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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cep20
centrosomal protein 20
MGI:1913336
18 phenotypes from 1 allele in 1 genetic background
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Allelic Composition
Genetic Background
Annotated Term Reference
Cep20tm1.1(KOMP)Vlcg/Cep20tm1.1(KOMP)Vlcg
B6(Cg)-Cep20tm1.1(KOMP)Vlcg
abnormal amniotic cavity morphology J:308526
abnormal angiogenesis J:308526
abnormal developmental vascular remodeling J:308526
abnormal direction of heart looping J:308526
abnormal heart development J:308526
abnormal left-right axis patterning J:308526
abnormal primitive node morphology J:308526
abnormal vitelline vasculature morphology J:308526
absent embryonic cilia J:308526
caudal body truncation J:308526
decreased embryo size J:308526
embryonic growth arrest J:308526
embryonic growth retardation J:308526
embryonic lethality during organogenesis, complete penetrance J:308526
enlarged pericardium J:308526
failure of chorioallantoic fusion J:308526
failure of initiation of embryo turning J:308526
pericardial edema J:308526

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
12/10/2024
MGI 6.24
The Jackson Laboratory