BAIT
C9ORF72
ALSFTD, FTDALS
chromosome 9 open reading frame 72
GO Process (2)
GO Function (2)
GO Component (9)
Gene Ontology Biological Process
Gene Ontology Molecular Function
Gene Ontology Cellular Component
Homo sapiens
PREY
IQGAP1
AA682088, D7Ertd237e, D7Ertd257e, mKIAA0051
IQ motif containing GTPase activating protein 1
GO Process (12)
GO Function (9)
GO Component (21)
Gene Ontology Biological Process
- cellular response to calcium ion [ISO]
- cellular response to epidermal growth factor stimulus [IMP, ISO]
- cellular response to fibroblast growth factor stimulus [IMP]
- cellular response to platelet-derived growth factor stimulus [IMP]
- epidermal growth factor receptor signaling pathway [IMP, ISO]
- fibroblast growth factor receptor signaling pathway [IMP]
- negative regulation of dephosphorylation [IGI]
- neuron projection extension [ISO]
- platelet-derived growth factor receptor signaling pathway [IMP]
- positive regulation of protein kinase activity [IMP, ISO]
- positive regulation of protein serine/threonine kinase activity [ISO]
- regulation of cytokine production [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
- actin cytoskeleton [ISO]
- axon [ISO]
- cell junction [ISO]
- cell leading edge [IGI]
- cell-cell junction [IDA]
- cytoplasm [IDA, ISO]
- cytoplasmic ribonucleoprotein granule [ISO]
- extracellular vesicular exosome [ISO]
- extrinsic component of cytoplasmic side of plasma membrane [ISO]
- focal adhesion [ISO]
- growth cone [ISO]
- lateral plasma membrane [IDA]
- membrane [IDA]
- microtubule [ISO]
- microtubule cytoskeleton [ISO]
- midbody [ISO]
- neuron projection [IGI, ISO]
- nucleoplasm [ISO]
- plasma membrane [ISO]
- protein complex [ISO]
- ribonucleoprotein complex [IDA, IGI]
Mus musculus
Affinity Capture-MS
An interaction is inferred when a bait protein is affinity captured from cell extracts by either polyclonal antibody or epitope tag and the associated interaction partner is identified by mass spectrometric methods.
Publication
Loss of C9ORF72 impairs autophagy and synergizes with polyQ Ataxin-2 to induce motor neuron dysfunction and cell death.
An intronic expansion of GGGGCC repeats within the C9ORF72 gene is the most common genetic cause of amyotrophic lateral sclerosis and frontotemporal dementia (ALS-FTD). Ataxin-2 with intermediate length of polyglutamine expansions (Ataxin-2 Q30x) is a genetic modifier of the disease. Here, we found that C9ORF72 forms a complex with the WDR41 and SMCR8 proteins to act as a GDP/GTP exchange ... [more]
EMBO J. Dec. 15, 2015; 35(12);1276-97 [Pubmed: 27103069]
Throughput
- Low Throughput
Curated By
- BioGRID