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 10001 - 10025 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0018799 Heart Diseases TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0018021 Goiter TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0238463 Papillary thyroid carcinoma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0006118 Brain Neoplasms TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0011884 Diabetic Retinopathy TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0024623 Malignant neoplasm of stomach TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0007766 Intracranial Aneurysm TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0035222 Respiratory Distress Syndrome, Adult TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0546837 Malignant neoplasm of esophagus TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0001339 Acute pancreatitis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0007131 Non-Small Cell Lung Carcinoma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C1800706 Idiopathic Pulmonary Fibrosis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0155626 Acute myocardial infarction TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0025500 Mesothelioma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C3203102 Idiopathic pulmonary arterial hypertension TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0011854 Diabetes Mellitus, Insulin-Dependent TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0028754 Obesity TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0019061 Hemolytic-Uremic Syndrome TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C1145628 Autonomic nervous system disorders TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0013264 Muscular Dystrophy, Duchenne TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C3714636 Pneumonitis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0023895 Liver diseases TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0239946 Fibrosis, Liver TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0038454 Cerebrovascular accident TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0009319 Colitis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062

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