Gene: TRIOBP ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 11078
Gene Symbol: TRIOBP
TRIOBP 		0.430 GeneticVariation phenotype BEFREE Broadening the phenotype of DFNB28: Mutations in TRIOBP are associated with moderate, stable hereditary hearing impairment. 28089734 2017
Entrez Id: 11078
Gene Symbol: TRIOBP
TRIOBP 		0.430 GeneticVariation phenotype BEFREE A delayed onset of hearing impairment due to TRIOBP pathogenic variants creates a potential therapeutic window for future targeted therapies. 29197352 2017
Entrez Id: 11078
Gene Symbol: TRIOBP
TRIOBP 		0.430 Biomarker phenotype GENOMICS_ENGLAND Actin-bundling protein TRIOBP forms resilient rootlets of hair cell stereocilia essential for hearing. 20510926 2010
Entrez Id: 11078
Gene Symbol: TRIOBP
TRIOBP 		0.430 GeneticVariation phenotype LHGDN Mutations in a novel isoform of TRIOBP that encodes a filamentous-actin binding protein are responsible for DFNB28 recessive nonsyndromic hearing loss. 16385458 2006
Entrez Id: 11078
Gene Symbol: TRIOBP
TRIOBP 		0.430 CausalMutation phenotype CLINVAR
Entrez Id: 11078
Gene Symbol: TRIOBP
TRIOBP 		0.430 GeneticVariation phenotype CLINVAR