ENSMUSG00000020230


Mus musculus

Features
Gene ID: ENSMUSG00000020230
  
Biological name :Prmt2
  
Synonyms : Prmt2 / protein arginine N-methyltransferase 2
  
Possible biological names infered from orthology : P55345 / protein arginine methyltransferase 2
  
Species: Mus musculus
  
Chr. number: 10
Strand: -1
Band: C1
Gene start: 76207222
Gene end: 76237865
  
Corresponding Affymetrix probe sets: 10370072 (MoGene1.0st)   1416844_at (Mouse Genome 430 2.0 Array)   1437234_x_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000097166
Ensembl peptide - ENSMUSP00000137725
Ensembl peptide - ENSMUSP00000020452
Ensembl peptide - ENSMUSP00000151456
Ensembl peptide - ENSMUSP00000097167
Ensembl peptide - ENSMUSP00000137707
NCBI entrez gene - 15468     See in Manteia.
MGI - MGI:1316652
RefSeq - NM_001077638
RefSeq - NM_001302965
RefSeq - NM_133182
RefSeq Peptide - NP_001289894
RefSeq Peptide - NP_573445
RefSeq Peptide - NP_001071106
swissprot - Q3UKX1
swissprot - A0A1W2P6Z3
swissprot - Q3UID4
swissprot - M0QW88
Ensembl - ENSMUSG00000020230
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 prmt2ENSDARG00000063212Danio rerio
 PRMT2ENSG00000160310Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Carm1 / Q9WVG6 / Histone-arginine methyltransferase CARM1 / Q86X55* / coactivator associated arginine methyltransferase 1*ENSMUSG0000003218527
Prmt3 / Q922H1 / protein arginine N-methyltransferase 3 / O60678* / protein arginine methyltransferase 3*ENSMUSG0000003050527
Prmt6 / Q6NZB1 / protein arginine N-methyltransferase 6 / Q96LA8* / protein arginine methyltransferase 6*ENSMUSG0000004930027
Prmt8 / Q6PAK3 / protein arginine N-methyltransferase 8 / Q9NR22* / protein arginine methyltransferase 8*ENSMUSG0000003035025
Prmt1 / Q9JIF0 / protein arginine N-methyltransferase 1 / Q99873* / protein arginine methyltransferase 1*ENSMUSG0000010932424


Protein motifs (from Interpro)
Interpro ID Name
 IPR001452  SH3 domain
 IPR007848  Methyltransferase small domain
 IPR025799  Protein arginine N-methyltransferase
 IPR029063  S-adenosyl-L-methionine-dependent methyltransferase
 IPR036028  SH3-like domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006479 protein methylation IEA
 biological_processGO:0016571 histone methylation IEA
 biological_processGO:0032088 negative regulation of NF-kappaB transcription factor activity IEA
 biological_processGO:0032259 methylation IEA
 biological_processGO:0043065 positive regulation of apoptotic process IEA
 biological_processGO:0045892 negative regulation of transcription, DNA-templated IEA
 biological_processGO:0045893 positive regulation of transcription, DNA-templated IEA
 biological_processGO:0060765 regulation of androgen receptor signaling pathway IEA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005654 nucleoplasm IEA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005829 cytosol IEA
 molecular_functionGO:0003713 transcription coactivator activity IEA
 molecular_functionGO:0005515 protein binding IEA
 molecular_functionGO:0008168 methyltransferase activity IEA
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0030331 estrogen receptor binding IEA
 molecular_functionGO:0033142 progesterone receptor binding IEA
 molecular_functionGO:0042054 histone methyltransferase activity IEA
 molecular_functionGO:0042803 protein homodimerization activity IEA
 molecular_functionGO:0042974 retinoic acid receptor binding IEA
 molecular_functionGO:0042975 peroxisome proliferator activated receptor binding IEA
 molecular_functionGO:0046966 thyroid hormone receptor binding IEA
 molecular_functionGO:0050681 androgen receptor binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0003077 abnormal cell cycle "failure to progress or abnormal progression through the stages of of the cell cycle" [smb:Susan M. Bello, Mouse Genome Informatics Curator, J:91266]
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Allelic Composition: Cdk4tm1Kiyo/Cdk4+,Lin9tm1Orc/Lin9+
Genetic Background: involves: 129S1/Sv

 MP:0004883 abnormal blood vessel healing "anomaly in the repair process of blood vessels after injury" [MGI:monikat "Monika Tomczuk, Mouse Genome Informatics Curator"]
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Allelic Composition: Cdk4tm1Kiyo/Cdk4+,Lin9tm1Orc/Lin9+
Genetic Background: involves: 129S1/Sv

 MP:0010101 increased sacral vertebrae number "increase of any or all of the four bony segments of the spine located posterior to the lumbar vertebrae and anterior to the caudal vertebrae" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Prkab1tm1a(KOMP)Wtsi/Prkab1tm1a(KOMP)Wtsi
Genetic Background: C57BL/6N-Prkab1tm1a(KOMP)Wtsi/Wtsi

  


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






 

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