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Phenotypes Associated with This Genotype
Genotype
MGI:3575011
Allelic
Composition
Gdf7tm1Tmj/Gdf7tm1Tmj
Genetic
Background
involves: 129
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gdf7tm1Tmj mutation (0 available); any Gdf7 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• incomplete penetrance; 20% of homozygous animals exhibited phenotype on an inbred 129 genetic background
• at postnatal day 15, 25% of mutant brains showed marked dilation of the lateral ventricles with no obvious defects in the morphology of the cerebellum or the cerebral cortex
• by postnatal day 40 severe hydroencephaly associated with dilation of the fourth and left ventricles was observed
• in all affected brains the cerebral cortex was thinned and the hippocampus was displaced dorsally, although the cellular organization of the cerebellum and the cerebral cortex was grossly normal
• the number of dorsal D1A commissural interneurons in E12.5, E13.5, and E14.5 spinal cord was reduced by ~92% compared with wild-type embryos, with no apparent change in the number of D1B neurons


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
12/30/2025
MGI 6.24
The Jackson Laboratory