Gene: TUBB2B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 347733
Gene Symbol: TUBB2B
TUBB2B 		0.310 GeneticVariation disease BEFREE These observations led us to ask whether axon dysinnervation is a primary phenotype, and why the E421K, but not other, TUBB2B substitutions cause CFEOM. 23001566 2012
Entrez Id: 347733
Gene Symbol: TUBB2B
TUBB2B 		0.310 GermlineCausalMutation disease ORPHANET These observations led us to ask whether axon dysinnervation is a primary phenotype, and why the E421K, but not other, TUBB2B substitutions cause CFEOM. 23001566 2012