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 9901 - 9925 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0001418 Adenocarcinoma ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0023903 Liver neoplasms ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0344315 Depressed mood ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0086133 Depressive Syndrome ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0242379 Malignant neoplasm of lung ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0025362 Mental Retardation ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0017638 Glioma ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0005586 Bipolar Disorder ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C2931498 Mental Retardation, X-Linked 1 ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0024141 Lupus Erythematosus, Systemic ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0243026 Sepsis ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0004936 Mental disorders ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0376358 Malignant neoplasm of prostate ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0338106 Adenocarcinoma of colon ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C1263846 Attention deficit hyperactivity disorder ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C4551686 Malignant neoplasm of soft tissue ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0015469 Facial paralysis ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0025193 Melancholia ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C1384666 hearing impairment ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0494475 Tonic - clonic seizures ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0011581 Depressive disorder ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0013264 Muscular Dystrophy, Duchenne ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0013902 Elliptocytosis, Hereditary ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0003467 Anxiety ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488
C0025037 Meckel Diverticulum ACSL4 2182 acyl-CoA synthetase long chain family member 4 O60488

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Last updated: August 19, 2024