Gene: FBXW7 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 55294
Gene Symbol: FBXW7
FBXW7 		0.010 GeneticVariation disease BEFREE Systemic heterozygous knockin of the Fbxw7 <sup>R468C</sup> mutation resulted in perinatal lethality due to defects in lung development, and occasionally caused an eyes-open at birth phenotype and cleft palate. 29386660 2018