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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Depdc5tm1c(EUCOMM)Hmgu
targeted mutation 1c, Helmholtz Zentrum Muenchen GmbH
MGI:5752552
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Depdc5tm1c(EUCOMM)Hmgu/Depdc5tm1c(EUCOMM)Hmgu
Tg(Syn1-cre)671Jxm/0
involves: C57BL/6N * CBA MGI:6154993
cn2
Depdc5tm1c(EUCOMM)Hmgu/Depdc5+
Tg(Syn1-cre)671Jxm/0
involves: C57BL/6N * CBA MGI:6154994


Genotype
MGI:6154993
cn1
Allelic
Composition
Depdc5tm1c(EUCOMM)Hmgu/Depdc5tm1c(EUCOMM)Hmgu
Tg(Syn1-cre)671Jxm/0
Genetic
Background
involves: C57BL/6N * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Depdc5tm1c(EUCOMM)Hmgu mutation (3 available); any Depdc5 mutation (120 available)
Tg(Syn1-cre)671Jxm mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• median survival is 115 days with no mice surviving past 175 days with no wounds or major pathology to explain sudden death

nervous system
• in three mice without detection of electroclinical seizures
• shorter latency to seizures induced by PTZ and increased death
• however, duration of seizures is normal
• in two mice
• in one mouse
• median survival is 115 days with no mice surviving past 175 days with no wounds or major pathology to explain sudden death
• thicker and disorganized in layer V cortical neurons
• enlarged and dysplastic neurons with abnormal cytoplasmic accumulation

behavior/neurological
N
• unlike constitutive knock-out mice, conditional knock-out mice do not exhibit a hunchback phenotype
• hindlimb clasping after 60 days of age
• in three mice without detection of electroclinical seizures
• shorter latency to seizures induced by PTZ and increased death
• however, duration of seizures is normal
• in two mice
• in one mouse

growth/size/body
• in male, but not female, mice from the time of weaning and persisting through adulthood

homeostasis/metabolism

skeleton
• with decreased neuronal density in deep layers




Genotype
MGI:6154994
cn2
Allelic
Composition
Depdc5tm1c(EUCOMM)Hmgu/Depdc5+
Tg(Syn1-cre)671Jxm/0
Genetic
Background
involves: C57BL/6N * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Depdc5tm1c(EUCOMM)Hmgu mutation (3 available); any Depdc5 mutation (120 available)
Tg(Syn1-cre)671Jxm mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
growth/size/body
• in male, but not female, mice after 3 months of age





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory