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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
congenital myasthenic syndrome 15
Summary
- Synonym
-
- CMS15
- congenital myasthenic syndrome 15 without tubular aggregates
- Definition
- A congenital myasthenic syndrome characterized by onset of progressive fatigable proximal muscle weakness in childhood that has_material_basis_in compound heterozygous mutation in the ALG14 gene on chromosome 1p21.
- Super Class
- autosomal recessive disease congenital myasthenic syndrome
External Links
- Disease Ontology
- DOID:0110658
- Mondo Disease Ontology
- OMIM
Related Genes
| Gene ID | Gene Symbol | Description | Source | Organism |
|---|---|---|---|---|
| 100379745 | alg14 | ALG14, UDP-N-acetylglucosaminyltransferase subunit | Xenopus tropicalis (tropical clawed frog) | |
| 108714370 | alg14.L | ALG14, UDP-N-acetylglucosaminyltransferase subunit L homeolog | Xenopus laevis (African clawed frog) | |
| 108715652 | alg14.S | ALG14, UDP-N-acetylglucosaminyltransferase subunit S homeolog | Xenopus laevis (African clawed frog) |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q96F25 | UDP-N-acetylglucosamine transferase subunit ALG14 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0009046 | Difficulty running |
| HP:0010628 | Facial palsy |
| HP:0100301 | Muscle fiber tubular inclusions |
| HP:0003677 | Slowly progressive |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0002828 | Multiple joint contractures |
| Gene ID | Gene Symbol | Description |
|---|---|---|
| 1798 | DPAGT1 | dolichyl-phosphate N-acetylglucosaminephosphotransferase 1 |
| 199857 | ALG14 | ALG14 UDP-N-acetylglucosaminyltransferase subunit |
| 2673 | GFPT1 | glutamine--fructose-6-phosphate transaminase 1 |
| 29925 | GMPPB | GDP-mannose pyrophosphorylase B |
| 85365 | ALG2 | ALG2 alpha-1,3/1,6-mannosyltransferase |
