Slc16a3 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc16a3
solute carrier family 16 (monocarboxylic acid transporters), member 3
MGI:1933438

10 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc16a3^tm1.1Lupel/Slc16a3^tm1.1Lupel C57BL/6J-Slc16a3^tm1.1Lupel	abnormal object recognition memory	J:296969
	normal behavior/neurological phenotype	J:296969
	impaired long-term object recognition memory	J:296969
	impaired spatial learning	J:296969
	normal nervous system phenotype	J:296969
Slc16a3^tm1Tac/Slc16a3^tm1Tac B6NTac.Cg-Slc16a3^tm1Tac/Tac	abnormal action potential	J:288233
	abnormal axon morphology	J:288233
	abnormal neuromuscular synapse morphology	J:288233
	impaired exercise endurance	J:288233
	normal muscle phenotype	J:288233

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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