Slc6a7 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc6a7
solute carrier family 6 (neurotransmitter transporter, L-proline), member 7
MGI:2147363

9 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc6a7^em1(IMPC)J/Slc6a7^em1(IMPC)J C57BL/6NJ-Slc6a7^em1(IMPC)J/Mmjax	increased exploration in new environment	J:211773
	increased grip strength	J:211773
	preweaning lethality, incomplete penetrance	J:211773
Slc6a7^tm1Veul/Slc6a7^tm1Veul B6.129P2-Slc6a7^tm1Veul	abnormal nervous system physiology	J:288931
	abnormal response to novel object	J:288931
	normal behavior/neurological phenotype	J:288931
	decreased exploration in new environment	J:288931
	decreased locomotor activity	J:288931
	impaired spatial memory extinction	J:288931

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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