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Protein Coding Gene : Myl3 myosin, light polypeptide 3
Primary Identifier  MGI:97268 Organism  mouse, laboratory
Chromosome  9 NCBI Gene Number  17897
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable actin monomer binding activity and cytoskeletal motor activity. Predicted to be involved in several processes, including cardiac muscle contraction; regulation of the force of heart contraction; and ventricular cardiac muscle tissue morphogenesis. Predicted to be located in A band and I band. Predicted to be part of myosin II complex. Is expressed in several structures, including diaphragm; eye; heart; limb segment; and skeletal musculature. Used to study osteoarthritis. Human ortholog(s) of this gene implicated in hypertrophic cardiomyopathy 8. Orthologous to human MYL3 (myosin light chain 3).
  • synonyms:
  • MLC1s,
  • slow skeletal,
  • Mylc,
  • alkali,
  • MGD-MRK-12766,
  • MLC1v,
  • ventricular,
  • Myl3,
  • myosin light chain, alkali, cardiac ventricles,
  • myosin, light polypeptide 3
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Genome

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

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2 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

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Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

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