Source: CURATED ×
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0242706
Disease: Hyperoxia
Hyperoxia
0.500 Biomarker phenotype CTD_human Mice deficient in the gene for cytochrome P450 (CYP)1A1 are more susceptible than wild-type to hyperoxic lung injury: evidence for protective role of CYP1A1 against oxidative stress. 24893714 2014
CUI: C0011853
Disease: Diabetes Mellitus, Experimental
Diabetes Mellitus, Experimental
0.500 Biomarker disease CTD_human Modulations of cytochrome P450 expression in diabetic mice by berberine. 22342832 2012
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.400 Biomarker group CTD_human Elevated blood pressure in cytochrome P4501A1 knockout mice is associated with reduced vasodilation to omega-3 polyunsaturated fatty acids. 22995157 2012
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.400 Biomarker group CTD_human Because TCDD induces cytochrome P4501A1 (CYP1A1) and CYP1A1 can increase ROS, we tested the hypothesis that TCDD-induced endothelial dysfunction and hypertension are mediated by CYP1A1. 20634294 2010
CUI: C0021364
Disease: Male infertility
Male infertility
0.400 Biomarker phenotype CTD_human Negative effects of serum p,p'-DDE on sperm parameters and modification by genetic polymorphisms. 19303595 2009
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.400 Biomarker disease CTD_human In conclusion, our study demonstrated that exon 3 of mEH and CYP1A1 T/C gene polymorphism are predisposing risk factors for susceptibility of sporadic PCa in northern India. 17919073 2007
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.400 Biomarker disease CTD_human Compared with women who had homozygous wild-type CYP1A1 m2 genotype, significantly increased risks of breast cancer were found for women with the CYP1A1 m2 homozygous variant genotype [odds ratio (OR) = 2.61, 95% confidence interval (CI): 1.00 - 6.80]. 16792888 2006
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.400 Biomarker disease CTD_human Compared with women who had homozygous wild-type CYP1A1 m2 genotype, significantly increased risks of breast cancer were found for women with the CYP1A1 m2 homozygous variant genotype [odds ratio (OR) = 2.61, 95% confidence interval (CI): 1.00 - 6.80]. 16792888 2006
CUI: C1458155
Disease: Mammary Neoplasms
Mammary Neoplasms
0.400 Biomarker group CTD_human [Study on serum organochlorines pesticides (DDTs) level, CYP1A1 genetic polymorphism and risk of breast cancer: a case control study]. 16792888 2006
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma
0.400 Biomarker disease CTD_human We found that the risk of HCC was elevated in women harboring either heterozygous or homozygous variants of the CYP1A1 gene and the respective OR (and 95% confidence interval) were 6.61 (1.35, 32.43) and 12.00 (1.73, 83.46). 15341023 2004
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate
0.400 Biomarker disease CTD_human This study suggests that the CYP1A1 polymorphism and its combination with GSTM1 may be associated with PCa susceptibility in the Japanese population. 11275366 2001
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease
0.370 Biomarker disease CTD_human Relation of PON1 and CYP1A1 genetic polymorphisms to clinical findings in a cross-sectional study of a Greek rural population professionally exposed to pesticides. 19022366 2009
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms
0.370 Biomarker group CTD_human Cytochrome P4501A1 and microsomal epoxide hydrolase gene polymorphisms: gene-environment interaction and risk of prostate cancer. 17919073 2007
CUI: C0033578
Disease: Prostatic Neoplasms
Prostatic Neoplasms
0.370 Biomarker group CTD_human Genetic polymorphisms in cytochrome P450 (CYP) 1A1, CYP1A2, CYP2E1, glutathione S-transferase (GST) M1 and GSTT1 and susceptibility to prostate cancer in the Japanese population. 11275366 2001
CUI: C4552766
Disease: Miscarriage
Miscarriage
0.330 Biomarker disease CTD_human Potential involvement of placental AhR in unexplained recurrent spontaneous abortion. 26593447 2016
CUI: C4552766
Disease: Miscarriage
Miscarriage
0.330 Biomarker disease CTD_human The CYP1A1*2A polymorphism was found to have significant association with chronic obstructive pneumonopathy (p=0.045), peripheral circulatory problems (trend p=0.042), arteritis (p=0.022), allergies (trend p=0.046), hemorrhoids (trend p=0.026), allergic dermatitis (p=0.0016) and miscarriages (p=0.012). 19022366 2009
CUI: C0018552
Disease: Hamartoma
Hamartoma
0.310 Biomarker disease CTD_human Hamartomas created a new compartment that concentrated TCDD up to 10-fold compared with serum and strongly expressed the TCDD-metabolizing enzyme cytochrome P450 1A1, thus representing a potentially significant source of enzymatic activity, which may add to the xenobiotic metabolism potential of the classical organs such as the liver. 21998131 2012
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms
0.310 Biomarker phenotype PSYGENET Among Caucasian women, those with the CYP1A1 rs2606345 CC and AC genotypes had approximately 2-fold greater odds of having depressive symptoms than did those with the AA genotype (95% confidence intervals [CIs], 1.33 to 4.66 and 1.25 to 3.14, respectively). 16949393 2006
CUI: C0740457
Disease: Malignant neoplasm of kidney
Malignant neoplasm of kidney
0.310 Biomarker disease CTD_human Somatic mutations in stilbene estrogen-induced Syrian hamster kidney tumors identified by DNA fingerprinting. 15003126 2004
CUI: C0019209
Disease: Hepatomegaly
Hepatomegaly
0.300 Biomarker phenotype CTD_human Discriminating between adaptive and carcinogenic liver hypertrophy in rat studies using logistic ridge regression analysis of toxicogenomic data: The mode of action and predictive models. 28108177 2017
CUI: C0000786
Disease: Spontaneous abortion
Spontaneous abortion
0.300 Biomarker phenotype CTD_human Potential involvement of placental AhR in unexplained recurrent spontaneous abortion. 26593447 2016
CUI: C0000822
Disease: Abortion, Tubal
Abortion, Tubal
0.300 Biomarker phenotype CTD_human Potential involvement of placental AhR in unexplained recurrent spontaneous abortion. 26593447 2016
CUI: C0005612
Disease: Birth Weight
Birth Weight
0.300 Biomarker phenotype CTD_human Combined effects of AHR, CYP1A1, and XRCC1 genotypes and prenatal maternal smoking on infant birth size: Biomarker assessment in the Hokkaido Study. 27592400 2016
CUI: C0023976
Disease: Long QT Syndrome
Long QT Syndrome
0.300 Biomarker disease CTD_human [Relationship of blood aryl hydrocarbon receptor mRNA and cytochrome P450 1A1 mRNA expression with corrected QT interval among residents exposed to arsenic via drinking water]. 26988683 2016
CUI: C0039239
Disease: Sinus Tachycardia
Sinus Tachycardia
0.300 Biomarker disease CTD_human CYP1A1 mRNA expression level was significantly higher in residents with sinus tachycardia or bradycardia than in residents with normal heart rate (1.47×10(-3)(0.87×10(-3), 2.77×10(-3)) vs.1.24×10(-3)(0.64×10(-3), 2.31×10(-3)), P<0.05). 26988683 2016