Motion Sickness Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_2951)
External Link https://www.disgenet.org/browser/0/1/0/C0026603
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Genes

25 genes associated with the disease Motion Sickness in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AUTS2 autism susceptibility candidate 2
CELF2 CUGBP, Elav-like family member 2
CNR1 cannabinoid receptor 1 (brain)
CNR2 cannabinoid receptor 2 (macrophage)
COPE coatomer protein complex, subunit epsilon
CPNE4 copine IV
CREB1 cAMP responsive element binding protein 1
EFHD2 EF-hand domain family, member D2
GHSR growth hormone secretagogue receptor
GPD2 glycerol-3-phosphate dehydrogenase 2 (mitochondrial)
HNMT histamine N-methyltransferase
HOXB3 homeobox B3
HOXD3 homeobox D3
HRH1 histamine receptor H1
LRP1B low density lipoprotein receptor-related protein 1B
MAP2K5 mitogen-activated protein kinase kinase 5
MAPK3 mitogen-activated protein kinase 3
NLGN1 neuroligin 1
PDZRN4 PDZ domain containing ring finger 4
POU6F2 POU class 6 homeobox 2
PRDM16 PR domain containing 16
SDK1 sidekick cell adhesion molecule 1
SMS spermine synthase
ST18 suppression of tumorigenicity 18, zinc finger
TRPV1 transient receptor potential cation channel, subfamily V, member 1