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 ▼ |
---|---|---|---|---|---|
C0020538 | Hypertensive disease | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0235527 | Heart Failure, Right-Sided | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C2239176 | Liver carcinoma | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C4551472 | Hypertrophic obstructive cardiomyopathy | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C2939447 | Right ventricular failure | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0009691 | Congenital cataract | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0011849 | Diabetes Mellitus | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0524620 | Metabolic Syndrome X | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C2675528 | Spastic Paraplegia 42, Autosomal Dominant | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0001418 | Adenocarcinoma | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0004096 | Asthma | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0003850 | Arteriosclerosis | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0018802 | Congestive heart failure | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0684249 | Carcinoma of lung | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0085580 | Essential Hypertension | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0006142 | Malignant neoplasm of breast | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0006111 | Brain Diseases | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0011570 | Mental Depression | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C3714756 | Intellectual Disability | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0027651 | Neoplasms | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0018801 | Heart failure | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0020540 | Malignant Hypertension | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0155626 | Acute myocardial infarction | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C1306459 | Primary malignant neoplasm | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0037773 | Spastic Paraplegia, Hereditary | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
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Last updated: August 19, 2024