About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:3575010
Allelic
Composition
Gdf7tm1Tmj/Gdf7tm1Tmj
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
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; 37% of homozygous mice exhibited this phenotype on a mixed 129P2/Ola Hsd and C57BL/6 genetic background
• by postnatal day 40 severe hydroencephaly associated with dilation of the fourth and left ventricles was observed
• 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
• 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 about 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
03/25/2025
MGI 6.24
The Jackson Laboratory