Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 22917
Gene Symbol: ZP1
ZP1
CUI: C4014291
Disease: OOCYTE MATURATION DEFECT 1
OOCYTE MATURATION DEFECT 1 		0.600 GermlineCausalMutation ORPHANET Mutant ZP1 in familial infertility. 24670168

2014
Entrez Id: 22917
Gene Symbol: ZP1
ZP1
CUI: C4014291
Disease: OOCYTE MATURATION DEFECT 1
OOCYTE MATURATION DEFECT 1 		0.600 Biomarker CTD_human

Entrez Id: 22917
Gene Symbol: ZP1
ZP1
CUI: C4014291
Disease: OOCYTE MATURATION DEFECT 1
OOCYTE MATURATION DEFECT 1 		0.600 CausalMutation CLINVAR

Entrez Id: 22917
Gene Symbol: ZP1
ZP1
CUI: C4540205
Disease: OOCYTE MATURATION DEFECT 3
OOCYTE MATURATION DEFECT 3 		0.300 GermlineCausalMutation ORPHANET Mutant ZP1 in familial infertility. 24670168

2014
Entrez Id: 22917
Gene Symbol: ZP1
ZP1
CUI: C0523465
Disease: Serum albumin measurement
Serum albumin measurement 		0.100 GeneticVariation GWASDB A genome-wide assessment of variability in human serum metabolism. 23281178

2013
Entrez Id: 22917
Gene Symbol: ZP1
ZP1
CUI: C0021359
Disease: Infertility
Infertility 		0.100 Biomarker HPO

Entrez Id: 22917
Gene Symbol: ZP1
ZP1
CUI: C1328577
Disease: Empty follicle syndrome
Empty follicle syndrome 		0.010 GeneticVariation BEFREE We thus propose that the specific mutations in ZP1 gene render a causality for the intractable EFS. 31292994

2019