distal arthrogryposis type 2B3

Summary
Synonym
  • DA2B3
  • distal arthrogryposis type 2B3 (Sheldon-Hall)
Definition
A distal arthrogryposis type 2B that has_material_basis_in heterozygous mutation in the MYH3 gene on chromosome 17p13.1.
Super Class
autosomal dominant disease distal arthrogryposis type 2B
Disease Ontology
DOID:0111602
Mondo Disease Ontology
OMIM
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
4619 MYH1 myosin heavy chain 1
4625 MYH7 myosin heavy chain 7
22989 MYH15 myosin heavy chain 15
Displaying all 8 entries
Gene ID Gene Symbol Description Source
17879 Myh1 myosin, heavy polypeptide 1, skeletal muscle, adult
17882 Myh2 myosin, heavy polypeptide 2, skeletal muscle, adult
17883 Myh3 myosin, heavy polypeptide 3, skeletal muscle, embryonic
17884 Myh4 myosin, heavy polypeptide 4, skeletal muscle
17888 Myh6 myosin, heavy polypeptide 6, cardiac muscle, alpha
140781 Myh7 myosin, heavy polypeptide 7, cardiac muscle, beta
544791 Myh13 myosin, heavy polypeptide 13, skeletal muscle
668940 Myh7b myosin, heavy chain 7B, cardiac muscle, beta

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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: December 9, 2024