Slc9a4 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc9a4
solute carrier family 9 (sodium/hydrogen exchanger), member 4
MGI:105074

14 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc9a4^{tm1b(EUCOMM)Wtsi}/Slc9a4^{tm1b(EUCOMM)Wtsi} C57BL/6N-Slc9a4^{tm1b(EUCOMM)Wtsi}/H	decreased bone mineral content	J:211773
	decreased bone mineral density	J:211773
	decreased prepulse inhibition	J:211773
	decreased startle reflex	J:211773
	increased circulating cholesterol level	J:211773
Slc9a4^tm1Ges/Slc9a4^tm1Ges involves: 129S6/SvEvTac * Black Swiss	abnormal gastric chief cell morphology	J:98566
	abnormal gastric parietal cell morphology	J:98566
	abnormal mucous neck cell morphology	J:98566
	abnormal stomach glandular epithelium morphology	J:98566
	abnormal stomach mucosa morphology	J:98566
	gastric necrosis	J:98566
	normal growth/size/body region phenotype	J:98566
	hypochlorhydria	J:98566
	stomach inflammation	J:98566

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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