Source: CURATED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
CUI: C4748135
Disease: INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES 		0.600 GeneticVariation UNIPROT De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies. 29796876

2018
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
CUI: C4748135
Disease: INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES 		0.600 GeneticVariation 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
CUI: C4748135
Disease: INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES 		0.600 Biomarker GENOMICS_ENGLAND De novo FBXO11 mutations are associated with intellectual disability and behavioural anomalies. 29796876

2018
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
CUI: C4748135
Disease: INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES 		0.600 GeneticVariation UNIPROT High diagnostic yield of syndromic intellectual disability by targeted next-generation sequencing. 27620904

2017
Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
CUI: C4748135
Disease: INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES 		0.600 Biomarker 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
CUI: C4748135
Disease: INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES
INTELLECTUAL DEVELOPMENTAL DISORDER WITH DYSMORPHIC FACIES AND BEHAVIORAL ABNORMALITIES 		0.600 Biomarker 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
CUI: C0079744
Disease: Diffuse Large B-Cell Lymphoma
Diffuse Large B-Cell Lymphoma 		0.320 CausalMutation CGI

Entrez Id: 80204
Gene Symbol: FBXO11
FBXO11
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		0.300 Biomarker GENOMICS_ENGLAND A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse. 17035249

2006