Slc22a12 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc22a12
solute carrier family 22 (organic anion/cation transporter), member 12
MGI:1195269

14 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc22a12^tm1Dgen/Slc22a12^tm1Dgen B6.129P2-Slc22a12^tm1Dgen	abnormal blood homeostasis	J:136005
	abnormal urine homeostasis	J:136005
	uraturia	J:136005
Slc22a12^tm1Dgen/Slc22a12^tm1Dgen involves: 129P2/OlaHsd * C57BL/6	normal behavior/neurological phenotype	J:101679
	normal cardiovascular system phenotype	J:101679
	normal digestive/alimentary phenotype	J:101679
	normal endocrine/exocrine gland phenotype	J:101679
	normal growth/size/body region phenotype	J:101679
	normal hematopoietic system phenotype	J:101679
	normal mortality/aging	J:101679
	normal nervous system phenotype	J:101679
	normal reproductive system phenotype	J:101679
Slc22a12^tm1Oka/Slc22a12^tm1Oka involves: 129 * C57BL/6J	abnormal renal reabsorption	J:260689
Slc22a12^tm1Oka/Slc22a12^tm1Oka involves: 129 * C57BL/6J	increased urine uric acid level	J:260689

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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