

Allelic Composition: Anks6tm1b(KOMP)Wtsi/Anks6tm1b(KOMP)Wtsi
Genetic Background: C57BL/6N-Anks6tm1b(KOMP)Wtsi/Wtsi

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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