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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 |
| Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name ▼ | UniProt ID |
|---|---|---|---|---|---|
| C0205696 | Anaplastic carcinoma | ACSL1 | 2180 | acyl-CoA synthetase long chain family member 1 | P33121 |
| C0033141 | Cardiomyopathies, Primary | ACSL1 | 2180 | acyl-CoA synthetase long chain family member 1 | P33121 |
| C1257958 | Glucose Metabolism Disorders | ACSL1 | 2180 | acyl-CoA synthetase long chain family member 1 | P33121 |
| 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 |
| 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 |
| C0022104 | Irritable Bowel Syndrome | ACSBG1 | 23205 | acyl-CoA synthetase bubblegum family member 1 | Q96GR2 |
| C0220597 | Adult Hodgkin Lymphoma | ACSBG1 | 23205 | acyl-CoA synthetase bubblegum family member 1 | Q96GR2 |
| C0678222 | Breast Carcinoma | ACSBG1 | 23205 | acyl-CoA synthetase bubblegum family member 1 | Q96GR2 |
| C0024291 | Lymphohistiocytosis, Hemophagocytic | ACSBG1 | 23205 | acyl-CoA synthetase bubblegum family member 1 | Q96GR2 |
