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 21 - 30 of 47 in total
Gene ID Gene Symbol Description Source
5373 PMM2 phosphomannomutase 2
5553 PRG2 proteoglycan 2, pro eosinophil major basic protein
6383 SDC2 syndecan 2
6476 SI sucrase-isomaltase
8813 DPM1 dolichyl-phosphate mannosyltransferase subunit 1, catalytic
8818 DPM2 dolichyl-phosphate mannosyltransferase subunit 2, regulatory
8867 SYNJ1 synaptojanin 1
8871 SYNJ2 synaptojanin 2
8972 MGAM maltase-glucoamylase
9215 LARGE1 LARGE xylosyl- and glucuronyltransferase 1

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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