Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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 |
|---|---|---|---|---|---|
| C0027651 | Neoplasms | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0038454 | Cerebrovascular accident | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0027092 | Myopia | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0037822 | Speech Disorders | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0221356 | Brachycephaly | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0154251 | Lipid Metabolism Disorders | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0524620 | Metabolic Syndrome X | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0018784 | Sensorineural Hearing Loss (disorder) | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C1332979 | Childhood Lymphoma | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C1332206 | Adult Lymphoma | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0029124 | Optic Atrophy | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0013421 | Dystonia | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0024299 | Lymphoma | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0038379 | Strabismus | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0035334 | Retinitis Pigmentosa | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0028738 | Nystagmus | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0009402 | Colorectal Carcinoma | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C3887523 | Very long chain acyl-CoA dehydrogenase deficiency | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0001627 | Congenital adrenal hyperplasia | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0028754 | Obesity | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0878544 | Cardiomyopathies | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C1282975 | von Willebrand Disease, Type 2N | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0031039 | Pericardial effusion | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0018784 | Sensorineural Hearing Loss (disorder) | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0007194 | Hypertrophic Cardiomyopathy | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
