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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc9a5
solute carrier family 9 (sodium/hydrogen exchanger), member 5
MGI:2685542
9 phenotypes from 2 alleles in 2 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc9a5em1(IMPC)J/Slc9a5em1(IMPC)J
C57BL/6NJ-Slc9a5em1(IMPC)J/Mmjax
decreased grip strength J:211773
decreased mean corpuscular hemoglobin concentration J:211773
Slc9a5tm1Smoc/Slc9a5tm1Smoc
involves: C57BL/6
abnormal nervous system physiology J:302075
abnormal object recognition memory J:302075
abnormal spatial reference memory J:302075
abnormal synapse morphology J:302075
normal behavior/neurological phenotype J:302075
enhanced learning J:302075
enhanced passive avoidance behavior J:302075

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
12/10/2024
MGI 6.24
The Jackson Laboratory