SLC10A2
This page contains an overview of the genetic variation in the SLC10A2 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:
SLC10A2 gene and transcript details
Gene Name
solute carrier family 10 (sodium/bile acid cotransporter family), member 2
Gene Links
Ensembl: ENSG00000125255 -
Locus Reference Genomic:
Genomic Location
Chromosome 13 : 103,698,483 - 103,718,599 (reverse strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (1044 bases) | Protein (348 aa) |
|---|---|---|
 |
ENST00000245312 | ENSP00000245312 |
 |
||
 |
NM_000452.2 | |
 |
Q12908 |
Summary of SLC10A2 in Cardiomyopathies
SLC10A2 variants in ExAC
Details of the protein-altering SLC10A2 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 | 252 | 0.00389 |
| Truncating | 26 | 0.00046 |
| Missense | 209 | 0.00323 |
| Inframe | 1 | 0.00003 |
| Splice Site | 16 | 0.00017 |