Symbol Name ID |
Slc6a19
solute carrier family 6 (neurotransmitter transporter), member 19 MGI:1921588 |
Darker colors indicate more annotations |
Human Phenotypes | Elevated urinary indoleacetic acid level |
Neutral hyperaminoaciduria |
Disease(s) Associated with SLC6A19 | ||
Hartnup disease |
Mouse Phenotypes | hyperthreoninuria |
aminoaciduria |
abnormal urine homeostasis |
abnormal renal transport |
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Availability | Mouse Genotype | ||||
Slc6a19bucp/Slc6a19bucp | |||||
Slc6a19tm1Dgen/Slc6a19tm1Dgen |
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 05/14/2024 MGI 6.23 |
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