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autosomal recessive limb-girdle muscular dystrophy type 2O
Summary
- Synonym
-
- LGMD2O
- MDDGC3
- muscular dystrophy-dystroglycanopathy (limb-girdle) type C3
- muscular dystrophy-dystroglycanopathy limb-girdle POMGNT1-related
- Definition
- An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in homozygous mutation in the gene encoding protein O-mannose beta-1,2-N-acetylglucosaminyltransferase (POMGNT1) on chromosome 1p34.
- Super Class
- autosomal recessive limb-girdle muscular dystrophy
External Links
- Disease Ontology
- DOID:0110292
- Mondo Disease Ontology
- ORDO
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source | Organism |
|---|---|---|---|---|
| 414570 | pomgnt1.L | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) L homeolog | Xenopus laevis (African clawed frog) | |
| 495292 | pomgnt1.S | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) S homeolog | Xenopus laevis (African clawed frog) | |
| 100158594 | pomgnt1 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) | Xenopus tropicalis (tropical clawed frog) |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003560 | Muscular dystrophy |
| HP:0100297 | Increased endomysial connective tissue |
| HP:0003307 | Hyperlordosis |
| HP:0003712 | Skeletal muscle hypertrophy |
| HP:0001270 | Motor delay |
| HP:0003676 | Progressive |
| HP:0011003 | High myopia |
| HP:0003551 | Difficulty climbing stairs |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0003621 | Juvenile onset |
