WHSC1
id:
whsc1-296-8487425
title:
WHSC1
text:
Probable histone-lysine N-methyltransferase NSD2 is an enzyme that in humans is encoded by the NSD2 gene. This gene encodes a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4. This gene maps to the 165 kb WHS critical
brand slug:
wiki
category slug:
encyclopedia
description:
Protein-coding gene in the species Homo sapiens
original url:
https://en.wikipedia.org/wiki/WHSC1
date created:
date modified:
2023-08-18T09:50:46Z
main entity:
{"identifier":"Q18032355","url":"https://www.wikidata.org/entity/Q18032355"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/0/04/Ideogram_human_chromosome_4.svg","width":474,"height":189}
fields total:
13
integrity:
15