Official Journal of the Human Genome Organisation
Table 1 Detailed information about the genes associated with congenital long QT syndrome
Disorders name | Gene symbol | Protein name | Chromosome number | Nucleotide position | Swiss-Prot ID | mRNA accession number |
|---|---|---|---|---|---|---|
Long QT syndrome 1 | KCNQ1 | Potassium voltage-gated channel subfamily KQT member 1 | 11 | 2439260–2826915 | P51787 | NM_181798 |
Long QT syndrome 2 | KCNH2 or HERG | Potassium voltage-gated channel subfamily H member 2 | 7 | 150079697–150090563 | Q12809 | NM_000238 |
Long QT syndrome 3 | SCN5A | Sodium channel protein type 5 subunit alpha | 3 | 38564558–38666167 | Q14524 | NM_000335 |
Long QT syndrome 5 | KCNE1 | Potassium voltage-gated channel subfamily E member 1 | 21 | 34740859–34806443 | P15382 | NM_000219 |
Long QT syndrome 6 | KCNE2 | Potassium voltage-gated channel subfamily E member 2 | 21 | 34658193–34665310 | Q9Y6J6 | NM_005136 |