HELZ2
This page contains an overview of the genetic variation in the HELZ2 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:
HELZ2 gene and transcript details
Gene Name
helicase with zinc finger 2, transcriptional coactivator
Gene Links
Ensembl: ENSG00000130589 -
Locus Reference Genomic:
Genomic Location
Chromosome 20 : 62,190,599 - 62,203,738 (reverse strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (7947 bases) | Protein (2649 aa) |
|---|---|---|
 |
ENST00000467148 | ENSP00000417401 |
 |
||
 |
NM_001037335.2 | |
 |
Q9BYK8 |
Summary of HELZ2 in Cardiomyopathies
HELZ2 variants in ExAC
Details of the protein-altering HELZ2 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 | 1218 | 0.02278 |
| Truncating | 36 | 0.00059 |
| Missense | 1125 | 0.02136 |
| Inframe | 3 | 0.00009 |
| Splice Site | 54 | 0.00076 |