ENSMUSG00000023943


Mus musculus

Features
Gene ID: ENSMUSG00000023943
  
Biological name :Sult1c1
  
Synonyms : Q80VR3 / Sulfotransferase 1C1 / Sult1c1
  
Possible biological names infered from orthology : Q6IMI6 / sulfotransferase family 1C member 3 / SULT1C3
  
Species: Mus musculus
  
Chr. number: 17
Strand: -1
Band: C
Gene start: 53961615
Gene end: 53990674
  
Corresponding Affymetrix probe sets: 10451828 (MoGene1.0st)   1420470_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000024738
NCBI entrez gene - 20888     See in Manteia.
MGI - MGI:102928
RefSeq - NM_018751
RefSeq Peptide - NP_061221
swissprot - Q80VR3
Ensembl - ENSMUSG00000023943
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 sult1st5ENSDARG00000003475Danio rerio
 sult1st6ENSDARG00000006811Danio rerio
 SULT1C3ENSGALG00000016805Gallus gallus
 Q6IMI6ENSG00000196228Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q9D939 / Sult1c2 / Sulfotransferase 1C2 / O00338* / sulfotransferase family 1C member 2*ENSMUSG0000002312258
Q3UZZ6 / Sult1d1 / Sulfotransferase 1 family member D1 ENSMUSG0000002927358
Q9QWG7 / Sult1b1 / Mus musculus sulfotransferase family 1B, member 1 (Sult1b1), transcript variant 1, mRNA. / O43704* / sulfotransferase family 1B member 1*ENSMUSG0000002926951
Sult1e1 / P49888* / AC108941.2* / sulfotransferase family 1E member 1*ENSMUSG0000002927246
Sult1a1 / sulfotransferase family 1A, phenol-preferring, member 1 / P50226* / P50225* / P0DMM9* / P0DMN0* / SULT1A4* / SULT1A2* / SULT1A3* / sulfotransferase family 1A member 2* / sulfotran...ENSMUSG0000003071145
P52843 / Sult2a1 / Bile salt sulfotransferase 1 / Q06520* / sulfotransferase family 2A member 1*ENSMUSG0000007879837
Sult2a4 / sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 4 / Q06520* / SULT2A1* / sulfotransferase family 2A member 1*ENSMUSG0000007437737
Sult2a5 / sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 5 / Q06520* / SULT2A1* / sulfotransferase family 2A member 1*ENSMUSG0000007879937
Sult2a3 / Q06520* / SULT2A1* / sulfotransferase family 2A member 1*ENSMUSG0000007437537
O35400 / Sult2b1 / Sulfotransferase family cytosolic 2B member 1 / O00204* / sulfotransferase family 2B member 1*ENSMUSG0000000327135
Sult2a6 / sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 6 / Q06520* / SULT2A1* / sulfotransferase family 2A member 1*ENSMUSG0000007081035
Sult3a1 / sulfotransferase family 3A, member 1ENSMUSG0000006966833
Sult2a7 / Q06520* / SULT2A1* / sulfotransferase family 2A member 1*ENSMUSG0000009415633
Sult3a2ENSMUSG0000009029832
Sult2a8 / sulfotransferase family 2A, dehydroepiandrosterone (DHEA)-preferring, member 8 / Q06520* / SULT2A1* / sulfotransferase family 2A member 1*ENSMUSG0000003037832
Sult5a1 / sulfotransferase family 5A, member 1ENSMUSG0000000073929


Protein motifs (from Interpro)
Interpro ID Name
 IPR000863  Sulfotransferase domain
 IPR027417  P-loop containing nucleoside triphosphate hydrolase


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006790 sulfur compound metabolic process IDA
 cellular_componentGO:0005737 cytoplasm IEA
 molecular_functionGO:0004027 alcohol sulfotransferase activity IEA
 molecular_functionGO:0004062 aryl sulfotransferase activity IDA
 molecular_functionGO:0008146 sulfotransferase activity IEA
 molecular_functionGO:0016740 transferase activity IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000150 abnormal rib morphology "malformed bones forming the bony wall of the chest" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:50311]
Show

Allelic Composition: Spns2tm1b(KOMP)Wtsi/Spns2tm1b(KOMP)Wtsi
Genetic Background: B6Brd;B6Dnk;B6N-Tyrc-Brd-Spns2tm1b(KOMP)Wtsi/WtsiH

 MP:0000223 decreased monocyte count "fewer than normal monocyte numbers" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
Show

Allelic Composition: Spns2tm1b(KOMP)Wtsi/Spns2tm1b(KOMP)Wtsi
Genetic Background: B6Brd;B6Dnk;B6N-Tyrc-Brd-Spns2tm1b(KOMP)Wtsi/WtsiH

 MP:0004647 decreased lumbar vertebrae number "reduced number of the six bony segments of the spine located anterior to the sacral vertebrae and posterior to the thoracic vertebrae" [MESH:National Library of Medicine_Medical Subject Headings]
Show

Allelic Composition: Spns2tm1b(KOMP)Wtsi/Spns2tm1b(KOMP)Wtsi
Genetic Background: B6Brd;B6Dnk;B6N-Tyrc-Brd-Spns2tm1b(KOMP)Wtsi/WtsiH

 MP:0008078 increased CD8-positive T cell number "greater number of the regulatory subset of T lymphocytes that are involved in MHC class I restricted interactions" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Spns2tm1b(KOMP)Wtsi/Spns2tm1b(KOMP)Wtsi
Genetic Background: B6Brd;B6Dnk;B6N-Tyrc-Brd-Spns2tm1b(KOMP)Wtsi/WtsiH

 MP:0010101 increased sacral vertebrae number "increase of any or all of the four bony segments of the spine located posterior to the lumbar vertebrae and anterior to the caudal vertebrae" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Spns2tm1b(KOMP)Wtsi/Spns2tm1b(KOMP)Wtsi
Genetic Background: B6Brd;B6Dnk;B6N-Tyrc-Brd-Spns2tm1b(KOMP)Wtsi/WtsiH

 MP:0013023 decreased Ly6C high monocyte number "decrease in the number of monocytes that express high levels of Ly6C and low MHC class II that represent a subset of circulating inflammatory monocytes that are recruited to infected or inflamed tissues" [MGI:Annie_Speak]
Show

Allelic Composition: Spns2tm1b(KOMP)Wtsi/Spns2tm1b(KOMP)Wtsi
Genetic Background: B6Brd;B6Dnk;B6N-Tyrc-Brd-Spns2tm1b(KOMP)Wtsi/WtsiH

  


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






 

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