Aliases for GPR89B Gene
External Ids for GPR89B Gene
Previous HGNC Symbols for GPR89B Gene
Previous GeneCards Identifiers for GPR89B Gene
GeneCards Summary for GPR89B Gene
GPR89B (G Protein-Coupled Receptor 89B) is a Protein Coding gene. Diseases associated with GPR89B include Chromosome 1Q21.1 Deletion Syndrome, 1.35-Mb and Hemochromatosis, Type 2A. 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 GPR89A.
UniProtKB/Swiss-Prot Summary for GPR89B Gene
Voltage dependent anion channel required for acidification and functions of the Golgi apparatus that may function in counter-ion conductance.