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Proper Citation: RRID:MGI:3027901
Description: Allele Detail: Spontaneous This is a legacy resource.
Species: Mus musculus
Notes: Allele Detail: Spontaneous This is a legacy resource.
Phenotype: thin cerebral cortex, absent olfactory bulb, encephalomeningocele, spongiform encephalopathy, abnormal neuronal migration, abnormal radial glial cell morphology, abnormal cerebral cortex morphology, hydrocephaly, absent olfactory bulb, absent olfactory bulb, absent hippocampal commissure, absent corpus callosum, absent anterior commissure, abnormal stratification in cerebral cortex, abnormal olfactory nerve morphology, abnormal cerebral hemisphere morphology, abnormal hippocampus development, hydrocephaly, abnormal hippocampus development, abnormal hypothalamus morphology, synostosis, abnormal hippocampus pyramidal cell layer, abnormal hippocampal fornix morphology, abnormal digit morphology, split sternal manubrium, absent corpus callosum, absent anterior commissure, abnormal thalamus morphology, abnormal olfactory nerve morphology, spongiform encephalopathy, absent pineal gland, cleft palate, exencephaly, eyelids open at birth, polydactyly, short fibula, short tibia, postnatal lethality
Affected Gene: Gli3
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Source: Integrated Animals
Source Database: MGI, Mouse Genome Informatics MGI
Data set from Kravitz, Owen and Kretizer's 2012 paper "Optogenetic identification of striatal projection neuron subtypes during in vivo recordings."
