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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ungtm1Mend
targeted mutation 1, Matthias Endres
MGI:3046503
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Ungtm1Mend/Ungtm1Mend involves: 129S4/SvJae * BALB/c MGI:3046508


Genotype
MGI:3046508
hm1
Allelic
Composition
Ungtm1Mend/Ungtm1Mend
Genetic
Background
involves: 129S4/SvJae * BALB/c
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Ungtm1Mend mutation (0 available); any Ung mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• homozygous MEF and primary cultures of cortical neurons are significantly more vulnerable to acute oxidative stress induced cell death

nervous system
• 72 hours after 20 minute long middle cerebral artery occlusion the volume of lesions formed in the brains of homozygous mice are larger (greater than 230%) and include both cortical tissue and striatum compared to wild-type and heterozygous littermates
• the density of viable neurons within a lesion is decreased in homozygous mice
• sensory-motor deficits are more severe in homozygous mice compared to wild-type and heterozygous littermates

homeostasis/metabolism
• 72 hours after 20 minute long middle cerebral artery occlusion the volume of lesions formed in the brains of homozygous mice are larger (greater than 230%) and include both cortical tissue and striatum compared to wild-type and heterozygous littermates
• the density of viable neurons within a lesion is decreased in homozygous mice
• sensory-motor deficits are more severe in homozygous mice compared to wild-type and heterozygous littermates





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory