| Name |
|---|
EKD2 GeneEpisodic kinesigenic dyskinesia 2 |
EMWX Geneepisodic muscle weakness, X-linked |
CILD4 GeneCiliary dyskinesia, primary, 4 |
PNKD2 Geneparoxysmal nonkinesigenic dyskinesia 2 |
PNKD Geneparoxysmal nonkinesigenic dyskinesia This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010] |
EA7 GeneEpisodic ataxia, type 7 |
CILD8 GeneCiliary dyskinesia, primary, 8 |
EA8 GeneEpisodic ataxia, type 8 |
EA3 GeneEpisodic ataxia, type 3 |
DPCD Genedeleted in primary ciliary dyskinesia homolog (mouse) This gene in mouse encodes a protein that may be involved in the generation and maintenance of ciliated cells. In mouse, expression of this gene increases during ciliated cell differentiation, and disruption of this gene has been linked to primary ciliary dyskinesia. [provided by RefSeq, Jul 2016] |
CSE Genechoreoathetosis/spasticity, episodic (paroxysmal choreoathetosis/spasticity) |