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 12876 - 12900 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0024809 Marijuana Abuse XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0038454 Cerebrovascular accident XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0037286 Skin Neoplasms XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0005695 Bladder Neoplasm XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0006826 Malignant Neoplasms XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0011570 Mental Depression XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0019348 Herpes Simplex Infections XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0005684 Malignant neoplasm of urinary bladder XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0021775 Intermittent Claudication XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0242383 Age related macular degeneration XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0473583 Nevus elasticus XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0553580 Ewings sarcoma XYLT2 64132 xylosyltransferase 2 Q9H1B5
C3714756 Intellectual Disability XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0011581 Depressive disorder XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0023480 Leukemia, Myelomonocytic, Chronic XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0008354 Cholera XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0018784 Sensorineural Hearing Loss (disorder) XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0085580 Essential Hypertension XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0376359 Gronblad-Strandberg Syndrome XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0022658 Kidney Diseases XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0018818 Ventricular Septal Defects XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0085669 Acute leukemia XYLT2 64132 xylosyltransferase 2 Q9H1B5
C1561643 Chronic Kidney Diseases XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0042769 Virus Diseases XYLT2 64132 xylosyltransferase 2 Q9H1B5
C0026267 Mitral Valve Prolapse Syndrome XYLT2 64132 xylosyltransferase 2 Q9H1B5

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