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rippling muscle disease 2
Summary
- Synonym
-
- autosomal dominant limb-girdle muscular dystrophy type 1C
- Definition
- A muscle tissue disease characterized by mechanically triggered contractions of skeletal muscle and that has_material_basis_in mutation in the caveolin-3 gene (CAV3) on chromosome 3p25.
- Super Class
- autosomal dominant disease muscle tissue disease
External Links
- Disease Ontology
- DOID:0060255
- Mondo Disease Ontology
- UMLS
- ORDO
- OMIM
- GARD
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 56983 | POGLUT1 | protein O-glucosyltransferase 1 | |
| 56994 | CHPT1 | choline phosphotransferase 1 | |
| 79147 | FKRP | fukutin related protein | |
| 79947 | DHDDS | dehydrodolichyl diphosphate synthase subunit | |
| 84197 | POMK | protein O-mannose kinase | |
| 84892 | POMGNT2 | protein O-linked mannose N-acetylglucosaminyltransferase 2 (beta 1,4-) | |
| 120071 | LARGE2 | LARGE xylosyl- and glucuronyltransferase 2 | |
| 124872 | B4GALNT2 | beta-1,4-N-acetyl-galactosaminyltransferase 2 (SID blood group) | |
| 148789 | B3GALNT2 | beta-1,3-N-acetylgalactosaminyltransferase 2 | |
| 729920 | CRPPA | CDP-L-ribitol pyrophosphorylase A |
Related Glycoprotein
