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Phenotypes Associated with This Genotype
Genotype
MGI:3823095
Allelic
Composition
Pou3f1tm1Mejr/Pou3f1tm1Mejr
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pou3f1tm1Mejr mutation (0 available); any Pou3f1 mutation (14 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• all but 2-4% of animals die soon after birth; survivors live for a longer period

growth/size/body
• by P5, surviving mutants can be identified by smaller size

nervous system
• nerve appears defective at P8 and P16
• no myelination of sciatic nerve is seen until second week postnatal whereas myelination is observed at P16 in wild-type
• myelination appears complete in adult nerves
• at P16, only larger axons are myelinated
• some Schwann cells show severely disrupted myelination, and fail to wrap myelin around the axon; other Schwann cells begin myelination before a 1:1 relation with axons is established
• sometimes myelination is seen in absence of axon

behavior/neurological
• by P5, surviving mutants exhibit tremors


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
05/07/2024
MGI 6.23
The Jackson Laboratory