ENSMUSG00000023393


Mus musculus

Features
Gene ID: ENSMUSG00000023393
  
Biological name :Slc17a9
  
Synonyms : Q8VCL5 / Slc17a9 / solute carrier family 17, member 9
  
Possible biological names infered from orthology : Q9BYT1
  
Species: Mus musculus
  
Chr. number: 2
Strand: 1
Band: H4
Gene start: 180725263
Gene end: 180742280
  
Corresponding Affymetrix probe sets: 10479463 (MoGene1.0st)   1425950_at (Mouse Genome 430 2.0 Array)   1432023_a_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000091771
NCBI entrez gene - 228993     See in Manteia.
MGI - MGI:1919107
RefSeq - XM_006500591
RefSeq - NM_183161
RefSeq - XM_006500589
RefSeq - XM_006500590
RefSeq Peptide - NP_898984
swissprot - Q8VCL5
Ensembl - ENSMUSG00000023393
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 slc17a9aENSDARG00000042954Danio rerio
 slc17a9bENSDARG00000011049Danio rerio
 SLC17A9ENSGALG00000028225Gallus gallus
 Q9BYT1ENSG00000101194Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q8BFU8 / Slc17a8 / Vesicular glutamate transporter 3 / Q8NDX2* / solute carrier family 17 member 8*ENSMUSG0000001993527
Q3TXX4 / Slc17a7 / Vesicular glutamate transporter 1 / Q9P2U7* / solute carrier family 17 member 7*ENSMUSG0000007057027
Q8BN82 / Sialin / Slc17a5 / Q9NRA2* / solute carrier family 17 member 5*ENSMUSG0000004962427
Slc17a6 / solute carrier family 17 member 6 / Q9P2U8*ENSMUSG0000003050026
Slc17a3 / solute carrier family 17 (sodium phosphate), member 3 / O00476* / solute carrier family 17 member 3*ENSMUSG0000003608324
Q61983 / Slc17a1 / solute carrier family 17 (sodium phosphate), member 1 / Q14916* / solute carrier family 17 member 1*ENSMUSG0000002133523
Q5NCM1 / Slc17a4 / Probable small intestine urate exporter / Q9Y2C5* / solute carrier family 17 member 4*ENSMUSG0000002133623
Q5SZA1 / Slc17a2 / solute carrier family 17 (sodium phosphate), member 2 / O00624* / solute carrier family 17 member 2*ENSMUSG0000003611021


Protein motifs (from Interpro)
Interpro ID Name
 IPR005829  Sugar transporter, conserved site
 IPR011701  Major facilitator superfamily
 IPR020846  Major facilitator superfamily domain
 IPR036259  MFS transporter superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006820 anion transport IBA
 biological_processGO:0006887 exocytosis IEA
 biological_processGO:0055085 transmembrane transport IBA
 biological_processGO:1903146 regulation of autophagy of mitochondrion IEA
 biological_processGO:1903955 positive regulation of protein targeting to mitochondrion IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IBA
 molecular_functionGO:0005215 transporter activity IEA
 molecular_functionGO:0022857 transmembrane transporter activity IBA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000189 hypoglycemia "low levels of plasma glucose in the circulating blood; this generally refers to a pathological state" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Prkag2tm1.1Geno/Prkag2tm1.1Geno,Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic Background: B6.Cg-Prkag2tm1.1Geno Edil3Tg(Sox2-cre)1Amc

 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]
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Allelic Composition: Rad9atm1.1(KOMP)Wtsi/Rad9atm1.1(KOMP)Wtsi
Genetic Background: C57BL/6N-Rad9atm1.1(KOMP)Wtsi/Bay

 MP:0002092 abnormal eye morphology "abnormal development of the eye tissues resulting in morphological abnormality or abnormal structure of the visual system" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Rad9atm1.1(KOMP)Wtsi/Rad9atm1.1(KOMP)Wtsi
Genetic Background: C57BL/6N-Rad9atm1.1(KOMP)Wtsi/Bay

 MP:0002169 no phenotype detected "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Otop1ied/Otop1ied
Genetic Background: involves: C3HeB/FeJ * C57BL/6

 MP:0002727 decreased circulating insulin level "less than normal levels of insulin in the blood" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, dlb:Donna Burkart , Mouse Genome Informatics Curator]
Show

Allelic Composition: Prkag2tm1.1Geno/Prkag2tm1.1Geno,Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic Background: B6.Cg-Prkag2tm1.1Geno Edil3Tg(Sox2-cre)1Amc

 MP:0002891 increased insulin sensitivity "greater ability to clear glucose from the bloodstream when given insulin than normal; can result in hypoglycemia" [RGD:Rat Genome Database submission]
Show

Allelic Composition: Prkag2tm1.1Geno/Prkag2tm1.1Geno,Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic Background: B6.Cg-Prkag2tm1.1Geno Edil3Tg(Sox2-cre)1Amc

 MP:0002909 abnormal adrenal gland physiology "altered ability of the surparenal gland to produce and secrete hormones " [hdene:Howard Dene , Mouse Genome Informatics Curator]
Show

Allelic Composition: Prkag2tm1.1Geno/Prkag2tm1.1Geno,Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic Background: B6.Cg-Prkag2tm1.1Geno Edil3Tg(Sox2-cre)1Amc

 MP:0005292 improved glucose tolerance "better than the normal response to oral consumption or intravenous injection of specified amounts of glucose and indicative of insulin sensitivity; measured by determining whole blood or plasma sugar level in a fasting state before and after taking glucose at specified intervals" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Prkag2tm1.1Geno/Prkag2tm1.1Geno,Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic Background: B6.Cg-Prkag2tm1.1Geno Edil3Tg(Sox2-cre)1Amc

 MP:0011479 abnormal catecholamine level "any anomaly in the amount of catecholamines, including adrenaline, noradrenaline and L-dopamine; catecholamines are act as hormones or neurotransmitters and are derived from the amino acid tyrosine" [MGI:csmith]
Show

Allelic Composition: Prkag2tm1.1Geno/Prkag2tm1.1Geno,Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic Background: B6.Cg-Prkag2tm1.1Geno Edil3Tg(Sox2-cre)1Amc

 MP:0013570 abnormal neuroendocrine gland physiology "any structural anomaly of any of the organized aggregations of cells that function as secretory or excretory organs and that release hormones in response to neural stimuli" [ISBN:0-683-40008-8]
Show

Allelic Composition: Prkag2tm1.1Geno/Prkag2tm1.1Geno,Edil3Tg(Sox2-cre)1Amc/Edil3+
Genetic Background: B6.Cg-Prkag2tm1.1Geno Edil3Tg(Sox2-cre)1Amc

  


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






 

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