Symbol Name ID |
Slc9a6
solute carrier family 9 (sodium/hydrogen exchanger), member 6 MGI:2443511 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Drooling |
Feeding difficulties in infancy |
Bowel incontinence |
Urinary incontinence |
Happy demeanor |
Conspicuously happy disposition |
Inappropriate laughter |
Autism |
Motor stereotypy |
Disease(s) Associated with SLC9A6 | |||||||||
Christianson syndrome |
Mouse Phenotypes | behavior/neurological phenotype |
increased susceptibility to pharmacologically induced seizures |
abnormal spatial reference memory |
ataxia |
impaired coordination |
increased vertical activity |
increased locomotor activity |
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Availability | Mouse Genotype | |||||||
Slc9a6tm1Dgen/Slc9a6tm1Dgen | * | |||||||
Slc9a6tm1Dgen/Slc9a6+ | ||||||||
Slc9a6tm1Dgen/Y | * |
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 04/16/2024 MGI 6.23 |
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