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Symbol
Name
ID
Foxg1
forkhead box G1
MGI:1347464
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Postnatal microcephaly
Progressive microcephaly
Short foot
Kyphosis
Scoliosis
Disease(s) Associated with FOXG1
Rett syndrome

Mouse Phenotypes
abnormal cranium morphology
Availability Mouse Genotype
Foxg1tm1M/Foxg1tm1M

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
10/08/2019
MGI 6.14
The Jackson Laboratory