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 |
---|---|---|---|---|---|
C0878544 | Cardiomyopathies | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0403766 | Acquired phimosis | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0013336 | Dwarfism | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0238461 | Anaplastic thyroid carcinoma | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0033975 | Psychotic Disorders | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0013595 | Eczema | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0015230 | Exanthema | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C1135196 | Heart Failure, Diastolic | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0162311 | Androgenetic Alopecia | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0027720 | Nephrosis | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0030567 | Parkinson Disease | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0027709 | Nephrocalcinosis | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0001403 | Addison Disease | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0007114 | Malignant neoplasm of skin | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0039621 | Tetany | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C1332986 | Childhood Osteosarcoma | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
C0014518 | Toxic Epidermal Necrolysis | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0041296 | Tuberculosis | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C1956346 | Coronary Artery Disease | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0006826 | Malignant Neoplasms | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0023895 | Liver diseases | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0019348 | Herpes Simplex Infections | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C2936791 | Antley-Bixler Syndrome, Autosomal Dominant | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0278996 | Malignant Head and Neck Neoplasm | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
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Last updated: August 19, 2024