×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Hydroxykynureninuria
0.710
Biomarker
GENOMICS_ENGLAND
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
28792876
2017
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Hydroxykynureninuria
0.710
GeneticVariation
UNIPROT
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
28792876
2017
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Hydroxykynureninuria
0.710
GeneticVariation
UNIPROT
This is the first report linking xanthurenic aciduria to a mutation in the gene encoding kynureninase .
17334708
2007
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Hydroxykynureninuria
0.710
GermlineCausalMutation
ORPHANET
This is the first report linking xanthurenic aciduria to a mutation in the gene encoding kynureninase .
17334708
2007
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Hydroxykynureninuria
0.710
Biomarker
CTD_human
This is the first report linking xanthurenic aciduria to a mutation in the gene encoding kynureninase .
17334708
2007
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Hydroxykynureninuria
0.710
GeneticVariation
BEFREE
This is the first report linking xanthurenic aciduria to a mutation in the gene encoding kynureninase .
17334708
2007
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Hydroxykynureninuria
0.710
CausalMutation
CLINVAR
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2
0.600
Biomarker
GENOMICS_ENGLAND
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
28792876
2017
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2
0.600
GermlineCausalMutation
ORPHANET
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
28792876
2017
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 2
0.600
CausalMutation
CLINVAR
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Major Depressive Disorder
0.310
Biomarker
BEFREE
Here we examined circulating concentrations of inflammatory cytokines (IFN-γ, TNF-α, IL-1β, IL-6), and the acute phase protein CRP alongside plasma tryptophan, kynurenine, kynurenic acid (KYNA) and 3-hydroxyanthranilic acid (3-HAA) concentrations, and whole blood mRNA expression of IDO, kynurenine aminotransferases (KAT I and II), kynurenine-3-monooxygenase (KMO), kynureninase and SERT in patients with major depressive disorder (MDD ) compared with age and sex-matched controls.
22683764
2012
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Multiple congenital anomalies
0.300
Biomarker
GENOMICS_ENGLAND
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
28792876
2017
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Congenital malformation syndrome
0.300
Biomarker
GENOMICS_ENGLAND
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
28792876
2017
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
VERTEBRAL, CARDIAC, RENAL, AND LIMB DEFECTS SYNDROME 1
0.300
GermlineCausalMutation
ORPHANET
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
28792876
2017
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Liver Cirrhosis, Experimental
0.300
Biomarker
CTD_human
Systems level analysis and identification of pathways and networks associated with liver fibrosis.
25380136
2014
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Inflammation
0.300
Biomarker
CTD_human
Gene expression changes by amyloid beta peptide-stimulated human postmortem brain microglia identify activation of multiple inflammatory processes.
16365156
2006
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Degenerative Diseases, Central Nervous System
0.300
Biomarker
CTD_human
Gene expression changes by amyloid beta peptide-stimulated human postmortem brain microglia identify activation of multiple inflammatory processes.
16365156
2006
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Neurodegenerative Disorders
0.300
Biomarker
CTD_human
Gene expression changes by amyloid beta peptide-stimulated human postmortem brain microglia identify activation of multiple inflammatory processes.
16365156
2006
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Degenerative Diseases, Spinal Cord
0.300
Biomarker
CTD_human
Gene expression changes by amyloid beta peptide-stimulated human postmortem brain microglia identify activation of multiple inflammatory processes.
16365156
2006
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Hypertensive disease
0.210
GeneticVariation
BEFREE
After having found no association with common polymorphisms, this study aimed to assess the role of 1 rare variant of KYNU , Arg188Gln , and kynureninase activity in relation to hypertension .
22012986
2011
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Hypertensive disease
0.210
Biomarker
RGD
Kynureninase is a novel candidate gene for hypertension in spontaneously hypertensive rats.
11924719
2002
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Blood Protein Measurement
0.100
GeneticVariation
GWASCAT
Genome and epigenome wide studies of neurological protein biomarkers in the Lothian Birth Cohort 1936.
31320639
2019
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Blood Protein Measurement
0.100
GeneticVariation
GWASCAT
Co-regulatory networks of human serum proteins link genetics to disease.
30072576
2018
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Blood Protein Measurement
0.100
GeneticVariation
GWASCAT
Genomic atlas of the human plasma proteome.
29875488
2018
×
Entrez Id:
8942
Gene Symbol:
KYNU
KYNU
Congenital clubfoot
0.100
CausalMutation
CLINVAR
NAD Deficiency, Congenital Malformations, and Niacin Supplementation.
28792876
2017