Gene: TUBB3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 10381
Gene Symbol: TUBB3
TUBB3 		0.900 Biomarker disease GENOMICS_ENGLAND Clinical heterogeneity associated with TUBB3 gene mutation in a Turkish family with congenital fibrosis of the extraocular muscles. 27428177 2017
Entrez Id: 10381
Gene Symbol: TUBB3
TUBB3 		0.900 CausalMutation disease CLINVAR Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance. 20074521 2010
Entrez Id: 10381
Gene Symbol: TUBB3
TUBB3 		0.900 Biomarker disease MGD Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance. 20074521 2010
Entrez Id: 10381
Gene Symbol: TUBB3
TUBB3 		0.900 GeneticVariation disease UNIPROT Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance. 20074521 2010
Entrez Id: 10381
Gene Symbol: TUBB3
TUBB3 		0.900 Biomarker disease GENOMICS_ENGLAND Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects. 20829227 2010
Entrez Id: 10381
Gene Symbol: TUBB3
TUBB3 		0.900 GeneticVariation disease CLINVAR
Entrez Id: 10381
Gene Symbol: TUBB3
TUBB3 		0.900 Biomarker disease CTD_human