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 |
|---|---|---|---|---|---|
| C0949541 | Hurthle Cell Tumor | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0008370 | Cholestasis | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0206695 | Carcinoma, Neuroendocrine | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0007112 | Adenocarcinoma of prostate | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0346255 | Oncocytoma, renal | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0027819 | Neuroblastoma | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0027888 | Hereditary Motor and Sensory Neuropathies | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0028754 | Obesity | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0043395 | Yellow Fever | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C2937421 | Prostatic Hyperplasia | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0018801 | Heart failure | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0009402 | Colorectal Carcinoma | AMDHD2 | 51005 | amidohydrolase domain containing 2 | Q9Y303 |
| C0751748 | Nonketotic Hyperglycinemia | AMT | 275 | aminomethyltransferase | P48728 |
| C0036572 | Seizures | AMT | 275 | aminomethyltransferase | P48728 |
| C0010043 | Corneal Ulcer | AMT | 275 | aminomethyltransferase | P48728 |
| C0030305 | Pancreatitis | AMT | 275 | aminomethyltransferase | P48728 |
| C0027066 | Myoclonus | AMT | 275 | aminomethyltransferase | P48728 |
| C0795830 | CHROMOSOME 9p DELETION SYNDROME | AMT | 275 | aminomethyltransferase | P48728 |
| C0001122 | Acidosis | AMT | 275 | aminomethyltransferase | P48728 |
| C0011570 | Mental Depression | AMT | 275 | aminomethyltransferase | P48728 |
| C0175693 | Russell-Silver syndrome | AMT | 275 | aminomethyltransferase | P48728 |
| C0017601 | Glaucoma | AMT | 275 | aminomethyltransferase | P48728 |
| C0024299 | Lymphoma | AMT | 275 | aminomethyltransferase | P48728 |
| C0344315 | Depressed mood | AMT | 275 | aminomethyltransferase | P48728 |
| C0270855 | Early myoclonic encephalopathy | AMT | 275 | aminomethyltransferase | P48728 |
