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MGI:Gpr98

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Contents

Species (Taxon ID) Mus musculus (house mouse) (taxon:10090)
Gene Name(s) Gpr98 ( synonyms: Mass1, Mgr1, VLGR1 )
Protein Name(s) G protein-coupled receptor 98,
External Links
MGI MGI:1274784

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0002142

stereocilia ankle link complex

MGI:MGI:3714249
PMID:17567809[1]

IDA: Inferred from Direct Assay

C

From MGI

GO:0004871

signal transducer activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0807

F

From MGI

GO:0004872

receptor activity

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0675

F

From MGI

GO:0004888

transmembrane signaling receptor activity

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR017981

F

From MGI

GO:0004930

G-protein coupled receptor activity

MGI:MGI:2156124
PMID:11606593[2]

NAS: Non-traceable Author Statement

F

From MGI

GO:0005509

calcium ion binding

MGI:MGI:2156124
PMID:11606593[2]

NAS: Non-traceable Author Statement

F

From MGI

GO:0005509

calcium ion binding

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8WXG9

F

From MGI

GO:0005576

extracellular region

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0964

C

From MGI

GO:0005737

cytoplasm

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8WXG9

C

From MGI

GO:0005886

plasma membrane

MGI:MGI:3629345
PMID:16775142[3]

IDA: Inferred from Direct Assay

C

From MGI

GO:0007154

cell communication

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR003644

P

From MGI

GO:0007165

signal transduction

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0807

P

From MGI

GO:0007166

cell surface receptor signaling pathway

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR017981

P

From MGI

GO:0007218

neuropeptide signaling pathway

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR000203

P

From MGI

GO:0007275

multicellular organismal development

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0217

P

From MGI

GO:0007399

nervous system development

MGI:MGI:2156124
PMID:11606593[2]

NAS: Non-traceable Author Statement

P

From MGI

GO:0007601

visual perception

MGI:MGI:3629345
PMID:16775142[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3046273

P

From MGI

GO:0007605

sensory perception of sound

MGI:MGI:3575610
PMID:15820310[4]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389570

P

From MGI

GO:0007605

sensory perception of sound

MGI:MGI:3695056
PMID:16137990[5]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389570

P

From MGI

GO:0007605

sensory perception of sound

MGI:MGI:3703302
PMID:17329413[6]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3708270

P

From MGI

GO:0007605

sensory perception of sound

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8WXG9

P

From MGI

GO:0009986

cell surface

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8WXG9

C

From MGI

GO:0016020

membrane

MGI:MGI:2156124
PMID:11606593[2]

NAS: Non-traceable Author Statement

C

From MGI

GO:0016021

integral to membrane

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0812

C

From MGI

GO:0016021

integral to membrane

MGI:MGI:2152098

IEA: Inferred from Electronic Annotation

InterPro:IPR003644
InterPro:IPR000832

C

From MGI

GO:0016337

cell-cell adhesion

MGI:MGI:2156124
PMID:11606593[2]

NAS: Non-traceable Author Statement

P

From MGI

GO:0017022

myosin binding

MGI:MGI:3714249
PMID:17567809[1]

IPI: Inferred from Physical Interaction

UniProtKB:P97479

F

From MGI

GO:0045494

photoreceptor cell maintenance

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8WXG9

P

From MGI

GO:0048496

maintenance of organ identity

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8WXG9

P

From MGI

GO:0048839

inner ear development

MGI:MGI:3629345
PMID:16775142[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3046273

P

From MGI

GO:0050877

neurological system process

MGI:MGI:2149857
PMID:11545713[7]

IMP: Inferred from Mutant Phenotype

MGI:MGI:2389570

P

From MGI

GO:0050877

neurological system process

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8WXG9

P

From MGI

GO:0050896

response to stimulus

MGI:MGI:1354194

IEA: Inferred from Electronic Annotation

UniProtKB-KW:KW-0716

P

From MGI

GO:0050910

detection of mechanical stimulus involved in sensory perception of sound

MGI:MGI:3629345
PMID:16775142[3]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3046273

P

From MGI

GO:0050953

sensory perception of light stimulus

MGI:MGI:4834177

ISO: Inferred from Sequence Orthology

UniProtKB:Q8WXG9

P

From MGI

GO:0060122

inner ear receptor stereocilium organization

MGI:MGI:3714249
PMID:17567809[1]

IMP: Inferred from Mutant Phenotype

MGI:MGI:3527179

P

From MGI


Notes

References

See Help:References for how to manage references in GONUTS.
  1. 1.0 1.1 1.2 Michalski N et al. (2007) Molecular characterization of the ankle-link complex in cochlear hair cells and its role in the hair bundle functioning. J Neurosci 27: 6478-88 PubMed GONUTS page
  2. 2.0 2.1 2.2 2.3 2.4 McMillan DR et al. (2002) Very large G protein-coupled receptor-1, the largest known cell surface protein, is highly expressed in the developing central nervous system. J Biol Chem 277: 785-92 PubMed GONUTS page
  3. 3.0 3.1 3.2 3.3 McGee J et al. (2006) The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles. J Neurosci 26: 6543-53 PubMed GONUTS page
  4. Johnson KR et al. (2005) The Mass1frings mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC. Genomics 85: 582-90 PubMed GONUTS page
  5. Klein BD et al. (2005) Auditory deficits associated with the frings mgr1 (mass1) mutation in mice. Dev Neurosci 27: 321-32 PubMed GONUTS page
  6. Schwander M et al. (2007) A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function. J Neurosci 27: 2163-75 PubMed GONUTS page
  7. Skradski SL et al. (2001) A novel gene causing a mendelian audiogenic mouse epilepsy. Neuron 31: 537-44 PubMed GONUTS page
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