myofibrillar myopathy 3

Summary
Synonym
  • LGMD 1A
  • autosomal dominant limb-girdle muscular dystrophy type 1A
  • myotilinopathy
  • spheroid body myopathy
Definition
A myofibrillar myopathy that has_material_basis_in heterozygous mutation in the MYOT gene on chromosome 5q31.
Super Class
autosomal dominant disease myofibrillar myopathy
External Links
Related Genes
Displaying entries 11 - 20 of 47 in total
Gene ID Gene Symbol Description Source
2023 ENO1 enolase 1
2218 FKTN fukutin
2710 GK glycerol kinase
2720 GLB1 galactosidase beta 1
3418 IDH2 isocitrate dehydrogenase (NADP(+)) 2
3612 IMPA1 inositol monophosphatase 1
3633 INPP5B inositol polyphosphate-5-phosphatase B
3958 LGALS3 galectin 3
4153 MBL2 mannose binding lectin 2
5286 PIK3C2A phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 alpha

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024