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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
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Allelic Composition
Genetic Background		 Annotated Term Reference
Slc6a7em1(IMPC)J/Slc6a7em1(IMPC)J
C57BL/6NJ-Slc6a7em1(IMPC)J/Mmjax 		increased exploration in new environment J:211773
increased grip strength J:211773
preweaning lethality, incomplete penetrance J:211773
Slc6a7tm1Veul/Slc6a7tm1Veul
B6.129P2-Slc6a7tm1Veul 		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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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory