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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gli3tm1.2Zllr
targeted mutation 1.2, Rolf Zeller
MGI:5425256
Summary 5 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Gli3tm1.2Zllr/Gli3tm1.2Zllr involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5523595
ht2
Gli3tm1.2Zllr/Gli3Xt-J involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J * NMRI MGI:5425260
cn3
Gli3tm1.1Zllr/Gli3tm1.2Zllr
Hoxa13tm1.1(cre)Makm/Hoxa13+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J MGI:5425261
cx4
Gli3tm1.2Zllr/Gli3tm1.2Zllr
Pkdcctm1.2Azun/Pkdcctm1.2Azun
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5523593
cx5
Gli3tm1.2Zllr/Gli3+
Pkdcctm1.2Azun/Pkdcctm1.2Azun
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 MGI:5523594


Genotype
MGI:5523595
hm1
Allelic
Composition
Gli3tm1.2Zllr/Gli3tm1.2Zllr
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli3tm1.2Zllr mutation (0 available); any Gli3 mutation (80 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• ossification centers in the limb bones are smaller at E16.5

limbs/digits/tail
• of the tibia




Genotype
MGI:5425260
ht2
Allelic
Composition
Gli3tm1.2Zllr/Gli3Xt-J
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J * NMRI
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli3tm1.2Zllr mutation (0 available); any Gli3 mutation (80 available)
Gli3Xt-J mutation (3 available); any Gli3 mutation (80 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• additional anterior digits are formed but the anterior most digit 1 is lost

nervous system
• brain abnormalities similar to mice homozygous for Gli3Xt-J

vision/eye
• eye abnormalities similar to mice homozygous for Gli3Xt-J




Genotype
MGI:5425261
cn3
Allelic
Composition
Gli3tm1.1Zllr/Gli3tm1.2Zllr
Hoxa13tm1.1(cre)Makm/Hoxa13+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli3tm1.1Zllr mutation (0 available); any Gli3 mutation (80 available)
Gli3tm1.2Zllr mutation (0 available); any Gli3 mutation (80 available)
Hoxa13tm1.1(cre)Makm mutation (0 available); any Hoxa13 mutation (29 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail




Genotype
MGI:5523593
cx4
Allelic
Composition
Gli3tm1.2Zllr/Gli3tm1.2Zllr
Pkdcctm1.2Azun/Pkdcctm1.2Azun
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli3tm1.2Zllr mutation (0 available); any Gli3 mutation (80 available)
Pkdcctm1.2Azun mutation (0 available); any Pkdcc mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• the primordia of the tibia and fibula are ectromelic at E16.5
• the primordia of the tibia and fibula are ectromelic at E16.5
• deformed in some mice at E16.5
• at E16.5 few or no columnar and hypertrophic chondrocytes are detected in the limbs
• hypertrophic differentiation is delayed
• expression analysis indicates the number of pre-hypertrophic chondrocytes is severely reduced in the limbs at E15.5 and E16.5
• at E16.5 no signs of ossification are seen in the humerus, tibia, fibula or digits and mineralization domains in other long bones are reduced
• delay is more severe than in mice homozygous for Pkdcctm1.2Azun alone

limbs/digits/tail
• the primordia of the tibia and fibula are ectromelic at E16.5
• the primordia of the tibia and fibula are ectromelic at E16.5




Genotype
MGI:5523594
cx5
Allelic
Composition
Gli3tm1.2Zllr/Gli3+
Pkdcctm1.2Azun/Pkdcctm1.2Azun
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli3tm1.2Zllr mutation (0 available); any Gli3 mutation (80 available)
Pkdcctm1.2Azun mutation (0 available); any Pkdcc mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
skeleton
• shorter ossified section at birth
• more severe than in mice homozygous for the Pkdcc mutation alone
• tibia and humerus are most severely affected
• tibia and humerus are most severely affected
• deformed in some mice at E16.5
• in long bones
• more severe than in mice homozygous for the Pkdcc mutation alone

limbs/digits/tail
• tibia and humerus are most severely affected
• tibia and humerus are most severely affected





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last database update
05/07/2024
MGI 6.23
The Jackson Laboratory