About   Help   FAQ
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
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Slc22a1tm1Ahs/Slc22a1tm1Ahs
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
Slc22a1tm1Kmgi/Slc22a1tm1Kmgi
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/30/2024
MGI 6.23
The Jackson Laboratory