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 62076 - 62100 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C1621958 Glioblastoma Multiforme ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C4551893 Toxemia of pregnancy ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0018801 Heart failure ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0011884 Diabetic Retinopathy ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0003635 Apraxias ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C1384514 Conn Syndrome ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0011570 Mental Depression ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0034069 Pulmonary Fibrosis ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0017638 Glioma ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0011581 Depressive disorder ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C1134719 Invasive Ductal Breast Carcinoma ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C1335302 Pancreatic Ductal Adenocarcinoma ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0524851 Neurodegenerative Disorders ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0524620 Metabolic Syndrome X ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0178664 Glomerulosclerosis (disorder) ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0036572 Seizures ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0013528 Echolalia ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0004364 Autoimmune Diseases ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0332915 Congenital failure of fusion ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0026691 Mucocutaneous Lymph Node Syndrome ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C1306459 Primary malignant neoplasm ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C1968949 Cakut ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0684249 Carcinoma of lung ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0242383 Age related macular degeneration ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0001418 Adenocarcinoma ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787

About Release Notes Help Feedback

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