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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Csnk2a1tm1Dcs
targeted mutation 1, David C Seldin
MGI:3769802
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Csnk2a1tm1Dcs/Csnk2a1tm1Dcs involves: 129S6/SvEvTac * C57BL/6 MGI:3769888


Genotype
MGI:3769888
hm1
Allelic
Composition
Csnk2a1tm1Dcs/Csnk2a1tm1Dcs
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Csnk2a1tm1Dcs mutation (1 available); any Csnk2a1 mutation (131 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

cardiovascular system
• at E10.5, trabeculation is reduced
• at E10.5, the open heart tube persists with an enlarged endomyocardial cavity with a thin and disorganized epithelium
• at E10.5, the presumptive parietal pericardial layer appears abnormal
• at E8.5, the primitive heart is enlarged
• at E9.5, hearts are enlarged and distended
• at E11, the pericardial sacs are edematous due to heart failure
• at E10.5, hearts are dilated
• at E10.5, some mice exhibit hemorrhaging in the thorax, abdomen and cranium
• by E11.5 hearts have stopped beating

nervous system
• at E9.5, neural tube closure is variable in severity with some mice exhibiting rostral closure with open cranial portions and few others exhibiting an entirely open neural tube
• at E10.5, mutant embryos typically show an open neural tube in the forebrain region, although it is closed but collapsed in the hindbrain region
• at E9.5, a few embryos exhibit an entirely open neural tube
• at E10.5, telencephalic vesicles have not expanded outwards
• forebrain region is smaller than in wild-type mice
• hindbrain region is smaller than in wild-type mice
• midbrain region is smaller than in wild-type mice

vision/eye
• retinal pigmentation is less pronounced in some embryos and virtually absent in others
• the eye field is indistinct and underdeveloped
• at E10.5, the optic stalk and vesicle have collapsed
• at E10.5, the optic stalk and vesicle have collapsed

embryo
• at E10.5, mice exhibit reduced numbers of branchial arches compared to wild-type mice
• at E10.5, the surface ectoderm appears abnormal
• at E9.5 and E10.5, limb bud development is delayed and never progresses beyond a limb bud paddle
• at E8.5, neural folds remain convex and fail to elevate and fuse unlike in wild-type mice
• at E9.5, neural tube closure is variable in severity with some mice exhibiting rostral closure with open cranial portions and few others exhibiting an entirely open neural tube
• at E10.5, mutant embryos typically show an open neural tube in the forebrain region, although it is closed but collapsed in the hindbrain region
• at E9.5, a few embryos exhibit an entirely open neural tube
• unlike in wild-type mice, the tail bud is short and terminates in a broad, blunt end

limbs/digits/tail
• at E9.5 and E10.5, limb bud development is delayed and never progresses beyond a limb bud paddle
• unlike in wild-type mice, the tail bud is short and terminates in a broad, blunt end

hearing/vestibular/ear
• at E10.5, the otic vesicles are rounder than in wild-type mice, lack the dorsal extension and the epithelium is thickened

growth/size/body
• at E8.5, the primitive heart is enlarged
• at E9.5, hearts are enlarged and distended
• at E11.5, branchial arches have not fused and the mouth is not formed
• the head shape is abnormal
• at E10.5

muscle
• at E10.5, trabeculation is reduced

craniofacial
• at E10.5, mice exhibit reduced numbers of branchial arches compared to wild-type mice
• at E11.5, branchial arches have not fused and the mouth is not formed
• the head shape is abnormal

pigmentation
• retinal pigmentation is less pronounced in some embryos and virtually absent in others

homeostasis/metabolism
• at E11, the pericardial sacs are edematous due to heart failure
• at E11





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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
04/23/2024
MGI 6.23
The Jackson Laboratory