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Search results 1 to 90 out of 90 for Gpr179

0.032s
Type Details Score
Gene
Type: gene
Organism: human
Gene
Type: gene
Organism: cattle
Gene
Type: gene
Organism: zebrafish
Gene
Type: gene
Organism: macaque, rhesus
Gene
Type: gene
Organism: frog, western clawed
Gene
Type: gene
Organism: chicken
Gene
Type: gene
Organism: rat
Gene
Type: gene
Organism: dog, domestic
Gene
Type: gene
Organism: chimpanzee
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Domain
Type: Family
Description: GPR179 is a probable G-protein coupled receptor that plays a critical role in DBC (depolarising bipolar cell) signal transduction []. Mutations in the GPR179 gene cause autosomal recessive complete congenital stationary night blindness (CSNB), which is characterised by an ON-bipolar retinal cell dysfunction [].
Publication
First Author: Peachey NS
Year: 2012
Journal: Am J Hum Genet
Title: GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindness.
Volume: 90
Issue: 2
Pages: 331-9
Publication  
First Author: Wilmet B
Year: 2022
Journal: Int J Mol Sci
Title: Mice Lacking Gpr179 with Complete Congenital Stationary Night Blindness Are a Good Model for Myopia.
Volume: 24
Issue: 1
Publication
First Author: Orlandi C
Year: 2013
Journal: Invest Ophthalmol Vis Sci
Title: Orphan receptor GPR179 forms macromolecular complexes with components of metabotropic signaling cascade in retina ON-bipolar neurons.
Volume: 54
Issue: 10
Pages: 7153-61
Publication
First Author: Ray TA
Year: 2014
Journal: J Neurosci
Title: GPR179 is required for high sensitivity of the mGluR6 signaling cascade in depolarizing bipolar cells.
Volume: 34
Issue: 18
Pages: 6334-43
Publication
First Author: Klooster J
Year: 2013
Journal: Invest Ophthalmol Vis Sci
Title: Ultrastructural localization of GPR179 and the impact of mutant forms on retinal function in CSNB1 patients and a mouse model.
Volume: 54
Issue: 10
Pages: 6973-81
Publication
First Author: Orhan E
Year: 2013
Journal: Invest Ophthalmol Vis Sci
Title: Further insights into GPR179: expression, localization, and associated pathogenic mechanisms leading to complete congenital stationary night blindness.
Volume: 54
Issue: 13
Pages: 8041-50
Publication
First Author: Orlandi C
Year: 2018
Journal: Cell Rep
Title: Transsynaptic Binding of Orphan Receptor GPR179 to Dystroglycan-Pikachurin Complex Is Essential for the Synaptic Organization of Photoreceptors.
Volume: 25
Issue: 1
Pages: 130-145.e5
Protein
Organism: Mus musculus/domesticus
Length: 333  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 2293  
Fragment?: false
Publication  
First Author: Orhan E
Year: 2021
Journal: Int J Mol Sci
Title: A New Mouse Model for Complete Congenital Stationary Night Blindness Due to Gpr179 Deficiency.
Volume: 22
Issue: 9
Publication
First Author: Orlandi C
Year: 2012
Journal: J Cell Biol
Title: GPR158/179 regulate G protein signaling by controlling localization and activity of the RGS7 complexes.
Volume: 197
Issue: 6
Pages: 711-9
Publication  
First Author: Bjarnadóttir TK
Year: 2005
Journal: Gene
Title: The gene repertoire and the common evolutionary history of glutamate, pheromone (V2R), taste(1) and other related G protein-coupled receptors.
Volume: 362
Pages: 70-84
Publication  
First Author: Chang B
Year: 2015
Journal: Mol Vis
Title: Survey of the nob5 mutation in C3H substrains.
Volume: 21
Pages: 1101-5
Publication  
First Author: Balmer J
Year: 2013
Journal: Mol Vis
Title: Presence of the Gpr179(nob5) allele in a C3H-derived transgenic mouse.
Volume: 19
Pages: 2615-25
Publication  
First Author: Nishiguchi KM
Year: 2015
Journal: Nat Commun
Title: Gene therapy restores vision in rd1 mice after removal of a confounding mutation in Gpr179.
