PDIA2
This page contains an overview of the genetic variation in the PDIA2 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:
PDIA2 gene and transcript details
Gene Name
protein disulfide isomerase family A, member 2
Gene Links
Ensembl: ENSG00000185615 -
Locus Reference Genomic:
Genomic Location
Chromosome 16 : 333,170 - 337,113 (forward strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (1575 bases) | Protein (525 aa) |
|---|---|---|
 |
ENST00000219406 | ENSP00000219406 |
 |
||
 |
NM_006849.2 | |
 |
Q13087 |
Summary of PDIA2 in Cardiomyopathies
PDIA2 variants in ExAC
Details of the protein-altering PDIA2 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 Variants | Combined frequency of rare variants | |
|---|---|---|
| All Variants | 435 | 0.00818 |
| Truncating | 59 | 0.00087 |
| Missense | 314 | 0.00615 |
| Inframe | 14 | 0.00022 |
| Splice Site | 48 | 0.00093 |