WBSCR22
id:
wbscr22-306-6838941
title:
WBSCR22
text:
Uncharacterized methyltransferase WBSCR22 is an enzyme that in humans is encoded by the WBSCR22 gene. This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.
brand slug:
wiki
category slug:
encyclopedia
description:
Protein-coding gene in the species Homo sapiens
original url:
https://en.wikipedia.org/wiki/WBSCR22
date created:
date modified:
2023-09-24T21:02:09Z
main entity:
{"identifier":"Q18048944","url":"https://www.wikidata.org/entity/Q18048944"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/9/99/Ideogram_human_chromosome_7.svg","width":474,"height":189}
fields total:
13
integrity:
15