SLCO1B1
This page contains an overview of the genetic variation in the SLCO1B1 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:
SLCO1B1 gene and transcript details
Gene Name
solute carrier organic anion transporter family, member 1B1
Gene Links
Ensembl: ENSG00000134538 -
Locus Reference Genomic:
Genomic Location
Chromosome 12 : 21,294,509 - 21,392,123 (forward strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (2073 bases) | Protein (691 aa) |
|---|---|---|
 |
ENST00000256958 | ENSP00000256958 |
 |
||
 |
NM_006446.4 | |
 |
Q9Y6L6 |
Summary of SLCO1B1 in Cardiomyopathies
SLCO1B1 variants in ExAC
Details of the protein-altering SLCO1B1 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 | 359 | 0.00574 |
| Truncating | 46 | 0.00063 |
| Missense | 280 | 0.00463 |
| Inframe | 2 | 0.00005 |
| Splice Site | 31 | 0.00044 |