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Gene: MAGEA3 (MAGE family member A3) Homo sapiens
Symbol: MAGEA3
Name: MAGE family member A3
Description: This gene is a member of the MAGEA gene family. The members of this family encode proteins with 50 to 80% sequence identity to each other. The promoters and first exons of the MAGEA genes show considerable variability, suggesting that the existence of this gene family enables the same function to be expressed under different transcriptional controls. The MAGEA genes are clustered at chromosomal location Xq28. They have been implicated in some hereditary disorders, such as dyskeratosis congenita. [provided by RefSeq, Jul 2008]
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: antigen MZ2-D; cancer/testis antigen 1.3; cancer/testis antigen family 1, member 3; CT1.3; HIP8; HYPD; MAGE-3 antigen; MAGE3; MAGEA6; melanoma antigen family A, 3; melanoma antigen family A3; melanoma-associated antigen 3; MGC14613
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Human AssemblyChrPosition (strand)SourceGenome Browsers
GRCh38X152,698,742 - 152,702,347 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X151,934,652 - 151,938,250 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X151,685,308 - 151,688,896 (-)NCBINCBI36hg18NCBI36
Build 34X151,605,220 - 151,608,808NCBI
CeleraX152,112,403 - 152,115,991 (+)NCBI
Cytogenetic MapXq28NCBI
HuRefX140,736,139 - 140,739,870 (-)NCBIHuRef
CHM1_1X151,741,886 - 151,745,481 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)

Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated


Comparative Map Data
Position Markers
miRNA Target Status


Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
More on MAGEA3
Alliance Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1353296
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-06-18
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.