Symbol Name ID |
Slc6a19
solute carrier family 6 (neurotransmitter transporter), member 19 MGI:1921588 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Elevated urinary indoleacetic acid level |
Neutral hyperaminoaciduria |
Disease(s) Associated with SLC6A19 | ||
Hartnup disease |
Mouse Phenotypes | homeostasis/metabolism phenotype |
abnormal homeostasis |
alaninuria |
hyperglutaminuria |
hyperglycinuria |
methioninuria |
phenylalaninuria |
hyperthreoninuria |
aminoaciduria |
decreased circulating insulin level |
insulin resistance |
abnormal urine homeostasis |
|
Availability | Mouse Genotype | ||||||||||||
Slc6a19bucp-2J/Slc6a19bucp-2J | * | ||||||||||||
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 08/02/2024 MGI 6.24 |
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