autosomal dominant Emery-Dreifuss muscular dystrophy 2

Summary
Synonym
  • EDMD2
  • EMD2
  • Emery-Dreifuss muscular dystrophy 2, autosomal dominant
  • Emery-Dreifuss muscular dystrophy, autosomal dominant
  • Hauptmann-Thannhauser muscular dystrophy
  • autosomal dominant limb-girdle muscular dystrophy type 1B
  • muscular dystrophy with early contractures and cardiomyopathy, autosomal dominant
  • scapuloilioperoneal atrophy with cardiopathy
Definition
An Emery-Dreifuss muscular dystrophy that has_material_basis_in an autosomal dominant mutation of the LMNA gene on chromosome 1q22.
Super Class
Emery-Dreifuss muscular dystrophy autosomal dominant disease
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
Related Glycoprotein
Displaying entries 41 - 42 of 42 in total
UniProt ID Protein Name Source
Q9Y5P6 Mannose-1-phosphate guanyltransferase beta
Q9Y6A1 Protein O-mannosyl-transferase 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