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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Csnk2a1
casein kinase 2, alpha 1 polypeptide
MGI:88543
32 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Csnk2a1tm1Dcs/Csnk2a1tm1Dcs
involves: 129S6/SvEvTac * C57BL/6
abnormal eye development J:129208
abnormal head shape J:129208
abnormal heart tube morphology J:129208
abnormal limb bud morphology J:129208
abnormal neural fold elevation formation J:129208
abnormal neural tube closure J:129208
abnormal optic stalk morphology J:129208
abnormal optic vesicle formation J:129208
abnormal otic vesicle development J:129208
abnormal pericardium development J:129208
abnormal pharyngeal arch morphology J:129208
abnormal retina pigmentation J:129208
abnormal surface ectoderm morphology J:129208
abnormal telencephalon development J:129208
absent heartbeat J:129208
absent mouth J:129208
craniorachischisis J:129208
decreased body length J:129208
decreased body size J:129208
decreased forebrain size J:129208
decreased hindbrain size J:129208
decreased midbrain size J:129208
dilated heart J:129208
embryonic lethality during organogenesis, incomplete penetrance J:129208
enlarged heart J:129208
hemorrhage J:129208
hydrops fetalis J:129208
incomplete rostral neuropore closure J:129208
pericardial edema J:129208
small second pharyngeal arch J:129208
trabecula carnea hypoplasia J:129208
truncated tail bud J:129208

Contributing Projects:
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
04/16/2024
MGI 6.23
The Jackson Laboratory