cholesterol-ester transfer protein deficiency

Summary
Synonym
  • CEPT deficiency
  • familial hyperalphalipoproteinemia
Definition
A lipid metabolism disorder characterized by elevated levels of alpha-lipoprotein in the blood.
Super Class
lipid metabolism disorder
External Links
Disease Ontology
DOID:0111368
ORDO
WikiPathways (from TogoID)
Related Genes
Displaying all 5 entries
Gene ID Gene Symbol Description Source
2590 GALNT2 polypeptide N-acetylgalactosaminyltransferase 2
3931 LCAT lecithin-cholesterol acyltransferase
3990 LIPC lipase C, hepatic type
4023 LPL lipoprotein lipase
9388 LIPG lipase G, endothelial type

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024