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congenital muscular dystrophy-dystroglycanopathy type A2
Summary
- Synonym
-
- MDDGA2
- Walker-Warburg syndrome or muscle-eye-brain disease, POMT2-related
- congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A2
- Definition
- A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in POMT2 on 14q24.3.
- Super Class
- congenital muscular dystrophy-dystroglycanopathy type A
External Links
- Disease Ontology
- DOID:0111240
- Mondo Disease Ontology
- OMIM
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9UKY4 | Protein O-mannosyl-transferase 2 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002084 | Encephalocele |
| HP:0010864 | Intellectual disability, severe |
| HP:0006829 | Severe muscular hypotonia |
| HP:0000540 | Hypermetropia |
| HP:0002803 | Congenital contracture |
| HP:0002187 | Intellectual disability, profound |
| HP:0003557 | Increased variability in muscle fiber diameter |
| HP:0000659 | Peters anomaly |
| Gene ID | Gene Symbol | Description |
|---|---|---|
| 10585 | POMT1 | protein O-mannosyltransferase 1 |
| 148789 | B3GALNT2 | beta-1,3-N-acetylgalactosaminyltransferase 2 |
| 2218 | FKTN | fukutin |
| 29925 | GMPPB | GDP-mannose pyrophosphorylase B |
| 29954 | POMT2 | protein O-mannosyltransferase 2 |
| 55624 | POMGNT1 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) |
| 729920 | CRPPA | CDP-L-ribitol pyrophosphorylase A |
| 79147 | FKRP | fukutin related protein |
| 9215 | LARGE1 | LARGE xylosyl- and glucuronyltransferase 1 |
| 10329 | RXYLT1 | ribitol xylosyltransferase 1 |
