ENSMUSG00000021612


Mus musculus

Features
Gene ID: ENSMUSG00000021612
  
Biological name :Slc6a18
  
Synonyms : O88576 / Slc6a18 / solute carrier family 6 (neurotransmitter transporter), member 18
  
Possible biological names infered from orthology : Q96N87 / solute carrier family 6 member 18
  
Species: Mus musculus
  
Chr. number: 13
Strand: -1
Band: C1
Gene start: 73661752
Gene end: 73678023
  
Corresponding Affymetrix probe sets: 10410513 (MoGene1.0st)   1451879_a_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000152403
Ensembl peptide - ENSMUSP00000152697
Ensembl peptide - ENSMUSP00000152605
Ensembl peptide - ENSMUSP00000152525
Ensembl peptide - ENSMUSP00000152516
Ensembl peptide - ENSMUSP00000022105
Ensembl peptide - ENSMUSP00000105301
Ensembl peptide - ENSMUSP00000105302
Ensembl peptide - ENSMUSP00000152146
Ensembl peptide - ENSMUSP00000152273
NCBI entrez gene - 22598     See in Manteia.
MGI - MGI:1336892
RefSeq - NM_001168644
RefSeq - NM_001168645
RefSeq - NM_001168643
RefSeq - NM_001040692
RefSeq - NM_001136087
RefSeq - NM_001168646
RefSeq Peptide - NP_001129559
RefSeq Peptide - NP_001162115
RefSeq Peptide - NP_001162116
RefSeq Peptide - NP_001162117
RefSeq Peptide - NP_001035782
RefSeq Peptide - NP_001162114
swissprot - O88576
swissprot - A0A1Y7VMA5
swissprot - A0A1Y7VJY3
swissprot - A0A1Y7VJ53
swissprot - A0A217FL56
Ensembl - ENSMUSG00000021612
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 slc6a18ENSDARG00000068387Danio rerio
 SLC6A18ENSGALG00000013180Gallus gallus
 Q96N87ENSG00000164363Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q9D687 / Slc6a19 / solute carrier family 6 (neurotransmitter transporter), member 19 / Q695T7* / solute carrier family 6 member 19*ENSMUSG0000002156553
O88575 / Slc6a20b / Sodium- and chloride-dependent transporter XTRP3B / Q9NP91* / SLC6A20* / solute carrier family 6 member 20*ENSMUSG0000002524345
Q8VDB9 / Slc6a20a / Sodium- and chloride-dependent transporter XTRP3A ENSMUSG0000003681445
Q8BG16 / Slc6a15 / Sodium-dependent neutral amino acid transporter B(0)AT2 / Q9H2J7* / solute carrier family 6 member 15*ENSMUSG0000001989442
Q8BJI1 / Slc6a17 / Sodium-dependent neutral amino acid transporter SLC6A17 / Q9H1V8* / solute carrier family 6 member 17*ENSMUSG0000002789441
Slc6a16 / Q9GZN6* / solute carrier family 6 member 16*ENSMUSG0000009415228
Slc6a21ENSMUSG0000007056814


Protein motifs (from Interpro)
Interpro ID Name
 IPR000175  Sodium:neurotransmitter symporter
 IPR002438  Sodium:neurotransmitter symporter, orphan
 IPR037272  Sodium:neurotransmitter symporter superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0003333 amino acid transmembrane transport IDA
 biological_processGO:0006836 neurotransmitter transport IEA
 biological_processGO:0006865 amino acid transport IEA
 biological_processGO:0015804 neutral amino acid transport IEA
 biological_processGO:0055085 transmembrane transport IEA
 cellular_componentGO:0005886 plasma membrane IDA
 cellular_componentGO:0005887 integral component of plasma membrane IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0031526 brush border membrane IDA
 molecular_functionGO:0005215 transporter activity TAS
 molecular_functionGO:0005328 neurotransmitter:sodium symporter activity IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0015175 neutral amino acid transmembrane transporter activity IMP
 molecular_functionGO:0015293 symporter activity IEA


Pathways (from Reactome)
Pathway description
Amino acid transport across the plasma membrane
Na+/Cl- dependent neurotransmitter transporters


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000231 hypertension "sustained high blood pressure at a level that is likely to result in cardiovascular disease and/or other pathological states" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Tmod1tm1Sung/Tmod1tm1Sung
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0003311 aminoaciduria "excretion of amino acids in the urine, especially in excessive amounts" [anna:Anna Anagnostopoulos, Mouse Genome Informatics Curator, J:66560]
Show

Allelic Composition: Tmod1tm1Sung/Tmod1tm1Sung
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0006144 increased systolic blood pressure "abnormal increase in the pressure in the arteries as the heart contracts and pumps blood into the arteries" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Tmod1tm1Sung/Tmod1tm1Sung
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0010107 abnormal renal reabsorption "any anomaly in the two-step process beginning with the active or passive extraction of substances (such as water, glucose, oligopeptides, amino acids, sodium (Na+) and other ions) from the renal tubule fluid into the renal interstitium, and the subsequent transport of these substances out of the renal interstitium back into the bloodstream; reabsorption begins in the proximal convoluted tubules and continues in the loop of Henle, distal convoluted tubules, and collecting tubules" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Tmod1tm1Sung/Tmod1tm1Sung
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

 MP:0011417 abnormal renal transport "any anomaly of the directed movement of substances through the kidney" [MGI:csmith]
Show

Allelic Composition: Tmod1tm1Sung/Tmod1tm1Sung
Genetic Background: involves: 129S1/Sv * 129X1/SvJ

  


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






 

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