AADAT, aminoadipate aminotransferase, 51166

N. diseases: 19; N. variants: 1
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.300 Biomarker disease CTD_human Computational Discovery of Niclosamide Ethanolamine, a Repurposed Drug Candidate That Reduces Growth of Hepatocellular Carcinoma Cells In Vitro and in Mice by Inhibiting Cell Division Cycle 37 Signaling. 28284560 2017
CUI: C0023893
Disease: Liver Cirrhosis, Experimental
Liver Cirrhosis, Experimental
0.300 Biomarker disease CTD_human Systems level analysis and identification of pathways and networks associated with liver fibrosis. 25380136 2014
CUI: C0341747
Disease: Detrusor and sphincter dyssynergia
Detrusor and sphincter dyssynergia
0.020 GeneticVariation disease BEFREE To investigate the effect of replication-defective herpes simplex virus (HSV) vectors encoding the kynurenine aminotransferase II (HSVrd-KATII) gene on detrusor-sphincter dyssynergia (DSD) in spinal cord injury (SCI) rats. 27995942 2017
CUI: C0341747
Disease: Detrusor and sphincter dyssynergia
Detrusor and sphincter dyssynergia
0.020 Biomarker disease BEFREE KAT II gene therapy effectively reduced the urethral pressure, improving detrusor-sphincter dyssynergia (DSD), and detrusor overactivity (DO), probably by blocking the N-methyl-D-aspartate receptor (NMDAr) in the L6-S1 spinal . 27391207 2017
CUI: C2930619
Disease: Sex Differentiation Disorders
Sex Differentiation Disorders
0.020 Biomarker group BEFREE KAT II gene therapy effectively reduced the urethral pressure, improving detrusor-sphincter dyssynergia (DSD), and detrusor overactivity (DO), probably by blocking the N-methyl-D-aspartate receptor (NMDAr) in the L6-S1 spinal . 27391207 2017
CUI: C2930619
Disease: Sex Differentiation Disorders
Sex Differentiation Disorders
0.020 GeneticVariation group BEFREE To investigate the effect of replication-defective herpes simplex virus (HSV) vectors encoding the kynurenine aminotransferase II (HSVrd-KATII) gene on detrusor-sphincter dyssynergia (DSD) in spinal cord injury (SCI) rats. 27995942 2017
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.010 AlteredExpression disease BEFREE Expression of KAT2 mRNA was enhanced in patients with UC and in patients with CD in remission. 31666808 2019
CUI: C0010346
Disease: Crohn Disease
Crohn Disease
0.010 AlteredExpression disease BEFREE Expression of KAT2 mRNA was enhanced in patients with UC and in patients with CD in remission. 31666808 2019
CUI: C0036341
Disease: Schizophrenia
Schizophrenia
0.010 Biomarker disease BEFREE Therefore, KAT2 could be exploited as a therapeutic target for the management of schizophrenia. 31308447 2019
CUI: C0233794
Disease: Memory impairment
Memory impairment
0.010 GeneticVariation phenotype BEFREE Acute administration of BFF816, a systemically active inhibitor of kynurenine aminotransferase II (KAT II), the major KYNA-synthesizing enzyme in the brain, normalized neurochemistry and prevented contextual memory deficits in adult EKyn animals. 30311334 2019
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.010 GeneticVariation disease BEFREE In this work, we assessed the relationship between single-nucleotide polymorphisms (SNPs) of KAT1, KAT2 and IDO1 gene encoding, and the risk of depression development. 29777939 2018
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.010 GeneticVariation disease BEFREE In this work, we assessed the relationship between single-nucleotide polymorphisms (SNPs) of KAT1, KAT2 and IDO1 gene encoding, and the risk of depression development. 29777939 2018
CUI: C0344315
Disease: Depressed mood
Depressed mood
0.010 GeneticVariation phenotype BEFREE In this work, we assessed the relationship between single-nucleotide polymorphisms (SNPs) of KAT1, KAT2 and IDO1 gene encoding, and the risk of depression development. 29777939 2018
CUI: C1510586
Disease: Autism Spectrum Disorders
Autism Spectrum Disorders
0.010 GeneticVariation disease BEFREE The novel de novo splice alteration c.664 + 2T > G in the DEAF1 gene and the novel de novo missense mutation c.95 C > T in the AADAT gene associated with ASD may be important clues for exploring the etiology of this disorder. 29366832 2018
CUI: C0019348
Disease: Herpes Simplex Infections
Herpes Simplex Infections
0.010 GeneticVariation group BEFREE To investigate the effect of replication-defective herpes simplex virus (HSV) vectors encoding the kynurenine aminotransferase II (HSVrd-KATII) gene on detrusor-sphincter dyssynergia (DSD) in spinal cord injury (SCI) rats. 27995942 2017
CUI: C0004936
Disease: Mental disorders
Mental disorders
0.010 Biomarker group BEFREE Reducing KYNA production through inhibiting kynurenine aminotransferase 2 (KAT2) would be a promising approach to understanding and treating the related neurological and mental disorders. 26773745 2016
CUI: C0019693
Disease: HIV Infections
HIV Infections
0.010 GeneticVariation group BEFREE The relationships between polymorphisms in KMO and KATII, psychopathological symptoms, and cerebrospinal fluid (CSF) [KYNA] were evaluated in subjects with and without HIV-infection. 27072370 2016
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.010 Biomarker group BEFREE We transfected A-431 tumour cells with the far red-emitting protein Katushka (Kat2), resulting in strong fluorescence allowing for the monitoring of tumour growth when implanted in BALB/c nu/nu mice with a CRi Maestro in vivo imager. 22350071 2012
CUI: C0025289
Disease: Meningitis
Meningitis
0.010 GeneticVariation disease BEFREE Association of kynurenine aminotransferase II gene C401T polymorphism with immune response in patients with meningitis. 21473761 2011
CUI: C0085437
Disease: Meningitis, Bacterial
Meningitis, Bacterial
0.010 GeneticVariation group BEFREE A significant decrease (p < 0.05) in TNF-α, IL-1β, IL-6, MIP-1αCCL3 and MIP-1β/CCL4 levels was observed in BM patients homozygous (TT) to the SNP AADAT+401C/T. 21473761 2011
CUI: C0020179
Disease: Huntington Disease
Huntington Disease
0.010 AlteredExpression disease BEFREE Genomic organization and expression analysis of mouse kynurenine aminotransferase II, a possible factor in the pathophysiology of Huntington's disease. 10441733 1999