myosin regulatory light chain 2, ventricular/cardiac muscle isoform; MLC-2v; MLC-2 (MYL2)
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Function
Structure
contains 3 EF-hand domains
Pathology
- defects in MYL2 are the cause of:
- familial hypertrophic cardiomyopathy type 10
- hypertrophic cardiomyopathy with mid-LV chamber-2
More general terms
Additional terms
References
- ↑ UniProt http://www.uniprot.org/uniprot/P10916.html
- ↑ Familial hypertrophic cardiomyopathy mutation database http://www.angis.org.au/Databases/heart/heartbreak.html
- ↑ GeneReviews https://www.genecards.org/cgi-bin/carddisp.pl?gene=MYL2