ENSMUSG00000095932


Mus musculus

Features
Gene ID: ENSMUSG00000095932
  
Biological name :Vmn1r49
  
Synonyms : Q9WUF1 / Vmn1r49 / vomeronasal 1, receptor 49
  
Possible biological names infered from orthology :
  
Species: Mus musculus
  
Chr. number: 6
Strand: -1
Band: D1
Gene start: 90071893
Gene end: 90078506
  
Corresponding Affymetrix probe sets: 10546240 (MoGene1.0st)   1421778_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000071762
Ensembl peptide - ENSMUSP00000145107
Ensembl peptide - ENSMUSP00000154456
NCBI entrez gene - 24112     See in Manteia.
MGI - MGI:1344384
RefSeq - NM_011911
RefSeq - XM_006506065
RefSeq Peptide - NP_036041
swissprot - Q9WUF1
Ensembl - ENSMUSG00000095932
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
No match


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
Q9EQ47 / Vmn1r44 / vomeronasal 1 receptor 44ENSMUSG0000006823483
Q9EQ46 / Vmn1r40 / vomeronasal 1 receptor 40ENSMUSG0000009605182
Q9EP51 / Vmn1r50 / vomeronasal 1 receptor 50ENSMUSG0000009455381
Vmn1r53 / vomeronasal 1 receptor 53ENSMUSG0000005769780
Vmn1r41 / vomeronasal 1 receptor 41ENSMUSG0000009458680
Q9EQ45 / Vmn1r46 / vomeronasal 1 receptor 46ENSMUSG0000006165376
Q8VIC7 / Vmn1r45 / vomeronasal 1 receptor 45ENSMUSG0000004424852
Q8VBS7 / Vmn1r42 / vomeronasal 1 receptor 42ENSMUSG0000006823251
Q9EQ52 / Vmn1r48 / vomeronasal 1 receptor 48ENSMUSG0000005759251
Vmn1r51 / vomeronasal 1 receptor 51ENSMUSG0000006281850
Q8VIC9 / Vmn1r43 / vomeronasal 1 receptor 43ENSMUSG0000006823150
Vmn1r47 / vomeronasal 1 receptor 47ENSMUSG0000006072450
Q9EPB8 / Vmn1r54 / vomeronasal 1 receptor 54ENSMUSG0000004720347
Vmn1r1 / vomeronasal 1 receptor 1ENSMUSG0000009101340
Q9EP79 / Vmn1r52 / vomeronasal 1 receptor 52ENSMUSG0000006081640
V1ra8 / Q9EQ48 / vomeronasal 1 receptor, A8ENSMUSG0000006254636


Protein motifs (from Interpro)
Interpro ID Name
 IPR004072  Vomeronasal receptor, type 1
 IPR017452  GPCR, rhodopsin-like, 7TM


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007165 signal transduction IEA
 biological_processGO:0007186 G-protein coupled receptor signaling pathway IEA
 biological_processGO:0007606 sensory perception of chemical stimulus TAS
 biological_processGO:0019236 response to pheromone IEA
 cellular_componentGO:0005886 plasma membrane IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 molecular_functionGO:0004871 obsolete signal transducer activity IEA
 molecular_functionGO:0004930 G-protein coupled receptor activity IEA
 molecular_functionGO:0016503 pheromone receptor activity IEA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000819 abnormal olfactory bulb morphology "malformation or absence of the forebrain region that coordinates neuronal signaling involved in the perception of smell; it receives input from the sensory neurons and outputs to the olfactory cortex" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, Principles of Neural Science:ISBN 0-8385-8034-3, J:16461]
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Allelic Composition: Nrp2tm1.2Mom/Nrp2tm1.2Mom,Vmn1r49tm1Mom/Vmn1r49tm1Mom
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

 MP:0009945 abnormal accessory olfactory bulb morphology "any structural anomaly of the forebrain region that coordinates sensory signaling arising from the vomeronasal organ; it is located on the dorsal-posterior portion of the main olfactory bulb, and the axons that leave the accessory olfactory bulb project to targets in the amygdala and hypothalamus" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Stx2tm1Dcru/Stx2+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

Allelic Composition: Vmn1r49tm4(Olfr151)Mom/Vmn1r49tm4(Olfr151)Mom
Genetic Background: involves: 129P2/OlaHsd * C57BL/6

Allelic Composition: Sema3ftm1Mom/Sema3ftm1Mom,Vmn1r49tm1Mom/Vmn1r49tm1Mom
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Sema3ftm1Mom/Sema3f+,Vmn1r49tm1Mom/Vmn1r49tm1Mom
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

 MP:0012014 abnormal olfactory neuron innervation pattern "any changes in the placement, morphology or number of axons from olfactory neurons to an effector tissue or to olfactory glomeruli or olfactory bulb" [MGI:csmith]
Show

Allelic Composition: Stx2tm1Dcru/Stx2+
Genetic Background: involves: 129X1/SvJ * C57BL/6J

  


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






 

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