FBXO32
This page contains an overview of the genetic variation in the FBXO32 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:
FBXO32 gene and transcript details
Gene Name
F-box protein 32
Gene Links
Ensembl: ENSG00000156804 -
Locus Reference Genomic:
Genomic Location
Chromosome 8 : 124,515,613 - 124,553,254 (reverse strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (1065 bases) | Protein (355 aa) |
|---|---|---|
 |
ENST00000517956 | ENSP00000428205 |
 |
||
 |
NM_148177.2 | |
 |
Q969P5 |
Summary of FBXO32 in Cardiomyopathies
FBXO32 variants in ExAC
Details of the protein-altering FBXO32 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 | 105 | 0.00158 |
| Truncating | 2 | 0.00002 |
| Missense | 83 | 0.00126 |
| Inframe | 0 | 0.00000 |
| Splice Site | 20 | 0.00031 |