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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(tetO-COX8A/PstI*)1Ctm
transgene insertion 1, Carlos T Moraes
MGI:5316004
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Slc6a3tm2(tTA)Xz/Slc6a3+
Tg(tetO-COX8A/PstI*)1Ctm/0
involves: 129X1/SvJ * C57BL/6 * C57BL/6J * SJL MGI:5316006
cx2
Tg(Camk2a-tTA)1Mmay/0
Tg(tetO-COX8A/PstI*)1Ctm/0
involves: C57BL/6 * CBA * SJL MGI:5316005


Genotype
MGI:5316006
cx1
Allelic
Composition
Slc6a3tm2(tTA)Xz/Slc6a3+
Tg(tetO-COX8A/PstI*)1Ctm/0
Genetic
Background
involves: 129X1/SvJ * C57BL/6 * C57BL/6J * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Slc6a3tm2(tTA)Xz mutation (0 available); any Slc6a3 mutation (32 available)
Tg(tetO-COX8A/PstI*)1Ctm mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mutants at 2 months of age exhibit a decrease in the exploration time in the activity cage, with this reduction lasting the duration of the dark cycle
• at 4 months of age, mutants exhibit an increased latency time to descend a pole from a fixed height, indicating poor motor coordination
• however, mutants show normal rotarod performance
• 4 month of mutants treated with L-DOPA and carbidopa, a common therapy for Parkinson Disease, exhibit improved performance on the pole test and the activity cage

growth/size/body
• mutants gain weight at a slower rate than controls; this slower weight gain is first observed at 2 months of age

homeostasis/metabolism
• mutants show a significant reduction in overall all amount of dopamine at both 4 and 12 months of age compared to controls
• mutants however show an increase in the amount of HVA and DOPA, downstream metabolites of dopamine, indicating altered dopamine metabolism in the striatum
• mutants over 12 months of age exhibit an increase in monoamine neurotransmitters, noradrenaline and serotonin
• mutants over 12 months of age exhibit an increase in monoamine neurotransmitters, noradrenaline and serotonin

nervous system
• mutants show a significant reduction in overall all amount of dopamine at both 4 and 12 months of age compared to controls
• mutants however show an increase in the amount of HVA and DOPA, downstream metabolites of dopamine, indicating altered dopamine metabolism in the striatum
• at 9 months of age, but not 4 months, mutants exhibit a 60% reduction in TH+ neurons in the substantia nigra, and by 12 months of age, very few TH+ neurons are left in the substantia nigra
• mutants exhibit a reduction in TH+ neurons in the striatum at 4 months of age
• mutants exhibit a reduction in dopamine transporter steady-state levels in the striatum, indicating a reduction of dopaminergic presynaptic terminals in the striatum at 4 months of age

Mouse Models of Human Disease
OMIM ID Ref(s)
Parkinson Disease, Late-Onset; PD 168600 J:178139




Genotype
MGI:5316005
cx2
Allelic
Composition
Tg(Camk2a-tTA)1Mmay/0
Tg(tetO-COX8A/PstI*)1Ctm/0
Genetic
Background
involves: C57BL/6 * CBA * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Camk2a-tTA)1Mmay mutation (7 available)
Tg(tetO-COX8A/PstI*)1Ctm mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mutants grown in the presence of Dox from E0 to P21 become progressively less active after the removal of Dox and die before 100 days of age

behavior/neurological
• mutants grown in the absence of Dox develop an abnormal limb-clasping behavior at 2 months of age
• mutants grown in the presence of Dox from E0 to P21, however, do not exhibit this limb-clasping behavior
• mutants grown in the presence of Dox from E0 to P21 become progressively less active after the removal of Dox and die before 100 days of age





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last database update
06/15/2016
MGI 6.04
The Jackson Laboratory