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Smchd1 regulates a subset of autosomal genes subject to monoallelic expression in addition to being critical for X inactivation

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Date

2013

Authors

Mould, Arne
Pang, Zhenyi
Pakusch, Miha
Tonks, Ian D.
Stark, Mitchell
Carrie, Dianne
Mukhopadhyay, Pamela
Seidel, Annica
Ellis, Jonathan J.
Deakin, Janine

Journal Title

Journal ISSN

Volume Title

Publisher

BioMed Central Ltd.

Abstract

Background: Smchd1 is an epigenetic modifier essential for X chromosome inactivation: female embryos lacking Smchd1 fail during midgestational development. Male mice are less affected by Smchd1-loss, with some (but not all) surviving to become fertile adu

Description

Keywords

Keywords: cadherin; cell protein; protocadherin alpha; protocadherin beta; protocadherin gamma; Smchd1 protein; unclassified drug; article; autosomal disorder; biallelic expression; chromosome; CpG island; embryo development; epigenetics; gene cluster; gene disrupt Clustered protocadherins; Genomic imprinting; Monoallelic expression; Smchd1; X inactivation

Citation

URI

http://hdl.handle.net/1885/73986

Collections

ANU Research Publications

Source

Epigenetics and Chromatin

Type

Journal article

Book Title

Entity type

Access Statement

License Rights

DOI

10.1186/1756-8935-6-19

Restricted until

2037-12-31

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01_Mould_Smchd1_regulates_a_subset_of_2013.pdf (3.72 MB)

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