Motion Sickness

8K3511

Motion sickness is the discomfort or nausea triggered by conflicting signals between your inner ear, eyes, and body during movement—commonly experienced in cars, boats, or planes. Research shows that variations near genes involved in vestibular function and neural signaling (like CTNNA2, CHRNA3, and GABRB3) can influe...

SNP Stats

Mapped
35
Positive
21 (60.0%)
Negative
14 (40.0%)

Genome Matching (1)

Public Results (7,972)

Connected Traits (1)

motion sickness

EFO_0006928

0 evidence35 SNPs1 traits0 studies0 positive · 0 negative

Connected Studies (1)

Genetic variants associated with motion sickness point to roles for inner ear development, neurological processes and glucose homeostasis.

PubMed 25628336

0 evidence35 SNPs1 traits1 studies0 positive · 0 negative

Connected Genes (22)

LRP1B

LDL receptor related protein 1B

This gene encodes a member of the low density lipoprotein (LDL) receptor family. These receptors play a wide variety of roles in normal cell function and development due to thei...

2 evidence237 SNPs0 traits0 studies2 positive · 0 negative

AUTS2

activator of transcription and developmental regulator AUTS2

This gene has been implicated in neurodevelopment and as a candidate gene for numerous neurological disorders, including autism spectrum disorders, intellectual disability, and...

1 evidence208 SNPs0 traits0 studies1 positive · 0 negative

SDK1

sidekick cell adhesion molecule 1

The protein encoded by this gene is a member of the immunoglobulin superfamily. The protein contains six immunoglobulin-like domains and thirteen fibronectin type III domains. F...

2 evidence205 SNPs0 traits0 studies1 positive · 1 negative

CPNE4

copine 4

This gene belongs to the highly conserved copine family. It encodes a calcium-dependent, phospholipid-binding protein, which may be involved in membrane trafficking, mitogenesis...

1 evidence137 SNPs0 traits0 studies0 positive · 1 negative

PRDM16

PR/SET domain 16

The reciprocal translocation t(1;3)(p36;q21) occurs in a subset of myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). This gene is located near the 1p36.3 breakpoi...

1 evidence133 SNPs0 traits0 studies1 positive · 0 negative

Connected SNPs (35)

rs705145

LINC02641

chr10additiveAlt C1.000

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