Gene: MID1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4281
Gene Symbol: MID1
MID1 		0.010 GeneticVariation group BEFREE Mutations of human MID1 are associated with X-linked Opitz G Syndrome (XLOS), which is characterized by midline birth defects. 28548391 2017