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Symbol
Name
ID
Scnn1a
sodium channel, nonvoltage-gated 1 alpha
MGI:101782
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties in infancy
Disease(s) Associated with SCNN1A
autosomal recessive pseudohypoaldosteronism type 1

Mouse Phenotypes
abnormal eating behavior
hypoactivity
Availability Mouse Genotype
Scnn1atm1Rss/Scnn1atm1Rss

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