About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:3784821
Allelic
Composition
Gli3Xt/Gli3Xt
Genetic
Background
involves: 101/H * C3H/HeH * C57BL/6 * CBA/H
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gli3Xt mutation (1 available); any Gli3 mutation (80 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• pituitary gland develops normally from floor of third ventricle
• chiasmatic recess develops normally
• mesencephalon does not appear enlarged relative to wild-type at 13.5 and 14.5 days of gestation
• anterior neuropore is still open to variable extent on day 11.5 of gestation in some embryos
• some embryos show normal closure while others display persistent open anterior neural folds spanning region of anterior neuropore to mesencephalon
• on day 13.5 of gestation, anterior neuropore remains open and brain ventricles openly communicate with the amniotic sac
• loss of diagnostic morphology of isthmus
• anterior isthmus region with characteristics of the cerebellum
• thicker than normal Purkinje region and axons disorganized
• dorsal mesencephalon, isthmus, and r1 not distinct at E10.5 and E12.5
• isthmus flexure less prominent
• in embryos with closed anterior neuropore, forebrain does not show anlage of a choroid plexus in telencephalon
• small unpaired choroid plexus is found in the circumference of an opening in dorsal wall of diencephalon, not associated with origin of telencephalic anlagen from diencephalon
• tegmentum unaffected
• ventral nuclei containing dopaminergic neurons appear normal
• expanded mesencephalic ventricle at E10.5 and E12.5
• loss of diagnostic morphology
• poorly formed
• loss of diagnostic morphology
• overgrown tectum
• on day 13.5, no choroid plexus is developing in forebrain
• hemispheres do not show any posterior elongation
• in embryos with closed anterior neuropore, anlage of a choroid plexus is missing from telencephalon
• telencephalon is represented by a broad-based lateral bulging from the median portion of the forebrain and does not display elongation posteriorly
• in embryos with closed anterior neuropore, forebrain does not show normal interhemispheric cleft
• display poorly defined origin that opens wide into the median third ventricle
• smaller than wild-type on day 13.5 of gestation
• at E15.5-16.5, cerebral hemispheres have very narrow rugged ventricles and do not show any lamination or cellular organization of the hemispheric walls
• bulb does not develop
• thickness of ventricular zone increased
• not clearly separated from the isthmus at E18.5
• poorly foliated
• thicker than normal
• axons disorganized in lateral regions

embryo
• anterior neuropore is still open to variable extent on day 11.5 of gestation in some embryos
• some embryos show normal closure while others display persistent open anterior neural folds spanning region of anterior neuropore to mesencephalon
• on day 13.5 of gestation, anterior neuropore remains open and brain ventricles openly communicate with the amniotic sac
• loss of diagnostic morphology of isthmus
• anterior isthmus region with characteristics of the cerebellum
• thicker than normal Purkinje region and axons disorganized
• dorsal mesencephalon, isthmus, and r1 not distinct at E10.5 and E12.5
• isthmus flexure less prominent


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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory