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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cfl1c5
c5
MGI:5473701
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cfl1c5/Cfl1c5 involves: C57BL/6J MGI:5473702
cx2
Cfl1c5/Cfl1c5
Dstncorn1/Dstncorn1
involves: A/WySn * C57BL/6J MGI:5473707
cx3
Cfl1c5/Cfl1c5
Dstncorn1/Dstn+
involves: A/WySn * C57BL/6J MGI:5473708
cx4
Cfl1c5/Cfl1c5
Vangl2Lp/Vangl2Lp
involves: C57BL/6J * LPT/LeJ MGI:5473703


Genotype
MGI:5473702
hm1
Allelic
Composition
Cfl1c5/Cfl1c5
Genetic
Background
involves: C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cfl1c5 mutation (0 available); any Cfl1 mutation (25 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• open cranial neural tube but closed in the trunk at E9.5

cardiovascular system

nervous system
• open cranial neural tube but closed in the trunk at E9.5
• open cranial neural tube but closed in the trunk at E9.5

homeostasis/metabolism




Genotype
MGI:5473707
cx2
Allelic
Composition
Cfl1c5/Cfl1c5
Dstncorn1/Dstncorn1
Genetic
Background
involves: A/WySn * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cfl1c5 mutation (0 available); any Cfl1 mutation (25 available)
Dstncorn1 mutation (0 available); any Dstn mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• unable to recover embryos at post-implantation stages




Genotype
MGI:5473708
cx3
Allelic
Composition
Cfl1c5/Cfl1c5
Dstncorn1/Dstn+
Genetic
Background
involves: A/WySn * C57BL/6J
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cfl1c5 mutation (0 available); any Cfl1 mutation (25 available)
Dstncorn1 mutation (0 available); any Dstn mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• most arrest prior to node formation

embryo
• most arrest prior to node formation
• in the 3 embryos that develop nodes apical trafficking of planar cell polarity proteins is disrupted




Genotype
MGI:5473703
cx4
Allelic
Composition
Cfl1c5/Cfl1c5
Vangl2Lp/Vangl2Lp
Genetic
Background
involves: C57BL/6J * LPT/LeJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cfl1c5 mutation (0 available); any Cfl1 mutation (25 available)
Vangl2Lp mutation (2 available); any Vangl2 mutation (34 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

embryo
• fail to undergo turning
• at E8.0 - E8.5 expression analysis indicates randomized left-right axis patterning
• at approximately E9.5
• shorter at E9.5
• open along the entire axis of the embryo at E9.5
• midline is shorter and wider at the 1 to 4 somite stage compared to either single mutant
• threefold shorter and wider compared to wild-type controls, twofold shorter and wider compared to Vangl2Lp single mutants
• change in size is not due to changes in cell shape
• expression analysis indicates many node cells lack posterior polarization
• cilia are normal in length but do not point uniformly to the posterior and their position on the cell is more variable than in controls
• significantly reduced length to width ratio compared to either single mutant

cardiovascular system
• in 2 of 6 embryos at E9.5
• a linear heart tube is seen at E9.5 in 1 of 6 embryos

growth/size/body
• shorter at E9.5
• at E8.0 - E8.5 expression analysis indicates randomized left-right axis patterning

nervous system
• open along the entire axis of the embryo at E9.5

cellular
• cilia are normal in length but do not point uniformly to the posterior and their position on the cell is more variable than in controls





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