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 |
---|---|---|---|---|---|
C1306459 | Primary malignant neoplasm | SQLE | 6713 | squalene epoxidase | Q14534 |
C0003811 | Cardiac Arrhythmia | SQLE | 6713 | squalene epoxidase | Q14534 |
C0023976 | Long QT Syndrome | SQLE | 6713 | squalene epoxidase | Q14534 |
C0030567 | Parkinson Disease | SPTSSB | 165679 | serine palmitoyltransferase small subunit B | Q8NFR3 |
C0752125 | Spinocerebellar Ataxia Type 7 | SPTLC3 | 55304 | serine palmitoyltransferase long chain base subunit 3 | Q9NUV7 |
C0524851 | Neurodegenerative Disorders | SPTLC3 | 55304 | serine palmitoyltransferase long chain base subunit 3 | Q9NUV7 |
C0151313 | Sensory neuropathy | SPTLC3 | 55304 | serine palmitoyltransferase long chain base subunit 3 | Q9NUV7 |
C1168401 | Squamous cell carcinoma of the head and neck | SPTLC3 | 55304 | serine palmitoyltransferase long chain base subunit 3 | Q9NUV7 |
C0031117 | Peripheral Neuropathy | SPTLC3 | 55304 | serine palmitoyltransferase long chain base subunit 3 | Q9NUV7 |
C0243026 | Sepsis | SPTLC3 | 55304 | serine palmitoyltransferase long chain base subunit 3 | Q9NUV7 |
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 |
C0004936 | Mental disorders | SPTLC1 | 10558 | serine palmitoyltransferase long chain base subunit 1 | O15269 |
C0020071 | Hereditary Sensory Autonomic Neuropathy, Type 1 | SPTLC1 | 10558 | serine palmitoyltransferase long chain base subunit 1 | O15269 |
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Last updated: August 19, 2024