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Symbol
Name
ID
Scn11a
sodium channel, voltage-gated, type XI, alpha
MGI:1345149
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Motor delay
Pain insensitivity
Abnormal autonomic nervous system physiology
Disease(s) Associated with SCN11A
familial episodic pain syndrome 3
hereditary sensory and autonomic neuropathy type 7

Mouse Phenotypes
abnormal nervous system electrophysiology
abnormal action potential
abnormal afterhyperpolarization
abnormal single cell response
abnormal miniature excitatory postsynaptic currents
abnormal channel response
Availability Mouse Genotype
Scn11atm1Gsk/Scn11atm1Gsk
Scn11atm1Mdba/Scn11atm1Mdba
Scn11atm1Wlf/Scn11atm1Wlf
Scn11aem1Akoi/Scn11a+
Scn11aem2Akoi/Scn11a+
Scn11aem3Akoi/Scn11a+
Scn11atm1.1Ikth/Scn11a+
Scn11atm1Mdba/Scn11atm1.1Ikth

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
04/23/2024
MGI 6.23
The Jackson Laboratory