ACYP2, acylphosphatase 2, 98

N. diseases: 42; N. variants: 20
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
HEARING LOSS, CISPLATIN-INDUCED, SUSCEPTIBILITY TO
0.300 Biomarker disease CTD_human Common variants in ACYP2 influence susceptibility to cisplatin-induced hearing loss. 25665007 2015
CUI: C0005890
Disease: Body Height
Body Height
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C2985280
Disease: Blood Protein Measurement
Blood Protein Measurement
0.100 GeneticVariation phenotype GWASCAT Co-regulatory networks of human serum proteins link genetics to disease. 30072576 2018
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms
0.100 GeneticVariation phenotype GWASCAT Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. 28604731 2017
High density lipoprotein measurement
0.100 GeneticVariation phenotype GWASCAT Exome-wide association study of plasma lipids in >300,000 individuals. 29083408 2017
CUI: C0008810
Disease: Circadian Rhythms
Circadian Rhythms
0.100 GeneticVariation phenotype GWASCAT Genome-Wide Association Analyses in 128,266 Individuals Identifies New Morningness and Sleep Duration Loci. 27494321 2016
CUI: C0085298
Disease: Sudden Cardiac Death
Sudden Cardiac Death
0.100 GeneticVariation phenotype GWASCAT GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
CUI: C1720824
Disease: Sudden Cardiac Arrest
Sudden Cardiac Arrest
0.100 GeneticVariation phenotype GWASDB GWAS for discovery and replication of genetic loci associated with sudden cardiac arrest in patients with coronary artery disease. 21658281 2011
CUI: C0008707
Disease: Chronic osteomyelitis
Chronic osteomyelitis
0.100 GeneticVariation disease CLINVAR
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 GeneticVariation group BEFREE Meta-analysis shown that ACYP2 rs1682111 was associated with the risk of cancer (OR = 0.90, 95% CI: 0.78-1.05, p = 0.02). 31124313 2019
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 Biomarker disease BEFREE It has been reported that ACYP2 gene was associated with the development of gastric cancer and colorectal cancer, but it is not clear that the relationship between ACYP2 gene and GI cancer in Chinese Han population. 31070019 2019
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 GeneticVariation group BEFREE Meta-analysis shown that ACYP2 rs1682111 was associated with the risk of cancer (OR = 0.90, 95% CI: 0.78-1.05, p = 0.02). 31124313 2019
Malignant neoplasm of colon and/or rectum
0.020 Biomarker disease BEFREE It has been reported that ACYP2 gene was associated with the development of gastric cancer and colorectal cancer, but it is not clear that the relationship between ACYP2 gene and GI cancer in Chinese Han population. 31070019 2019
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 GeneticVariation disease BEFREE Single Nucleotide Polymorphisms in the Acylphosphatase 2 Gene and The SNP-SNP Interactions on the Risk of Breast Cancer in Chinese Han Women. 29033240 2018
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 GeneticVariation disease BEFREE Single Nucleotide Polymorphisms in the Acylphosphatase 2 Gene and The SNP-SNP Interactions on the Risk of Breast Cancer in Chinese Han Women. 29033240 2018
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 GeneticVariation group BEFREE We investigated the association between single nucleotide polymorphisms (SNPs) in ACYP2, which has been associated with telomere length in several types of cancer, and the risk of CRC in a Chinese Han population. 28039478 2017
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma
0.020 GeneticVariation disease BEFREE Genetic polymorphisms in the telomere length-related gene ACYP2 are associated with the risk of colorectal cancer in a Chinese Han population. 28039478 2017
CUI: C0340100
Disease: High altitude pulmonary edema
High altitude pulmonary edema
0.020 GeneticVariation disease BEFREE The CC genotype of rs17045754 had a protect effect on HAPE patients, and it was found to have a 0.29-fold reduced risk of HAPE in the recessive model.Although additional, larger population-based studies are needed to confirm these findings, our study shed light on the association between ACYP2 variant and HAPE risk in Han Chinese population for the first time. 28353602 2017
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 GeneticVariation group BEFREE We investigated the association between single nucleotide polymorphisms (SNPs) in ACYP2, which has been associated with telomere length in several types of cancer, and the risk of CRC in a Chinese Han population. 28039478 2017
Malignant neoplasm of colon and/or rectum
0.020 GeneticVariation disease BEFREE Genetic polymorphisms in the telomere length-related gene ACYP2 are associated with the risk of colorectal cancer in a Chinese Han population. 28039478 2017
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
0.020 GeneticVariation group BEFREE The variant rs1872328 in the ACYP2 gene was recently identified as a risk factor for the development of cisplatin-induced ototoxicity in children with brain tumors. 26928270 2016
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 GeneticVariation disease BEFREE In sum, our findings reveal significant associations between SNPs in the ACYP2 gene and BC risk in a Han Chinese population. 27894080 2016
CUI: C0340100
Disease: High altitude pulmonary edema
High altitude pulmonary edema
0.020 GeneticVariation disease BEFREE The present study aimed to determine whethher there is any association between ACYP2 polymorphism and the risk of HAPE. 27552709 2016
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 GeneticVariation disease BEFREE In sum, our findings reveal significant associations between SNPs in the ACYP2 gene and BC risk in a Han Chinese population. 27894080 2016
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms
0.020 GeneticVariation group BEFREE Taking a genome-wide association study approach, we identified inherited genetic variations in ACYP2 associated with cisplatin-related ototoxicity (rs1872328: P = 3.9 × 10(-8), hazard ratio = 4.5) in 238 children with newly diagnosed brain tumors, with independent replication in 68 similarly treated children. 25665007 2015