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 |
---|---|---|---|---|---|
C0023903 | Liver neoplasms | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0023269 | leiomyosarcoma | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0003467 | Anxiety | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C3888198 | BESTROPHINOPATHY, AUTOSOMAL RECESSIVE | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0036572 | Seizures | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0520679 | Sleep Apnea, Obstructive | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0011265 | Presenile dementia | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0151313 | Sensory neuropathy | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0000768 | Congenital Abnormality | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0028738 | Nystagmus | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C1857276 | Trichohepatoenteric Syndrome | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C0009319 | Colitis | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
C1970344 | Congenital Disorder Of Glycosylation, Type IIF | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C4552000 | Episodic Kinesigenic Dyskinesia 1 | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C0004153 | Atherosclerosis | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C0270764 | Motor Neuron Disease, Lower | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C2931826 | Potassium aggravated myotonia | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C0032285 | Pneumonia | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C0011847 | Diabetes | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C0007222 | Cardiovascular Diseases | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C0017638 | Glioma | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C0033687 | Proteinuria | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C0002395 | Alzheimer's Disease | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C0020538 | Hypertensive disease | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
C0003850 | Arteriosclerosis | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
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Last updated: August 19, 2024