Symbol Name ID |
Slc17a5
solute carrier family 17 (anion/sugar transporter), member 5 MGI:1924105 |
Darker colors indicate more annotations |
Human Phenotypes | Attention deficit hyperactivity disorder |
Disease(s) Associated with SLC17A5 | |
sialuria |
Mouse Phenotypes | decreased exploration in new environment |
behavioral despair |
tremors |
weakness |
abnormal locomotor behavior |
abnormal gait |
short stride length |
environmentally induced seizures |
tonic-clonic seizures |
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Availability | Mouse Genotype | |||||||||
Slc17a5tm1Lex/Slc17a5tm1Lex |
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 09/03/2024 MGI 6.24 |
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