RecName: Full=Potassium voltage-gated channel subfamily E member 2; Al - Protein

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Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation? [Circ Arrhythm Electrophysiol. ...]
Loss-of-Function KCNE2 Variants: True Monogenic Culprits of Long-QT Syndrome or Proarrhythmic Variants Requiring Secondary Provocation?
Roberts JD, Krahn AD, Ackerman MJ, Rohatgi RK, Moss AJ, Nazer B, Tadros R, Gerull B, Sanatani S, Wijeyeratne YD, et al. Circ Arrhythm Electrophysiol. 2017 Aug; 10(8).
Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation. [Biomark Med. 2014]
Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation.
Nielsen JB, Bentzen BH, Olesen MS, David JP, Olesen SP, Haunsø S, Svendsen JH, Schmitt N. Biomark Med. 2014; 8(4):557-70.
In silico screening of the impact of hERG channel kinetic abnormalities on channel block and susceptibility to acquired long QT syndrome. [J Mol Cell Cardiol. 2014]
In silico screening of the impact of hERG channel kinetic abnormalities on channel block and susceptibility to acquired long QT syndrome.
Romero L, Trenor B, Yang PC, Saiz J, Clancy CE. J Mol Cell Cardiol. 2014 Jul; 72:126-37. Epub 2014 Mar 11.

RefSeq genomic sequence
See the genomic reference sequence for the KCNE2 gene (NG_008804.1).
RefSeq protein
See the reference protein sequence for potassium voltage-gated channel subfamily E member 2 (NP_751951.1).

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Q9Y6J6 [Domain Mapping of Disease Mut...]
Q9Y6J6
Domain Mapping of Disease Mutations
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RecName: Full=Potassium voltage-gated channel subfamily E member 2; AltName: Ful...
RecName: Full=Potassium voltage-gated channel subfamily E member 2; AltName: Full=MinK-related peptide 1; AltName: Full=Minimum potassium ion channel-related peptide 1; AltName: Full=Potassium channel subunit beta MiRP1
gi|6685661|sp|Q9Y6J6.1|KCNE2_HUMAN

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