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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Ccnf
cyclin F
MGI:102551
23 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Ccnftm1.1Sje/Ccnftm1.1Sje
involves: 129S7/SvEvBrd * C57BL/6
abnormal allantois morphology J:89060
abnormal cell cycle J:89060
abnormal hindbrain development J:89060
abnormal neural tube closure J:89060
abnormal placenta development J:89060
abnormal rostral-caudal axis patterning J:89060
abnormal visceral yolk sac morphology J:89060
abnormal vitelline vascular remodeling J:89060
abnormal vitelline vasculature morphology J:89060
absent vitelline blood vessels J:89060
decreased cell proliferation J:89060
decreased embryo size J:89060
delayed brain development J:89060
disorganized yolk sac vascular plexus J:89060
embryonic lethality during organogenesis, complete penetrance J:89060
failure of chorioallantoic fusion J:89060
forebrain hypoplasia J:89060
incomplete embryo turning J:89060
kinked neural tube J:89060
midbrain hypoplasia J:89060
small hindlimb buds J:89060
Ccnftm1Sje/Ccnftm1.1Sje
Tg(Col1a1-cre)1Kry/0
involves: 129S7/SvEvBrd * C57BL/6 * FVB
normal skeleton phenotype J:89060
Ccnftm1Sje/Ccnftm1.1Sje
Tg(Fabp1-cre)1Jig/0
involves: 129S7/SvEvBrd * C57BL/6 * FVB/N
normal digestive/alimentary phenotype J:89060

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
01/14/2020
MGI 6.14
The Jackson Laboratory