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 ▲ |
---|---|---|---|---|---|
C0003742 | Arcus Senilis | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0524620 | Metabolic Syndrome X | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0004238 | Atrial Fibrillation | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0023817 | Hyperlipoproteinemia Type I | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0020473 | Hyperlipidemia | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0023895 | Liver diseases | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0742343 | Acute Chest Syndrome | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0020474 | Hyperlipidemia, Familial Combined | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0025517 | Metabolic Diseases | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0002871 | Anemia | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C1561643 | Chronic Kidney Diseases | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0154251 | Lipid Metabolism Disorders | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0002878 | Anemia, Hemolytic | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0010054 | Coronary Arteriosclerosis | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
C0342883 | Cholesteryl Ester Transfer Protein Deficiency | LCAT | 3931 | lecithin-cholesterol acyltransferase | P04180 |
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 |
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