Symbol Name ID |
Scn11a
sodium channel, voltage-gated, type XI, alpha MGI:1345149 |
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 |
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Availability | Mouse Genotype | ||||||
Scn11atm1Gsk/Scn11atm1Gsk | |||||||
Scn11atm1Mdba/Scn11atm1Mdba | |||||||
Scn11atm1Wlf/Scn11atm1Wlf | |||||||
Scn11aem1Akoi/Scn11a+ | |||||||
Scn11aem2Akoi/Scn11a+ | |||||||
Scn11aem3Akoi/Scn11a+ | |||||||
Scn11atm1.1Ikth/Scn11a+ | |||||||
Scn11atm1Mdba/Scn11atm1.1Ikth |
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 08/02/2024 MGI 6.24 |
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