FBXO11, F-box protein 11, 80204

N. diseases: 93; N. variants: 619
Disease: Otitis Media ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0029882
Disease: Otitis Media
Otitis Media 		0.220 GeneticVariation disease BEFREE Single-nucleotide polymorphisms (SNPs) within FBXO11 (family-based association testing Z-Score=2.61; P(best)=0.009) were associated with severe OM in family-based analysis of 434 families (561 affected individuals) from the Western Australian Family Study of OM. 21293382 2011
CUI: C0029882
Disease: Otitis Media
Otitis Media 		0.220 Biomarker disease MGD A hearing and vestibular phenotyping pipeline to identify mouse mutants with hearing impairment. 20057387 2010
CUI: C0029882
Disease: Otitis Media
Otitis Media 		0.220 Biomarker disease MGD A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse. 17035249 2006
CUI: C0029882
Disease: Otitis Media
Otitis Media 		0.220 GeneticVariation disease LHGDN The FBXO11 gene is the human homologue of the gene mutated in the novel deaf mouse mutant jeff (Jf), a single gene model of otitis media. 16847180 2006