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Protein-coding gene in the species Homo sapiens
Spartan (SPRTN ) is a protein that in humans is encoded by the SPRTN gene . It is involved in DNA repair .[ 5] [ 6] [ 7] Ruijs-Aalfs syndrome is an autosomal recessive genetic disorder . Characteristics of this disorder are features of premature aging , chromosome instability and development of hepatocellular carcinoma .[ 8] Ruijs-Aalfs syndrome arises as a result of mutations in the SPRTN gene that encodes a metalloproteinase employed in the repair of protein-linked DNA breaks.[ 8]
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