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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Pvalb-cre)1Tama
transgene insertion 1, Nobuaki Tamamaki
MGI:3837553
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Scn1atm2.1Kzy/Scn1a+
Tg(Pvalb-cre)1Tama/0
involves: 129P2/OlaHsd * C57BL/6 * DBA MGI:5523888
cn2
Scn1atm2.1Kzy/Scn1atm2.1Kzy
Tg(Pvalb-cre)1Tama/0
involves: 129P2/OlaHsd * C57BL/6 * DBA MGI:5523889
cx3
Tg(CAG-mRFP,-GFP)1Tama/?
Tg(Pvalb-cre)1Tama/?
involves: C57BL/6 * DBA MGI:3837561


Genotype
MGI:5523888
cn1
Allelic
Composition
Scn1atm2.1Kzy/Scn1a+
Tg(Pvalb-cre)1Tama/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * DBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scn1atm2.1Kzy mutation (1 available); any Scn1a mutation (114 available)
Tg(Pvalb-cre)1Tama mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• some mice develop recurrent seizures after P16

mortality/aging
• some mice develop recurrent seizures after P16 and experience sporadic sudden death

nervous system
• some mice develop recurrent seizures after P16

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Dravet syndrome DOID:0080422 OMIM:607208
J:202863




Genotype
MGI:5523889
cn2
Allelic
Composition
Scn1atm2.1Kzy/Scn1atm2.1Kzy
Tg(Pvalb-cre)1Tama/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6 * DBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Scn1atm2.1Kzy mutation (1 available); any Scn1a mutation (114 available)
Tg(Pvalb-cre)1Tama mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all animals die before P30

behavior/neurological
• develops around P14
• mice are physically normal for first week postnatal, but around P10 develop spontaneous generalized convulsive seizures

nervous system
• mice are physically normal for first week postnatal, but around P10 develop spontaneous generalized convulsive seizures

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
Dravet syndrome DOID:0080422 OMIM:607208
J:202863




Genotype
MGI:3837561
cx3
Allelic
Composition
Tg(CAG-mRFP,-GFP)1Tama/?
Tg(Pvalb-cre)1Tama/?
Genetic
Background
involves: C57BL/6 * DBA
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype





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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
09/03/2024
MGI 6.24
The Jackson Laboratory