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 |
---|---|---|---|---|---|
C0344315 | Depressed mood | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C4290140 | recurrent myocardial infarction | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0004238 | Atrial Fibrillation | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0005684 | Malignant neoplasm of urinary bladder | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0600139 | Prostate carcinoma | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0023452 | Childhood Acute Lymphoblastic Leukemia | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0687720 | Central Diabetes Insipidus | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0001175 | Acquired Immunodeficiency Syndrome | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C2919828 | Chronic ulcerative colitis | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0028754 | Obesity | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0037221 | Situs Inversus | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0751606 | Adult Acute Lymphocytic Leukemia | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0751177 | Cancer of Head | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0595989 | Carcinoma of larynx | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0014852 | Esophageal Diseases | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0000768 | Congenital Abnormality | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0745103 | Hyperlipoproteinemia Type IIa | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0476089 | Endometrial Carcinoma | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0037930 | Spinal Cord Neoplasms | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0034155 | Purpura, Thrombotic Thrombocytopenic | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0018799 | Heart Diseases | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0018802 | Congestive heart failure | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0546837 | Malignant neoplasm of esophagus | ACSS2 | 55902 | acyl-CoA synthetase short chain family member 2 | Q9NR19 |
C0024117 | Chronic Obstructive Airway Disease | 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