UNC45B
This page contains an overview of the genetic variation in the UNC45B 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:
UNC45B gene and transcript details
Gene Name
unc-45 homolog B (C. elegans)
Gene Links
Ensembl: ENSG00000141161 -
Locus Reference Genomic:
Genomic Location
Chromosome 17 : 33,475,283 - 33,513,578 (forward strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (2793 bases) | Protein (931 aa) |
|---|---|---|
 |
ENST00000268876 | ENSP00000268876 |
 |
||
 |
NM_173167.2 | |
 |
Q8IWX7 |
Summary of UNC45B in Cardiomyopathies
UNC45B variants in ExAC
Details of the protein-altering UNC45B 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 | 463 | 0.00767 |
| Truncating | 24 | 0.00029 |
| Missense | 388 | 0.00666 |
| Inframe | 3 | 0.00009 |
| Splice Site | 48 | 0.00062 |