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. 2016 Jun 15;3(2):22. doi: 10.3390/jcdd3020022

Table 1.

Cardiac and skeletal muscle functions of Popdc proteins.

Function Reference
POPDC genes are predominantly expressed in striated muscle [1]
Popdc1−/− mice display a reduction in the number and an increase in the size of caveolae [33]
Popdc1−/− mice display an increased vulnerability to ischemia-reperfusion injury [33]
Popdc1 controls membrane trafficking of TREK-1 [10]
Popdc1 or Popdc2 null mutant mice display an age-dependent stress-induced bradycardia phenotype [10]
Depletion of either Popdc1 or Popdc2 in mice results in structural remodelling of SAN tissue [10]
Depletion of popdc1 or popdc2 in zebrafish causes AV-block and muscular dystrophy [9,12]
Popdc1 in zebrafish controls the formation of the myotendinous junction [12]
The missense mutation POPDC1S191F causes cardiac arrhythmia and muscular dystrophy in patients [12]
POPDC1 and POPDC3 are downregulated in human heart failure [40]
POPDC1 has been associated with atrial fibrillation [38]
POPDC1 is a novel genetic determinant of the QT interval and the QRS time [39]