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CFAP53 gene

Known as: CFAP53, CCDC11, FLJ32743 
 
National Institutes of Health

Papers overview

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2018
2018
GW29-e1822 CCDC11 Promotes Cardiac Hypertrophy and Dysfunction in Response to Pressure Overload
Mutations in CCDC11, a coiled-coil domain containing protein, are associated with embryonic asymmetry including situs inversus… Expand
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2017
2017
Roles of the cilium-associated gene CCDC11 in left-right patterning and in laterality disorders in humans.
Axial determination occurs during early stages of embryogenesis. Flaws in laterality patterning result in abnormal positioning of… Expand
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2016
2016
Ccdc11 is a novel centriolar satellite protein essential for ciliogenesis and establishment of left–right asymmetry
Mutations in CCDC11 cause aberrant placement of internal organs and congenital heart disease in humans. Ccdc11 is a novel… Expand
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2016
2016
A Zebrafish Loss-of-Function Model for Human CFAP53 Mutations Reveals Its Specific Role in Laterality Organ Function.
Establishing correct left-right asymmetry during embryonic development is crucial for proper asymmetric positioning of the organs… Expand
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2015
2015
Mutations in CCDC11, which encodes a coiled-coil containing ciliary protein, causes situs inversus due to dysmotility of monocilia in the left-right organizer.
In vertebrates, establishment of left-right (LR) asymmetry is dependent on cilia-driven fluid flow within the LR organizer… Expand
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2012
2012
A human laterality disorder associated with recessive CCDC11 mutation
Background Significant advancements in understanding the molecular pathophysiology of laterality determination were recently made… Expand
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