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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Keshan disease
Summary
- Definition
- A nutritional deficiency that is disease characterized by a cardiomyopathy secondary to selenium deficiency.
- Super Class
- nutritional deficiency disease
External Links
- Disease Ontology
- DOID:0050083
- Mondo Disease Ontology
- MeSH
- GARD
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 142 | PARP1 | poly(ADP-ribose) polymerase 1 | |
| 1543 | CYP1A1 | cytochrome P450 family 1 subfamily A member 1 | |
| 1557 | CYP2C19 | cytochrome P450 family 2 subfamily C member 19 | |
| 1636 | ACE | angiotensin I converting enzyme | |
| 2597 | GAPDH | glyceraldehyde-3-phosphate dehydrogenase | |
| 2876 | GPX1 | glutathione peroxidase 1 | |
| 3383 | ICAM1 | intercellular adhesion molecule 1 | |
| 3418 | IDH2 | isocitrate dehydrogenase (NADP(+)) 2 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P04406 | Glyceraldehyde-3-phosphate dehydrogenase | |
| P05362 | Intercellular adhesion molecule 1 | |
| P07203 | Glutathione peroxidase 1 | |
| P09874 | Poly [ADP-ribose] polymerase 1 | |
| P12821 | Angiotensin-converting enzyme | |
| P48735 | Isocitrate dehydrogenase [NADP], mitochondrial |
