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 |
---|---|---|---|---|---|
C0241910 | Autoimmune Chronic Hepatitis | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C1858142 | ICHTHYOSIS, LAMELLAR, 3 | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0013336 | Dwarfism | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0017605 | Angle Closure Glaucoma | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0563625 | Agnosia for Pain | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C1291245 | Cortisone reductase deficiency | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C2919945 | Cavernous Hemangioma of Brain | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0549622 | Sexual Dysfunction | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0026848 | Myopathy | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0266362 | Ambiguous Genitalia | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C1860042 | Antley-Bixler Syndrome with Disordered Steroidogenesis | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0279626 | Squamous cell carcinoma of esophagus | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0038580 | Substance Dependence | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0024809 | Marijuana Abuse | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0019158 | Hepatitis | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0235974 | Pancreatic carcinoma | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0013080 | Down Syndrome | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0020437 | Hypercalcemia | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C4721532 | Lymphoma, Non-Hodgkin, Familial | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0010278 | Craniosynostosis | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0206726 | gliosarcoma | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0037773 | Spastic Paraplegia, Hereditary | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0279607 | Adult Hepatocellular Carcinoma | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0033975 | Psychotic Disorders | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0405580 | Adrenal cortical hypofunction | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
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Last updated: August 19, 2024