Aliases for GPR89A Gene
External Ids for GPR89A Gene
Previous GeneCards Identifiers for GPR89A Gene
GPR89A is a nearly identical copy of the GPR89B gene (MIM 612806).[supplied by OMIM, Jun 2009]
GeneCards Summary for GPR89A Gene
GPR89A (G Protein-Coupled Receptor 89A) is a Protein Coding gene. Diseases associated with GPR89A include Chromosome 1Q21.1 Deletion Syndrome, 1.35-Mb and Thrombocytopenia-Absent Radius Syndrome. Gene Ontology (GO) annotations related to this gene include obsolete signal transducer activity and voltage-gated anion channel activity. An important paralog of this gene is GPR89B.
UniProtKB/Swiss-Prot Summary for GPR89A Gene
Voltage dependent anion channel required for acidification and functions of the Golgi apparatus that may function in counter-ion conductance.