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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fgf8tm1.1Jyhl
targeted mutation 1.1, James Y H Li
MGI:4430251
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl involves: CD-1 MGI:4430255
cn2
En1tm7(cre/ESR1)Alj/0
Fgf8tm1.1Jyhl/Fgf8tm1.3Mrt
involves: 129P2/OlaHsd * 129S6/SvEvTac MGI:4437222
cx3
Fgf17tm1Dor/Fgf17tm1Dor
Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl
involves: 129S6/SvEvTac MGI:4437230


Genotype
MGI:4430255
hm1
Allelic
Composition
Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl
Genetic
Background
involves: CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf8tm1.1Jyhl mutation (0 available); any Fgf8 mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
embryo
• malformed branchial arches at E9.5
• the anteroposterior (AP) axis aligns with the short, rather than the long, transverse axis of the embryo at E6.5
• the AP axis of the embryo is parallel with the long uterine axis at E6.5
• normal long axis of the embryo in register with the long uterine axis at E6.5
• abnormal embryonic mesoderm derived structures at E8.5 in 21.6% of the mutant (11/51)
• normal somites and cardiomesoderm at E8.5 in 78.4% of the mutant (40/51)
• smaller in size than wild-type at E9.5
• at E9.5
• accumulation of mesodermal cells at the primitive streak at E7.5
• lack of morphologically distinct node structure at E7.5
• the amniotic membrane appears rough and fluffy

growth/size/body
• smaller in size than wild-type at E9.5

nervous system
• at E9.5

craniofacial
• malformed branchial arches at E9.5

cardiovascular system
• malformed heart tubes at E9.5




Genotype
MGI:4437222
cn2
Allelic
Composition
En1tm7(cre/ESR1)Alj/0
Fgf8tm1.1Jyhl/Fgf8tm1.3Mrt
Genetic
Background
involves: 129P2/OlaHsd * 129S6/SvEvTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
En1tm7(cre/ESR1)Alj mutation (1 available); any En1 mutation (34 available)
Fgf8tm1.1Jyhl mutation (0 available); any Fgf8 mutation (21 available)
Fgf8tm1.3Mrt mutation (1 available); any Fgf8 mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging

nervous system
• a significant increase in the number of dead cells in the mesencephalon and to a less extent in rhombomere of the neural tube of embryos at the 13-somite stage
• a significant increase in the number of dead cells in rhombomere of the neural tube of embryos at the 13-somite stage
• a reduction of serotonergic neurons in raphe nuclei
• E18.5 revealed a nearly complete loss of the midbrain and the cerebellum
• a significant increase in the number of dead cells in the mesencephalon at the 13-somite stage
• depletion of dopaminergic neurons at E18.5
• E18.5 revealed a nearly complete loss of the midbrain and the cerebellum
• at E18.5 in the substantia nigra and ventral tegmental area
• at E18.5 a reduction of serotonergic neurons in the raphe nucleus

embryo
• a significant increase in the number of dead cells in the mesencephalon and to a less extent in rhombomere of the neural tube of embryos at the 13-somite stage
• a significant increase in the number of dead cells in rhombomere of the neural tube of embryos at the 13-somite stage




Genotype
MGI:4437230
cx3
Allelic
Composition
Fgf17tm1Dor/Fgf17tm1Dor
Fgf8tm1.1Jyhl/Fgf8tm1.1Jyhl
Genetic
Background
involves: 129S6/SvEvTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fgf17tm1Dor mutation (1 available); any Fgf17 mutation (35 available)
Fgf8tm1.1Jyhl mutation (0 available); any Fgf8 mutation (21 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• the tissue between the inferior colliculus and the anterior cerebellum is significantly reduced in adult mice
• lobules I-III are truncated and considerably smaller in size in adult mice





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory