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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Ythdf1tm1.1Sjj
targeted mutation 1.1, Sheng-Jian Ji
MGI:6356298
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Ythdf1tm1.1Sjj/Ythdf1tm1.1Sjj
Tg(Atoh1-cre/Esr1*)14Fsh/0
involves: FVB/N MGI:6719337


Genotype
MGI:6719337
cn1
Allelic
Composition
Ythdf1tm1.1Sjj/Ythdf1tm1.1Sjj
Tg(Atoh1-cre/Esr1*)14Fsh/0
Genetic
Background
involves: FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(Atoh1-cre/Esr1*)14Fsh mutation (1 available)
Ythdf1tm1.1Sjj mutation (0 available); any Ythdf1 mutation (37 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• embryos exhibit defects in pre-crossing commissural axon guidance, with significantly more commissural axons misprojecting into motor columns at E11.5
• pre-crossing axon guidance defects include stalling and pre-crossing turning phenotypes
• however, patterning of the spinal cord and development of dI1 commissural neurons is normal

homeostasis/metabolism
• however, Robo3.1 mRNA level is not affected in the spinal cord
• when dorsal spinal cord (DSC) explants are dissected from pre-crossing E10.5 spinal cord and cultured in vitro, dorsal commissural axons show a dramatic reduction in Robo3.1 protein level relative to controls

cellular
• embryos exhibit defects in pre-crossing commissural axon guidance, with significantly more commissural axons misprojecting into motor columns at E11.5
• pre-crossing axon guidance defects include stalling and pre-crossing turning phenotypes
• however, patterning of the spinal cord and development of dI1 commissural neurons is normal





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