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Phenotypes Associated with This Genotype
Genotype
MGI:2678685
Allelic
Composition
Gli2tm1Alj/Gli2tm1Alj
Gli3Xt-J/Gli3+
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C3H * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli2tm1Alj mutation (0 available); any Gli2 mutation (173 available)
Gli3Xt-J mutation (3 available); any Gli3 mutation (84 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
craniofacial
• coronoid, condylar, angular and dental processes are hypoplastic

limbs/digits/tail
• on forelimbs, there is a postaxial stub of an extra digit
• display more severe preaxial polydactyly compared to Gli2 homozygotes
• shortening of the humerus
• shortening of the radius; shortening is more severe than in the ulna
• shortening of the ulna, although not as severe as the radius
• not as severe as the tibia

skeleton
• show an exacerbated phenotype in various skeletal elements with respect to Gli2 nulls
• coronoid, condylar, angular and dental processes are hypoplastic
• shortening of the humerus
• shortening of the radius; shortening is more severe than in the ulna
• shortening of the ulna, although not as severe as the radius
• not as severe as the tibia
• sternum is split rostrally and improperly segmented
• there are severe abnormalities in chondrogenesis of ventral vertebral components
• there are severe abnormalities in chondrogenesis of ventral vertebral components

growth/size/body
• coronoid, condylar, angular and dental processes are hypoplastic


Contributing Projects:
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
01/28/2026
MGI 6.24
The Jackson Laboratory