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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
neonatal jaundice
Summary
- Synonym
-
- neonatal hyperbilirubinemia
- neonatal icterus
- Definition
- A pigmentation disease characterized by a high level of bilirubin in the blood, causing a yellowing of the skin and other tissues of a newborn infant.
- Super Class
- pigmentation disease
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 28 | ABO | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | |
| 847 | CAT | catalase | |
| 2203 | FBP1 | fructose-bisphosphatase 1 | |
| 2539 | G6PD | glucose-6-phosphate dehydrogenase | |
| 2592 | GALT | galactose-1-phosphate uridylyltransferase | |
| 2678 | GGT1 | gamma-glutamyltransferase 1 | |
| 2821 | GPI | glucose-6-phosphate isomerase | |
| 2876 | GPX1 | glutathione peroxidase 1 | |
| 3098 | HK1 | hexokinase 1 | |
| 7355 | SLC35A2 | solute carrier family 35 member A2 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P19440 | Glutathione hydrolase 1 proenzyme | |
| P22309 | UDP-glucuronosyltransferase 1A1 | |
| P22310 | UDP-glucuronosyltransferase 1A4 | |
| P35503 | UDP-glucuronosyltransferase 1A3 | |
| P35504 | UDP-glucuronosyltransferase 1A5 | |
| Q9HAW7 | UDP-glucuronosyltransferase 1A7 | |
| Q9HAW8 | UDP-glucuronosyltransferase 1A10 | |
| Q9HAW9 | UDP-glucuronosyltransferase 1A8 | |
| Q9NYU2 | UDP-glucose:glycoprotein glucosyltransferase 1 |
