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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
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc22a3em1(IMPC)Mbp/Slc22a3em1(IMPC)Mbp
C57BL/6N-Slc22a3em1(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
Slc22a3tm1Dpb/Slc22a3tm1Dpb
involves: 129P2/OlaHsd
abnormal dopamine level J:180517
increased susceptibility to dopaminergic neuron neurotoxicity J:180517
Slc22a3tm1Dpb/Slc22a3tm1Dpb
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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last database update
06/12/2024
MGI 6.13
The Jackson Laboratory