abnormal linear vestibular evoked potential Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the biphasic response elicited by linear acceleration transients (usually jerk pulses to an animal's head); normally, this response is measured by electrophysiological activity of the peripheral vestibular nerve; this assesses the function of the gravity receptor system including the utricles and saccules of the inner ear (Mammalian Phenotype Ontology, MP_0004812)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004812
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Genes

29 gene mutations causing the abnormal linear vestibular evoked potential phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
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
CDH23 cadherin-related 23
CLRN1 clarin 1
COCH cochlin
CTNNA2 catenin (cadherin-associated protein), alpha 2
CYBA cytochrome b-245, alpha polypeptide
ESPN espin
GRID2 glutamate receptor, ionotropic, delta 2
HR hair growth associated
KCNA10 potassium channel, voltage gated shaker related subfamily A, member 10
LOC102723475 putative uncharacterized protein LOC388820
MBP myelin basic protein
MYO6 myosin VI
MYO7A myosin VIIA
NOX3 NADPH oxidase 3
OTOP1 otopetrin 1
PCDH15 protocadherin-related 15
POU3F4 POU class 3 homeobox 4
QKI QKI, KH domain containing, RNA binding
SLC30A4 solute carrier family 30 (zinc transporter), member 4
SLC4A11 solute carrier family 4, sodium borate transporter, member 11
SOBP sine oculis binding protein homolog (Drosophila)
SPTBN4 spectrin, beta, non-erythrocytic 4
TMIE transmembrane inner ear
USH1G Usher syndrome 1G (autosomal recessive)
WNT1 wingless-type MMTV integration site family, member 1