Slc22a1 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc22a1
solute carrier family 22 (organic cation transporter), member 1
MGI:108111

8 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc22a1^tm1Ahs/Slc22a1^tm1Ahs involves: 129P2/OlaHsd * FVB	abnormal digestive system physiology	J:70604
	abnormal hepatobiliary system physiology	J:70604
	abnormal liver physiology	J:70604
	abnormal urine organic cation level	J:70604
	abnormal xenobiotic pharmacokinetics	J:70604
Slc22a1^tm1Kmgi/Slc22a1^tm1Kmgi involves: 129P2/OlaHsd * C57BL/6J * FVB/N	abnormal fasting circulating glucose level	J:122106
	abnormal hepatic glucose production	J:122106
	abnormal physiological response to xenobiotic	J:122106
	abnormal xenobiotic pharmacokinetics	J:122106

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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