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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
lipid storage disease
Summary
- Synonym
-
- Lipoid storage diseas
- inborn lipid storage disorder
- lipoidosis
- Definition
- A lysosomal storage disease that involves the accumulation of harmful amounts of lipids (fats) in some of the body's cells and tissues.
- Super Class
- lysosomal storage disease
External Links
- Disease Ontology
- DOID:9455
- Mondo Disease Ontology
- MeSH
- UMLS
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 8435 | SOAT2 | sterol O-acyltransferase 2 | |
| 8513 | LIPF | lipase F, gastric type | |
| 8972 | MGAM | maltase-glucoamylase | |
| 9415 | FADS2 | fatty acid desaturase 2 | |
| 10724 | OGA | O-GlcNAcase | |
| 23583 | SMUG1 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | |
| 51172 | NAGPA | N-acetylglucosamine-1-phosphodiester alpha-N-acetylglucosaminidase | |
| 54658 | UGT1A1 | UDP glucuronosyltransferase family 1 member A1 | |
| 79153 | GDPD3 | glycerophosphodiester phosphodiesterase domain containing 3 | |
| 79158 | GNPTAB | N-acetylglucosamine-1-phosphate transferase subunits alpha and beta |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P07098 | Gastric triacylglycerol lipase | |
| P07911 | Uromodulin | |
| P08236 | Beta-glucuronidase | |
| P10253 | Lysosomal alpha-glucosidase | |
| P10619 | Lysosomal protective protein | |
| P11169 | Solute carrier family 2, facilitated glucose transporter member 3 | |
| P11413 | Glucose-6-phosphate 1-dehydrogenase | |
| P13591 | Neural cell adhesion molecule 1 | |
| P14410 | Sucrase-isomaltase, intestinal | |
| P15289 | Arylsulfatase A |
