Homo sapiens Protein: GPR98
Summary
InnateDB Protein IDBP-373298.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol GPR98
Protein Name G protein-coupled receptor 98
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000392618
InnateDB Gene IDBG-33218 (GPR98)
Protein Structure
UniProt Annotation
Function Receptor that may have an important role in the development of the central nervous system.
Subcellular Localization Cell membrane; Multi-pass membrane protein.
Disease Associations Usher syndrome 2C (USH2C) [MIM:605472]: USH is a genetically heterogeneous condition characterized by the association of retinitis pigmentosa with sensorineural deafness. Age at onset and differences in auditory and vestibular function distinguish Usher syndrome type 1 (USH1), Usher syndrome type 2 (USH2) and Usher syndrome type 3 (USH3). USH2 is characterized by congenital mild hearing impairment with normal vestibular responses. {ECO:0000269PubMed:14740321, ECO:0000269PubMed:22147658}. Note=The disease is caused by mutations affecting the gene represented in this entry.Febrile seizures, familial, 4 (FEB4) [MIM:604352]: Seizures associated with febrile episodes in childhood without any evidence of intracranial infection or defined pathologic or traumatic cause. It is a common condition, affecting 2-5% of children aged 3 months to 5 years. The majority are simple febrile seizures (generally defined as generalized onset, single seizures with a duration of less than 30 minutes). Complex febrile seizures are characterized by focal onset, duration greater than 30 minutes, and/or more than one seizure in a 24 hour period. The likelihood of developing epilepsy following simple febrile seizures is low. Complex febrile seizures are associated with a moderately increased incidence of epilepsy. Note=The disease may be caused by mutations affecting the gene represented in this entry.
Tissue Specificity Expressed at low levels in adult tissues. {ECO:0000269PubMed:10976914}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0004888 transmembrane signaling receptor activity
GO:0004930 G-protein coupled receptor activity
GO:0005509 calcium ion binding
GO:0005515 protein binding
Biological Process
GO:0007154 cell communication
GO:0007166 cell surface receptor signaling pathway
GO:0007186 G-protein coupled receptor signaling pathway
GO:0007218 neuropeptide signaling pathway
GO:0007399 nervous system development
GO:0007605 sensory perception of sound
GO:0016337 single organismal cell-cell adhesion
GO:0045494 photoreceptor cell maintenance
GO:0048496 maintenance of organ identity
GO:0050877 neurological system process
GO:0050953 sensory perception of light stimulus
Cellular Component
GO:0005737 cytoplasm
GO:0005886 plasma membrane
GO:0009986 cell surface
GO:0016020 membrane
GO:0016021 integral component of membrane
GO:0043235 receptor complex
GO:0070062 extracellular vesicular exosome
Protein Structure and Domains
PDB ID
InterPro IPR000203 GPS motif
IPR000832 GPCR, family 2, secretin-like
IPR003644 Na-Ca exchanger/integrin-beta4
IPR017981 GPCR, family 2-like
PFAM PF01825
PF00002
PF03160
PRINTS PR00249
PIRSF
SMART SM00303
SM00237
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8WXG9
PhosphoSite PhosphoSite-Q8WXG9
TrEMBL
UniProt Splice Variant
Entrez Gene 84059
UniGene Hs.613157
RefSeq
HUGO HGNC:17416
OMIM 602851
CCDS
HPRD 09111
IMGT
EMBL AB014586 AB075823 AC027323 AC034215 AC074132 AC093281 AC093529 AC094109 AC099512 AF055084 AF435925 AL136541
GenPept AAD55586 AAL30811 BAA31661 BAB85529 CAB66476