Slc41a3 Phenotype Annotations

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 12/30/2025 MGI 6.24