Gene description for CCDC88C
Gene name coiled-coil domain containing 88C
Gene symbol CCDC88C
Other names/aliases DAPLE
HKRP2
KIAA1509
SCA40
Species Homo sapiens
 Database cross references - CCDC88C
ExoCarta ExoCarta_440193
Entrez Gene 440193
HGNC 19967
MIM 611204
UniProt Q9P219  
 CCDC88C identified in exosomes derived from the following tissue/cell type
Hepatocytes 26054723    
 Gene ontology annotations for CCDC88C
Molecular Function
    PDZ domain binding GO:0030165 ISS
    protein self-association GO:0043621 ISS
Biological Process
    Wnt signaling pathway GO:0016055 IEA
    stress-activated protein kinase signaling cascade GO:0031098 IMP
    regulation of protein phosphorylation GO:0001932 ISS
    protein destabilization GO:0031648 ISS
    protein homooligomerization GO:0051260 ISS
Subcellular Localization
    cytoplasm GO:0005737 IDA
 Experiment description of studies that identified CCDC88C in exosomes
1
Experiment ID 237
ISEV standards
EM
EV Biophysical techniques
TSG101|Alix|HSC70|GAPDH
EV Cytosolic markers
EV Membrane markers
HSP90B1
EV Negative markers
qNano
EV Particle analysis
Identified molecule mRNA
Identification method RNA Sequencing
PubMed ID 26054723    
Organism Homo sapiens
Experiment description Hepatocellular carcinoma-derived exosomes promote motility of immortalized hepatocyte through transfer of oncogenic proteins and RNAs
Authors He M, Qin H, Poon TC, Sze SC, Ding X, Co NN, Ngai SM, Chan TF, Wong N
Journal name Carcinogenesis
Publication year 2015
Sample Hepatocytes
Sample name MIHA
Isolation/purification methods Differential centrifugation
Filtration
Ultracentrifugation
Sucrose density gradient
Flotation density 1.13-1.19 g/mL
Molecules identified in the study Protein
RNA
Methods used in the study Western blotting
Mass spectrometry
RNA Sequencing
 Protein-protein interactions for CCDC88C
  Protein Interactor ExoCarta ID Identification method PubMed Species
No interactions are found.
 Pathways in which CCDC88C is involved
PathwayEvidenceSource
negative regulation of TCF-dependent signaling by DVL-interacting proteins TAS Reactome





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