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 57326 - 57350 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0036341 Schizophrenia RBKS 64080 ribokinase Q9H477
C0041296 Tuberculosis RBKS 64080 ribokinase Q9H477
C0009402 Colorectal Carcinoma POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C4552092 Dowling-Degos disease 1 POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0027651 Neoplasms POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C3714534 dowling-degos disease POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0011603 Dermatitis POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C3809147 DOWLING-DEGOS DISEASE 2 POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0024117 Chronic Obstructive Airway Disease POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0242379 Malignant neoplasm of lung POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C2239176 Liver carcinoma POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0037274 Dermatologic disorders POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C1134719 Invasive Ductal Breast Carcinoma POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0023895 Liver diseases POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0027051 Myocardial Infarction POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0406811 Reticulate acropigmentation of Kitamura POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0684249 Carcinoma of lung POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0007124 Noninfiltrating Intraductal Carcinoma POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0018801 Heart failure POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0678222 Breast Carcinoma POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0018802 Congestive heart failure POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0036341 Schizophrenia POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0158623 Congenital anomaly of coronary artery POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C0025958 Microcephaly POFUT1 23509 protein O-fucosyltransferase 1 Q9H488
C1292778 Chronic myeloproliferative disorder POFUT1 23509 protein O-fucosyltransferase 1 Q9H488

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