HNRNPH2-related disorders
id:
hnrnph2-related-disorders-237-3942078
title:
HNRNPH2-related disorders
text:
HNRNPH2-related disorder is considered as a neurodevelopmental disorder (NDD) caused by heterozygous mutation in the HNRNPH2 gene on the chromosome Xq22. This gene encodes a member of a family of ubiquitous heterogeneous nuclear ribonucleoproteins (HNRNP). The HNRNPs are a large group of RNA binding proteins with distinct nucleic acid binding properties. These ribonucleoproteins act as a shuttle between the nucleus and the cytoplasm and act on pre-mRNA to positively or negatively affect spliceos
brand slug:
wiki
category slug:
encyclopedia
description:
Medical condition
original url:
https://en.wikipedia.org/wiki/HNRNPH2-related_disorders
date created:
date modified:
2022-07-05T03:16:13Z
main entity:
{"identifier":"Q55782521","url":"https://www.wikidata.org/entity/Q55782521"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/6/62/X-linked_dominant.svg","width":1525,"height":1283}
fields total:
13
integrity:
15