ENSMUSG00000028825


Mus musculus

Features
Gene ID: ENSMUSG00000028825
  
Biological name :Rhd
  
Synonyms : Rhd
  
Possible biological names infered from orthology : P18577 / Q02161 / Rh blood group CcEe antigens / Rh blood group D antigen / RHCE
  
Species: Mus musculus
  
Chr. number: 4
Strand: 1
Band: D3
Gene start: 134864536
Gene end: 134896172
  
Corresponding Affymetrix probe sets: 10509002 (MoGene1.0st)   1417049_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000030627
NCBI entrez gene - 19746     See in Manteia.
MGI - MGI:1202882
RefSeq - NM_011270
RefSeq Peptide - NP_035400
swissprot - A0A0R4J0A2
Ensembl - ENSMUSG00000028825
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 rhdENSDARG00000002194Danio rerio
 RHCEENSGALG00000040279Gallus gallus
 RHCEENSG00000188672Homo sapiens
 RHDENSG00000187010Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Rhag / Q9QUT0 / Ammonium transporter Rh type A / Q02094* / Rh associated glycoprotein*ENSMUSG0000002392633
Rhbg / Q8BUX5 / Ammonium transporter Rh type B / Q9H310* / Rh family B glycoprotein (gene/pseudogene)*ENSMUSG0000010444532
Rhcg / Q9QXP0 / Ammonium transporter Rh type C / Q9UBD6* / Rh family C glycoprotein*ENSMUSG0000003054930
Gm38392 / RHBG* / Q9H310* / Rh family B glycoprotein (gene/pseudogene)*ENSMUSG0000010376630


Protein motifs (from Interpro)
Interpro ID Name
 IPR002229  Blood group Rhesus C/E/D polypeptide
 IPR024041  Ammonium transporter AmtB-like domain
 IPR029020  Ammonium/urea transporter


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0015696 ammonium transport IEA
 biological_processGO:0072488 ammonium transmembrane transport IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 molecular_functionGO:0008519 ammonium transmembrane transporter activity IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0001191 abnormal skin condition "anomalous state of the skin" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Prkab1tm1a(KOMP)Wtsi/Prkab1tm1a(KOMP)Wtsi
Genetic Background: C57BL/6N-Prkab1tm1a(KOMP)Wtsi/Wtsi

 MP:0002591 decreased mean corpuscular volume "less than the average amount of space occupied by each red blood cell, calculated from the hematocrit and red cell count, in erythrocyte indices" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, Stedman s Medical Dictionary:ISBN 0-683-40008-8]
Show

Allelic Composition: Prkab1tm1a(KOMP)Wtsi/Prkab1tm1a(KOMP)Wtsi
Genetic Background: C57BL/6N-Prkab1tm1a(KOMP)Wtsi/Wtsi

 MP:0002874 decreased hemoglobin content "decrease in the total hemoglobin content in the circulating blood" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Prkab1tm1a(KOMP)Wtsi/Prkab1tm1a(KOMP)Wtsi
Genetic Background: C57BL/6N-Prkab1tm1a(KOMP)Wtsi/Wtsi

 MP:0002966 decreased circulating alkaline phosphatase level "reduced activity of this enzyme, which hydrolyzes orthophosphoric monoesters, found in the blood" [RGD:Rat Genome Database submission, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Prkab1tm1a(KOMP)Wtsi/Prkab1tm1a(KOMP)Wtsi
Genetic Background: C57BL/6N-Prkab1tm1a(KOMP)Wtsi/Wtsi

 MP:0003656 abnormal erythrocyte physiology "functional anomaly of the cells in the blood that carry oxygen, red blood cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Gt(ROSA)26Sortm1(Thy1-FBXL2)Wata/Gt(ROSA)26Sor+,Tg(Thy1-PSEN1*M146V,-APP*Swe)10Arte/0
Genetic Background: involves: C57BL/6 * C57BL/6N * CBA

 MP:0005642 decreased mean corpuscular hemoglobin concentration "less than the normal Hgb/Hct; the average hemoglobin concentration in a given volume of packed red cells, calculated from the hemoglobin therein and the hematocrit, in erythrocyte indices" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:8936]
Show

Allelic Composition: Prkab1tm1a(KOMP)Wtsi/Prkab1tm1a(KOMP)Wtsi
Genetic Background: C57BL/6N-Prkab1tm1a(KOMP)Wtsi/Wtsi

 MP:0008810 increased circulating iron level "elevation in the concentration of iron in the blood" [MGI:smb "Susan M. Bello, Mouse Genome Informatics Curator"]
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Allelic Composition: Gt(ROSA)26Sortm1(Thy1-FBXL2)Wata/Gt(ROSA)26Sor+,Tg(Thy1-PSEN1*M146V,-APP*Swe)10Arte/0
Genetic Background: involves: C57BL/6 * C57BL/6N * CBA

  


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






 

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