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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Prkg1tm2Naw
targeted mutation 2, Hermann Nawrath
MGI:2668652
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Prkg1tm2Naw/Prkg1tm2Naw either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) MGI:2668654
cn2
Myl7tm1(cre)Krc/Myl7+
Prkg1tm2Naw/Prkg1tm2Naw
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) MGI:2668843
cn3
Prkg1tm2Naw/Prkg1tm2Naw
Tg(Pcp2-cre)2Mpin/?
involves: 129/Sv * C57BL/6 MGI:2680086
cn4
Kittm1(cre/ERT2)Dsa/Kit+
Prkg1tm2Naw/Prkg1tm2Naw
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 MGI:5545743
cn5
Neurod6tm1(cre)Kan/Neurod6+
Prkg1tm2Naw/Prkg1tm2.1Naw
involves: 129S1/Sv * 129X1/SvJ MGI:2668663


Genotype
MGI:2668654
hm1
Allelic
Composition
Prkg1tm2Naw/Prkg1tm2Naw
Genetic
Background
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prkg1tm2Naw mutation (0 available); any Prkg1 mutation (60 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype




Genotype
MGI:2668843
cn2
Allelic
Composition
Myl7tm1(cre)Krc/Myl7+
Prkg1tm2Naw/Prkg1tm2Naw
Genetic
Background
either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Myl7tm1(cre)Krc mutation (0 available); any Myl7 mutation (7 available)
Prkg1tm2Naw mutation (0 available); any Prkg1 mutation (60 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cardiovascular system
• cGMP analogues reduce the force of contraction in cardiac muscle from adult controls but not from adult mutants

muscle
• cGMP analogues reduce the force of contraction in cardiac muscle from adult controls but not from adult mutants




Genotype
MGI:2680086
cn3
Allelic
Composition
Prkg1tm2Naw/Prkg1tm2Naw
Tg(Pcp2-cre)2Mpin/?
Genetic
Background
involves: 129/Sv * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prkg1tm2Naw mutation (0 available); any Prkg1 mutation (60 available)
Tg(Pcp2-cre)2Mpin mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• long term depression in the cerebellum is suppressed
• motor coordination as determined by footprint, runway, and rotarod tests was normal
• less vestibulo-occular reflex adaptation than in controls




Genotype
MGI:5545743
cn4
Allelic
Composition
Kittm1(cre/ERT2)Dsa/Kit+
Prkg1tm2Naw/Prkg1tm2Naw
Genetic
Background
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Kittm1(cre/ERT2)Dsa mutation (0 available); any Kit mutation (182 available)
Prkg1tm2Naw mutation (0 available); any Prkg1 mutation (60 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
digestive/alimentary system
• significant GI motor dysfunction is observed with tamoxifen treatment
• change in contraction frequency is observed in tamoxifen-treated mutants
• nitric oxide-dependent nitrergic slow component of the inhibitory junction potential in circular smooth muscle cells of the colon is abolished in tamoxifen-treated mice
• GI transit time is increased by about 2 hours in treated mutants

muscle
• change in contraction frequency is observed in tamoxifen-treated mutants
• nitric oxide-dependent nitrergic slow component of the inhibitory junction potential in circular smooth muscle cells of the colon is abolished in tamoxifen-treated mice




Genotype
MGI:2668663
cn5
Allelic
Composition
Neurod6tm1(cre)Kan/Neurod6+
Prkg1tm2Naw/Prkg1tm2.1Naw
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Neurod6tm1(cre)Kan mutation (0 available); any Neurod6 mutation (18 available)
Prkg1tm2.1Naw mutation (0 available); any Prkg1 mutation (60 available)
Prkg1tm2Naw mutation (0 available); any Prkg1 mutation (60 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
N
• unlike Prkg1tm1Hfm homozygotes, conditional mutant mice have a normal life expectancy

nervous system
N
• adult conditional mutant mice display no significant differences in baseline synaptic transmission relative to control littermates
• adult (12-14 weeks of age) but not juvenile (3-4 weeks of age) conditional mutant mice display reduced hippocampal LTP after repetitive episodes of theta burst stimulation (TBS)
• the difference in LTP between adult conditional and control mice is abolished by anisomycin (a protein synthesis inhibitor), suggesting a defect in late-phase LTP
• however, both juvenile and adult conditional mutant mice show a normal LTP in response to a single episode of tetanic stimulation, regardless of whether a weak TBS or a strong tetanic stimulus is used

behavior/neurological
N
• despite a deficit in late-phase LTP, adult conditional mutant mice exhibit normal performance in hippocampus-dependent behavioral tests, i.e., contextual fear conditioning and spatial learning, with no significant differences in the freezing response to the conditioning context, in acquisition of a spatial searching strategy, or in storage and retrieval of spatial memory relative to control mice

cardiovascular system
N
• unlike Prkg1tm1Hfm homozygotes, conditional mutant mice display no detectable cardiovascular abnormalities

digestive/alimentary system
N
• unlike Prkg1tm1Hfm homozygotes, conditional mutant mice display no detectable gastrointestinal abnormalities





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