Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0042571
Disease: Vertigo
Vertigo
0.010 Biomarker phenotype BEFREE Women and CYP3A5*1/*1 subjects showed more often dizziness (p = 0.034; p = 0.009). 29325225 2018
CUI: C1861172
Disease: Venous Thromboembolism
Venous Thromboembolism
0.010 GeneticVariation phenotype BEFREE The objective was to investigate the impact of CYP3A5 and CYP1A2 genetic polymorphisms on the association of VTE with hormone therapy. 18628519 2008
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.040 GeneticVariation disease BEFREE Impact of CYP3A5 genetic polymorphisms on the pharmacokinetics and short-term remission in patients with ulcerative colitis treated with tacrolimus. 24033383 2014
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.040 Biomarker disease BEFREE In this study, in order to evaluate UC-specific components in UC mouse serum, we analyzed the influence of serum derived from UC mice on the results of fluorescent P450 inhibition assays based on 12 human P450 enzymes, such as CYP1A1, CYP2C8, CYP2E1,CYP3A4, CYP1A2, CYP2D6, CYP2A13, CYP2B6, CYP2C9, CYP2C18, CYP2C19, and CYP3A5. 29842871 2018
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.040 GeneticVariation disease BEFREE Because Tac response in patients who have undergone solid-organ transplantation has been associated with the presence of variants in CYP3A and ABCB1, we elucidated the contributions of CYP3A4*1B and CYP3A5*3 and of ABCB1 1236C>T, 2677G>T,A, and 3435C>T polymorphisms to Tac response in 89 patients with UC. 21289623 2011
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis
0.040 GeneticVariation disease BEFREE We investigated the correlation between CYP3A5 genetic polymorphisms and the adverse events in patients with UC. 27717793 2017
CUI: C1269955
Disease: Tumor Cell Invasion
Tumor Cell Invasion
0.010 AlteredExpression phenotype BEFREE Mechanistic investigations showed that CYP3A5 overexpression limited MMP2/9 function and suppressed HCC migration and invasion in vitro and in vivo by inhibiting AKT signaling. 25649767 2015
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.020 GeneticVariation disease BEFREE The data suggested that CYP2C19 and CYP3A5 polymorphisms affect susceptibility to paediatric TB. 22771593 2012
CUI: C0041296
Disease: Tuberculosis
Tuberculosis
0.020 GeneticVariation disease BEFREE The aim of this study was to examine the effect of two gene polymorphisms, one in the CYP2B6 (rs3745274) gene and one in the CYP3A5 (rs776746) gene, on the development of hepatotoxicity in patients treated with anti-TB drugs in a Brazilian Amazon population. 25271170 2015
CUI: C0154659
Disease: Toxic Encephalitis
Toxic Encephalitis
0.300 Therapeutic disease CTD_human Increased risk of vincristine neurotoxicity associated with low CYP3A5 expression genotype in children with acute lymphoblastic leukemia. 21225912 2011
CUI: C0087086
Disease: Thrombus
Thrombus
0.300 Biomarker phenotype CTD_human Increased risk of atherothrombotic events associated with cytochrome P450 3A5 polymorphism in patients taking clopidogrel. 16754899 2006
CUI: C0040053
Disease: Thrombosis
Thrombosis
0.300 Biomarker phenotype CTD_human Increased risk of atherothrombotic events associated with cytochrome P450 3A5 polymorphism in patients taking clopidogrel. 16754899 2006
Therapy-related acute myeloid leukemia and myelodysplastic syndrome
0.010 GeneticVariation disease BEFREE Our data do not support an association between common CYP3A4, NQO1 or CYP3A5 polymorphisms and the risk of t-ML in children treated for ALL. 12439220 2002
CUI: C0686347
Disease: Tardive Dyskinesia
Tardive Dyskinesia
0.010 Biomarker disease BEFREE Polymorphic variations in GSTM1, GSTT1, PgP, CYP2D6, CYP3A5, and dopamine D2 and D3 receptors and their association with tardive dyskinesia in severe mental illness. 16160620 2005
CUI: C0038433
Disease: Streptozotocin Diabetes
Streptozotocin Diabetes
0.200 Biomarker disease CTD_mouse Modulations of cytochrome P450 expression in diabetic mice by berberine. 22342832 2012
CUI: C0280280
Disease: stage, prostate cancer
stage, prostate cancer
0.010 GeneticVariation disease BEFREE The CYP3A5 A6986G polymorphism may be specifically associated with a decreased risk of low-grade or early stage prostate cancer. 15876487 2005
Squamous cell carcinoma of esophagus
0.020 GeneticVariation disease BEFREE However, six individual genes (including SULT2B1, CYP1B1, CYP3A7, CYP3A5, SHBG and CYP11A1) were significantly associated with ESCC risk (P < 0.05). 23358850 2013
Squamous cell carcinoma of esophagus
0.020 AlteredExpression disease BEFREE mRNA expression of CYP2E1, CYP2C, CYP3A4, and CYP3A5 was determined using RT-PCR in both normal and malignant esophageal tissues of patients with untreated esophageal SCC (n = 21) and in controls (n = 10). 17373732 2007
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.020 GeneticVariation disease BEFREE Gene-environment interaction: the role of SULT1A1 and CYP3A5 polymorphisms as risk modifiers for squamous cell carcinoma of the oesophagus. 16272171 2006
CUI: C0007137
Disease: Squamous cell carcinoma
Squamous cell carcinoma
0.020 Biomarker disease BEFREE CYP2C8, CYP3A4, CYP3A5, and CYP2E1) between SCC patients and healthy subjects and may contribute to the development of SCC in the esophagus. 17373732 2007
CUI: C0280100
Disease: Solid Neoplasm
Solid Neoplasm
0.010 Biomarker phenotype BEFREE Recently, it was published that CYP3A5 contributes to chemotherapeutic drug resistance in a wide range of solid tumors, including hepatocellular carcinoma. 31588878 2019
CUI: C0149925
Disease: Small cell carcinoma of lung
Small cell carcinoma of lung
0.010 GeneticVariation disease BEFREE Certain combined CYP3A4/CYP3A5 haplotypes show differential susceptibility to prostate cancer and there is a nonsignificant increase in the risk of small-cell lung cancer for a CYP3A5*1/*1 genotype. 16430309 2006
CUI: C0520680
Disease: Sleep Apnea, Central
Sleep Apnea, Central
0.010 Biomarker disease BEFREE CYP3A5 genotyping is a new approach to detecting FK506 dose requirement and a predictive index for the FK506 or CsA treatment selection in kidney recipients. 29113387 2017
CUI: C2939419
Disease: Secondary Neoplasm
Secondary Neoplasm
0.010 Biomarker group BEFREE In this study, we investigated whether single nucleotide polymorphisms (SNPs) identified by genome-wide association study (GWAS) (MAP3K1, FGFR2, TNRC9, HCN1, and 5p12), and SNPs involved in the metabolism of estrogen (CYP19, COMT, ESR1, and UGT1A1), tamoxifen (CYP2C9, CYP2C19, CYP3A5, and CYP2D6), and chemotherapeutic agents (ABCB1, ALDH3A1, and CYP2B6) are associated with the prognoses of 414 hormone receptor (HR)-positive early breast cancers with negative or 1 to 3 nodal metastases. 28178648 2017
Secondary malignant neoplasm of colon and/or rectum
0.010 GeneticVariation disease BEFREE CYP3A5 rs776746 A>G polymorphisms have a prognostic contribution toward FOLFIRI regimen in mCRC. 25934339 2015