Slc41a3 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc41a3
solute carrier family 41, member 3
MGI:1918949

8 phenotypes from 1 allele in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc41a3^{tm1a(KOMP)Wtsi}/Slc41a3^{tm1a(KOMP)Wtsi} B6JTyr;B6N-Slc41a3^{tm1a(KOMP)Wtsi}/Wtsi	limb grasping	J:175295
Slc41a3^{tm1a(KOMP)Wtsi}/Slc41a3^{tm1a(KOMP)Wtsi} involves: C57BL/6 * C57BL/6N	decreased circulating magnesium level	J:344881
Slc41a3^{tm1a(KOMP)Wtsi}/Slc41a3^{tm1a(KOMP)Wtsi} involves: C57BL/6J * C57BL/6N	abnormal magnesium ion homeostasis	J:236099
	normal behavior/neurological phenotype	J:236099
	decreased circulating magnesium level	J:236099
	enlarged kidney	J:236099
	normal homeostasis/metabolism phenotype	J:236099
	hydronephrosis	J:236099
	ureter stenosis	J:236099

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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