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