BAIT
PRRT2
1500031I19Rik, AI195361, DSPB3
proline-rich transmembrane protein 2
GO Process (1)
GO Function (0)
GO Component (1)
Gene Ontology Biological Process
Mus musculus
PREY
ATP1A2
AW060654, Atpa-3, mKIAA0778
ATPase, Na+/K+ transporting, alpha 2 polypeptide
GO Process (30)
GO Function (6)
GO Component (15)
Gene Ontology Biological Process
- ATP catabolic process [ISO]
- ATP hydrolysis coupled proton transport [ISO]
- adult locomotory behavior [IMP]
- cellular potassium ion homeostasis [ISO]
- cellular response to mechanical stimulus [ISO]
- cellular response to steroid hormone stimulus [IDA, ISO]
- cellular sodium ion homeostasis [ISO]
- locomotion [IMP]
- negative regulation of calcium ion transmembrane transport [ISO]
- negative regulation of calcium:sodium antiporter activity [ISO]
- negative regulation of cytosolic calcium ion concentration [IMP]
- negative regulation of heart contraction [IMP]
- negative regulation of striated muscle contraction [IMP]
- neurotransmitter uptake [IMP]
- potassium ion import [ISO]
- potassium ion transport [ISO]
- regulation of blood pressure [IGI]
- regulation of cardiac muscle cell contraction [ISO]
- regulation of muscle contraction [IMP]
- regulation of respiratory gaseous exchange by neurological system process [IMP]
- regulation of smooth muscle contraction [IMP]
- regulation of striated muscle contraction [IMP]
- regulation of the force of heart contraction [IMP]
- regulation of vasoconstriction [IGI, IMP]
- response to glycoside [IMP, ISO]
- response to nicotine [ISO]
- sodium ion export from cell [ISO]
- sodium ion transmembrane transport [ISO]
- sodium ion transport [ISO]
- visual learning [IMP]
Gene Ontology Molecular Function
Gene Ontology Cellular Component
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
Rescue of neuropsychiatric phenotypes in a mouse model of 16p11.2 duplication syndrome by genetic correction of an epilepsy network hub.
Neuropsychiatric disorders (NPDs) are frequently co-morbid with epilepsy, but the biological basis of shared risk remains poorly understood. The 16p11.2 duplication is a copy number variant that confers risk for diverse NPDs including autism spectrum disorder, schizophrenia, intellectual disability and epilepsy. We used a mouse model of the 16p11.2 duplication (16p11.2dup/+) to uncover molecular and circuit properties associated with this ... [more]
Nat Commun Feb. 17, 2023; 14(1);825 [Pubmed: 36808153]
Throughput
- High Throughput
Additional Notes
- High confidence interactions included proteins that bound to anti-PRRT2 antibodies with a cut off of P<0.1 compared to an IgG control.
Curated By
- BioGRID