Gene description for 2810417H13Rik
Gene name RIKEN cDNA 2810417H13 gene
Gene symbol 2810417H13Rik
Other names/aliases AA409629
Ns5apt9
Ns5atp9
PAF15
Paf
mKIAA0101
p15(PAF)
Species Mus musculus
 Database cross references - 2810417H13Rik
ExoCarta ExoCarta_68026
Entrez Gene 68026
UniProt Q9CQX4  
 2810417H13Rik identified in exosomes derived from the following tissue/cell type
Mast cells 17486113    
 Gene ontology annotations for 2810417H13Rik
Molecular Function
    chromatin binding GO:0003682 ISO
Biological Process
    regulation of cell cycle GO:0051726 ISO
    centrosome organization GO:0051297 ISO
    cellular response to DNA damage stimulus GO:0006974 ISO
    translesion synthesis GO:0019985 ISO
    DNA replication GO:0006260 ISO
    response to UV GO:0009411 ISO
    DNA repair GO:0006281 IEA
Subcellular Localization
    nucleus GO:0005634 ISO
    cytoplasm GO:0005737 ISO
    perinuclear region of cytoplasm GO:0048471 ISO
 Experiment description of studies that identified 2810417H13Rik in exosomes
1
Experiment ID 15
ISEV standards
EM
EV Biophysical techniques
EV Cytosolic markers
CD63
EV Membrane markers
EV Negative markers
EV Particle analysis
Identified molecule mrna
Identification method Microarray
PubMed ID 17486113    
Organism Mus musculus
Homo sapiens
Experiment description Exosome-mediated transfer of mRNAs and microRNAs is a novel mechanism of genetic exchange between cells.
Authors Valadi H, Ekstrom K, Bossios A, Sjostrand M, Lee JJ, Lotvall JO
Journal name NCB
Publication year 2007
Sample Mast cells
Sample name MC9
Bone marrow-derived mast cells
HMC-1
Isolation/purification methods Filtration
Ultracentrifugation
Sucrose density gradient
Flotation density 1.11-1.21 g/mL
Molecules identified in the study Protein
mRNA
miRNA
Methods used in the study Mass spectrometry [MALDI TOF]
Western blotting
Microarray
miRCURY LNA Array
 Protein-protein interactions for 2810417H13Rik
  Protein Interactor ExoCarta ID Identification method PubMed Species
No interactions are found.
 Pathways in which 2810417H13Rik is involved
PathwayEvidenceSource
Termination of translesion DNA synthesis IEA Reactome





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