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 |
---|---|---|---|---|---|
C0400966 | Non-alcoholic Fatty Liver Disease | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0041696 | Unipolar Depression | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0034194 | Pyloric Stenosis | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0023269 | leiomyosarcoma | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C1306459 | Primary malignant neoplasm | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0033687 | Proteinuria | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0009402 | Colorectal Carcinoma | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0036341 | Schizophrenia | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C3714756 | Intellectual Disability | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0268731 | Renal glomerular disease | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C1136249 | Mental Retardation, X-Linked | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0016202 | Flatfoot | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0011570 | Mental Depression | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C2239176 | Liver carcinoma | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0038379 | Strabismus | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0027868 | Neuromuscular Diseases | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0027092 | Myopia | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C1261473 | Sarcoma | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C1845672 | Mental Retardation, X-Linked 63 | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0235991 | Small for gestational age (disorder) | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0699791 | Stomach Carcinoma | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0006826 | Malignant Neoplasms | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0678222 | Breast Carcinoma | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C1567741 | Alport Syndrome | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
C0282126 | Depression, Neurotic | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
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Last updated: August 19, 2024