ADORA3

This page contains an overview of the genetic variation in the ADORA3 gene, including its role in inherited cardiac disease. For more details, click on the links below, or for a specific variant, enter the HGVS variant here:

ADORA3 gene and transcript details

Gene Name
adenosine A3 receptor

Gene Links
Ensembl: ENSG00000121933 - Locus Reference Genomic: LRG_424

Genomic Location
Chromosome 1 : 112,042,572 - 112,045,976 (reverse strand)
View in: Ensembl - UCSC Genome Browser


Canonical Seqs Transcript (954 bases)Protein (318 aa)
ENST00000241356 ENSP00000241356
LRG_424t1LRG_424p1
NM_000677.3
P33765

Summary of ADORA3 in Cardiomyopathies


ADORA3 variants in ExAC

Details of the protein-altering ADORA3 variants (missense, loss of function truncating, inframe indels and splice site regions) found in the ExAC database are shown below. To view lists of specific variants with links to detailed population frequency data, click on the variant numbers - for all or a particular variant class.

Total VariantsCombined frequency of rare variants
All Variants1290.00213
Truncating60.00006
Missense1180.00192
Inframe10.00003
Splice Site40.00012

Rare variants are defined as having a mean allelic frequency of less than 0.0001.