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 |
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 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024