Gene: MEIOB ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 254528
Gene Symbol: MEIOB
MEIOB 		0.010 GeneticVariation disease BEFREE A truncating MEIOB mutation responsible for familial primary ovarian insufficiency abolishes its interaction with its partner SPATA22 and their recruitment to DNA double-strand breaks. 31000419 2019