STRING 9.05 
USH1G [ENSP00000320076]
 
Usher syndrome 1G (autosomal recessive); Unknown. Required for normal hearing. May have a role in the development and maintenance of the stereocilia bundles. Might function as an anchoring/scaffolding protein in hair cells. Could be involved in the functional network formed by USH1C, CDH23 and MYO7A that is required for cohesion of the growing hair bundle
USH1C [ENSP00000005226]
 
Usher syndrome 1C (autosomal recessive, severe); May be involved in protein-protein interaction
Evidence suggesting a functional link:
Neighborhood in the Genome:  
none / insignificant.
    
Gene Fusions:  
none / insignificant.
    
Cooccurence Across Genomes:  
none / insignificant.
    
Co-Expression:  
none / insignificant.
    
Experimental/Biochemical Data:   yes (score 0.983). In addition, putative homologs were found interacting in other species (score 0.257).  
Association in Curated Databases:  
none / insignificant.
    
Co-Mentioned in PubMed Abstracts:   yes (score 0.870).  
Combined Score:
 
0.998
 
Evidence for specific actions:
Binding:yes (score: 0.970)