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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 |
|---|---|---|
| Q92819 | Hyaluronan synthase 2 | |
| Q92835 | Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 1 | |
| Q96AD5 | Patatin-like phospholipase domain-containing protein 2 | |
| Q9NRA2 | Sialin | |
| Q9UEF7 | Klotho | |
| Q9Y286 | Sialic acid-binding Ig-like lectin 7 |
