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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Plk2tm1Rle
targeted mutation 1, Raymond L Erikson
MGI:2678106
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Plk2tm1Rle/Plk2tm1Rle either: (involves: 129/Sv * 129S6/SvEvTac) or (involves: 129S6/SvEvTac * MF1) MGI:2678107


Genotype
MGI:2678107
hm1
Allelic
Composition
Plk2tm1Rle/Plk2tm1Rle
Genetic
Background
either: (involves: 129/Sv * 129S6/SvEvTac) or (involves: 129S6/SvEvTac * MF1)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Plk2tm1Rle mutation (0 available); any Plk2 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• growth rate is similar to that of wild-type, and dwarfism is putatively due to defects in embryonic development
• labyrinthine zone at E18.5 is significantly smaller and exhibits reduced cell proliferation
• average weight of placentas is about 70% of that of wild-type at E16.5 and this difference is maintained until birth
• decreased cell proliferation in the labyrinth

growth/size/body
• growth rate is similar to that of wild-type, and dwarfism is putatively due to defects in embryonic development
• on average about 20% smaller than wild-type mice
• fetuses are about 94% of the weight of normal embryos at E16.5 and E17.5 and reach 86% at E18.5

skeleton
• ossification is delayed in the sternebrae and xiphoid process
• ossification of other bones occurs at the same time as it did in wild-type fetuses

vision/eye
• ~30% are born with incompletely closed eyelids

cellular
• the cell cycle appears to be slightly delayed in embryonic fibroblasts cultured in vitro during early passages but by passage 6, they divide at the same rate as controls
• delay for cells in entering S phase from G1

integument
• skin is pale, although mutants do not appear to be anemic





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