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Symbol Name ID |
Slc9a9
solute carrier family 9 (sodium/hydrogen exchanger), member 9 MGI:2679732 |
| Darker colors indicate more annotations |
| Human Phenotypes | EEG abnormality |
Abnormal nonverbal communicative behavior |
Delayed speech and language development |
Lack of spontaneous play |
Impaired ability to form peer relationships |
Autism |
Inflexible adherence to routines |
Motor stereotypy |
Restrictive behavior |
Intellectual disability |
Seizure |
| Disease(s) Associated with SLC9A9 | |||||||||||
| autistic disorder |
| Mouse Phenotypes | abnormal synaptic vesicle exocytosis |
abnormal brain wave pattern |
abnormal neuron physiology |
abnormal CNS synaptic transmission |
abnormal excitatory postsynaptic potential |
abnormal miniature excitatory postsynaptic currents |
decreased miniature inhibitory postsynaptic current amplitude |
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| Availability | Mouse Genotype | |||||||
| Slc9a9tm2d(KOMP)Wtsi/Slc9a9tm2d(KOMP)Wtsi | ||||||||
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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