ENSMUSG00000019984


Mus musculus

Features
Gene ID: ENSMUSG00000019984
  
Biological name :Med23
  
Synonyms : Med23 / mediator complex subunit 23
  
Possible biological names infered from orthology : Q9ULK4
  
Species: Mus musculus
  
Chr. number: 10
Strand: 1
Band: A4
Gene start: 24869986
Gene end: 24913681
  
Corresponding Affymetrix probe sets: 10362210 (MoGene1.0st)   1452064_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000090316
Ensembl peptide - ENSMUSP00000135232
Ensembl peptide - ENSMUSP00000020159
Ensembl peptide - ENSMUSP00000135751
Ensembl peptide - ENSMUSP00000134836
Ensembl peptide - ENSMUSP00000134866
NCBI entrez gene - 70208     See in Manteia.
MGI - MGI:1917458
RefSeq - NM_027347
RefSeq - NM_001166416
RefSeq Peptide - NP_081623
RefSeq Peptide - NP_001159888
swissprot - H3BLE0
swissprot - H3BJ66
swissprot - H3BJ42
swissprot - F8WJB0
swissprot - E9QNV2
swissprot - H3BK33
Ensembl - ENSMUSG00000019984
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 med23ENSDARG00000029157Danio rerio
 MED23ENSGALG00000040607Gallus gallus
 MED23ENSG00000112282Homo sapiens


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR021629  Mediator complex, subunit Med23


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006355 regulation of transcription, DNA-templated IEA
 cellular_componentGO:0005667 transcription factor complex IEA


Pathways (from Reactome)
Pathway description
Generic Transcription Pathway


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000259 abnormal vascular development "malformation or aberrant differentiation of the blood vessels" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:17509]
Show

Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac

 MP:0002169 no phenotype detected "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Artm2.1Reb/Ar+,Tg(Amh-cre)8815Reb/?
Genetic Background: 129S(FVB)-Artm2.1Reb

 MP:0003861 abnormal nervous system development "impaired or altered growth of the components of the nervous system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac

 MP:0003984 embryonic growth retardation "slow or limited development before birth" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac

 MP:0005076 abnormal cell differentiation "anomaly in the process whereby relatively unspecialized cells, e. g. embryonic or regenerative cells, acquire specialized structural and/or functional features that characterize the cells, tissues, or organs of the mature organism or some other relatively stable phase of the organism s life history" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac

 MP:0011098 complete embryonic lethality during organogenesis "death of all organisms of a given genotype in a population between embryo turning and the completion of organogenesis (Mus: E9 to less than E14)" [MGI:csmith]
Show

Allelic Composition: Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph
Genetic Background: involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac

  


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






 

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