Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C4225234
Disease: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn 		0.710 CausalMutation CLINVAR

Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.160 GeneticVariation GWASCAT Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank data. 30664745

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.160 GeneticVariation GWASCAT Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. 29483656

2018
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.160 GeneticVariation GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764

2015
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0740279
Disease: Cerebellar atrophy
Cerebellar atrophy 		0.120 Biomarker HPO

Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0018801
Disease: Heart failure
Heart failure 		0.110 GeneticVariation GWASCAT Pleiotropic Meta-Analyses of Longitudinal Studies Discover Novel Genetic Variants Associated with Age-Related Diseases. 27790247

2016
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0013336
Disease: Dwarfism
Dwarfism 		0.110 Biomarker HPO

Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0013421
Disease: Dystonia
Dystonia 		0.110 Biomarker HPO

Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0001948
Disease: Alcohol consumption
Alcohol consumption 		0.100 GeneticVariation GWASCAT Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. 30698716

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic 		0.100 GeneticVariation GWASCAT Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. 30940813

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0005890
Disease: Body Height
Body Height 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0013595
Disease: Eczema
Eczema 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0014772
Disease: Red Blood Cell Count measurement
Red Blood Cell Count measurement 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0021704
Disease: Intelligence
Intelligence 		0.100 GeneticVariation GWASCAT A combined analysis of genetically correlated traits identifies 187 loci and a role for neurogenesis and myelination in intelligence. 29326435

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0236664
Disease: Alcohol-Related Disorders
Alcohol-Related Disorders 		0.100 GeneticVariation GWASCAT Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. 30940813

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0236970
Disease: Alcohol-Induced Disorders
Alcohol-Induced Disorders 		0.100 GeneticVariation GWASCAT Genome-wide association study of alcohol consumption and use disorder in 274,424 individuals from multiple populations. 30940813

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.100 GeneticVariation GWASCAT Multiancestry Genome-Wide Association Study of Lipid Levels Incorporating Gene-Alcohol Interactions. 30698716

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies genetic loci for self-reported habitual sleep duration supported by accelerometer-derived estimates. 30846698

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0427460
Disease: Red cell distribution width determination
Red cell distribution width determination 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.100 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0518026
Disease: body fat percentage (physical finding)
body fat percentage (physical finding) 		0.100 GeneticVariation GWASCAT Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. 30593698

2019
Entrez Id: 64116
Gene Symbol: SLC39A8
SLC39A8
CUI: C0871470
Disease: Systolic Pressure
Systolic Pressure 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019