Symbol Name ID |
Foxp2
forkhead box P2 MGI:2148705 |
Darker colors indicate more annotations |
Human Phenotypes | Increased serum serotonin |
Disease(s) Associated with FOXP2 | |
autistic disorder |
Mouse Phenotypes | abnormal circulating mineral level |
increased circulating ferritin level |
decreased dopamine level |
increased dopamine level |
abnormal energy homeostasis |
increased serotonin level |
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Availability | Mouse Genotype | ||||||
Foxp2tm2.1Woen/Foxp2tm2.1Woen | |||||||
Foxp2tm2.2Woen/Foxp2+ |
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 05/14/2024 MGI 6.23 |
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