ENSMUSG00000029484


Mus musculus

Features
Gene ID: ENSMUSG00000029484
  
Biological name :Anxa3
  
Synonyms : Annexin A3 / Anxa3 / O35639
  
Possible biological names infered from orthology : P12429
  
Species: Mus musculus
  
Chr. number: 5
Strand: 1
Band: E3
Gene start: 96793339
Gene end: 96845966
  
Corresponding Affymetrix probe sets: 10523451 (MoGene1.0st)   1460330_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000142527
Ensembl peptide - ENSMUSP00000143615
Ensembl peptide - ENSMUSP00000143491
Ensembl peptide - ENSMUSP00000143103
Ensembl peptide - ENSMUSP00000031447
NCBI entrez gene - 11745     See in Manteia.
MGI - MGI:1201378
RefSeq - NM_013470
RefSeq Peptide - NP_038498
swissprot - O35639
swissprot - A0A0G2JGL7
swissprot - Q3TET3
swissprot - A0A0G2JFB3
swissprot - A0A0G2JDV9
Ensembl - ENSMUSG00000029484
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 anxa3aENSDARG00000009196Danio rerio
 anxa3bENSDARG00000044254Danio rerio
 ANXA3ENSG00000138772Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Anxa11 / P97384 / Annexin A11 / P50995*ENSMUSG0000002186652
Anxa4 / P97429 / Mus musculus annexin A4 (Anxa4), transcript variant 1, mRNA. / P09525* / annexin A4*ENSMUSG0000002999451
Anxa6 / P14824 / Annexin A6 / P08133*ENSMUSG0000001834048
Anxa1 / P10107 / Annexin A1 / P04083*ENSMUSG0000002465948
Anxa5 / P48036 / Annexin A5 / P08758*ENSMUSG0000002771247
Anxa8 / O35640 / Annexin A8 / P13928* / Q5VT79* / ANXA8L1* / annexin A8 like 1*ENSMUSG0000002195046
Anxa2 / P07356 / Annexin A2 / P07355*ENSMUSG0000003223146
Anxa7 / Q07076 / Annexin A7 / P20073*ENSMUSG0000002181444


Protein motifs (from Interpro)
Interpro ID Name
 IPR001464  Annexin
 IPR002390  Annexin A3
 IPR018252  Annexin repeat, conserved site
 IPR018502  Annexin repeat
 IPR037104  Annexin superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006909 phagocytosis IEA
 biological_processGO:0010595 positive regulation of endothelial cell migration IEA
 biological_processGO:0021766 hippocampus development IEA
 biological_processGO:0031100 animal organ regeneration IEA
 biological_processGO:0042742 defense response to bacterium IEA
 biological_processGO:0043086 negative regulation of catalytic activity IEA
 biological_processGO:0043312 neutrophil degranulation IEA
 biological_processGO:0045766 positive regulation of angiogenesis IEA
 biological_processGO:0051054 positive regulation of DNA metabolic process IEA
 biological_processGO:0051091 positive regulation of DNA-binding transcription factor activity IEA
 biological_processGO:0051384 response to glucocorticoid IEA
 biological_processGO:0070848 response to growth factor IEA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005829 cytosol IEA
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0030424 axon IEA
 cellular_componentGO:0030425 dendrite IEA
 cellular_componentGO:0030670 phagocytic vesicle membrane IEA
 cellular_componentGO:0042581 specific granule IEA
 cellular_componentGO:0043025 neuronal cell body IEA
 molecular_functionGO:0004859 phospholipase inhibitor activity IEA
 molecular_functionGO:0005509 calcium ion binding IEA
 molecular_functionGO:0005544 calcium-dependent phospholipid binding IEA
 molecular_functionGO:0019834 phospholipase A2 inhibitor activity IEA
 molecular_functionGO:0048306 calcium-dependent protein binding IEA


Pathways (from Reactome)
Pathway description
No match


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:0002110 abnormal digit morphology "abnormal development of the digits resulting in structural abnormality" [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:0010097 abnormal retinal blood vessel morphology "any structural anomaly of the blood vessels supplying the retina" [MGI: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

  


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






 

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