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 52601 - 52625 of 62743 in total
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

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Last updated: August 19, 2024