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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 |
|---|---|---|---|
| 28 | ABO | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | |
| 98 | ACYP2 | acylphosphatase 2 | |
| 142 | PARP1 | poly(ADP-ribose) polymerase 1 | |
| 353 | APRT | adenine phosphoribosyltransferase | |
| 410 | ARSA | arylsulfatase A | |
| 501 | ALDH7A1 | aldehyde dehydrogenase 7 family member A1 | |
| 811 | CALR | calreticulin | |
| 952 | CD38 | CD38 molecule | |
| 960 | CD44 | CD44 molecule (IN blood group) | |
| 1048 | CEACAM5 | CEA cell adhesion molecule 5 |
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 |
