Source: GWASCAT

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder
0.110 GeneticVariation GWASCAT Genomic predictors of combat stress vulnerability and resilience in U.S. Marines: A genome-wide association study across multiple ancestries implicates PRTFDC1 as a potential PTSD gene. 25456346

2015

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0005890
Disease: Body Height
Body Height
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
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: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0424678
Disease: Lean body mass
Lean body mass
0.100 GeneticVariation GWASCAT Genomics of body fat percentage may contribute to sex bias in anorexia nervosa. 30593698

2019

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
Red cell distribution width determination
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
RDW - Red blood cell distribution width result
0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0040420
Disease: Tonometry
Tonometry
0.100 GeneticVariation GWASCAT Genome-wide association analyses identify new loci influencing intraocular pressure. 29617998

2018

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation
0.100 GeneticVariation GWASCAT Identification of a novel locus associated with skin colour in African-admixed populations. 28300201

2017

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0023508
Disease: White Blood Cell Count procedure
White Blood Cell Count procedure
0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0032181
Disease: Platelet Count measurement
Platelet Count measurement
0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0200633
Disease: Neutrophil count (procedure)
Neutrophil count (procedure)
0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0200635
Disease: Lymphocyte Count measurement
Lymphocyte Count measurement
0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0200637
Disease: Monocyte count procedure
Monocyte count procedure
0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0200638
Disease: Eosinophil count procedure
Eosinophil count procedure
0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0200641
Disease: Blood basophil count (lab test)
Blood basophil count (lab test)
0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0206161
Disease: Reticulocyte count (procedure)
Reticulocyte count (procedure)
0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
Red cell distribution width determination
0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0750880
Disease: Monocyte count result
Monocyte count result
0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016

Entrez Id: 56952
Gene Symbol: PRTFDC1
PRTFDC1
RDW - Red blood cell distribution width result
0.100 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252

2016