absent linear vestibular evoked potential Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of the biphasic response elicited by linear acceleration transients (usually jerk pulses to an animal's head) (Mammalian Phenotype Ontology, MP_0004813)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004813
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Genes

20 gene mutations causing the absent 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
CDH23 cadherin-related 23
CYBA cytochrome b-245, alpha polypeptide
ESPN espin
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
SLC30A4 solute carrier family 30 (zinc transporter), member 4
SOBP sine oculis binding protein homolog (Drosophila)
SPTBN4 spectrin, beta, non-erythrocytic 4
TMIE transmembrane inner ear
USH1G Usher syndrome 1G (autosomal recessive)