Symbol Name ID |
Slc9a1
solute carrier family 9 (sodium/hydrogen exchanger), member 1 MGI:102462 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Short stature |
Disease(s) Associated with SLC9A1 | |
autosomal recessive spinocerebellar ataxia 19 |
Mouse Phenotypes | growth/size/body region phenotype |
decreased body weight |
polycystic kidney |
decreased body size |
|
Availability | Mouse Genotype | ||||
Slc9a1swe/Slc9a1swe | * | ||||
Slc9a1tm1Smb/Slc9a1tm1Smb | |||||
Slc9a1em1(IMPC)Mbp/Slc9a1+ |
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 03/19/2024 MGI 6.23 |
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