Symbol Name ID |
Slc9a9
solute carrier family 9 (sodium/hydrogen exchanger), member 9 MGI:2679732 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Lack of spontaneous play |
Impaired ability to form peer relationships |
Autism |
Inflexible adherence to routines |
Motor stereotypy |
Restrictive behavior |
Disease(s) Associated with SLC9A9 | ||||||
autistic disorder |
Mouse Phenotypes | behavior/neurological phenotype |
abnormal behavior |
abnormal habituation |
abnormal olfactory behavior |
abnormal response to social novelty |
abnormal allogrooming behavior |
increased grooming behavior |
increased grip strength |
increased stereotypic behavior |
decreased thermal nociceptive threshold |
abnormal social/conspecific interaction behavior |
abnormal social investigation |
abnormal social recognition |
abnormal social play behavior |
decreased vocalization |
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Availability | Mouse Genotype | |||||||||||||||
Slc9a9em1(IMPC)J/Slc9a9em1(IMPC)J | ||||||||||||||||
Slc9a9tm1.1Yzj/Slc9a9tm1.1Yzj | * | |||||||||||||||
Slc9a9tm2d(KOMP)Wtsi/Slc9a9tm2d(KOMP)Wtsi | ||||||||||||||||
Slc9a9tm2c(KOMP)Wtsi/Slc9a9tm2c(KOMP)Wtsi Tg(Nes-cre)1Kln/0 (conditional) |
* | |||||||||||||||
Slc9a9tm2c(KOMP)Wtsi/Slc9a9+ Tg(Nes-cre)1Kln/0 (conditional) |
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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