lipid metabolism disorder

Summary
Synonym
  • dyslipidemia
  • fatty acid metabolism disorder
Definition
An inherited metabolic disorder that involves the creation and degradation of lipids.
Super Class
inherited metabolic disorder
External Links
Disease Ontology
DOID:3146
MeSH
UMLS
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 1 - 10 of 16 in total
Gene ID Gene Symbol Description Source
224 ALDH3A2 aldehyde dehydrogenase 3 family member A2
1374 CPT1A carnitine palmitoyltransferase 1A
1376 CPT2 carnitine palmitoyltransferase 2
1718 DHCR24 24-dehydrocholesterol reductase
3030 HADHA hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha
3032 HADHB hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta
3295 HSD17B4 hydroxysteroid 17-beta dehydrogenase 4
3952 LEP leptin
3990 LIPC lipase C, hepatic type
5465 PPARA peroxisome proliferator activated receptor alpha
Displaying all 3 entries
Gene ID Gene Symbol Description Source
12894 Cpt1a carnitine palmitoyltransferase 1a, liver
16846 Lep leptin
19013 Ppara peroxisome proliferator activated receptor alpha
Displaying all 3 entries
Gene ID Gene Symbol Description Source
25608 Lep leptin
25747 Ppara peroxisome proliferator activated receptor alpha
25757 Cpt1a carnitine palmitoyltransferase 1A
Displaying 1 entry
Gene ID Gene Symbol Description Source
38355 CPT2 Carnitine palmitoyltransferase 2
Related Glycoprotein

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024