Slc47a1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc47a1
solute carrier family 47, member 1
MGI:1914723

10 phenotypes from 3 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc47a1^{Gt(IST12634F2)Tigm}/Slc47a1^{Gt(IST12634F2)Tigm} B6.B6N-Slc47a1^{Gt(IST12634F2)Tigm}	abnormal liver morphology	J:206792
	abnormal xenobiotic pharmacokinetics	J:206792
	increased body weight	J:206792
	increased physiological sensitivity to xenobiotic	J:206792
	kidney degeneration	J:206792
Slc47a1^{tm1b(EUCOMM)Wtsi}/Slc47a1^{tm1b(EUCOMM)Wtsi} C57BL/6N-Slc47a1^{tm1b(EUCOMM)Wtsi}/Ieg	abnormal vocalization	J:211773
	decreased circulating phosphate level	J:211773
	increased circulating total protein level	J:211773
Slc47a1^tm1Kinu/Slc47a1^tm1Kinu C57BL/6-Slc47a1^tm1Kinu	abnormal xenobiotic pharmacokinetics	J:163959
	increased blood urea nitrogen level	J:163959
	increased circulating creatinine level	J:163959

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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