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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Fmn2tm1Led
targeted mutation 1, Philip Leder
MGI:2448909
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Fmn2tm1Led/Fmn2tm1Led either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss) MGI:2654511


Genotype
MGI:2654511
hm1
Allelic
Composition
Fmn2tm1Led/Fmn2tm1Led
Genetic
Background
either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fmn2tm1Led mutation (1 available); any Fmn2 mutation (75 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
reproductive system
• meiotic incompetence in oocytes results in polyploid embryos
• mutant oocytes cannot correctly position the metaphase spindle during meiosis I and form the first polar body
• homozygous females ovulate oocytes that fail to progress through metaphase I and to correctly position the metaphase I spindle at the cortex of the oocyte, resulting in the ovulation of oocytes that have not formed the first polar body
• homozygous females mated to wild-type male exhibit recurrent pregnancy loss during early and mid-gestational stages of development
• homozygous females rarely carry embryos to term and give birth
• homozygous females mated with wild-type males contain a normal number of uterine decidua but most decidua contain grossly abnormal embryos

behavior/neurological
• few pups that are born die from inadequate nursing as a result of a small litter size

cellular
• meiotic incompetence in oocytes results in polyploid embryos
• mutant oocytes cannot correctly position the metaphase spindle during meiosis I and form the first polar body





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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory