XB-FEAT-923189: Difference between revisions

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=mybpc2=  
=mybpc2=  
This is the community wiki page for the gene ''mybpc2'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase
This is the community wiki page for the gene ''mybpc2'' please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.
 
=nomenclature changes=
10.18.2019
Human name has changed for Entrez Gene: 4606. From myosin binding protein C, fast type to myosin binding protein C2
 
 
=Summary for human MYBPC2 from NCBI=
 
This gene encodes a member of the myosin-binding protein C family. This family includes the fast-, slow- and cardiac-type isoforms, each of which is a myosin-associated protein found in the cross-bridge-bearing zone (C region) of A bands in striated muscle. The protein encoded by this locus is referred to as the fast-type isoform. Mutations in the related but distinct genes encoding the slow-type and cardiac-type isoforms have been associated with distal arthrogryposis, type 1 and hypertrophic cardiomyopathy, respectively. [provided by RefSeq, Jul 2012]

Latest revision as of 11:43, 23 October 2019

mybpc2

This is the community wiki page for the gene mybpc2 please feel free to add any information that is relevant to this gene that is not already captured elsewhere in Xenbase.

nomenclature changes

10.18.2019 Human name has changed for Entrez Gene: 4606. From myosin binding protein C, fast type to myosin binding protein C2


Summary for human MYBPC2 from NCBI

This gene encodes a member of the myosin-binding protein C family. This family includes the fast-, slow- and cardiac-type isoforms, each of which is a myosin-associated protein found in the cross-bridge-bearing zone (C region) of A bands in striated muscle. The protein encoded by this locus is referred to as the fast-type isoform. Mutations in the related but distinct genes encoding the slow-type and cardiac-type isoforms have been associated with distal arthrogryposis, type 1 and hypertrophic cardiomyopathy, respectively. [provided by RefSeq, Jul 2012]