HAP1, huntingtin associated protein 1, 9001

N. diseases: 65; N. variants: 2
Disease: Congenital failure of fusion ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0332915
Disease: Congenital failure of fusion
Congenital failure of fusion 		0.010 Biomarker disease BEFREE Loss of HAPLESS 2/GENERATIVE CELL SPECIFIC 1 (HAP2/GCS1) proteins results in gamete fusion failure in diverse organisms, but their exact role is unclear. 28137780 2017