ENSMUSG00000019303


Mus musculus

Features
Gene ID: ENSMUSG00000019303
  
Biological name :Psmc3ip
  
Synonyms : O35047 / proteasome (prosome, macropain) 26S subunit, ATPase 3, interacting protein / Psmc3ip
  
Possible biological names infered from orthology : PSMC3 interacting protein / Q9P2W1
  
Species: Mus musculus
  
Chr. number: 11
Strand: -1
Band: D
Gene start: 101091823
Gene end: 101095436
  
Corresponding Affymetrix probe sets: 10391339 (MoGene1.0st)   1425271_at (Mouse Genome 430 2.0 Array)   1442058_s_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000019447
Ensembl peptide - ENSMUSP00000117100
NCBI entrez gene - 19183     See in Manteia.
MGI - MGI:1098610
RefSeq - NM_008949
RefSeq - XM_006532524
RefSeq Peptide - NP_032975
swissprot - D6RFC4
swissprot - C4PFH5
swissprot - O35047
Ensembl - ENSMUSG00000019303
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 psmc3ipENSDARG00000037892Danio rerio
 PSMC3IPENSGALG00000019741Gallus gallus
 Q9P2W1ENSG00000131470Homo sapiens


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR010776  Homologous-pairing protein 2
 IPR036388  Winged helix-like DNA-binding domain superfamily
 IPR036390  Winged helix DNA-binding domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006310 DNA recombination IEA
 biological_processGO:0007131 reciprocal meiotic recombination IEA
 biological_processGO:0051321 meiotic cell cycle IEA
 biological_processGO:1903506 regulation of nucleic acid-templated transcription IEA
 cellular_componentGO:0000502 proteasome complex IEA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005654 nucleoplasm IEA
 molecular_functionGO:0003677 DNA binding IEA
 molecular_functionGO:0030374 nuclear receptor transcription coactivator activity IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0001117 absence of gametes "missing mature reproductive cells, ovum or spermatozoon, capable of fusing with a cell of similar origin, but opposite sex to give a zygote" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:34193]
Show

Allelic Composition: KitlSl-21J/Kitl+
Genetic Background: B10.BR H2k H2-T18a/SgSnJ-KitlSl-21J/GrsrJ

 MP:0001924 infertility "inability to produce live offspring" [J:47225]
Show

Allelic Composition: KitlSl-21J/Kitl+
Genetic Background: B10.BR H2k H2-T18a/SgSnJ-KitlSl-21J/GrsrJ

 MP:0001930 abnormal meiosis "malfunction in the process of nuclear division that results in gametes with one half the normal number of the original cell" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: KitlSl-21J/Kitl+
Genetic Background: B10.BR H2k H2-T18a/SgSnJ-KitlSl-21J/GrsrJ

 MP:0001940 testicular hypoplasia "decreased cell number in the testicles" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: KitlSl-21J/Kitl+
Genetic Background: B10.BR H2k H2-T18a/SgSnJ-KitlSl-21J/GrsrJ

 MP:0002777 absent ovarian follicles "lack of the sac-like structures in the ovaries that surround the ova" [J:42612, pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator]
Show

Allelic Composition: KitlSl-21J/Kitl+
Genetic Background: B10.BR H2k H2-T18a/SgSnJ-KitlSl-21J/GrsrJ

 MP:0003582 abnormal ovary development "abnormal morphogenesis of the female reproductive gland containing the germ cells" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: KitlSl-21J/Kitl+
Genetic Background: B10.BR H2k H2-T18a/SgSnJ-KitlSl-21J/GrsrJ

 MP:0005159 azoospermia "absence of living spermatozoa " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: KitlSl-21J/Kitl+
Genetic Background: B10.BR H2k H2-T18a/SgSnJ-KitlSl-21J/GrsrJ

 MP:0005169 abnormal male meiosis "malfunction in the process of nuclear division that results in sperm with one half the normal chromosome number of the original cell" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: KitlSl-21J/Kitl+
Genetic Background: B10.BR H2k H2-T18a/SgSnJ-KitlSl-21J/GrsrJ

Allelic Composition: Mnd1Gt(RRS590)Byg/Mnd1Gt(RRS590)Byg,Psmc3iptm1Rdco/Psmc3iptm1Rdco
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6

 MP:0008261 arrest of male meiosis "cessation of the progression of the process of nuclear division that results in sperm with one half the normal chromosome number of the original cell" [ISBN:0-683-40008-8 "Stedman s Medical Dictionary, 27th edition"]
Show

Allelic Composition: KitlSl-21J/Kitl+
Genetic Background: B10.BR H2k H2-T18a/SgSnJ-KitlSl-21J/GrsrJ

 MP:0010948 abnormal double-strand DNA break repair "any annomaly in the process of repair of double-strand breaks in DNA via homologous and nonhomologous mechanisms to reform a continuous DNA helix" [GO:0006302]
Show

Allelic Composition: Psmc3iptm1Rdco/Psmc3iptm1Rdco,Spo11tm1.1Gvpc/Spo11tm1.1Gvpc
Genetic Background: involves: 129S6/SvEvTac * C57BL/6

Allelic Composition: Mnd1Gt(RRS590)Byg/Mnd1Gt(RRS590)Byg,Psmc3iptm1Rdco/Psmc3iptm1Rdco
Genetic Background: involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6

  


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






 

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