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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
crn
cranioschisis
MGI:1856835
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
crn/crn Not Specified MGI:4367738


Genotype
MGI:4367738
hm1
Allelic
Composition
crn/crn
Genetic
Background
Not Specified
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phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• newborns do not nurse and die or are killed by mother

nervous system
• in region of primary brain vesicles, and cervical and cephalic flexures
• due to neural tube supporting mesenchyme defect
• disorganized neural overgrowth accompanies cases of extreme anencephaly
• degree varies from 1mm diameter skin and frontal cranium defect to absence of calvarium above level of orbit
• affected fetuses with this condition suffer petechiae and abrasions to the brain; at birth neural tissue is necrotic or becomes damaged

limbs/digits/tail
• reduced numbers of calcified vertebrae

craniofacial
• minimal defect is a 1mm diameter skin and frontal cranium abnormality

skeleton
• minimal defect is a 1mm diameter skin and frontal cranium abnormality
• reduced numbers of calcified vertebrae

digestive/alimentary system

embryo
• neural tube supporting mesenchyme loses normal stellate cellular inerconnections for not more than 24 hours but long enough to disrupt important cell/matrix interactions
• in region of primary brain vesicles, and cervical and cephalic flexures
• due to neural tube supporting mesenchyme defect

growth/size/body





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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
12/10/2024
MGI 6.24
The Jackson Laboratory