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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 | impaired granulosa cell differentiation |
decreased granulosa cell proliferation |
abnormal ovary morphology |
decreased corpora lutea number |
abnormal ovarian follicle morphology |
absent mature ovarian follicles |
absent primordial ovarian follicles |
absent secondary ovarian follicles |
increased atretic ovarian follicle number |
impaired ovarian folliculogenesis |
abnormal ovary size |
decreased ovary weight |
small ovary |
abnormal seminiferous tubule morphology |
decreased Sertoli cell number |
decreased testis weight |
small testis |
abnormal ovary physiology |
abnormal testis physiology |
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| Availability | Mouse Genotype | |||||||||||||||||||
| Foxl2tm1Gpil/Foxl2tm1Gpil | ||||||||||||||||||||
| Foxl2tm1Tre/Foxl2tm1Tre | ||||||||||||||||||||
| Foxl2tm4(cre)Tre/Foxl2tm4(cre)Tre | ||||||||||||||||||||
| Foxl2tm2.1Tre/Foxl2tm2.1Tre Gt(ROSA)26Sortm9(cre/ESR1)Arte/? (conditional) |
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| Foxl2tm2.1Tre/Foxl2tm2.1Tre Tg(Cga-cre)3Sac/0 (conditional) |
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| Foxl2tm2.1Tre/Foxl2tm2.1Tre Gnrhrtm1.1(cre)Uboe/Gnrhr+ (conditional) |
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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 04/23/2024 MGI 6.23 |
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