decreased synaptic depression Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description decrease in the duration of the reduction of effectiveness of synaptic connections between neurons and target after repetitive stimulation (Mammalian Phenotype Ontology, MP_0002917)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002917
Similar Terms
Downloads & Tools

Genes

10 gene mutations causing the decreased synaptic depression phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ADORA1 adenosine A1 receptor
BSN bassoon presynaptic cytomatrix protein
CNR1 cannabinoid receptor 1 (brain)
PCDH17 protocadherin 17
PRKACB protein kinase, cAMP-dependent, catalytic, beta
SHANK3 SH3 and multiple ankyrin repeat domains 3
STX1A syntaxin 1A (brain)
SYN2 synapsin II
TRPV1 transient receptor potential cation channel, subfamily V, member 1
UNC13A unc-13 homolog A (C. elegans)