Automated description from the Alliance of Genome Resources (Release 4.0)
Predicted to have several functions, including molybdopterin adenylyltransferase activity; molybdopterin cofactor binding activity; and molybdopterin molybdotransferase activity. Involved in Mo-molybdopterin cofactor biosynthetic process; establishment of synaptic specificity at neuromuscular junction; and protein localization to membrane. Localizes to several cellular components, including GABA-ergic synapse; anchored component of synaptic membrane; and postsynaptic specialization. Is expressed in several structures, including central nervous system and retina. Human ortholog(s) of this gene implicated in inherited metabolic disorder and molybdenum cofactor deficiency type C. Orthologous to human GPHN (gephyrin).