Automated description from the Alliance of Genome Resources (Release 9.0.0)
Enables glutamine synthetase activity. Involved in several processes, including intracellular ammonium homeostasis; positive regulation of erythrocyte differentiation; and regulation of sprouting angiogenesis. Acts upstream of or within cellular response to starvation and response to glucose. Located in cell body; cytoplasm; and glial cell projection. Is expressed in several structures, including alimentary system; central nervous system; respiratory system; sensory organ; and urinary system. Used to study temporal lobe epilepsy. Human ortholog(s) of this gene implicated in Alzheimer's disease; Huntington's disease; congenital glutamine deficiency; developmental and epileptic encephalopathy 116; and heart disease. Orthologous to human GLUL (glutamate-ammonia ligase).
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