Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
myofibrillar myopathy 1
Summary
- Synonym
-
- autosomal recessive limb-girdle muscular dystrophy type 2R
- desminopathy
- Definition
- A myofibrillar myopathy that has_material_basis_in heterozygous, homozygous, or compound heterozygous mutation in the desmin gene on chromosome 2q35.
- Super Class
- autosomal dominant disease autosomal recessive disease myofibrillar myopathy
External Links
- Disease Ontology
- DOID:0080092
- Mondo Disease Ontology
- ORDO
- OMIM
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 5286 | PIK3C2A | phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha | |
| 5373 | PMM2 | phosphomannomutase 2 | |
| 5553 | PRG2 | proteoglycan 2, pro eosinophil major basic protein | |
| 6383 | SDC2 | syndecan 2 | |
| 6390 | SDHB | succinate dehydrogenase complex iron sulfur subunit B | |
| 6476 | SI | sucrase-isomaltase | |
| 6652 | SORD | sorbitol dehydrogenase | |
| 8813 | DPM1 | dolichyl-phosphate mannosyltransferase subunit 1, catalytic | |
| 8818 | DPM2 | dolichyl-phosphate mannosyltransferase subunit 2, regulatory | |
| 8867 | SYNJ1 | synaptojanin 1 |
Related Glycoprotein
