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muscular dystrophy-dystroglycanopathy type B5
Summary
- Synonym
-
- FKRP-related congenital muscular dystrophy
- MDC1C
- MDDGB5
- congenital muscular dystrophy 1C
- muscular dystrophy-dystroglycanopathy (congenital with or without impaired intellectual development), type B, 5
- muscular dystrophy-dystroglycanopathy (congenital with or without mental retardation), type B, 5
- Definition
- A congenital muscular dystrophy characterized by autosomal recessive inheritance of muscular dystrophy with variable penetrance of intellectual disability and structural brain abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the FKRP gene on chromosome 19q13.3.
- Super Class
- autosomal recessive disease muscular dystrophy-dystroglycanopathy type B
External Links
- Disease Ontology
- DOID:0110635
- Mondo Disease Ontology
- ORDO
- OMIM
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 31 | ACACA | acetyl-CoA carboxylase alpha | |
| 43 | ACHE | acetylcholinesterase (Yt blood group) | |
| 217 | ALDH2 | aldehyde dehydrogenase 2 family member | |
| 952 | CD38 | CD38 molecule | |
| 1120 | CHKB | choline kinase beta | |
| 1272 | CNTN1 | contactin 1 | |
| 1605 | DAG1 | dystroglycan 1 | |
| 2218 | FKTN | fukutin | |
| 2632 | GBE1 | 1,4-alpha-glucan branching enzyme 1 | |
| 3098 | HK1 | hexokinase 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q12860 | Contactin-1 | |
| Q13085 | Acetyl-CoA carboxylase 1 | |
| Q14118 | Dystroglycan 1 | |
| Q8NCE2 | Myotubularin-related protein 14 | |
| Q9H9S5 | Ribitol 5-phosphate transferase FKRP | |
| Q9Y259 | Choline/ethanolamine kinase | |
| Q9Y6A1 | Protein O-mannosyl-transferase 1 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0003701 | Proximal muscle weakness |
| HP:0003707 | Calf muscle pseudohypertrophy |
| HP:0003712 | Skeletal muscle hypertrophy |
| HP:0003797 | Limb-girdle muscle atrophy |
| HP:0004637 | Decreased cervical spine mobility |
| HP:0006899 | Fusion of the cerebellar hemispheres |
| HP:0006955 | Olivopontocerebellar hypoplasia |
| HP:0007015 | Poor gross motor coordination |
| HP:0007126 | Proximal amyotrophy |
| HP:0007204 | Diffuse white matter abnormalities |
| Gene ID | Gene Symbol | Description |
|---|---|---|
| 10585 | POMT1 | protein O-mannosyltransferase 1 |
| 29925 | GMPPB | GDP-mannose pyrophosphorylase B |
| 29954 | POMT2 | protein O-mannosyltransferase 2 |
| 79147 | FKRP | fukutin related protein |
| 9215 | LARGE1 | LARGE xylosyl- and glucuronyltransferase 1 |
| 55624 | POMGNT1 | protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-) |
| 84197 | POMK | protein O-mannose kinase |
| 2218 | FKTN | fukutin |
| 729920 | CRPPA | CDP-L-ribitol pyrophosphorylase A |
