SLC2A10
This page contains an overview of the genetic variation in the SLC2A10 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:
SLC2A10 gene and transcript details
Gene Name
solute carrier family 2 (facilitated glucose transporter), member 10
Gene Links
Ensembl: ENSG00000197496 -
Locus Reference Genomic:
Genomic Location
Chromosome 20 : 45,338,376 - 45,362,473 (forward strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (1623 bases) | Protein (541 aa) |
|---|---|---|
 |
ENST00000359271 | ENSP00000352216 |
 |
||
 |
NM_030777.3 | |
 |
O95528 |
Summary of SLC2A10 in Cardiomyopathies
SLC2A10 variants in ExAC
Details of the protein-altering SLC2A10 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 | 255 | 0.00450 |
| Truncating | 9 | 0.00017 |
| Missense | 232 | 0.00419 |
| Inframe | 0 | 0.00000 |
| Splice Site | 14 | 0.00014 |