ENSMUSG00000032131


Mus musculus

Features
Gene ID: ENSMUSG00000032131
  
Biological name :Abcg4
  
Synonyms : Abcg4 / ATP binding cassette subfamily G member 4
  
Possible biological names infered from orthology : Q9H172
  
Species: Mus musculus
  
Chr. number: 9
Strand: -1
Band: A5.2
Gene start: 44273188
Gene end: 44288615
  
Corresponding Affymetrix probe sets: 10592772 (MoGene1.0st)   1424437_s_at (Mouse Genome 430 2.0 Array)   1427732_s_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000124154
Ensembl peptide - ENSMUSP00000124647
Ensembl peptide - ENSMUSP00000124583
Ensembl peptide - ENSMUSP00000034648
Ensembl peptide - ENSMUSP00000123999
NCBI entrez gene - 192663     See in Manteia.
MGI - MGI:1890594
RefSeq - XM_011242421
RefSeq - NM_138955
RefSeq Peptide - NP_620405
swissprot - E0CY02
swissprot - E0CYI8
swissprot - Q91WA9
swissprot - F6XWY6
Ensembl - ENSMUSG00000032131
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 abcg4aENSDARG00000061047Danio rerio
 abcg4bENSDARG00000078068Danio rerio
 ABCG4ENSGALG00000006795Gallus gallus
 ABCG4ENSG00000172350Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Abcg1 / Q64343 / ATP binding cassette subfamily G member 1 / P45844*ENSMUSG0000002403070
Abcg2 / ATP binding cassette subfamily G member 2 (Junior blood group) / Q9UNQ0*ENSMUSG0000002980227
Abcg5 / Q99PE8 / ATP binding cassette subfamily G member 5 / Q9H222*ENSMUSG0000004050524
Abcg3 / Q99P81 / ATP binding cassette subfamily G member 3 / ABCG2* / Q9UNQ0* / ATP binding cassette subfamily G member 2 (Junior blood group)*ENSMUSG0000002929922


Protein motifs (from Interpro)
Interpro ID Name
 IPR003439  ABC transporter-like
 IPR003593  AAA+ ATPase domain
 IPR013525  ABC-2 type transporter
 IPR017871  ABC transporter, conserved site
 IPR027417  P-loop containing nucleoside triphosphate hydrolase


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0015918 sterol transport IEA
 biological_processGO:0030301 cholesterol transport IEA
 biological_processGO:1990830 cellular response to leukemia inhibitory factor IEP
 cellular_componentGO:0005886 plasma membrane IBA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IBA
 molecular_functionGO:0000166 nucleotide binding IEA
 molecular_functionGO:0005524 ATP binding IEA
 molecular_functionGO:0016887 ATPase activity IEA
 molecular_functionGO:0017127 cholesterol transporter activity IBA
 molecular_functionGO:0034041 sterol-transporting ATPase activity IBA
 molecular_functionGO:0042803 protein homodimerization activity ISO
 molecular_functionGO:0046982 protein heterodimerization activity ISO


Pathways (from Reactome)
Pathway description
ABC transporters in lipid homeostasis


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0001547 abnormal lipid level "anomalous concentrations of fat-soluble substances (molecules composed of carbon and hydrogen and are characteristically insoluble in water) in the body" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Dag1tm4.1Kcam/Dag1tm4.1Kcam
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

Allelic Composition: Abcg1tm1Dgen/Abcg1+,Abcg4tm1Dgen/Abcg4tm1Dgen
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Abcg1tm1Dgen/Abcg1tm1Dgen,Abcg4tm1Dgen/Abcg4tm1Dgen
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Abcg1tm1Dgen/Abcg1tm1Dgen,Abcg4tm1Dgen/Abcg4+
Genetic Background: involves: 129P2/OlaHsd

 MP:0002118 abnormal lipid homeostasis "anomaly in the state of equilibrium in the body with respect to lipids in the fluids and tissues" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Dag1tm4.1Kcam/Dag1tm4.1Kcam
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

Allelic Composition: Abcg1tm1Dgen/Abcg1tm1Dgen,Abcg4tm1Dgen/Abcg4tm1Dgen
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Abcg1tm1Dgen/Abcg1tm1Dgen,Abcg4tm1Dgen/Abcg4+
Genetic Background: involves: 129P2/OlaHsd

 MP:0003193 decreased cholesterol efflux "reduced level of removal of excess cholesterol from cells by an active transport pathway" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, RGD:Rat Genome Database submission]
Show

Allelic Composition: Abcg1tm1Dgen/Abcg1+,Abcg4tm1Dgen/Abcg4tm1Dgen
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Abcg1tm1Dgen/Abcg1tm1Dgen,Abcg4tm1Dgen/Abcg4tm1Dgen
Genetic Background: involves: 129P2/OlaHsd

Allelic Composition: Abcg1tm1Dgen/Abcg1tm1Dgen,Abcg4tm1Dgen/Abcg4+
Genetic Background: involves: 129P2/OlaHsd

 MP:0005278 abnormal cholesterol homeostasis "anomaly in the state of equilibrium in the body of these most abundant steroids in animal tissues, and precursors to steroid hormones and bile salts; also components of plasma membranes" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:71350]
Show

Allelic Composition: Abcg1tm1Dgen/Abcg1tm1Dgen,Abcg4tm1Dgen/Abcg4tm1Dgen
Genetic Background: involves: 129P2/OlaHsd

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000032131 Abcg4 / ATP binding cassette subfamily G member 4 / Q9H172*  / complex






 

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