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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 |
|---|---|---|---|---|---|
| C0007282 | Carotid Stenosis | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
| C0006142 | Malignant neoplasm of breast | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
| C1961102 | Precursor Cell Lymphoblastic Leukemia Lymphoma | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
| C0234533 | Generalized seizures | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
| C0003873 | Rheumatoid Arthritis | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
| C0342276 | Maturity onset diabetes mellitus in young | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
| C0011849 | Diabetes Mellitus | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
| C0751955 | Brain Infarction | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
| C0020538 | Hypertensive disease | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
| C1956346 | Coronary Artery Disease | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
| C0003467 | Anxiety | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0036341 | Schizophrenia | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0026703 | Mucopolysaccharidoses | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0033578 | Prostatic Neoplasms | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0376358 | Malignant neoplasm of prostate | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C1306459 | Primary malignant neoplasm | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0018784 | Sensorineural Hearing Loss (disorder) | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0027877 | Neuronal Ceroid-Lipofuscinoses | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0013421 | Dystonia | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0393593 | Dystonia Disorders | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0154676 | Organic writer's cramp | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C1568248 | Usher Syndrome, Type III | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C1283601 | Deficiency of sulfatase | ARSG | 22901 | arylsulfatase G | Q96EG1 |
| C0521694 | Atrophic retina | ARSG | 22901 | arylsulfatase G | Q96EG1 |
