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FLASH GENE
Symbol MYL3 contributors: - updated : 13-07-2006
HGNC name myosin, light polypeptide 3, alkali; ventricular, skeletal, slow
HGNC id 7584
Corresponding disease
CMH8 cardiomyopathy, familial, hypertrophic, 8
Location 3p21.3      Physical location : 46.899.356 - 46.904.973
Synonym name essential myosin light chain,ventricular
Synonym symbol(s) ELC, MLC1-SB, MLC1V, MYL1V
DNA
TYPE functioning gene
STRUCTURE 5.00 kb     7 Exon(s)
10 Kb 5' upstream gene genomic sequence study
MAPPING cloned Y linked   status confirmed
RNA
TRANSCRIPTS type messenger
EXPRESSION
Type restricted
constitutive of
   expressed in (based on citations)
organ(s)
SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
blood / hematopoieticthymus   highly
Cardiovascularheart   highly
Digestiveliver    
Respiratorylung   moderately
tissue
SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
Lymphoid    
Muscularstriatumcardiac  
Muscularstriatumskeletal  
cell lineage
cell lines
fluid/secretion
at STAGE
physiological period fetal
Text muscle
PROTEIN
PHYSICAL PROPERTIES
STRUCTURE
motifs/domains
three EF-hand domains
secondary structure two heavy chains and four light chains
mono polymer hexamer
HOMOLOGY
interspecies homolog to murine Mylc
Homologene
FAMILY
CATEGORY motor/contractile , structural protein
SUBCELLULAR LOCALIZATION     intracellular
intracellular,cytoplasm,cytoskeleton
basic FUNCTION modulating the interaction between myosin and actin
CELLULAR PROCESS
PHYSIOLOGICAL PROCESS cardiovascular
PATHWAY
metabolism
signaling
a component myosin is an hexamer of 2 heavy chains and 4 light chains
INTERACTION
DNA
RNA
small molecule
protein CASP3 (cleavage of MYL3 contributing to depression of myocyte function)
cell & other
REGULATION
ASSOCIATED DISORDERS
corresponding disease(s) CMH8
related resource FHC Mutation Database
Susceptibility
Variant & Polymorphism
Candidate gene
Marker
Therapy target
ANIMAL & CELL MODELS