Orr et al., 2016 - A mutation in the atrial-specific myosin light chain gene (MYL4) causes familial atrial fibrillation. Nature communications   7:11303 Full text @ Nat. Commun.
16 Genes / Markers
Marker Type Symbol Name
Gene actn2b actinin, alpha 2b
Gene atp2a2a ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2a
Gene cacna1c calcium channel, voltage-dependent, L type, alpha 1C subunit
Gene cacna1da calcium channel, voltage-dependent, L type, alpha 1D subunit, a
Gene cmlc1 cardiac myosin light chain-1
Gene cryaa crystallin, alpha A
Gene ilk integrin-linked kinase
Gene kcnh6a potassium voltage-gated channel, subfamily H (eag-related), member 6a
Gene myh6 myosin, heavy chain 6, cardiac muscle, alpha
Gene myl4 myosin, light chain 4, alkali; atrial, embryonic
Gene nfatc3a nuclear factor of activated T cells 3a
Gene ryr2b ryanodine receptor 2b (cardiac)
Gene slc8a1a solute carrier family 8 member 1a
Gene tnnc1a troponin C type 1a (slow)
Gene tnnc1b troponin C type 1b (slow)
Gene ttn.2 titin, tandem duplicate 2
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