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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gli2tm3(Gli1)Alj
targeted mutation 3, Alexandra L Joyner
MGI:2158719
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Gli2tm3(Gli1)Alj/Gli2tm3(Gli1)Alj either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss) MGI:3846350
hm2
Gli2tm3(Gli1)Alj/Gli2tm3(Gli1)Alj involves: 129S6/SvEvTac * Black Swiss * Swiss Webster MGI:3795686
ht3
Gli2tm2.1Alj/Gli2tm3(Gli1)Alj either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss) MGI:3846348
cx4
Gli2tm3(Gli1)Alj/Gli2tm3(Gli1)Alj
Gli3Xt-J/Gli3+
involves: 129S6/SvEvTac * Black Swiss * C3H/HeJ * C57BL/6 * Swiss Webster MGI:3795687


Genotype
MGI:3846350
hm1
Allelic
Composition
Gli2tm3(Gli1)Alj/Gli2tm3(Gli1)Alj
Genetic
Background
either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli2tm3(Gli1)Alj mutation (0 available); any Gli2 mutation (169 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most mice that survive past weaning die by 3 months of age
• fewer than expected mice are found at weaning

growth/size/body
• about 40% smaller than controls by 3 months of age

behavior/neurological
• impaired hindlimb coordination is seen at 3 months of age
• stiffness in the hindlimbs is seen at 3 months of age

integument
• loss of hair beginning on the dorsal neck
• hair loss is more severe than in mice carrying Gli2tm3.1(Gli2)Alj and Gli2tm2.1Alj




Genotype
MGI:3795686
hm2
Allelic
Composition
Gli2tm3(Gli1)Alj/Gli2tm3(Gli1)Alj
Genetic
Background
involves: 129S6/SvEvTac * Black Swiss * Swiss Webster
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli2tm3(Gli1)Alj mutation (0 available); any Gli2 mutation (169 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
N
• embryos show normal mammary gland development




Genotype
MGI:3846348
ht3
Allelic
Composition
Gli2tm2.1Alj/Gli2tm3(Gli1)Alj
Genetic
Background
either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli2tm2.1Alj mutation (1 available); any Gli2 mutation (169 available)
Gli2tm3(Gli1)Alj mutation (0 available); any Gli2 mutation (169 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• viable with no gross abnormalities
• unlike in homozygous null mice, at E10.5 the floor plate is present, interneurons are found in the appropriate location, and notochord regression is normal
• unlike in homozygous null mice, at E12.5 lung size is normal and the accessory lobe is present




Genotype
MGI:3795687
cx4
Allelic
Composition
Gli2tm3(Gli1)Alj/Gli2tm3(Gli1)Alj
Gli3Xt-J/Gli3+
Genetic
Background
involves: 129S6/SvEvTac * Black Swiss * C3H/HeJ * C57BL/6 * Swiss Webster
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli2tm3(Gli1)Alj mutation (0 available); any Gli2 mutation (169 available)
Gli3Xt-J mutation (3 available); any Gli3 mutation (81 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
• most embryos lack mammary bud pair number 3 and number 5

integument
• most embryos lack mammary bud pair number 3 and number 5





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