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DisGeNET

DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.

Source Last Updated
DisGeNET July 29, 2024
Displaying entries 7051 - 7075 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0009402 Colorectal Carcinoma CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0699885 Carcinoma of bladder CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C1269683 Major Depressive Disorder CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0279680 Transitional cell carcinoma of bladder CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0014175 Endometriosis CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0023895 Liver diseases CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0009404 Colorectal Neoplasms CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0023452 Childhood Acute Lymphoblastic Leukemia CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0086565 Liver Dysfunction CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0600139 Prostate carcinoma CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0005695 Bladder Neoplasm CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0028754 Obesity CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0023890 Liver Cirrhosis CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0011991 Diarrhea CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0085580 Essential Hypertension CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0007137 Squamous cell carcinoma CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0027051 Myocardial Infarction CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0023467 Leukemia, Myelocytic, Acute CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0220668 Congenital contractural arachnodactyly CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0035220 Respiratory Distress Syndrome, Newborn CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0241910 Autoimmune Chronic Hepatitis CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0014544 Epilepsy CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0011847 Diabetes CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0085859 Polyglandular Type I Autoimmune Syndrome CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
C0039590 Testicular Neoplasms CYP1A2 1544 cytochrome P450 family 1 subfamily A member 2 P05177
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Last updated: August 19, 2024