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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 |
|---|---|---|---|---|---|
| C0021053 | Immune System Diseases | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0015934 | Fetal Growth Retardation | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0282577 | Congenital Disorders of Glycosylation | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0152115 | Lingual-Facial-Buccal Dyskinesia | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0004943 | Behcet Syndrome | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0029408 | Degenerative polyarthritis | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0011849 | Diabetes Mellitus | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C4317224 | Congenital disorder of glycosylation type 1q | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0013146 | Drug abuse | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0006826 | Malignant Neoplasms | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0003504 | Aortic Valve Insufficiency | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0028754 | Obesity | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0085580 | Essential Hypertension | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0007785 | Cerebral Infarction | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C1306459 | Primary malignant neoplasm | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0040034 | Thrombocytopenia | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0003028 | Anhidrosis | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C3714756 | Intellectual Disability | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0027947 | Neutropenia | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0024796 | Marfan Syndrome | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C1956346 | Coronary Artery Disease | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| 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 |
| C0033975 | Psychotic Disorders | SPTLC1 | 10558 | serine palmitoyltransferase long chain base subunit 1 | O15269 |
