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 |
---|---|---|---|---|---|
C0023492 | Leukemia, T-Cell | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
C0011847 | Diabetes | SACM1L | 22908 | SAC1 like phosphatidylinositide phosphatase | Q9NTJ5 |
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 |
C0031117 | Peripheral Neuropathy | SARM1 | 23098 | sterile alpha and TIR motif containing 1 | Q6SZW1 |
C0013146 | Drug abuse | SARM1 | 23098 | sterile alpha and TIR motif containing 1 | Q6SZW1 |
C0600139 | Prostate carcinoma | SARM1 | 23098 | sterile alpha and TIR motif containing 1 | Q6SZW1 |
C0002736 | Amyotrophic Lateral Sclerosis | SARM1 | 23098 | sterile alpha and TIR motif containing 1 | Q6SZW1 |
C3160718 | PARKINSON DISEASE, LATE-ONSET | SARM1 | 23098 | sterile alpha and TIR motif containing 1 | Q6SZW1 |
C0025517 | Metabolic Diseases | SARM1 | 23098 | sterile alpha and TIR motif containing 1 | Q6SZW1 |
C0027765 | nervous system disorder | SARM1 | 23098 | sterile alpha and TIR motif containing 1 | Q6SZW1 |
C0024117 | Chronic Obstructive Airway Disease | SARM1 | 23098 | sterile alpha and TIR motif containing 1 | Q6SZW1 |
C0030567 | Parkinson Disease | SARM1 | 23098 | sterile alpha and TIR motif containing 1 | Q6SZW1 |
C4721453 | Peripheral Nervous System Diseases | SARM1 | 23098 | sterile alpha and TIR motif containing 1 | Q6SZW1 |
C1842675 | AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder) | SARM1 | 23098 | sterile alpha and TIR motif containing 1 | Q6SZW1 |
C0243026 | Sepsis | SARM1 | 23098 | sterile alpha and TIR motif containing 1 | Q6SZW1 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024