abnormal paired-pulse inhibition Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description defects in the suppressive response of central synapses when activated twice in rapid succession; indicative of defects in short-term plasticity due to lack of inhibition of neurotransmitter release at the second stimulus (Mammalian Phenotype Ontology, MP_0004807)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004807
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7 gene mutations causing the abnormal paired-pulse inhibition phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGRN agrin
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CPLX1 complexin 1
PCDH17 protocadherin 17
RIMS1 regulating synaptic membrane exocytosis 1
RLN3 relaxin 3
STX1B syntaxin 1B