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Symbol
Name
ID
Scnn1b
sodium channel, nonvoltage-gated 1 beta
MGI:104696
Phenotype annotations related to renal/urinary system
Darker colors indicate more annotations
Human Phenotypes
Renal salt wasting
Renal insufficiency
Disease(s) Associated with SCNN1B
autosomal recessive pseudohypoaldosteronism type 1
Liddle syndrome

Mouse Phenotypes
abnormal urine homeostasis
abnormal kidney morphology
Availability Mouse Genotype
Scnn1btm1.1Ipt/Scnn1btm1.1Ipt
Scnn1btm1Wsh/Scnn1btm1Wsh
Scnn1btm1.1Ipt/Scnn1b+

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
11/14/2017
MGI 6.11
The Jackson Laboratory