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Vmn1r51 Gene Detail
Summary
  • Symbol
    Vmn1r51
  • Name
    vomeronasal 1 receptor 51
  • Synonyms
    V1r1, V1ra1, VN12
  • Feature Type
    protein coding gene
  • IDs
    MGI:1333759
    NCBI Gene: 22296
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr6:90122643-90130645 bp, + strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 6, 40.02 cM, cytoband D2
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    75 from dbSNP Build 142
  • Strain Annotations
    16
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1333759
protein coding gene Chr6:90122596-90132264 (+)
129S1/SvImJ MGP_129S1SvImJ_G0031030
protein coding gene Chr6:91608861-91617199 (+)
A/J MGP_AJ_G0030999
protein coding gene Chr6:88132772-88135338 (+)
AKR/J MGP_AKRJ_G0030930
protein coding gene Chr6:90617544-90620110 (+)
BALB/cJ MGP_BALBcJ_G0031008
protein coding gene Chr6:87996440-88113715 (+)
C3H/HeJ MGP_C3HHeJ_G0030699
protein coding gene Chr6:93843393-93845959 (-)
C57BL/6NJ MGP_C57BL6NJ_G0031468
protein coding gene Chr6:94038288-94046635 (+)
CAROLI/EiJ no annotation
CAST/EiJ no annotation
CBA/J MGP_CBAJ_G0030696
protein coding gene Chr6:97583089-97585655 (+)
DBA/2J MGP_DBA2J_G0030850
protein coding gene Chr6:87335986-87338552 (+)
FVB/NJ MGP_FVBNJ_G0030803
protein coding gene Chr6:86535284-86543631 (+)
LP/J MGP_LPJ_G0030929
protein coding gene Chr6:91579458-91587796 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0030837
protein coding gene Chr6:101642657-101651004 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0031494
protein coding gene Chr6:90474078-90482409 (+)
PWK/PhJ MGP_PWKPhJ_G0029834
protein coding gene Chr6:86319098-86327647 (+)
SPRET/EiJ MGP_SPRETEiJ_G0029663
protein coding gene Chr6:89368226-89370799 (-)
WSB/EiJ MGP_WSBEiJ_G0030200
protein coding gene Chr6:90881943-90890282 (+)



Homology
less
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    1 phenotype from multigenic genotypes
    13 phenotype references
  • All Mutations and Alleles
    5
  • Radiation induced
    1
  • Spontaneous
    1
  • Targeted
    3
  • Genomic Mutations
    3 involving Vmn1r51
  • Incidental Mutations
    APF
  • Find Mice (IMSR)
Homozygotes and heterozygotes for a null mutation exhibit axons that fail to converge on multiple discrete glomeruli, but rather, appear widely distributed throughout the glomerular layer of the accessory olfactory bulb.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell death
cell differentiation
cell population proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
nucleic acid-templated transcription
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
non-membrane-bounded organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
synapse
vacuole
Click cells to view annotations.
Expression
less
  • cDNA Data
  • Literature Summary
Interactions
less
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic 22296 NCBI Gene Model | MGI Sequence Detail 8003 C57BL/6J ±  kb
transcript NM_011683 RefSeq | MGI Sequence Detail 2359 C57BL/6  
polypeptide Q8VIC6 UniProt | EBI | MGI Sequence Detail 319 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 3
    cDNA 3

    Microarray probesets 3
References
more
  • Summaries
    All 34
    Developmental Gene Expression 3
    Gene Ontology 3
    Phenotypes 13
  • Earliest
    J:21726 Champion KM, et al., Identification of a heritable deficiency of the folate-dependent enzyme 10-formyltetrahydrofolate dehydrogenase in mice. Proc Natl Acad Sci U S A. 1994 Nov 22;91(24):11338-42
  • Latest
    J:198564 Prince JE, et al., Kirrel3 is required for the coalescence of vomeronasal sensory neuron axons into glomeruli and for male-male aggression. Development. 2013 Jun;140(11):2398-408

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
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last database update
06/11/2019
MGI 6.14
The Jackson Laboratory