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congenital muscular dystrophy-dystroglycanopathy type A11
Summary
- Synonym
-
- MDDGA11
- Walker-Warburg syndrome or muscle-eye-brain disease B3GALNT2-related
- congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A11
- Definition
- A congenital muscular dystrophy-dystroglycanopathy type A that has_material_basis_in homozygous or compound heterozygous mutation in B3GALNT2 on 1q42.3.
- Super Class
- congenital muscular dystrophy-dystroglycanopathy type A
External Links
- Disease Ontology
- DOID:0111230
Related Genes
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q8NCR0 | UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 2 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003202 | Skeletal muscle atrophy |
| HP:0003560 | Muscular dystrophy |
| HP:0007731 | Chorioretinal dysplasia |
| HP:0007957 | Corneal opacity |
| HP:0007973 | Retinal dysplasia |
| HP:0008736 | Hypoplasia of penis |
| HP:0010508 | Metatarsus valgus |
| HP:0012400 | Abnormal circulating aldolase concentration |
| HP:0002435 | Meningocele |
| HP:0000505 | Visual impairment |
| Gene ID | Gene Symbol | Description |
|---|---|---|
| 10329 | RXYLT1 | ribitol xylosyltransferase 1 |
| 10585 | POMT1 | protein O-mannosyltransferase 1 |
| 11041 | B4GAT1 | beta-1,4-glucuronyltransferase 1 |
| 148789 | B3GALNT2 | beta-1,3-N-acetylgalactosaminyltransferase 2 |
| 1605 | DAG1 | dystroglycan 1 |
| 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 |
