abnormal vestibular system physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the sensory system responsible for the sense of head position and movement of the body through space; such anomalies may result in impaired balance, dizziness, poor regulation of postural muscle tone and inability to detect quick movements of the head (Mammalian Phenotype Ontology, MP_0004742)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004742
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44 gene mutations causing the abnormal vestibular system physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AHR aryl hydrocarbon receptor
AP3D1 adaptor-related protein complex 3, delta 1 subunit
ATP2B2 ATPase, Ca++ transporting, plasma membrane 2
BLOC1S5 biogenesis of lysosomal organelles complex-1, subunit 5, muted
BLOC1S6 biogenesis of lysosomal organelles complex-1, subunit 6, pallidin
BMP4 bone morphogenetic protein 4
CDH23 cadherin-related 23
CLRN1 clarin 1
COCH cochlin
CSF1 colony stimulating factor 1 (macrophage)
CTNNA2 catenin (cadherin-associated protein), alpha 2
CYBA cytochrome b-245, alpha polypeptide
EPHB2 EPH receptor B2
EPS8L2 EPS8-like 2
ESPN espin
GFI1 growth factor independent 1 transcription repressor
GRID2 glutamate receptor, ionotropic, delta 2
GRXCR1 glutaredoxin, cysteine rich 1
HR hair growth associated
IREB2 iron-responsive element binding protein 2
KCNA10 potassium channel, voltage gated shaker related subfamily A, member 10
LOC102723475 putative uncharacterized protein LOC388820
LYST lysosomal trafficking regulator
MBP myelin basic protein
MYO6 myosin VI
MYO7A myosin VIIA
NOX3 NADPH oxidase 3
NR4A3 nuclear receptor subfamily 4, group A, member 3
OTOP1 otopetrin 1
PCDH15 protocadherin-related 15
POU3F4 POU class 3 homeobox 4
POU4F3 POU class 4 homeobox 3
QKI QKI, KH domain containing, RNA binding
S1PR2 sphingosine-1-phosphate receptor 2
SLC26A4 solute carrier family 26 (anion exchanger), member 4
SLC30A4 solute carrier family 30 (zinc transporter), member 4
SLC4A11 solute carrier family 4, sodium borate transporter, member 11
SLITRK6 SLIT and NTRK-like family, member 6
SOBP sine oculis binding protein homolog (Drosophila)
SPTBN4 spectrin, beta, non-erythrocytic 4
TMIE transmembrane inner ear
TMPRSS3 transmembrane protease, serine 3
USH1G Usher syndrome 1G (autosomal recessive)
WNT1 wingless-type MMTV integration site family, member 1