ENSMUSG00000042197


Mus musculus

Features
Gene ID: ENSMUSG00000042197
  
Biological name :Zfp451
  
Synonyms : Q8C0P7 / Zfp451 / zinc finger protein 451
  
Possible biological names infered from orthology : Q9Y4E5 / ZNF451
  
Species: Mus musculus
  
Chr. number: 1
Strand: -1
Band: B
Gene start: 33761545
Gene end: 33814595
  
Corresponding Affymetrix probe sets: 10353754 (MoGene1.0st)   1427208_at (Mouse Genome 430 2.0 Array)   1451816_at (Mouse Genome 430 2.0 Array)   1455943_at (Mouse Genome 430 2.0 Array)   1456350_at (Mouse Genome 430 2.0 Array)   1456415_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000141714
Ensembl peptide - ENSMUSP00000110821
Ensembl peptide - ENSMUSP00000141813
Ensembl peptide - ENSMUSP00000137992
Ensembl peptide - ENSMUSP00000019861
Ensembl peptide - ENSMUSP00000044372
NCBI entrez gene - 98403     See in Manteia.
MGI - MGI:2137896
RefSeq - NM_133817
RefSeq - XM_017313044
RefSeq - XM_011238626
RefSeq - XM_006496370
RefSeq - NM_001290699
RefSeq - NM_001290700
RefSeq Peptide - NP_001277628
RefSeq Peptide - NP_001277629
RefSeq Peptide - NP_598578
swissprot - A0A0A6YX30
swissprot - Q8C0P7
swissprot - Q8VCL4
swissprot - A0A0A6YWV3
swissprot - E9Q9H6
swissprot - M0QWT6
Ensembl - ENSMUSG00000042197
  

This gene has been taged as a transcription factor by TFT
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 znf451ENSDARG00000076939Danio rerio
 ZNF451ENSGALG00000016282Gallus gallus
 Q9Y4E5ENSG00000112200Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR013087  Zinc finger C2H2-type
 IPR021623  Lamina-associated polypeptide 2 alpha, C-terminal


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006351 transcription, DNA-templated IEA
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 biological_processGO:0016925 protein sumoylation ISO
 biological_processGO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway IEA
 biological_processGO:0060633 negative regulation of transcription initiation from RNA polymerase II promoter IEA
 biological_processGO:2000616 negative regulation of histone H3-K9 acetylation IEA
 cellular_componentGO:0005634 nucleus ISO
 cellular_componentGO:0005654 nucleoplasm IEA
 cellular_componentGO:0016605 PML body IEA
 molecular_functionGO:0003676 nucleic acid binding IEA
 molecular_functionGO:0003677 DNA binding IEA
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0046872 metal ion binding IEA
 molecular_functionGO:0061665 SUMO ligase activity IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0001402 hypoactivity "reduced movement from one place to another" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, J:64289]
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Allelic Composition: Nsd3tm1b(EUCOMM)Hmgu/Nsd3tm1b(EUCOMM)Hmgu
Genetic Background: C57BL/6N-Nsd3tm1b(EUCOMM)Hmgu/H

 MP:0001944 abnormal pancreas morphology "malformation of the organ that secretes pancreatic juice into the duodenum and secretes glucagon and insulin into the bloodstream" [il:Ira Lu , Mouse Genome Informatics Curator]
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Allelic Composition: Nsd3tm1b(EUCOMM)Hmgu/Nsd3tm1b(EUCOMM)Hmgu
Genetic Background: C57BL/6N-Nsd3tm1b(EUCOMM)Hmgu/H

 MP:0002060 abnormal skin morphology "malformation or atypical structure of the membranous protective covering of the body" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:56777]
Show

Allelic Composition: Nsd3tm1b(EUCOMM)Hmgu/Nsd3tm1b(EUCOMM)Hmgu
Genetic Background: C57BL/6N-Nsd3tm1b(EUCOMM)Hmgu/H

 MP:0002875 decreased erythrocyte count "reduced number of the cells in the blood that carry oxygen, red blood cells, per unit" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Nsd3tm1b(EUCOMM)Hmgu/Nsd3tm1b(EUCOMM)Hmgu
Genetic Background: C57BL/6N-Nsd3tm1b(EUCOMM)Hmgu/H

 MP:0005561 increased mean corpuscular hemoglobin "greater than the average levels of hemoglobin contained in an erythrocyte" [RGD:Rat Genome Database submission, Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Nsd3tm1b(EUCOMM)Hmgu/Nsd3tm1b(EUCOMM)Hmgu
Genetic Background: C57BL/6N-Nsd3tm1b(EUCOMM)Hmgu/H

  


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






 

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