Gene description for MYO1A
Gene name myosin IA
Gene symbol MYO1A
Other names/aliases BBMI
DFNA48
MIHC
MYHL
Species Homo sapiens
 Database cross references - MYO1A
ExoCarta ExoCarta_4640
Entrez Gene 4640
HGNC 7595
MIM 601478
UniProt Q9UBC5  
 MYO1A identified in exosomes derived from the following tissue/cell type
Colorectal cancer cells 25890246    
Neuroblastoma cells 25944692    
 Gene ontology annotations for MYO1A
Molecular Function
    actin binding GO:0003779 IEA
    motor activity GO:0003774 IEA
    ATP binding GO:0005524 IEA
    calmodulin binding GO:0005516 IEA
Biological Process
    metabolic process GO:0008152 IEA
    microvillus assembly GO:0030033 IEA
    sensory perception of sound GO:0007605 IMP
    vesicle localization GO:0051648 IMP
Subcellular Localization
    myosin complex GO:0016459 IEA
    microvillus GO:0005902 IDA
    filamentous actin GO:0031941 IDA
    basolateral plasma membrane GO:0016323 IDA
    apical plasma membrane GO:0016324 IEA
    lateral plasma membrane GO:0016328 IDA
    cortical actin cytoskeleton GO:0030864 IDA
    basal plasma membrane GO:0009925 IEA
    brush border GO:0005903 IDA
    cytoplasm GO:0005737 IDA
 Experiment description of studies that identified MYO1A in exosomes
1
Experiment ID 286
ISEV standards
CEM
EV Biophysical techniques
Alix|TSG101
EV Cytosolic markers
CD63|CD81|EpCAM
EV Membrane markers
EV Negative markers
DLS
EV Particle analysis
Identified molecule protein
Identification method Mass spectrometry
PubMed ID 25890246    
Organism Homo sapiens
Experiment description Highly-purified exosomes and shed microvesicles isolated from the human colon cancer cell line LIM1863 by sequential centrifugal ultrafiltration are biochemically and functionally distinct.
Authors Xu R, Greening DW, Rai A, Ji H, Simpson RJ.
Journal name Methods
Publication year 2015
Sample Colorectal cancer cells
Sample name LIM1863 - Sequential centrifugal ultrafiltration - Rep 2
Isolation/purification methods Differential centrifugation
Filtration
Sequential centrifugal ultrafiltration
Centrifugal concentration
Flotation density -
Molecules identified in the study Protein
Methods used in the study Mass spectrometry
Western blotting
2
Experiment ID 224
ISEV standards
EM|AFM
EV Biophysical techniques
Alix|TSG101
EV Cytosolic markers
CD63|CD81
EV Membrane markers
GOLGA2
EV Negative markers
EV Particle analysis
Identified molecule protein
Identification method Mass spectrometry
PubMed ID 25944692    
Organism Homo sapiens
Experiment description Proteogenomic analysis reveals exosomes are more oncogenic than ectosomes
Authors Keerthikumar S, Gangoda L, Liem M, Fonseka P, Atukorala I, Ozcitti C, Mechler A, Adda CG, Ang CS, Mathivanan S
Journal name Oncotarget
Publication year 2015
Sample Neuroblastoma cells
Sample name SH-SY5Y
Isolation/purification methods Differential centrifugation
Ultracentrifugation
OptiPrep density gradient
Flotation density 1.10 g/mL
Molecules identified in the study Protein
Methods used in the study Mass spectrometry
Western blotting
 Protein-protein interactions for MYO1A
  Protein Interactor ExoCarta ID Identification method PubMed Species
1 CNN1 1264
Reconstituted Complex Homo sapiens
2 DISC1 27185
Two-hybrid Homo sapiens
View the network image/svg+xml
 Pathways in which MYO1A is involved
No pathways found





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