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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
agnosia
Summary
- Synonym
-
- Dyspraxia
- Dyspraxia syndrome
- Definition
- A communication disorder that is a loss of ability to recognize objects, persons, sounds, shapes, or smells while the specific sense is not defective nor is there any significant memory loss.
- Super Class
- communication disorder
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 8869 | ST3GAL5 | ST3 beta-galactoside alpha-2,3-sialyltransferase 5 | |
| 8898 | MTMR2 | myotubularin related protein 2 | |
| 9200 | HACD1 | 3-hydroxyacyl-CoA dehydratase 1 | |
| 9215 | LARGE1 | LARGE xylosyl- and glucuronyltransferase 1 | |
| 9254 | CACNA2D2 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | |
| 9469 | CHST3 | carbohydrate sulfotransferase 3 | |
| 9524 | TECR | trans-2,3-enoyl-CoA reductase | |
| 10159 | ATP6AP2 | ATPase H+ transporting accessory protein 2 | |
| 10466 | COG5 | component of oligomeric golgi complex 5 | |
| 10585 | POMT1 | protein O-mannosyltransferase 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9UKY4 | Protein O-mannosyl-transferase 2 | |
| Q9UNP4 | Lactosylceramide alpha-2,3-sialyltransferase | |
| Q9UP83 | Conserved oligomeric Golgi complex subunit 5 | |
| Q9Y259 | Choline/ethanolamine kinase | |
| Q9Y487 | V-type proton ATPase 116 kDa subunit a 2 | |
| Q9Y5P6 | Mannose-1-phosphate guanyltransferase beta | |
| Q9Y6A1 | Protein O-mannosyl-transferase 1 |
