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The protein encoded by this gene catalyzes the penultimate step of the arginine biosynthetic pathway. There are approximately 10 to 14 copies of this gene including the pseudogenes scattered across the human genome, among which the one located on chromosome 9 appears to be the only functional gene for argininosuccinate synthetase. Mutations in the chromosome 9 copy of ASS cause citrullinemia. Two transcript variants encoding the same protein have been found for this gene.
AA408052; arginino succinate synthetase; argininosuccinate synthase; argininosuccinate synthase 1; argininosuccinate synthetase; argininosuccinate synthetase 1; arginosuccinate synthetase 1; ASS; Ass1; Ass-1; ASSA; citrulline-aspartate ligase; citrulline--aspartate ligase; citrullinemia; CN; CTLN1; fold; mutant arginino succinate synthetase; RP11-618A20.2
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