Aliases for CNIH3 Gene
External Ids for CNIH3 Gene
Previous GeneCards Identifiers for CNIH3 Gene
GeneCards Summary for CNIH3 Gene
CNIH3 (Cornichon Family AMPA Receptor Auxiliary Protein 3) is a Protein Coding gene. Diseases associated with CNIH3 include Tarp Syndrome and Schizophrenia. Among its related pathways are Vesicle-mediated transport and Metabolism of proteins. Gene Ontology (GO) annotations related to this gene include channel regulator activity. An important paralog of this gene is CNIH2.
UniProtKB/Swiss-Prot Summary for CNIH3 Gene
Regulates the trafficking and gating properties of AMPA-selective glutamate receptors (AMPARs). Promotes their targeting to the cell membrane and synapses and modulates their gating properties by regulating their rates of activation, deactivation and desensitization.