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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Th-cre)#Gsat
transgene insertion, GENSAT Project at Rockefeller University
MGI:5607431
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Trp53inp2tm1c(KOMP)Mbp/Trp53inp2tm1c(KOMP)Mbp
Tg(Th-cre)#Gsat/0
involves: 129S4/SvJaeSor * C57BL/6N * FVB/N MGI:6507407
cn2
Wnt5atm1.1Krvl/Wnt5atm1.1Krvl
Tg(Th-cre)#Gsat/0
involves: 129S6/SvEvTac * C57BL/6 * FVB/N MGI:5607432


Genotype
MGI:6507407
cn1
Allelic
Composition
Trp53inp2tm1c(KOMP)Mbp/Trp53inp2tm1c(KOMP)Mbp
Tg(Th-cre)#Gsat/0
Genetic
Background
involves: 129S4/SvJaeSor * C57BL/6N * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Th-cre)#Gsat mutation (0 available)
Trp53inp2tm1c(KOMP)Mbp mutation (0 available); any Trp53inp2 mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• defects in axon growth of NGF-responsive sympathetic neurons are observed in the heart at E16.5
• analysis of superior cervical ganglia (SCGs) revealed normal numbers of sympathetic neurons at E16.5 but significant cell loss at birth (P0.5) and 3 weeks after birth (P21) relative to control littermates
• although no neuronal loss is detected at E16.5, sympathetic innervation of the heart is already decreased with a significant reduction in both density of innervation and axonal branching
• analysis of superior cervical ganglia (SCGs) revealed normal numbers of sympathetic neurons at E16.5 but significant cell loss at birth (P0.5) and 3 weeks after birth (P21) relative to control littermates
• neuronal loss is likely due to the axons failing to reach target tissues and gain access to adequate levels of nerve growth factor (NGF)

cellular
• defects in axon growth of NGF-responsive sympathetic neurons are observed in the heart at E16.5




Genotype
MGI:5607432
cn2
Allelic
Composition
Wnt5atm1.1Krvl/Wnt5atm1.1Krvl
Tg(Th-cre)#Gsat/0
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Th-cre)#Gsat mutation (0 available)
Wnt5atm1.1Krvl mutation (1 available); any Wnt5a mutation (40 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• reduced innervation of peripheral tissues
• 30% decrease in numbers of superior cervical ganglia neurons by P7





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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
04/23/2024
MGI 6.23
The Jackson Laboratory