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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 60751 - 60775 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▼ UniProt ID
C0030567 Parkinson Disease ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0017921 Glycogen storage disease type II ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0007820 Cerebrovascular Disorders ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0687720 Central Diabetes Insipidus ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0007103 Malignant neoplasm of endometrium ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0011860 Diabetes Mellitus, Non-Insulin-Dependent ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0035078 Kidney Failure ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0027651 Neoplasms ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0520947 Clumsiness - motor delay ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0376358 Malignant neoplasm of prostate ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0016202 Flatfoot ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C1561643 Chronic Kidney Diseases ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0013537 Eclampsia ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0678222 Breast Carcinoma ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C1136249 Mental Retardation, X-Linked ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C1563705 Nephrogenic Diabetes Insipidus, Type I ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
C0018213 Graves Disease ATP6AP2 10159 ATPase H+ transporting accessory protein 2 O75787
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
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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Supported by JST NBDC Grant Number JPMJND2204

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

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Last updated: August 19, 2024