Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0028754
Disease: Obesity
Obesity
0.030 GeneticVariation disease BEFREE Erythrocyte acid phosphatase (ACP locus 1), also known as low-molecular-weight protein tyrosine phosphatase, has previously been associated to glycemia, dyslipidemia, and obesity. 19570551 2009
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
0.010 GeneticVariation group BEFREE The Cardiff survey did show a significant relationship between ACP-1 genotypes and the presence or absence of congenital abnormalities, but since this was largely attributable to an excess of ACP-1 CA individuals with abnormalities, a category with a small expected value, further data are required to confirm the validity of this observation. 3208680 1989
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated
0.010 GeneticVariation group BEFREE Cardiac-specific deletion of Ndufab1 in mice caused defective bioenergetics and elevated ROS levels, leading to progressive dilated cardiomyopathy and eventual heart failure and sudden death. 31366990 2019
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis
0.010 GeneticVariation disease BEFREE p53 codon 72 polymorphism and coronary artery disease: evidence of interaction with ACP₁. 23197232 2012
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 GeneticVariation disease BEFREE p53 codon 72 polymorphism and coronary artery disease: evidence of interaction with ACP₁. 23197232 2012
CUI: C0015702
Disease: Favism
Favism
0.010 GeneticVariation disease BEFREE Association between ACP(1) genetic polymorphism and favism. 21644204 2011
CUI: C0235575
Disease: Hemolytic reaction
Hemolytic reaction
0.010 GeneticVariation phenotype BEFREE An association between favism (a hemolytic reaction to consumption of fava beans), glucose-6-phosphate dehydrogenase deficiency (G6PD(-)) and acid phosphatase locus 1 (ACP(1)) phenotypes has been reported; the frequency of carriers of the p(a) and p(c) ACP(1) alleles was found to be significantly higher in G6PD(-) individuals showing favism than in the general population. 21644204 2011
CUI: C0267026
Disease: Actinic cheilitis
Actinic cheilitis
0.010 GeneticVariation disease BEFREE Strong associations between alcoholic cirrhosis and alpha-1-antitrypsin PI*Z allele, haptoglobin HP*1 allele and acid phosphatase ACP AC phenotype were observed. 1512005 1992
CUI: C0476089
Disease: Endometrial Carcinoma
Endometrial Carcinoma
0.010 GeneticVariation disease BEFREE In this article, the authors have studied the relationship between ACP(1) genotype and grade in colon and endometrium cancers. 22692348 2012
Hereditary Nonpolyposis Colorectal Cancer
0.010 GeneticVariation disease BEFREE Because both beta-catenin and ACP gene mutations have recently been shown to activate the same signaling pathway, we analyzed beta-catenin mutation in HNPCC tumors. 10493496 1999
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 GeneticVariation disease BEFREE p53 codon 72 polymorphism and coronary artery disease: evidence of interaction with ACP₁. 23197232 2012
Deficiency of glucose-6-phosphate dehydrogenase
0.010 GeneticVariation disease BEFREE An association between favism (a hemolytic reaction to consumption of fava beans), glucose-6-phosphate dehydrogenase deficiency (G6PD(-)) and acid phosphatase locus 1 (ACP(1)) phenotypes has been reported; the frequency of carriers of the p(a) and p(c) ACP(1) alleles was found to be significantly higher in G6PD(-) individuals showing favism than in the general population. 21644204 2011
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.050 Biomarker disease BEFREE Chemical synthesis and in silico molecular modeling of novel pyrrolyl benzohydrazide derivatives: Their biological evaluation against enoyl ACP reductase (InhA) and Mycobacterium tuberculosis. 28961440 2017
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.050 Biomarker disease BEFREE The pharmacophore features were then filtered by Surflex-dock study using enoyl ACP reductase from M. tuberculosis. 27889632 2017
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.050 Biomarker disease BEFREE The site of action of isoniazid, used in the treatment of tuberculosis for 50 years, and the consumer antimicrobial agent triclosan were revealed recently to be the enoyl-ACP reductase of the type II FAS. 11591436 2001
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.050 Biomarker disease BEFREE Slow-onset inhibition of 2-trans-enoyl-ACP (CoA) reductase from Mycobacterium tuberculosis by an inorganic complex. 16842188 2006
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.050 Biomarker disease BEFREE The pentacyano(isoniazid)ferrate(II) compound, named IQG-607, inhibits the enzyme 2-trans-enoyl-ACP(CoA) reductase from M. tuberculosis, a key component in the FASII system. 29281707 2017
CUI: C0394005
Disease: Ataxic cerebral palsy
Ataxic cerebral palsy
0.040 Biomarker disease BEFREE In the absence of FXN, the NFS1-ISD11-ACP (SDA) complex was reportedly inhibited by binding of recombinant ISCU. 30031876 2018
CUI: C0394005
Disease: Ataxic cerebral palsy
Ataxic cerebral palsy
0.040 Biomarker disease BEFREE Slow-onset inhibition of 2-trans-enoyl-ACP (CoA) reductase from Mycobacterium tuberculosis by an inorganic complex. 16842188 2006
CUI: C0394005
Disease: Ataxic cerebral palsy
Ataxic cerebral palsy
0.040 Biomarker disease BEFREE In this study, we have investigated the influence of the quaternary structure of 2-trans-enoyl-ACP (CoA) reductase or InhA, from Mycobacterium tuberculosis, to its flexibility. 31548581 2019
CUI: C0431129
Disease: Adamantinous Craniopharyngioma
Adamantinous Craniopharyngioma
0.040 Biomarker disease BEFREE In the absence of FXN, the NFS1-ISD11-ACP (SDA) complex was reportedly inhibited by binding of recombinant ISCU. 30031876 2018
CUI: C0431129
Disease: Adamantinous Craniopharyngioma
Adamantinous Craniopharyngioma
0.040 Biomarker disease BEFREE Slow-onset inhibition of 2-trans-enoyl-ACP (CoA) reductase from Mycobacterium tuberculosis by an inorganic complex. 16842188 2006
CUI: C0431129
Disease: Adamantinous Craniopharyngioma
Adamantinous Craniopharyngioma
0.040 Biomarker disease BEFREE In this study, we have investigated the influence of the quaternary structure of 2-trans-enoyl-ACP (CoA) reductase or InhA, from Mycobacterium tuberculosis, to its flexibility. 31548581 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.030 Biomarker disease BEFREE Relative to white persons with dementia, African American persons with dementia were reported to have a lower preference for comfort care (81% vs. 58%) and lower rates of completion of legal ACP (89% vs. 73%). 31309906 2019
CUI: C0011265
Disease: Presenile dementia
Presenile dementia
0.030 Biomarker disease BEFREE We therefore aimed to further explore barriers and facilitators for ACP with community-dwelling people with dementia. 30115008 2018