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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 |
|---|---|---|---|---|---|
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | ACACA | 31 | acetyl-CoA carboxylase alpha | Q13085 |
| C1862939 | AMYOTROPHIC LATERAL SCLEROSIS 1 | ACACA | 31 | acetyl-CoA carboxylase alpha | Q13085 |
| C0007134 | Renal Cell Carcinoma | ACACA | 31 | acetyl-CoA carboxylase alpha | Q13085 |
| C0037286 | Skin Neoplasms | ACACA | 31 | acetyl-CoA carboxylase alpha | Q13085 |
| C0007194 | Hypertrophic Cardiomyopathy | ACACA | 31 | acetyl-CoA carboxylase alpha | Q13085 |
| C1536500 | Deficiency of acetyl-CoA acetyltransferase | ACAA2 | 10449 | acetyl-CoA acyltransferase 2 | P42765 |
| C0035222 | Respiratory Distress Syndrome, Adult | ACAA2 | 10449 | acetyl-CoA acyltransferase 2 | P42765 |
| C0029408 | Degenerative polyarthritis | ACAA2 | 10449 | acetyl-CoA acyltransferase 2 | P42765 |
| C2239176 | Liver carcinoma | ACAA2 | 10449 | acetyl-CoA acyltransferase 2 | P42765 |
| C0004096 | Asthma | ACAA1 | 30 | acetyl-CoA acyltransferase 1 | P09110 |
| C0577631 | Carotid Atherosclerosis | ACAA1 | 30 | acetyl-CoA acyltransferase 1 | P09110 |
| C3658299 | Zellweger Spectrum | ACAA1 | 30 | acetyl-CoA acyltransferase 1 | P09110 |
| C1536500 | Deficiency of acetyl-CoA acetyltransferase | ACAA1 | 30 | acetyl-CoA acyltransferase 1 | P09110 |
| C0264408 | Childhood asthma | ACAA1 | 30 | acetyl-CoA acyltransferase 1 | P09110 |
| C0024305 | Lymphoma, Non-Hodgkin | ACAA1 | 30 | acetyl-CoA acyltransferase 1 | P09110 |
| C2239176 | Liver carcinoma | ACAA1 | 30 | acetyl-CoA acyltransferase 1 | P09110 |
| C0027051 | Myocardial Infarction | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
| C0018889 | Helminthiasis | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
| C0020445 | Hypercholesterolemia, Familial | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
| C0006826 | Malignant Neoplasms | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
| C0007138 | Carcinoma, Transitional Cell | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
| C0677886 | Epithelial ovarian cancer | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
| C0007097 | Carcinoma | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
| C0346647 | Malignant neoplasm of pancreas | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
| C0010068 | Coronary heart disease | ABO | 28 | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | P16442 |
