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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc16a7
solute carrier family 16 (monocarboxylic acid transporters), member 7
MGI:1330284
6 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc16a7tm1.1Lupel/Slc16a7tm1.1Lupel
C57BL/6J-Slc16a7tm1.1Lupel
abnormal object recognition memory J:296969
argyrophilic inclusion bodies J:296969
normal behavior/neurological phenotype J:296969
impaired long-term object recognition memory J:296969
impaired neuron differentiation J:296969
impaired spatial learning J:296969

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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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory