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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc9a3r1
solute carrier family 9 (sodium/hydrogen exchanger), member 3 regulator 1
MGI:1349482
15 phenotypes from 2 alleles in 4 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc9a3r1tm1Geo/Slc9a3r1tm1Geo
involves: C57BL/6J
abnormal intestinal epithelium morphology J:95282
abnormal intestinal goblet cell morphology J:95282
abnormal intestine morphology J:95282
decreased circulating phosphate level J:95282
premature death J:95282
Slc9a3r1tm1Ssl/Slc9a3r1tm1Ssl
FVB.129-Slc9a3r1tm1Ssl
abnormal physiological response to xenobiotic J:128912
normal reproductive system phenotype J:128912
Slc9a3r1tm1Ssl/Slc9a3r1tm1Ssl
involves: 129X1/SvJ
decreased litter size J:78606
reduced fertility J:78606
Slc9a3r1tm1Ssl/Slc9a3r1tm1Ssl
involves: 129X1/SvJ * C57BL/6
abnormal locomotor behavior J:78606
decreased bone mineral content J:78606
decreased bone mineral density J:78606
decreased litter size J:78606
hydrocephaly J:78606
increased urine phosphate level J:78606
premature death J:78606
prenatal lethality, incomplete penetrance J:78606

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
11/05/2019
MGI 6.14
The Jackson Laboratory