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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Gli3Pdn
polydactyly Nagoya
MGI:1856282
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Gli3Pdn/Gli3Pdn involves: Jcl:ICR MGI:3027901
ht2
Gli3Pdn/Gli3+ involves: Jcl:ICR MGI:2656898


Genotype
MGI:3027901
hm1
Allelic
Composition
Gli3Pdn/Gli3Pdn
Genetic
Background
involves: Jcl:ICR
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli3Pdn mutation (1 available); any Gli3 mutation (80 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands

mortality/aging
• mice die within 2 days of birth

nervous system
• abnormal radial glial fibers are arranged in an irregular pattern compared to in wild-type mice
• mice are deficient in the commissure anterior, fornix, and commissura fornicis unlike wild-type mice
• the fiber of the anterior commissure does not decussate on day 14 of gestation (J:17581)
• lack of massa commissuralis on day 15 of gestation (J:17581)
• regression of hypothalamus
• regression of thalamus
• mice exhibit expansion of cerebrum compared with wild-type mice
• 8 of 10 mice exhibit fissuration of cerebral hemisphere unlike wild-type mice
• mice exhibit an expansion of ventriculus lateralis, tertius, and quartus, and aquaeductus cerebri are expanded compared with wild-type mice
• hippocampal primordia and posterior of the telencephalon show wavy and/or rosette-like structures on day 14 of gestation (J:17581)
• pyramidal layers in regio superior and inferior are disorganized compared to in wild-type mice (J:38885)
• disorganized pyramidal layers
• mice exhibit abnormal fissures and proturberances in the caudo-dorsal cortex compared to in wild-type mice
• olfactory bulb is never induced from the telencephalon (J:17581)
• observed in 20.7% of mice
• olfactory nerve never attaches to the rostroventral telencephalon (J:17581)
• mice exhibit an irregular mass of the olfactory nerve on the cribriform plate unlike in wild-type mice (J:38885)
• protrusion of cortical tissue
• pyknotic and spongy degeneration were observed in the septal nucleus and the mesencephalon around the aqueduct of Sylvius at E16, the periventricular thalamus and hypothalamus at E18 and the corpus callosum and fimbria hippocampi at birth (J:17581)
• of the periventricular white matter at the posterior horn of the lateral ventricle in some mice (J:38885)

limbs/digits/tail
• displayed an extra tab on the postaxial side of the forelimb
• 2 to 3 extra preaxial digits on the forelimbs
• 1 to 3 extra preaxial digits on the hindlimbs
• however the radii and ulnae are of normal length

skeleton
• however the radii and ulnae are of normal length
• bifurcation of the manubrium

vision/eye
• observed in 12.1% of mice

digestive/alimentary system
• observed in 12.1% of mice

craniofacial
• observed in 12.1% of mice

cellular
• abnormal radial glial fibers are arranged in an irregular pattern compared to in wild-type mice

growth/size/body
• observed in 12.1% of mice




Genotype
MGI:2656898
ht2
Allelic
Composition
Gli3Pdn/Gli3+
Genetic
Background
involves: Jcl:ICR
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli3Pdn mutation (1 available); any Gli3 mutation (80 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• enlarged first digit on the forelimb, often showing a bifurcated distal phalanx
• often displayed an extra tab on the postaxial side of the forelimb, which regressed with age
• 1 extra preaxial digits on the hindlimb, that remained rudimentary with age





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory