Slc22a3 Phenotype Annotations

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Slc22a3
solute carrier family 22 (organic cation transporter), member 3
MGI:1333817

15 phenotypes from 2 alleles in 3 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Slc22a3^em1(IMPC)Mbp/Slc22a3^em1(IMPC)Mbp C57BL/6N-Slc22a3^em1(IMPC)Mbp/MbpMmucd	abnormal behavior	J:211773
	abnormal eye morphology	J:211773
	anophthalmia	J:211773
	decreased anxiety-related response	J:211773
	decreased locomotor activity	J:211773
	decreased thigmotaxis	J:211773
	hyperactivity	J:211773
Slc22a3^tm1Dpb/Slc22a3^tm1Dpb involves: 129P2/OlaHsd	abnormal dopamine level	J:180517
Slc22a3^tm1Dpb/Slc22a3^tm1Dpb involves: 129P2/OlaHsd	increased susceptibility to dopaminergic neuron neurotoxicity	J:180517
Slc22a3^tm1Dpb/Slc22a3^tm1Dpb involves: 129P2/OlaHsd * FVB/N	normal behavior/neurological phenotype	J:69978
	normal cardiovascular system phenotype	J:69978
	normal growth/size/body region phenotype	J:69978
	normal mortality/aging	J:69978
	normal nervous system phenotype	J:69978
	normal reproductive system phenotype	J:69978

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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