Symbol Name ID |
Kcnk9
potassium channel, subfamily K, member 9 MGI:3521816 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Dysphagia |
Intellectual disability |
Global developmental delay |
Disease(s) Associated with KCNK9 | |||
Birk-Barel syndrome |
Mouse Phenotypes | nervous system phenotype |
abnormal action potential |
|
Availability | Mouse Genotype | ||
Kcnk9tm1.1Daba/Kcnk9tm1.1Daba | * | ||
Kcnk9tm1.1Fles/Kcnk9tm1.1Fles | * |
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 08/02/2024 MGI 6.24 |
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