Symbol Name ID |
Foxl2
forkhead box L2 MGI:1349428 |
Darker colors indicate more annotations |
Human Phenotypes | Increased circulating gonadotropin level |
Disease(s) Associated with FOXL2 | |
blepharophimosis, ptosis, and epicanthus inversus syndrome |
Mouse Phenotypes | decreased circulating follicle stimulating hormone level |
decreased circulating luteinizing hormone level |
increased circulating luteinizing hormone level |
decreased circulating insulin-like growth factor I level |
decreased follicle stimulating hormone level |
|
Availability | Mouse Genotype | |||||
Foxl2tm1Gpil/Foxl2tm1Gpil | ||||||
Foxl2tm2.1Tre/Foxl2tm2.1Tre Gnrhrtm1.1(cre)Uboe/Gnrhr+ (conditional) |
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 08/02/2024 MGI 6.24 |
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