Homo sapiens Protein: GPR98 | |||||||||||||||||||||||
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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.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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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 |
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PFAM |
PF01825
PF00002 PF03160 |
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PRINTS |
PR00249
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PIRSF | |||||||||||||||||||||||
SMART |
SM00303
SM00237 |
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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 | ||||||||||||||||||||||