Volume: 6
Pages: 6006
Publication
First Author: Sarria I
Year: 2016
Journal: J Neurosci
Title: Intermolecular Interaction between Anchoring Subunits Specify Subcellular Targeting and Function of RGS Proteins in Retina ON-Bipolar Neurons.
Volume: 36
Issue: 10
Pages: 2915-25
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus caroli
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus pahari
Protein Coding Gene
Type: protein_coding_gene
Organism: Mus spretus
GXD Expression    
Probe: MGI:6148994
Assay Type: RNA in situ
Annotation Date: 2018-04-04
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:3277028
Stage: TS28
Assay Id: MGI:6149144
Age: postnatal day 10
Image: 2C
Specimen Label: 2C
Detected: false
Specimen Num: 1
Publication
First Author: Peachey NS
Year: 2012
Journal: Doc Ophthalmol
Title: Response properties of slow PIII in the Large (vls) mutant.
Volume: 125
Issue: 3
Pages: 203-9
Publication
First Author: Peachey NS
Year: 2012
Journal: J Neurophysiol
Title: Depolarizing bipolar cell dysfunction due to a Trpm1 point mutation.
Volume: 108
Issue: 9
Pages: 2442-51
Publication  
First Author: Hasan N
Year: 2020
Journal: eNeuro
Title: LRIT3 is Required for Nyctalopin Expression and Normal ON and OFF Pathway Signaling in the Retina.
Volume: 7
Issue: 1
Publication
First Author: Neuillé M
Year: 2015
Journal: Eur J Neurosci
Title: LRIT3 is essential to localize TRPM1 to the dendritic tips of depolarizing bipolar cells and may play a role in cone synapse formation.
Volume: 42
Issue: 3
Pages: 1966-75
Publication
First Author: Wang Y
Year: 2017
Journal: Neuron
Title: The Auxiliary Calcium Channel Subunit α2δ4 Is Required for Axonal Elaboration, Synaptic Transmission, and Wiring of Rod Photoreceptors.
Volume: 93
Issue: 6
Pages: 1359-1374.e6
Publication
First Author: Cao Y
Year: 2022
Journal: Curr Biol
Title: Post-developmental plasticity of the primary rod pathway allows restoration of visually guided behaviors.
Volume: 32
Issue: 22
Pages: 4783-4796.e3
Publication
First Author: Khrimian L
Year: 2017
Journal: J Exp Med
Title: Gpr158 mediates osteocalcin's regulation of cognition.
Volume: 214
Issue: 10
Pages: 2859-2873
Publication  
First Author: Gong Y
Year: 2022
Journal: Cells
Title: Peroxisome Metabolism Contributes to PIEZO2-Mediated Mechanical Allodynia.
Volume: 11
Issue: 11
Publication      
First Author: Taconic
Year: 2006
Journal: MGI Direct Data Submission
Title: Information obtained from Taconic website.
Publication      
First Author: University of California, Davis
Year: 2010
Journal: MGI Direct Data Submission
Title: Alleles produced for the KOMP project by the University of California, Davis
Publication      
First Author: International Mouse Strain Resource
Year: 2014
Journal: Database Download
Title: MGI download of germline transmission data for alleles from IMSR strain data
Publication        
First Author: MGD Nomenclature Committee
Year: 1995
Title: Nomenclature Committee Use
Publication      
First Author: Mouse Genome Informatics (MGI) and National Center for Biotechnology Information (NCBI)
Year: 2008
Journal: Database Download
Title: Mouse Gene Trap Data Load from dbGSS
Publication
First Author: Zambrowicz BP
Year: 2003
Journal: Proc Natl Acad Sci U S A
Title: Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention.
Volume: 100
Issue: 24
Pages: 14109-14
Publication        
First Author: GemPharmatech
Year: 2020
Title: GemPharmatech Website.
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2000
Title: Gene Ontology Annotation by electronic association of SwissProt Keywords with GO terms
Publication
First Author: Okazaki Y
Year: 2002
Journal: Nature
Title: Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs.
