Symbol Name ID |
Scn1a
sodium channel, voltage-gated, type I, alpha MGI:98246 |
! | Indicates phenotype varies with strain background. |
Darker colors indicate more annotations |
Human Phenotypes | Sudden unexpected death in epilepsy |
Disease(s) Associated with SCN1A | |
developmental and epileptic encephalopathy 6B |
Mouse Phenotypes | increased susceptibility to induced morbidity/mortality |
premature death |
lethality throughout fetal growth and development, incomplete penetrance |
neonatal lethality |
postnatal lethality |
postnatal lethality, complete penetrance |
postnatal lethality, incomplete penetrance |
preweaning lethality, incomplete penetrance |
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Availability | Mouse Genotype | ||||||||
Scn1aem1Anord/Scn1aem1Anord | |||||||||
Scn1atm1.1Aesc/Scn1atm1.1Aesc | |||||||||
Scn1atm1.1Swl/Scn1atm1.1Swl | |||||||||
Scn1atm1Kzy/Scn1atm1Kzy | |||||||||
Scn1atm1Wac/Scn1atm1Wac | |||||||||
Scn1atm1Wac/Scn1atm1Wac Tg(Scn1a*)RH9Aesc/0 |
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Scn1atm2.2Kzy/Scn1atm2.2Kzy | |||||||||
Scn1atm1.1Kzy/Scn1a+ | |||||||||
Scn1atm1.1Swl/Scn1a+ | ! | ||||||||
Scn1atm1Kea/Scn1a+ | ! | ||||||||
Scn1atm1Kzy/Scn1a+ | |||||||||
Scn1atm1Wac/Scn1a+ | ! | ||||||||
Scn1atm1Wac/Scn1a+ Tg(Scn1a*)RH9Aesc/0 |
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Scn1atm2.2Kzy/Scn1a+ | |||||||||
Scn1atm2.1Kzy/Scn1atm2.1Kzy Tg(Slc32a1-cre)65Kzy/0 (conditional) |
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Emx1tm1.1(cre)Ito/Emx1+ Scn1atm2.1Kzy/Scn1atm2.1Kzy Tg(Slc32a1-cre)65Kzy/0 (conditional) |
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Scn1atm2.1Kzy/Scn1atm2.1Kzy Tg(Pvalb-cre)1Tama/0 (conditional) |
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Scn1atm2.1Kzy/Scn1a+ Tg(Slc32a1-cre)65Kzy/0 (conditional) |
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Scn1atm2.1Kzy/Scn1a+ Tg(Pvalb-cre)1Tama/0 (conditional) |
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Scn1atm2.1Wac/Scn1a+ Tg(I12b-cre)1Jlr/0 (conditional) |
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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