AMMECR1
id:
ammecr1-0-14510122
title:
AMMECR1
text:
In molecular biology, the AMMECR1 protein is a protein encoded by the AMMECR1 gene on human chromosome Xq22.3. The contiguous gene deletion syndrome is characterised by Alport syndrome (A), intellectual disability (M), midface hypoplasia (M), and elliptocytosis (E), as well as generalized hypoplasia and cardiac abnormalities. It is caused by a deletion in Xq22.3, comprising several genes including AMME chromosomal region gene 1 (AMMECR1), which encodes a protein with a nuclear location and prese
brand slug:
wiki
category slug:
encyclopedia
description:
original url:
https://en.wikipedia.org/wiki/AMMECR1
date created:
date modified:
2020-12-30T18:53:44Z
main entity:
{"identifier":"Q24770794","url":"https://www.wikidata.org/entity/Q24770794"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/3/37/PDB_1zq7_EBI.jpg","width":800,"height":600}
fields total:
13
integrity:
14