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 |
Disease ID | Disease Name | Gene Symbol ▲ | Gene ID | Gene Name | UniProt ID |
---|---|---|---|---|---|
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 |
C0036631 | Seminoma | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0025202 | melanoma | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0524662 | Opiate Addiction | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0033860 | Psoriasis | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0011581 | Depressive disorder | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0003469 | Anxiety Disorders | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
C0025149 | Medulloblastoma | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024