Symbol Name ID |
Scnn1a
sodium channel, nonvoltage-gated 1 alpha MGI:101782 |
Darker colors indicate more annotations |
Human Phenotypes | Renal insufficiency |
Disease(s) Associated with SCNN1A | |
Liddle syndrome |
Mouse Phenotypes | abnormal renal transport |
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Availability | Mouse Genotype | |
Scnn1atm1.1Hum/Scnn1atm1.1Hum Tg(Hoxb7-cre)13Amc/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 09/03/2024 MGI 6.24 |
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