Bos taurus Gene: MYO5A
Summary
InnateDB Gene IDBG-646647.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol MYO5A
Gene Name Uncharacterized protein
Synonyms
Species Bos taurus
Ensembl Gene ENSBTAG00000006489
Encoded Proteins
myosin VA (heavy chain 12, myoxin)
myosin VA (heavy chain 12, myoxin)
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 ENSG00000197535:
This gene is one of three myosin V heavy-chain genes, belonging to the myosin gene superfamily. Myosin V is a class of actin-based motor proteins involved in cytoplasmic vesicle transport and anchorage, spindle-pole alignment and mRNA translocation. The protein encoded by this gene is abundant in melanocytes and nerve cells. Mutations in this gene cause Griscelli syndrome type-1 (GS1), Griscelli syndrome type-3 (GS3) and neuroectodermal melanolysosomal disease, or Elejalde disease. Multiple alternatively spliced transcript variants encoding different isoforms have been reported, but the full-length nature of some variants has not been determined. [provided by RefSeq, Dec 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 10:58026028-58152577
Strand Forward strand
Band
Transcripts
ENSBTAT00000008516 ENSBTAP00000008516
ENSBTAT00000063531 ENSBTAP00000054970
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 29 interaction(s) predicted by orthology.
Predicted by orthology
Total 29 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000146 microfilament motor activity
GO:0003774 motor activity
GO:0003779 actin binding
GO:0005509 calcium ion binding
GO:0005515 protein binding
GO:0005516 calmodulin binding
GO:0005524 ATP binding
GO:0017137 Rab GTPase binding
GO:0044822 poly(A) RNA binding
GO:0051015 actin filament binding
Biological Process
GO:0006511 ubiquitin-dependent protein catabolic process
GO:0006582 melanin metabolic process
GO:0006887 exocytosis
GO:0007268 synaptic transmission
GO:0007601 visual perception
GO:0008152 metabolic process
GO:0016192 vesicle-mediated transport
GO:0030048 actin filament-based movement
GO:0030073 insulin secretion
GO:0030318 melanocyte differentiation
GO:0031585 regulation of inositol 1,4,5-trisphosphate-sensitive calcium-release channel activity
GO:0031987 locomotion involved in locomotory behavior
GO:0032252 secretory granule localization
GO:0032400 melanosome localization
GO:0032402 melanosome transport
GO:0032869 cellular response to insulin stimulus
GO:0042438 melanin biosynthetic process
GO:0042476 odontogenesis
GO:0042552 myelination
GO:0042640 anagen
GO:0042759 long-chain fatty acid biosynthetic process
GO:0048066 developmental pigmentation
GO:0050808 synapse organization
GO:0051643 endoplasmic reticulum localization
GO:0072659 protein localization to plasma membrane
Cellular Component
GO:0001726 ruffle
GO:0001750 photoreceptor outer segment
GO:0005737 cytoplasm
GO:0005794 Golgi apparatus
GO:0005882 intermediate filament
GO:0016020 membrane
GO:0016459 myosin complex
GO:0030141 secretory granule
GO:0032593 insulin-responsive compartment
GO:0035371 microtubule plus-end
GO:0042470 melanosome
GO:0042641 actomyosin
GO:0043025 neuronal cell body
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Regulation of actin dynamics for phagocytic cup formation pathway
Insulin processing pathway
Translocation of GLUT4 to the plasma membrane pathway
Innate Immune System pathway
Metabolism of proteins pathway
Immune System pathway
Fcgamma receptor (FCGR) dependent phagocytosis pathway
Peptide hormone metabolism pathway
Membrane Trafficking pathway
Membrane Trafficking pathway
Metabolism of proteins pathway
Peptide hormone metabolism pathway
Insulin processing pathway
Translocation of GLUT4 to the plasma membrane pathway
KEGG
INOH
PID NCI
Cross-References
SwissProt
TrEMBL F1MHT3
UniProt Splice Variant
Entrez Gene 541234
UniGene
RefSeq XM_005211878
HUGO HGNC:7602
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02028993
GenPept
RNA Seq Atlas 101908382 541234