Slc22a3 Phenotype Annotations

About Help FAQ

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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23