Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.110 GeneticVariation GWASCAT Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes. 29221444

2017
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma 		0.110 GeneticVariation GWASCAT Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer. 29059430

2017
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
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: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0021704
Disease: Intelligence
Intelligence 		0.100 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203

2019
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.100 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203

2019
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.100 GeneticVariation GWASCAT Genetic architecture of human plasma lipidome and its link to cardiovascular disease. 31551469

2019
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C1305855
Disease: Body mass index
Body mass index 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0021704
Disease: Intelligence
Intelligence 		0.100 GeneticVariation GWASCAT Study of 300,486 individuals identifies 148 independent genetic loci influencing general cognitive function. 29844566

2018
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0022661
Disease: Kidney Failure, Chronic
Kidney Failure, Chronic 		0.100 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		0.100 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117

2018
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0596887
Disease: mathematical ability
mathematical ability 		0.100 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396

2018
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C1561643
Disease: Chronic Kidney Diseases
Chronic Kidney Diseases 		0.100 GeneticVariation GWASCAT Genome-Wide Association Studies of Metabolites in Patients with CKD Identify Multiple Loci and Illuminate Tubular Transport Mechanisms. 29545352

2018
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C1837461
Disease: SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3
SCOLIOSIS, ISOLATED, SUSCEPTIBILITY TO, 3 		0.100 GeneticVariation GWASCAT The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease. 30019117

2018
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0278704
Disease: Malignant Childhood Neoplasm
Malignant Childhood Neoplasm 		0.100 GeneticVariation GWASCAT Genome-Wide Association Study to Identify Susceptibility Loci That Modify Radiation-Related Risk for Breast Cancer After Childhood Cancer. 29059430

2017
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0428883
Disease: Diastolic blood pressure
Diastolic blood pressure 		0.100 GeneticVariation GWASCAT Genome-wide association analyses using electronic health records identify new loci influencing blood pressure variation. 27841878

2017
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.100 GeneticVariation GWASCAT Genome-wide association study of coronary artery calcified atherosclerotic plaque in African Americans with type 2 diabetes. 29221444

2017
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0011615
Disease: Dermatitis, Atopic
Dermatitis, Atopic 		0.100 GeneticVariation GWASCAT Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms. 25574825

2015
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.100 GeneticVariation GWASCAT Genome-wide comparative analysis of atopic dermatitis and psoriasis gives insight into opposing genetic mechanisms. 25574825

2015
Entrez Id: 5799
Gene Symbol: PTPRN2
PTPRN2
CUI: C0154778
Disease: Myopia, Degenerative
Myopia, Degenerative 		0.100 GeneticVariation GWASCAT A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French Population. 23049088

2012