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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name ▼ | UniProt ID |
---|---|---|---|---|---|
C0001430 | Adenoma | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0036875 | Disorders of Sex Development | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0008354 | Cholera | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0015934 | Fetal Growth Retardation | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0002395 | Alzheimer's Disease | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0020456 | Hyperglycemia | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0020428 | Hyperaldosteronism | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0038220 | Status Epilepticus | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C1384583 | Congenital absence of germinal epithelium of testes | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0270824 | Visual seizure | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0027651 | Neoplasms | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C0006142 | Malignant neoplasm of breast | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C0006826 | Malignant Neoplasms | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C4551507 | Buphthalmos | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C1306459 | Primary malignant neoplasm | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C1332977 | Childhood Leukemia | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C0086132 | Depressive Symptoms | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C0007104 | Female Breast Carcinoma | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C0235974 | Pancreatic carcinoma | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C0678222 | Breast Carcinoma | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C1856439 | GLAUCOMA 3, PRIMARY CONGENITAL, A | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C0242379 | Malignant neoplasm of lung | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C0344559 | Irido-corneo-trabecular dysgenesis (disorder) | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
C0085207 | Gestational Diabetes | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
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Last updated: August 19, 2024