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
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
344 APOC2 apolipoprotein C2
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
4144 MAT2A methionine adenosyltransferase 2A
4598 MVK mevalonate kinase
Displaying all 8 entries
Gene ID Gene Symbol Description Source
12894 Cpt1a carnitine palmitoyltransferase 1a, liver
12896 Cpt2 carnitine palmitoyltransferase 2
15488 Hsd17b4 hydroxysteroid (17-beta) dehydrogenase 4
16846 Lep leptin
18168 Npy5r neuropeptide Y receptor Y5
19013 Ppara peroxisome proliferator activated receptor alpha
76267 Fads1 fatty acid desaturase 1
97212 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha
Displaying all 7 entries
Gene ID Gene Symbol Description Source
25340 Npy5r neuropeptide Y receptor Y5
25413 Cpt2 carnitine palmitoyltransferase 2
25608 Lep leptin
25747 Ppara peroxisome proliferator activated receptor alpha
25757 Cpt1a carnitine palmitoyltransferase 1A
170670 Hadha hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha
171155 Hadhb hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta
Displaying 1 entry
Gene ID Gene Symbol Description Source
38355 CPT2 Carnitine palmitoyltransferase 2

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Last updated: December 9, 2024