abnormal sensorimotor gating Gene Set

Dataset	MPO Gene-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
Description	malfunction of the process by which inhibitory neural pathways filter multiple stimuli and allow attention to be focused on one stimulus; usually measured by pre-pulse inhibition (PPI) (Mammalian Phenotype Ontology, MP_0002634)
External Link	http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002634
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Genes

12 gene mutations causing the abnormal sensorimotor gating phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol	Name
AP3D1	adaptor-related protein complex 3, delta 1 subunit
ATP1A3	ATPase, Na+/K+ transporting, alpha 3 polypeptide
CDS2	CDP-diacylglycerol synthase (phosphatidate cytidylyltransferase) 2
DHRS3	dehydrogenase/reductase (SDR family) member 3
DVL1	dishevelled segment polarity protein 1
FZD3	frizzled class receptor 3
ICAM5	intercellular adhesion molecule 5, telencephalin
POMK	protein-O-mannose kinase
SLC6A1	solute carrier family 6 (neurotransmitter transporter), member 1
SLC6A9	solute carrier family 6 (neurotransmitter transporter, glycine), member 9
SP4	Sp4 transcription factor
TYROBP	TYRO protein tyrosine kinase binding protein