ENSMUSG00000042167


Mus musculus

Features
Gene ID: ENSMUSG00000042167
  
Biological name :Papd4
  
Synonyms : PAP associated domain containing 4 / Papd4 / Q91YI6
  
Possible biological names infered from orthology : poly(A) RNA polymerase D4, non-canonical / Q6PIY7
  
Species: Mus musculus
  
Chr. number: 13
Strand: -1
Band: C3
Gene start: 93146282
Gene end: 93192385
  
Corresponding Affymetrix probe sets: 10411119 (MoGene1.0st)   10521966 (MoGene1.0st)   1419183_at (Mouse Genome 430 2.0 Array)   1433568_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000153060
Ensembl peptide - ENSMUSP00000153703
Ensembl peptide - ENSMUSP00000153685
Ensembl peptide - ENSMUSP00000153339
Ensembl peptide - ENSMUSP00000048124
NCBI entrez gene - 100715     See in Manteia.
MGI - MGI:2140950
RefSeq - XM_006517510
RefSeq - XM_017315331
RefSeq - XM_006517511
RefSeq - NM_133905
RefSeq Peptide - NP_598666
swissprot - Q91YI6
swissprot - A0A286YED5
swissprot - A0A286YCM6
swissprot - A0A286YDA7
Ensembl - ENSMUSG00000042167
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 papd4ENSDARG00000099679Danio rerio
 PAPD4ENSGALG00000014810Gallus gallus
 PAPD4ENSG00000164329Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
B2RX14 / Zcchc11 / zinc finger, CCHC domain containing 11 / Q5TAX3* / zinc finger CCHC-type containing 11*ENSMUSG0000003461029
Zcchc6 / zinc finger, CCHC domain containing 6 / Q5VYS8* / zinc finger CCHC-type containing 6*ENSMUSG0000003524828
Tut1 / Q8R3F9 / terminal uridylyl transferase 1, U6 snRNA-specific / Q9H6E5* / AP002990.1*ENSMUSG0000007164518
Mtpap / Q9D0D3 / Poly(A) RNA polymerase, mitochondrial / Q9NVV4* / mitochondrial poly(A) polymerase*ENSMUSG0000002423417


Protein motifs (from Interpro)
Interpro ID Name
 IPR002058  PAP/25A-associated


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0002244 hematopoietic progenitor cell differentiation IMP
 biological_processGO:0006397 mRNA processing IEA
 biological_processGO:0021766 hippocampus development IEA
 biological_processGO:0030182 neuron differentiation IEA
 biological_processGO:0043631 RNA polyadenylation IEA
 biological_processGO:0060041 retina development in camera-type eye IEA
 biological_processGO:0071044 histone mRNA catabolic process IEA
 biological_processGO:1990603 dark adaptation IEA
 cellular_componentGO:0005634 nucleus IDA
 cellular_componentGO:0005737 cytoplasm IEA
 cellular_componentGO:0005829 cytosol IEA
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0004652 polynucleotide adenylyltransferase activity ISO
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0005524 ATP binding IEA
 molecular_functionGO:0016740 transferase activity IEA
 molecular_functionGO:0046872 metal ion binding IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0005621 abnormal cell physiology "aberration in the vital processes of the cell " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, hdene:Howard Dene , Mouse Genome Informatics Curator]
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Allelic Composition: Bcl11btm1Avram/Bcl11btm1Avram,Tg(Cd4-cre)1Cwi/?,Tg(LCKprBCL2)36Sjk/?
Genetic Background: involves: 129 * C57BL/6 * DBA/2

  


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






 

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