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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 |
|---|---|---|---|
| 84197 | POMK | protein O-mannose kinase | |
| 85365 | ALG2 | ALG2 alpha-1,3/1,6-mannosyltransferase | |
| 113189 | CHST14 | carbohydrate sulfotransferase 14 | |
| 113612 | CYP2U1 | cytochrome P450 family 2 subfamily U member 1 | |
| 120227 | CYP2R1 | cytochrome P450 family 2 subfamily R member 1 | |
| 138050 | HGSNAT | heparan-alpha-glucosaminide N-acetyltransferase | |
| 139189 | DGKK | diacylglycerol kinase kappa | |
| 148789 | B3GALNT2 | beta-1,3-N-acetylgalactosaminyltransferase 2 | |
| 159371 | SLC35G1 | solute carrier family 35 member G1 | |
| 199857 | ALG14 | ALG14 UDP-N-acetylglucosaminyltransferase subunit |
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 |
