FKTN
This page contains an overview of the genetic variation in the FKTN 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:
FKTN gene and transcript details
Gene Name
fukutin
Gene Links
Ensembl: ENSG00000106692 -
Locus Reference Genomic: LRG_434
Genomic Location
Chromosome 9 : 108,337,314 - 108,397,545 (forward strand)
View in: Ensembl -
UCSC Genome Browser
| Canonical Seqs | Transcript (1383 bases) | Protein (461 aa) |
|---|---|---|
 |
ENST00000223528 | ENSP00000223528 |
 |
LRG_434t2 | LRG_434p2 |
 |
NM_001079802.1 | |
 |
O75072 |
Summary of FKTN in Cardiomyopathies
FKTN variants in ExAC
Details of the protein-altering FKTN 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 | 187 | 0.00303 |
| Truncating | 17 | 0.00024 |
| Missense | 155 | 0.00263 |
| Inframe | 0 | 0.00000 |
| Splice Site | 15 | 0.00015 |