Symbol Name ID |
Gli3
GLI-Kruppel family member GLI3 MGI:95729 |
Darker colors indicate more annotations |
Human Phenotypes | Abnormal calvaria morphology |
Frontal bossing |
Craniosynostosis |
Dolichocephaly |
Scaphocephaly |
Trigonocephaly |
Macrocephaly |
Metopic synostosis |
Delayed cranial suture closure |
Midline facial capillary hemangioma |
High forehead |
Cleft upper lip |
Cleft palate |
Microglossia |
Anodontia |
Natal tooth |
Anteverted nares |
Depressed nasal bridge |
Wide nasal bridge |
Short nose |
Choanal atresia |
Downslanted palpebral fissures |
Disease(s) Associated with GLI3 | ||||||||||||||||||||||
anodontia | ||||||||||||||||||||||
Greig cephalopolysyndactyly syndrome | ||||||||||||||||||||||
Pallister-Hall syndrome |
Mouse Phenotypes | abnormal craniofacial morphology |
abnormal lambdoid suture morphology |
wide metopic suture |
wide sagittal suture |
abnormal cranium morphology |
abnormal basisphenoid bone morphology |
basisphenoid bone foramen |
small basisphenoid bone |
enlarged cranium |
abnormal neurocranium morphology |
abnormal interfrontal bone morphology |
absent neurocranium |
abnormal tooth development |
abnormal maxilla morphology |
abnormal palatine bone horizontal plate morphology |
abnormal craniofacial development |
abnormal facial morphology |
bilateral cleft upper lip |
unilateral cleft upper lip |
cleft palate |
abnormal ear position |
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Availability | Mouse Genotype | |||||||||||||||||||||
Gli3Pdn/Gli3Pdn | ||||||||||||||||||||||
Gli3TgBR/Gli3TgBR | ||||||||||||||||||||||
Gli3tm1Urt/Gli3tm1Urt | ||||||||||||||||||||||
Gli3Xt-3H/Gli3Xt-3H | ||||||||||||||||||||||
Gli3Xt-J/Gli3Xt-J | ||||||||||||||||||||||
Gli3Xt-3H/Gli3+ |
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 03/19/2024 MGI 6.23 |
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