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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cep55tm1a(EUCOMM)Hmgu
targeted mutation 1a, Helmholtz Zentrum Muenchen GmbH
MGI:4951017
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cep55tm1a(EUCOMM)Hmgu/Cep55tm1a(EUCOMM)Hmgu involves: C57BL/6N MGI:6458514


Genotype
MGI:6458514
hm1
Allelic
Composition
Cep55tm1a(EUCOMM)Hmgu/Cep55tm1a(EUCOMM)Hmgu
Genetic
Background
involves: C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cep55tm1a(EUCOMM)Hmgu mutation (0 available); any Cep55 mutation (71 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• from P1 to P14, mice are cannibalized by parents with few survivors with only 3 of 74 mice alive at P14

nervous system
• of neural progenitor cells at E16.5 in the subventricular zone, intermediate zone and cortical plate
• decreased length, thickness, and cellularity during embryonic development and at birth
• thinner and more transparent than control cortices
• of neural progenitor cells at E16.5 in the subventricular zone, intermediate zone and cortical plate

renal/urinary system
• thin with glomeruli in the superficial cortex in rare surviving mice at P14
• small and hypercellular

cellular
• binucleated cells in the cortex and a slight increase in binucleated cells in tail tip fibroblast
• neural progenitor cells exhibit impaired cytokinesis compared to in control cells
• of neural progenitor cells at E16.5 in the subventricular zone, intermediate zone and cortical plate

behavior/neurological

craniofacial
• flat skull in newborn mice

growth/size/body
• at E18.5 and P0
• at E18.5

integument
• at E18.5

skeleton
• flat skull in newborn mice





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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
11/12/2024
MGI 6.24
The Jackson Laboratory