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 |
---|---|---|---|---|---|
C1956346 | Coronary Artery Disease | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0011570 | Mental Depression | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0020445 | Hypercholesterolemia, Familial | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0007103 | Malignant neoplasm of endometrium | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0281361 | Adenocarcinoma of pancreas | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0004153 | Atherosclerosis | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0267725 | Paraesophageal hernia | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0018790 | Cardiac Arrest | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0585129 | Retroperitoneal sarcoma | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0345904 | Malignant neoplasm of liver | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0002395 | Alzheimer's Disease | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0279626 | Squamous cell carcinoma of esophagus | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0699790 | Colon Carcinoma | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0032285 | Pneumonia | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0015695 | Fatty Liver | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0162871 | Aortic Aneurysm, Abdominal | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0155626 | Acute myocardial infarction | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0220668 | Congenital contractural arachnodactyly | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0243026 | Sepsis | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0035078 | Kidney Failure | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0010054 | Coronary Arteriosclerosis | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0016065 | Polyostotic fibrous dysplasia | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0701818 | Choledocholithiasis | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0019322 | Umbilical hernia | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0003850 | Arteriosclerosis | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
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