Bos taurus Gene: MYL3
Summary
InnateDB Gene IDBG-646222.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MYL3
Gene Name Myosin light chain 3
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000008394
Encoded Proteins
Myosin light chain 3
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000160808:
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 Information
Type Protein coding
Genomic Location Chromosome 22:53202766-53208551
Strand Forward strand
Band
Transcripts
ENSBTAT00000011047 ENSBTAP00000011047
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 5 interaction(s) predicted by orthology.
Predicted by orthology
Total 5 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003785 actin monomer binding
GO:0005509 calcium ion binding
Biological Process
GO:0002026 regulation of the force of heart contraction
GO:0006942 regulation of striated muscle contraction
GO:0055010 ventricular cardiac muscle tissue morphogenesis
GO:0060048 cardiac muscle contraction
Cellular Component
GO:0016459 myosin complex
GO:0031672 A band
GO:0031674 I band
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathways
NETPATH
REACTOME
Muscle contraction pathway
Striated Muscle Contraction pathway
KEGG
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Striated Muscle Contraction pathway
Muscle contraction pathway
Striated Muscle Contraction pathway
Muscle contraction pathway
KEGG
Hypertrophic cardiomyopathy (HCM) pathway
Cardiac muscle contraction pathway
Dilated cardiomyopathy pathway
Cardiac muscle contraction pathway
Hypertrophic cardiomyopathy (HCM) pathway
Dilated cardiomyopathy pathway
INOH
PID NCI
Cross-References
SwissProt P85100
TrEMBL
UniProt Splice Variant
Entrez Gene 618352
UniGene Bt.23497
RefSeq NM_001076501
HUGO
OMIM
CCDS
HPRD
IMGT
EMBL AAFC03056301
GenPept
RNA Seq Atlas 618352