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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 |
|---|---|---|---|
| 6713 | SQLE | squalene epoxidase | |
| 7412 | VCAM1 | vascular cell adhesion molecule 1 | |
| 8050 | PDHX | pyruvate dehydrogenase complex component X | |
| 8473 | OGT | O-linked N-acetylglucosamine (GlcNAc) transferase | |
| 8505 | PARG | poly(ADP-ribose) glycohydrolase | |
| 8692 | HYAL2 | hyaluronidase 2 | |
| 9365 | KL | klotho | |
| 10232 | MSLN | mesothelin | |
| 10724 | OGA | O-GlcNAcase | |
| 23417 | MLYCD | malonyl-CoA decarboxylase |
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 |
