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

Mapeados
35
Positivos
21 (60.0%)
Negativos
14 (40.0%)

Genome Matching (1)

Resultados Públicos (7.972)

Traços Conectados (1)

motion sickness

EFO_0006928

0 evidências35 SNPs1 traços0 estudos0 positivos · 0 negativos

Estudos Conectados (1)

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

PubMed 25628336

0 evidências35 SNPs1 traços1 estudos0 positivos · 0 negativos

Genes Conectados (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 evidências237 SNPs0 traços0 estudos2 positivos · 0 negativos

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 evidências208 SNPs0 traços0 estudos1 positivos · 0 negativos

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 evidências205 SNPs0 traços0 estudos1 positivos · 1 negativos

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 evidências137 SNPs0 traços0 estudos0 positivos · 1 negativos

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 evidências133 SNPs0 traços0 estudos1 positivos · 0 negativos

SNPs Conectados (35)

rs705145

LINC02641

chr10additiveAlt C1.000

Explore fenótipos no Genodex

Instale o app para comparar este fenótipo com seus genomas, inspecionar resultados privados e explorar o contexto completo de evidências.

Baixar o app