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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
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Allelic Composition
Genetic Background		 Annotated Term Reference
Slc9a4tm1b(EUCOMM)Wtsi/Slc9a4tm1b(EUCOMM)Wtsi
C57BL/6N-Slc9a4tm1b(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
Slc9a4tm1Ges/Slc9a4tm1Ges
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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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory