Symbol Name ID |
Foxc1
forkhead box C1 MGI:1347466 |
Darker colors indicate more annotations |
Human Phenotypes | Hypospadias |
Disease(s) Associated with FOXC1 | |
Axenfeld-Rieger syndrome |
Mouse Phenotypes | ovary hemorrhage |
decreased oocyte number |
oocyte degeneration |
abnormal primordial germ cell migration |
abnormal ovary morphology |
abnormal ovarian cortex morphology |
abnormal ovarian follicle morphology |
impaired ovarian folliculogenesis |
polyovular ovarian follicle |
abnormal ovarian medulla morphology |
small ovary |
ectopic ovary |
ovary cyst |
disorganized testis cords |
small testis |
abnormal testis tunica albuginea morphology |
ectopic testis |
abnormal reproductive system morphology |
abnormal oviduct morphology |
short oviduct |
small gonad |
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Availability | Mouse Genotype | |||||||||||||||||||||
Foxc1ch/Foxc1ch | ||||||||||||||||||||||
Foxc1tm1Blh/Foxc1tm1Blh | ||||||||||||||||||||||
Foxc1ch/Foxc1+ |
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 09/03/2024 MGI 6.24 |
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