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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Dbptm1Schb
targeted mutation 1, Ueli Schibler
MGI:2183196
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Dbptm1Schb/Dbptm1Schb 129P2/OlaHsd-Dbptm1Schb MGI:3845760
cx2
Dbptm1Schb/Dbptm1Schb
Hlftm1Schb/Hlftm1Schb
Teftm1Schb/Teftm1Schb
involves: 129P2/OlaHsd * 129S2/SvPas MGI:3045596
cx3
Dbptm1Schb/Dbptm1Schb
Hlftm1Schb/Hlftm1Schb
Teftm1Schb/Tef+
involves: 129P2/OlaHsd * 129S2/SvPas MGI:3843511
cx4
Dbptm1Schb/Dbptm1Schb
Teftm1Schb/Teftm1Schb
involves: 129P2/OlaHsd * 129S2/SvPas MGI:3843512


Genotype
MGI:3845760
hm1
Allelic
Composition
Dbptm1Schb/Dbptm1Schb
Genetic
Background
129P2/OlaHsd-Dbptm1Schb
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dbptm1Schb mutation (2 available); any Dbp mutation (23 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• generate about 40% fewer wheel revolutions and show less spontaneous activity under light/dark conditions
• overall decrease in activity is mostly the result of decreased activity during the dark phase
• moderately but significantly shorter compared to controls under dark/dark conditions




Genotype
MGI:3045596
cx2
Allelic
Composition
Dbptm1Schb/Dbptm1Schb
Hlftm1Schb/Hlftm1Schb
Teftm1Schb/Teftm1Schb
Genetic
Background
involves: 129P2/OlaHsd * 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dbptm1Schb mutation (2 available); any Dbp mutation (23 available)
Hlftm1Schb mutation (2 available); any Hlf mutation (17 available)
Teftm1Schb mutation (2 available); any Tef mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system

liver/biliary system
• increased liver mass

mortality/aging
• 50% of mice die within the first 2 months of age due to lethal seizures

behavior/neurological
• mice are hypersensitive to xenobiotic compounds including pentobarbital
• a circadian trend of seizure occurance is observed, with 4-times more seizures occuring during early light period hours (major sleep period) than during early dark period hours (major active period)
• observed in some mice; audiogenic seizures account for about 25% of all deceased mice
• spontaneous tonic-clonic seizures that occur predominantly within slow-wave sleep during the first 2 min after transition to sleep
• observe a few absence-like seizures without any sign of EEG hypoactivity

nervous system
• a circadian trend of seizure occurance is observed, with 4-times more seizures occuring during early light period hours (major sleep period) than during early dark period hours (major active period)
• observed in some mice; audiogenic seizures account for about 25% of all deceased mice
• spontaneous tonic-clonic seizures that occur predominantly within slow-wave sleep during the first 2 min after transition to sleep
• observe a few absence-like seizures without any sign of EEG hypoactivity
• reduction in levels of serotonin and dopamine and increase in levels of histamine in the brain
• analysis of sleep EEG of a 12-hour light period shows a significant increase in slow-wave delta activity and a significant decrease in theta activity
• activity in all frequency bins greater than 15 Hz (the beta frequency range) is significantly increased during all vigilance states

homeostasis/metabolism
• increased plasma levels of alanine aminotransferase
• reduction in levels of dopamine in the brain
• reduction in the levels of serotonin in the brain
• mice are hypersensitive to xenobiotic compounds including pentobarbital, mitoxantrone and cyclophosphamide

growth/size/body
• increased liver mass




Genotype
MGI:3843511
cx3
Allelic
Composition
Dbptm1Schb/Dbptm1Schb
Hlftm1Schb/Hlftm1Schb
Teftm1Schb/Tef+
Genetic
Background
involves: 129P2/OlaHsd * 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dbptm1Schb mutation (2 available); any Dbp mutation (23 available)
Hlftm1Schb mutation (2 available); any Hlf mutation (17 available)
Teftm1Schb mutation (2 available); any Tef mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• several seizure-like activities are observed in mutants, however they never develop into generalized epilepsies
• several absence-like seizures without any sign of EEG hypoactivity are seen

nervous system
• several seizure-like activities are observed in mutants, however they never develop into generalized epilepsies
• several absence-like seizures without any sign of EEG hypoactivity are seen
• analysis of sleep EEG of a 12-hour light period shows an increase in slow-wave delta activity and a decrease in theta activity, however this is much less pronounced than in triple homozygous mutants
• activity in all frequency bins greater than 15 Hz (the beta frequency range) is increased in waking mutants




Genotype
MGI:3843512
cx4
Allelic
Composition
Dbptm1Schb/Dbptm1Schb
Teftm1Schb/Teftm1Schb
Genetic
Background
involves: 129P2/OlaHsd * 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dbptm1Schb mutation (2 available); any Dbp mutation (23 available)
Teftm1Schb mutation (2 available); any Tef mutation (13 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• succumb to sudden death





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory