Gene description for Gltscr1l
Gene name GLTSCR1-like
Gene symbol Gltscr1l
Other names/aliases mKIAA0240
Species Mus musculus
 Database cross references - Gltscr1l
ExoCarta ExoCarta_210982
Vesiclepedia VP_210982
Entrez Gene 210982
UniProt Q8CHH5  
 Gltscr1l identified in sEVs derived from the following tissue/cell type
Mast cells 17486113    
 Gene ontology annotations for Gltscr1l
Biological Process
    chromatin remodeling GO:0006338 NAS
    regulation of transcription by RNA polymerase II GO:0006357 NAS
    positive regulation of cell population proliferation GO:0008284 NAS
    negative regulation of cell differentiation GO:0045596 NAS
    positive regulation of DNA-templated transcription GO:0045893 IBA
    positive regulation of stem cell population maintenance GO:1902459 NAS
Subcellular Localization
    chromatin GO:0000785 NAS
    SWI/SNF complex GO:0016514 IBA
    SWI/SNF complex GO:0016514 IDA
    SWI/SNF complex GO:0016514 ISO
    GBAF complex GO:0140288 NAS
 Experiment description of studies that identified Gltscr1l in sEVs
1
Experiment ID 15
MISEV standards
EM
Biophysical techniques
CD63
Enriched markers
Negative markers
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 Gltscr1l
  Protein Interactor ExoCarta ID Identification method PubMed Species
No interactions are found.
 Pathways in which Gltscr1l is involved
No pathways found





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