MYL3, myosin light chain 3

MYL3, myosin light chain 3

• MYL3 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, Jul 2008]

• Gene Synonyms (CMH8, MLC-lV/sb, MLC1SB, MLC1V, VLC1, VLCl, myosin light chain 3, CMLC1, cardiac myosin light chain 1, myosin light chain 1, slow-twitch muscle B/ventricular isoform, myosin, light chain 3, alkali; ventricular, skeletal, slow, myosin, light polypeptide 3, alkali; ventricular, skeletal, slow, ventricular myosin alkali light chain, ventricular myosin light chain 1, ventricular/slow twitch myosin alkali light chain,)
• NCBI Gene ID: 4634
• Species: Homo sapiens (Human)
• UNIPROT ID#>>P08590
  UNIPROT ID#>>A0A024R2Q5
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

myosin light chain 3 interacts with:

• agrin
  autophagy related 101
  IQ motif containing GTPase activating protein 1
  myosin heavy chain 14
  myosin XVIIIA
  Sp1 transcription factor
  tyrosine 3-monooxygenase/tryptophan 5-monooxygenase activation protein theta
  ubiquitin C

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.