Volume: 420
Issue: 6915
Pages: 563-73
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2010
Title: Human to Mouse ISO GO annotation transfer
Publication
First Author: Diez-Roux G
Year: 2011
Journal: PLoS Biol
Title: A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Volume: 9
Issue: 1
Pages: e1000582
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2002
Title: Mouse Genome Informatics Computational Sequence to Gene Associations
Publication      
First Author: Bairoch A
Year: 1999
Journal: Database Release
Title: SWISS-PROT Annotated protein sequence database
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and Loading Genome Assembly Coordinates from Ensembl Annotations
Publication        
First Author: Mouse Genome Informatics Scientific Curators
Year: 2005
Title: Obtaining and loading genome assembly coordinates from NCBI annotations
Publication      
First Author: Mouse Genome Informatics (MGI) and The National Center for Biotechnology Information (NCBI)
Year: 2010
Journal: Database Download
Title: Consensus CDS project
Publication      
First Author: Mouse Genome Informatics
Year: 2010
Journal: Database Release
Title: Protein Ontology Association Load.
Publication      
First Author: Mouse Genome Database and National Center for Biotechnology Information
Year: 2000
Journal: Database Release
Title: Entrez Gene Load
Publication      
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Gene 1.0 ST Array Platform
Publication      
First Author: Mouse Genome Informatics Group
Year: 2003
Journal: Database Procedure
Title: Automatic Encodes (AutoE) Reference
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
Publication
First Author: Audo I
Year: 2012
Journal: Am J Hum Genet
Title: Whole-exome sequencing identifies mutations in GPR179 leading to autosomal-recessive complete congenital stationary night blindness.
Volume: 90
Issue: 2
Pages: 321-30
Allele  
Name: G protein-coupled receptor 179; no b wave 5
Allele Type: Spontaneous
Genotype
Symbol: Gpr179/Gpr179
Background: involves: C3H
Zygosity: hm
Has Mutant Allele: true
DO Term
Protein
Organism: Mus musculus/domesticus
Length: 474  
Fragment?: false
Publication
First Author: Patel N
Year: 2013
Journal: PLoS One
Title: GPR158, an orphan member of G protein-coupled receptor Family C: glucocorticoid-stimulated expression and novel nuclear role.
Volume: 8
Issue: 2
Pages: e57843
Publication
First Author: Itakura T
Year: 2019
Journal: J Ocul Pharmacol Ther
Title: GPR158 in the Visual System: Homeostatic Role in Regulation of Intraocular Pressure.
Volume: 35
Issue: 4
Pages: 203-215
Publication
First Author: Patel N
Year: 2015
Journal: PLoS One
Title: Expression and functional role of orphan receptor GPR158 in prostate cancer growth and progression.
Volume: 10
Issue: 2
Pages: e0117758
Publication    
First Author: Sutton LP
Year: 2018
Journal: Elife
Title: Orphan receptor GPR158 controls stress-induced depression.
Volume: 7
Protein Domain
Type: Family
Description: This group includes orphan receptors GPR158, GPR158-like (also called GPR179) and similar proteins. These orphan receptors are closely related to the type B receptor for gamma-aminobutyric acid (GABA-B), which is activated by its endogenous ligand GABA, the principal inhibitory neurotransmitter []. Both GPR179 and GPR158 were shown to recruit regulator of G protein signaling (RGS) complexes and thus regulate activity of other GPCRs []. GPR158 has been suggested to act as a homeostatic regulator of intraocular pressure and could be a pharmacological target for managing ocular hypertension [, ]. It has been linked to prostate cancer growth and progression []. It also serves as a novel regulator operating in the prefrontal cortex (PFC) that links chronic stress to depression []. GPR179 has been shown to play a critical role in depolarizing bipolar cell signal transduction. It is mutated in autosomal-recessive complete congenital stationary night blindness [].
Publication
First Author: Hunter DD
Year: 2019
Journal: J Comp Neurol
Title: CNS synapses are stabilized trans-synaptically by laminins and laminin-interacting proteins.
Volume: 527
Issue: 1
Pages: 67-86
Protein
Organism: Mus musculus/domesticus
Length: 1200  
Fragment?: false
Protein
Organism: Mus musculus/domesticus
Length: 631  
Fragment?: false