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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Chrna4tm1Dra
targeted mutation 1, John Drago
MGI:1888964
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Chrna4tm1Dra/Chrna4tm1Dra involves: 129S4/SvJae * C57BL/6 MGI:3587441


Genotype
MGI:3587441
hm1
Allelic
Composition
Chrna4tm1Dra/Chrna4tm1Dra
Genetic
Background
involves: 129S4/SvJae * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Chrna4tm1Dra mutation (1 available); any Chrna4 mutation (42 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
N
• mutant mice do not display DAC (which consists of three distinct stereotypic behaviors - saccadic behavior, forelimb dystonia, Straub tail) after injection with 2, 6, or 8 mg/kg nicotine
• under an unhabituated or habituated condition, nicotine administration produced a smaller and delayed decline in sniffing, locomotion, total rearing, and sifting than in wild-type
• under normal conditions, homozygous null mice do not develop spontaneous seizures, however following administration of the GABA antagonist, pentylenetetrazole (PTZ), homozygous null mice show increased mortality, greater number of generalized clonic seizures, and EEGs with increased spikes, multi-spike complexes and continuous fast activity
• over an initial 1 hour phase of exploratory behavior in a novel environment, exhibit increased sniffing and decreased grooming
• over a subsequent phase of habituation, mice also exhibit increased sniffing, increased locomotion, and a reduced rate of habituation
• spend less time in open arms and make fewer open-arm entries in an elevated plus-maze, indicating increased anxiety
• exhibit decreased grooming over an initial 1 hour phase of exploratory behavior in a novel environment
• over a subsequent phase of habituation in a new environment, exhibit increased locomotion
• over a subsequent phase of habituation, exhibit an increase in total rearing, rearing seated, rearing to wall, and rearing free

nervous system
• under normal conditions, homozygous null mice do not develop spontaneous seizures, however following administration of the GABA antagonist, pentylenetetrazole (PTZ), homozygous null mice show increased mortality, greater number of generalized clonic seizures, and EEGs with increased spikes, multi-spike complexes and continuous fast activity
• EEGs with increased spikes, multi-spike complexes and continuous fast activity are observed when mice receive a GABA antagonist

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
NOT autosomal dominant nocturnal frontal lobe epilepsy 1 DOID:0060682 OMIM:600513
J:64208 , J:97020





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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory