increased synaptic depression Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increase in the duration of the reduction of effectiveness of synaptic connections between neurons and target after repetitive stimulation (Mammalian Phenotype Ontology, MP_0002916)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002916
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Genes

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

Symbol Name
FGF22 fibroblast growth factor 22
KCNMA1 potassium channel, calcium activated large conductance subfamily M alpha, member 1
PCLO piccolo presynaptic cytomatrix protein
PIP5K1C phosphatidylinositol-4-phosphate 5-kinase, type I, gamma
RAB3A RAB3A, member RAS oncogene family
SYN1 synapsin I
SYN2 synapsin II
SYN3 synapsin III
SYNJ1 synaptojanin 1
SYT1 synaptotagmin I
UCHL1 ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
USP14 ubiquitin specific peptidase 14 (tRNA-guanine transglycosylase)