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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Vcltm1.1Whz
targeted mutation 1.1, Wolfgang H Ziegler
MGI:4822196
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Vcltm1.1Whz/Vcltm1.1Whz involves: 129/Sv * C57BL/6 * SJL MGI:4822197


Genotype
MGI:4822197
hm1
Allelic
Composition
Vcltm1.1Whz/Vcltm1.1Whz
Genetic
Background
involves: 129/Sv * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Vcltm1.1Whz mutation (0 available); any Vcl mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Vcltm1.1Whz/Vcltm1.1Whz embryos are not viable and show exencephaly and increased cell death

mortality/aging

nervous system
• cranial neural folds fail to fuse by E10.5
• absent at E10.5
• at E10.5

embryo
• head mesenchyme is loosely organized and contains massively dilated blood vessels at E10.5
• cranial neural folds fail to fuse by E10.5
• at E10.5 apoptosis is greatly increased primarily in mesenchymal tissues ventral to the spinal cord and in the neuroepithelium

cardiovascular system
• head mesenchyme is loosely organized and contains massively dilated blood vessels at E10.5

cellular
• MEFs display an increase in the size of adhesion sites
• at E10.5 apoptosis is greatly increased primarily in mesenchymal tissues ventral to the spinal cord and in the neuroepithelium

growth/size/body
• at E10.5 head structures fail to fuse along the cranial midline
• head mesenchyme is loosely organized and contains massively dilated blood vessels at E10.5





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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
04/30/2024
MGI 6.23
The Jackson Laboratory