SPRTN
id:
sprtn-266-10373461
title:
SPRTN
text:
Spartan (SPRTN) is a protein that in humans is encoded by the SPRTN gene. It is involved in DNA repair. 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. 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.
brand slug:
wiki
category slug:
encyclopedia
description:
Protein-coding gene in the species Homo sapiens
original url:
https://en.wikipedia.org/wiki/SPRTN
date created:
date modified:
2022-04-08T20:14:38Z
main entity:
{"identifier":"Q18047333","url":"https://www.wikidata.org/entity/Q18047333"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/d/d6/Ideogram_human_chromosome_1.svg","width":474,"height":189}
fields total:
13
integrity:
15