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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 |
|---|---|---|---|---|---|
| C1956346 | Coronary Artery Disease | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0010068 | Coronary heart disease | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1510586 | Autism Spectrum Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0009081 | Congenital clubfoot | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0030044 | Acrocephaly | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0004352 | Autistic Disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0003864 | Arthritis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0040332 | Tobacco Dependence | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0848558 | Hypospadias | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0013080 | Down Syndrome | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1378703 | Renal carcinoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0003850 | Arteriosclerosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C1838244 | TIBIAL MUSCULAR DYSTROPHY, TARDIVE | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C4552000 | Episodic Kinesigenic Dyskinesia 1 | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0004153 | Atherosclerosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0019569 | Hirschsprung Disease | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0022680 | Polycystic Kidney Diseases | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0005587 | Depression, Bipolar | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0024299 | Lymphoma | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0795907 | CONOTRUNCAL ANOMALY FACE SYNDROME | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0020626 | Hypoparathyroidism | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C3160718 | PARKINSON DISEASE, LATE-ONSET | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0010054 | Coronary Arteriosclerosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0026269 | Mitral Valve Stenosis | COMT | 1312 | catechol-O-methyltransferase | P21964 |
| C0032914 | Pre-Eclampsia | COMT | 1312 | catechol-O-methyltransferase | P21964 |
