About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc6a19
solute carrier family 6 (neurotransmitter transporter), member 19
MGI:1921588
18 phenotypes from 3 alleles in 4 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Slc6a19bucp-2J/Slc6a19bucp-2J
FVB/NJ-Slc6a19bucp-2J/GrsrJ
abnormal coat appearance J:237832
abnormal coat/hair pigmentation J:237832
normal hearing/vestibular/ear phenotype J:237832
normal homeostasis/metabolism phenotype J:237832
Slc6a19bucp/Slc6a19bucp
A/J-Slc6a19bucp/GrsrJ
abnormal coat appearance J:237831
abnormal coat/hair pigmentation J:237831
abnormal homeostasis J:237831
abnormal urine homeostasis J:237831
Slc6a19tm1Dgen/Slc6a19+
involves: 129 * C57BL/6J
abnormal intestine physiology J:175382
Slc6a19tm1Dgen/Slc6a19tm1Dgen
B6.129-Slc6a19tm1Dgen
decreased body weight J:175382
Slc6a19tm1Dgen/Slc6a19tm1Dgen
involves: 129 * C57BL/6J
abnormal intestine physiology J:175382
abnormal renal transport J:175382
aminoaciduria J:175382
decreased body size J:175382
decreased body weight J:175382
decreased circulating insulin level J:175382
decreased lean body mass J:175382
decreased total body fat amount J:175382
normal digestive/alimentary phenotype J:175382
hyperthreoninuria J:175382
insulin resistance J:175382
weight loss J:175382

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
04/16/2024
MGI 6.23
The Jackson Laboratory