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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 |
|---|---|---|---|---|---|
| C0029434 | Osteogenesis Imperfecta | CD38 | 952 | CD38 molecule | P28907 |
| C0036439 | Scoliosis, unspecified | CD38 | 952 | CD38 molecule | P28907 |
| C0021400 | Influenza | CD38 | 952 | CD38 molecule | P28907 |
| C0278878 | Adult Glioblastoma | CD38 | 952 | CD38 molecule | P28907 |
| C0020071 | Hereditary Sensory Autonomic Neuropathy, Type 1 | SPTLC2 | 9517 | serine palmitoyltransferase long chain base subunit 2 | O15270 |
| C3150896 | NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IC | SPTLC2 | 9517 | serine palmitoyltransferase long chain base subunit 2 | O15270 |
| C0033860 | Psoriasis | SPTLC2 | 9517 | serine palmitoyltransferase long chain base subunit 2 | O15270 |
| C0027651 | Neoplasms | SPTLC2 | 9517 | serine palmitoyltransferase long chain base subunit 2 | O15270 |
| C0206664 | Teratocarcinoma | SPTLC2 | 9517 | serine palmitoyltransferase long chain base subunit 2 | O15270 |
| C0027051 | Myocardial Infarction | SPTLC2 | 9517 | serine palmitoyltransferase long chain base subunit 2 | O15270 |
| C0699739 | Sensory Neuropathy, Hereditary | SPTLC2 | 9517 | serine palmitoyltransferase long chain base subunit 2 | O15270 |
| C0011991 | Diarrhea | SPTLC2 | 9517 | serine palmitoyltransferase long chain base subunit 2 | O15270 |
| C0007959 | Charcot-Marie-Tooth Disease | SPTLC2 | 9517 | serine palmitoyltransferase long chain base subunit 2 | O15270 |
| C4721453 | Peripheral Nervous System Diseases | SPTLC2 | 9517 | serine palmitoyltransferase long chain base subunit 2 | O15270 |
| C2239176 | Liver carcinoma | SPTLC2 | 9517 | serine palmitoyltransferase long chain base subunit 2 | O15270 |
| C0003028 | Anhidrosis | SPTLC2 | 9517 | serine palmitoyltransferase long chain base subunit 2 | O15270 |
| C0029443 | Osteomyelitis | SPTLC2 | 9517 | serine palmitoyltransferase long chain base subunit 2 | O15270 |
| C0001418 | Adenocarcinoma | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
| C0003028 | Anhidrosis | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
| C0024796 | Marfan Syndrome | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
| C0004153 | Atherosclerosis | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
| C0013146 | Drug abuse | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
| C0270764 | Motor Neuron Disease, Lower | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
| C0004943 | Behcet Syndrome | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
| C0007222 | Cardiovascular Diseases | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
