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 2126 - 2150 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0041296 Tuberculosis ACSBG2 81616 acyl-CoA synthetase bubblegum family member 2 Q5FVE4
C0162309 Adrenoleukodystrophy ACSBG2 81616 acyl-CoA synthetase bubblegum family member 2 Q5FVE4
C0021364 Male infertility ACSBG2 81616 acyl-CoA synthetase bubblegum family member 2 Q5FVE4
C3280314 Combined Malonic and Methylmalonic Aciduria ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C0013421 Dystonia ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C0268583 Methylmalonic acidemia ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C0024299 Lymphoma ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C0011991 Diarrhea ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C0025521 Inborn Errors of Metabolism ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C0085584 Encephalopathies ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C0020615 Hypoglycemia ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C0025517 Metabolic Diseases ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C1332206 Adult Lymphoma ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C1332979 Childhood Lymphoma ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C0025958 Microcephaly ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C0233794 Memory impairment ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C0149931 Migraine Disorders ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C0079731 B-Cell Lymphomas ACSF3 197322 acyl-CoA synthetase family member 3 Q4G176
C0699790 Colon Carcinoma ACSL1 2180 acyl-CoA synthetase long chain family member 1 P33121
C0007102 Malignant tumor of colon ACSL1 2180 acyl-CoA synthetase long chain family member 1 P33121
C0279702 Conventional (Clear Cell) Renal Cell Carcinoma ACSL1 2180 acyl-CoA synthetase long chain family member 1 P33121
C0243026 Sepsis ACSL1 2180 acyl-CoA synthetase long chain family member 1 P33121
C0017638 Glioma ACSL1 2180 acyl-CoA synthetase long chain family member 1 P33121
C0684249 Carcinoma of lung ACSL1 2180 acyl-CoA synthetase long chain family member 1 P33121
C0011882 Diabetic Neuropathies ACSL1 2180 acyl-CoA synthetase long chain family member 1 P33121

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Last updated: August 19, 2024