Symbol Name ID |
Foxc1
forkhead box C1 MGI:1347466 |
Darker colors indicate more annotations |
Human Phenotypes | Hypoplasia of the maxilla |
Malar flattening |
Midface retrusion |
Prominent forehead |
Everted lower lip vermilion |
Microdontia |
Hypodontia |
Concave nasal ridge |
Depressed nasal bridge |
Wide nasal bridge |
Telecanthus |
Disease(s) Associated with FOXC1 | |||||||||||
Axenfeld-Rieger syndrome | |||||||||||
Axenfeld-Rieger syndrome type 3 |
Mouse Phenotypes | abnormal pharyngeal arch artery morphology |
abnormal fourth pharyngeal arch artery morphology |
abnormal craniofacial bone morphology |
small basisphenoid bone |
abnormal foramen magnum morphology |
short basicranium |
small Meckel's cartilage |
abnormal neurocranium morphology |
abnormal frontal bone morphology |
absent frontal bone |
abnormal occipital bone morphology |
abnormal sphenoid bone morphology |
absent neurocranium |
abnormal hyoid bone morphology |
short mandible |
abnormal maxillary zygomatic process morphology |
enlarged maxillary zygomatic process |
abnormal craniofacial development |
abnormal Reichert's cartilage morphology |
abnormal nasal capsule morphology |
short snout |
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Availability | Mouse Genotype | |||||||||||||||||||||
Foxc1ch/Foxc1ch | ||||||||||||||||||||||
Foxc1hith/Foxc1hith | ||||||||||||||||||||||
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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