Source: INFERRED

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0857379
Disease: Abnormality of the pinna
Abnormality of the pinna 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
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: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement 		0.100 GeneticVariation GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576

2018
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0426429
Disease: Broad nasal tip
Broad nasal tip 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C1611184
Disease: Calcification of coronary artery
Calcification of coronary artery 		0.100 GeneticVariation GWASCAT Novel Loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis. 22916037

2012
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.100 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370

2019
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		0.100 GeneticVariation GWASDB Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia. 18179892

2008
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C3810365
Disease: Central visual impairment
Central visual impairment 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.100 GeneticVariation GWASCAT Association analyses identify 38 susceptibility loci for inflammatory bowel disease and highlight shared genetic risk across populations. 26192919

2015
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.100 CausalMutation CLINVAR The Rac activator DOCK7 regulates neuronal polarity through local phosphorylation of stathmin/Op18. 16982419

2006
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.100 GeneticVariation CLINVAR The Rac activator DOCK7 regulates neuronal polarity through local phosphorylation of stathmin/Op18. 16982419

2006
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.100 CausalMutation CLINVAR Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness. 24814191

2014
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0432072
Disease: Dysmorphic features
Dysmorphic features 		0.100 GeneticVariation CLINVAR Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical blindness. 24814191

2014
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy 		0.110 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C4014492
Disease: EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23
EPILEPTIC ENCEPHALOPATHY, EARLY INFANTILE, 23 		0.700 CausalMutation CLINVAR

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0557874
Disease: Global developmental delay
Global developmental delay 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
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: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.100 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531

2018
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C1857970
Disease: Hypobetalipoproteinemia, Familial, 2
Hypobetalipoproteinemia, Familial, 2 		0.100 CausalMutation CLINVAR

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0344482
Disease: Hypoplasia of corpus callosum
Hypoplasia of corpus callosum 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C1848529
Disease: Hypoplasia of the pons
Hypoplasia of the pons 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia 		0.100 Biomarker HPO

Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.100 GeneticVariation GWASDB Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219

2012
Entrez Id: 85440
Gene Symbol: DOCK7
DOCK7
CUI: C0523744
Disease: Lipids measurement
Lipids measurement 		0.100 GeneticVariation GWASCAT Genome-wide association study identifies multiple loci influencing human serum metabolite levels. 22286219

2012