Gene: FBXO28 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23219
Gene Symbol: FBXO28
FBXO28 		0.010 GeneticVariation phenotype BEFREE A novel FBXO28 frameshift mutation in a child with developmental delay, dysmorphic features, and intractable epilepsy: A second gene that may contribute to the 1q41-q42 deletion phenotype. 30160831 2018