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 ▼ |
---|---|---|---|---|---|
C0024439 | Macular corneal dystrophy | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0033687 | Proteinuria | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0013238 | Dry Eye Syndromes | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C3665347 | Visual Impairment | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0039292 | Tangier Disease | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C2239176 | Liver carcinoma | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0155733 | Atherosclerosis of aorta | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0022658 | Kidney Diseases | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C4721610 | Carcinoma, Ovarian Epithelial | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0002895 | Anemia, Sickle Cell | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0027888 | Hereditary Motor and Sensory Neuropathies | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C3665365 | Arteriosclerotic cardiovascular disease, NOS | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0005859 | Bloom Syndrome | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0018802 | Congestive heart failure | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0178664 | Glomerulosclerosis (disorder) | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C1140680 | Malignant neoplasm of ovary | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C1636149 | Macular dystrophy, corneal type 1 | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0577631 | Carotid Atherosclerosis | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0027051 | Myocardial Infarction | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0524851 | Neurodegenerative Disorders | PRNP | 5621 | prion protein | P04156 |
C1852467 | Creutzfeldt-Jakob Disease, Sporadic | PRNP | 5621 | prion protein | P04156 |
C0162534 | Prion Diseases | PRNP | 5621 | prion protein | P04156 |
C0002395 | Alzheimer's Disease | PRNP | 5621 | prion protein | P04156 |
C0006142 | Malignant neoplasm of breast | PRNP | 5621 | prion protein | P04156 |
C0017495 | Gerstmann-Straussler-Scheinker Disease | PRNP | 5621 | prion protein | P04156 |
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Last updated: August 19, 2024