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 |
|---|---|---|---|---|---|
| C0040921 | Trichomonas Infections | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0086543 | Cataract | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0338473 | Neuroaxonal Dystrophies | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0027765 | nervous system disorder | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C1306459 | Primary malignant neoplasm | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0024236 | Lymphedema | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0036572 | Seizures | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0028738 | Nystagmus | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0870082 | Hyperkeratosis | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0042571 | Vertigo | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0036857 | Severe intellectual disability | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0235946 | Cerebral atrophy | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0038379 | Strabismus | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0027066 | Myoclonus | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0007194 | Hypertrophic Cardiomyopathy | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0282160 | Aplasia Cutis Congenita | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C3714756 | Intellectual Disability | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0878544 | Cardiomyopathies | NAGA | 4668 | alpha-N-acetylgalactosaminidase | P17050 |
| C0007134 | Renal Cell Carcinoma | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0600139 | Prostate carcinoma | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0027651 | Neoplasms | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C0376358 | Malignant neoplasm of prostate | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C1858328 | Bile acid synthesis defect, congenital, 4 | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C1704272 | Benign Prostatic Hyperplasia | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
| C1306459 | Primary malignant neoplasm | AMACR | 23600 | alpha-methylacyl-CoA racemase | Q9UHK6 |
