MTA2

metastasis associated 1 family member 2

Summary

This gene encodes a protein that has been identified as a component of NuRD, a nucleosome remodeling deacetylase complex identified in the nucleus of human cells. It shows a very broad expression pattern and is strongly expressed in many tissues. It may represent one member of a small gene family that encode different but related proteins involved either directly or indirectly in transcriptional regulation. Their indirect effects on transcriptional regulation may include chromatin remodeling. It is closely related to another member of this family, a protein that has been correlated with the metastatic potential of certain carcinomas. These two proteins are so closely related that they share the same types of domains. These domains include two DNA binding domains, a dimerization domain, and a domain commonly found in proteins that methylate DNA. One of the proteins known to be a target protein for this gene product is p53. Deacetylation of p53 is correlated with a loss of growth inhibition in transformed cells supporting a connection between these gene family members and metastasis. [provided by RefSeq, May 2011]

Known Variants22 total

rsidPosition (GRCh37)AllelesClassClinVar
rs77854813111:62,361,415G/C—uncertain significance
rs105433642611:62,361,423G/A—uncertain significance
rs249596874011:62,361,430G/T—uncertain significance
rs76005974611:62,361,466G/A—uncertain significance
rs143579266311:62,361,479C/T—uncertain significance
rs14206375011:62,361,816T/C—uncertain significance
rs36880148611:62,361,821C/T—uncertain significance
rs74650441911:62,362,028C/T—uncertain significance
rs77049041411:62,362,029G/A—uncertain significance
rs76845284511:62,362,073C/T—uncertain significance
rs14949780911:62,362,465C/T—uncertain significance
rs77956781911:62,362,519C/T—uncertain significance
rs77365008311:62,362,924T/G—uncertain significance
rs194209053011:62,363,235G/A—uncertain significance
rs14057762411:62,363,312C/T—uncertain significance
rs156504418711:62,363,797C/A—uncertain significance
rs131483056311:62,363,961A/G—uncertain significance
rs249597735111:62,364,207G/A—uncertain significance
rs77392908411:62,365,150C/G—uncertain significance
rs249598195111:62,366,028G/C—uncertain significance
rs1222362711:62,368,557G/Cregulatory region variant—
rs7149039411:62,370,155G/Asplice region variant—

Gene information from NCBI Gene. Variant classifications from ClinVar.