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Symbol
Name
ID
Scnn1b
sodium channel, nonvoltage-gated 1 beta
MGI:104696
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Osteomyelitis
Disease(s) Associated with SCNN1B
autosomal recessive pseudohypoaldosteronism type 1

Mouse Phenotypes
abnormal pelvic girdle bone morphology
Availability Mouse Genotype
Scnn1btm1b(EUCOMM)Hmgu/Scnn1b+

Contributing Projects:
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
03/31/2020
MGI 6.15
The Jackson Laboratory