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 40901 - 40925 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0031117 Peripheral Neuropathy CYP2C8 1558 cytochrome P450 family 2 subfamily C member 8 P10632
C1458155 Mammary Neoplasms CYP2C8 1558 cytochrome P450 family 2 subfamily C member 8 P10632
C1961102 Precursor Cell Lymphoblastic Leukemia Lymphoma CYP2C8 1558 cytochrome P450 family 2 subfamily C member 8 P10632
C0023453 L2 Acute Lymphoblastic Leukemia CYP2C8 1558 cytochrome P450 family 2 subfamily C member 8 P10632
C0023452 Childhood Acute Lymphoblastic Leukemia CYP2C8 1558 cytochrome P450 family 2 subfamily C member 8 P10632
C0027765 nervous system disorder CYP2C8 1558 cytochrome P450 family 2 subfamily C member 8 P10632
C0007137 Squamous cell carcinoma CYP2C8 1558 cytochrome P450 family 2 subfamily C member 8 P10632
C0006826 Malignant Neoplasms CYP2C8 1558 cytochrome P450 family 2 subfamily C member 8 P10632
C0238198 Gastrointestinal Stromal Tumors CYP2C8 1558 cytochrome P450 family 2 subfamily C member 8 P10632
C0029445 Bone necrosis CYP2C8 1558 cytochrome P450 family 2 subfamily C member 8 P10632
C0019189 Hepatitis, Chronic CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0010054 Coronary Arteriosclerosis CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0024623 Malignant neoplasm of stomach CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0038454 Cerebrovascular accident CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C1956346 Coronary Artery Disease CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0027051 Myocardial Infarction CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0011847 Diabetes CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0011849 Diabetes Mellitus CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0003850 Arteriosclerosis CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0339573 Glaucoma, Primary Open Angle CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0003872 Arthritis, Psoriatic CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0006142 Malignant neoplasm of breast CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0011570 Mental Depression CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0948008 Ischemic stroke CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261
C0007787 Transient Ischemic Attack CYP2C19 1557 cytochrome P450 family 2 subfamily C member 19 P33261

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024