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Symbol Name ID |
Slc17a5
solute carrier family 17 (anion/sugar transporter), member 5 MGI:1924105 |
| Darker colors indicate more annotations |
| Human Phenotypes | Spasticity |
Ataxia |
Poor fine motor coordination |
Athetosis |
Delayed speech and language development |
Dysarthria |
Attention deficit hyperactivity disorder |
Intellectual disability |
Intellectual disability, mild |
Sleep apnea |
Inability to walk |
Global developmental delay |
Seizure |
| Disease(s) Associated with SLC17A5 | |||||||||||||
| sialuria |
| Mouse Phenotypes | environmentally induced seizures |
tonic-clonic seizures |
decreased oligodendrocyte progenitor number |
abnormal corpus callosum morphology |
abnormal optic tract morphology |
abnormal brainstem morphology |
brain vacuoles |
abnormal neuron morphology |
abnormal myelin sheath morphology |
abnormal optic nerve morphology |
abnormal nervous system physiology |
abnormal myelination |
demyelination |
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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 04/23/2024 MGI 6.23 |
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