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Gene Protein Transcript Promoter Expression GO/PPI PubMed Cross reference

Gene information for MYL3 (Homo sapiens)
(Information is obtained from NCBI Gene database)
Entrez gene ID4634
Official gene symbolMYL3
Full namemyosin, light chain 3, alkali; ventricular, skeletal, slow
Aliases,CMH8,MLC1SB,MLC1V,VLC1,
Gene summaryMYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq]
LocationChromosome: 3   Locus: 3p21.3-p21.2
Gene position46904973 - 46899357  Map Viewer
Gene orientationminus
Gene size5617 bp
Gene sequence
OMIM ID160790