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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
obsolete Matthew-Wood syndrome
Summary
- Definition
- A syndrome that is characterized by microphthalmia or anophthalmia, pulmonary agenesis, and diaphragmatic defect.
External Links
- Disease Ontology
- DOID:0050819
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2813 | GP2 | glycoprotein 2 | |
| 2817 | GPC1 | glypican 1 | |
| 2821 | GPI | glucose-6-phosphate isomerase | |
| 2876 | GPX1 | glutathione peroxidase 1 | |
| 3037 | HAS2 | hyaluronan synthase 2 | |
| 3098 | HK1 | hexokinase 1 | |
| 3099 | HK2 | hexokinase 2 | |
| 3161 | HMMR | hyaluronan mediated motility receptor | |
| 3417 | IDH1 | isocitrate dehydrogenase (NADP(+)) 1 | |
| 3635 | INPP5D | inositol polyphosphate-5-phosphatase D |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P16444 | Dipeptidase 1 | |
| P17931 | Galectin-3 | |
| P18669 | Phosphoglycerate mutase 1 | |
| P18827 | Syndecan-1 | |
| P19320 | Vascular cell adhesion protein 1 | |
| P19367 | Hexokinase-1 | |
| P19835 | Bile salt-activated lipase | |
| P20815 | Cytochrome P450 3A5 | |
| P21217 | 3-galactosyl-N-acetylglucosaminide 4-alpha-L-fucosyltransferase FUT3 | |
| P21589 | 5'-nucleotidase |
