Slc18a3 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc18a3
solute carrier family 18 (vesicular monoamine), member 3
MGI:1101061

10 phenotypes from 1 allele in 1 genetic background

Allelic Composition Genetic Background	Annotated Term	Reference
Slc18a3^tm1Mca/Slc18a3⁺ involves: 129S4/SvJae * C57BL/6J	abnormal miniature endplate potential	J:137284
	abnormal object recognition memory	J:137284
	abnormal social investigation	J:137284
	abnormal synaptic acetylcholine release	J:137284
	normal behavior/neurological phenotype	J:137284
	impaired coordination	J:137284
Slc18a3^tm1Mca/Slc18a3^tm1Mca involves: 129S4/SvJae * C57BL/6J	abnormal endplate potential	J:137284
	abnormal miniature endplate potential	J:137284
	abnormal social investigation	J:137284
	abnormal synaptic acetylcholine release	J:137284
	decreased grip strength	J:137284
	impaired coordination	J:137284
	impaired exercise endurance	J:137284
	increased susceptibility to pharmacologically induced seizures	J:136620

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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