LQT6: Difference between revisions

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==LQT6 Subtype==
==LQT6 Subtype==
{| class="wikitable"
| '''Type''' || '''OMIM''' || '''Mutation'''
|-
| [[LQT6]] || {{OMIM2|603796}} || beta subunit MiRP1 (or [[KCNE2]]) which coassembles with [[HERG]] || -
|}
[[LQT6]] is an [[autosomal dominant]] relatively uncommon form of LQTS. It involves mutations in the gene KCNE2 which encodes for the potassium channel beta subunit MiRP1, constituting part of the I<sub>Kr</sub> repolarizing K<sup>+</sup> current.
[[LQT6]] is an [[autosomal dominant]] relatively uncommon form of LQTS. It involves mutations in the gene KCNE2 which encodes for the potassium channel beta subunit MiRP1, constituting part of the I<sub>Kr</sub> repolarizing K<sup>+</sup> current.



Revision as of 16:54, 7 October 2012