Slc22a4 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc22a4
solute carrier family 22 (organic cation transporter), member 4
MGI:1353479

6 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc22a4^{tm1.1(KOMP)Vlcg}/Slc22a4^{tm1.1(KOMP)Vlcg} C57BL/6N-Slc22a4^{tm1.1(KOMP)Vlcg}/Ieg	enlarged cecum	J:211773
Slc22a4^tm1Atsu/Slc22a4^tm1Atsu involves: C57BL/6J	abnormal amino acid level	J:207006
	abnormal small intestinal villus morphology	J:207006
	increased susceptibility to induced morbidity/mortality	J:207006
	increased susceptibility to injury	J:207006
	intestinal inflammation	J:207006

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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