Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.600 GeneticVariation disease UNIPROT De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies. 29796876 2018
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.600 GeneticVariation disease UNIPROT De Novo Variants in the F-Box Protein FBXO11 in 20 Individuals with a Variable Neurodevelopmental Disorder. 30057029 2018
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.600 Biomarker disease GENOMICS_ENGLAND De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies. 29796876 2018
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.600 GeneticVariation disease UNIPROT High diagnostic yield of syndromic intellectual disability by targeted next-generation sequencing. 27620904 2017
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.600 Biomarker disease GENOMICS_ENGLAND Diagnostic Yield and Novel Candidate Genes by Exome Sequencing in 152 Consanguineous Families With Neurodevelopmental Disorders. 28097321 2017
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.600 Biomarker disease GENOMICS_ENGLAND A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse. 17035249 2006
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11 		0.600 CausalMutation disease CLINVAR
Entrez Id: 2956
Gene Symbol: MSH6
MSH6 		0.100 CausalMutation disease CLINVAR