PLCZ1, phospholipase C zeta 1, 89869

N. diseases: 5; N. variants: 1
Disease: SPERMATOGENIC FAILURE 17 ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C4310666
Disease: SPERMATOGENIC FAILURE 17
SPERMATOGENIC FAILURE 17 		0.500 GeneticVariation disease UNIPROT Homozygous mutation of PLCZ1 leads to defective human oocyte activation and infertility that is not rescued by the WW-binding protein PAWP. 26721930 2016
CUI: C4310666
Disease: SPERMATOGENIC FAILURE 17
SPERMATOGENIC FAILURE 17 		0.500 Biomarker disease CTD_human