Slc9a5 Phenotype Annotations

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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

8 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc9a5^em1(IMPC)J/Slc9a5^em1(IMPC)J C57BL/6NJ-Slc9a5^em1(IMPC)J/Mmjax	decreased mean corpuscular hemoglobin concentration	J:211773
Slc9a5^tm1Smoc/Slc9a5^tm1Smoc 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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