Symbol Name ID |
Wdr19
WD repeat domain 19 MGI:2443231 |
Darker colors indicate more annotations |
Human Phenotypes | Frontal bossing |
Sagittal craniosynostosis |
Full cheeks |
Smooth philtrum |
Thin upper lip vermilion |
Thin vermilion border |
Taurodontia |
Anteverted nares |
Wide nasal bridge |
Epicanthus |
Disease(s) Associated with WDR19 | ||||||||||
asphyxiating thoracic dystrophy 5 | ||||||||||
cranioectodermal dysplasia 4 |
Mouse Phenotypes | abnormal cranium morphology |
absent frontal bone |
interparietal bone hypoplasia |
absent supraoccipital bone |
parietal bone hypoplasia |
abnormal mandibular angle morphology |
short mandible |
abnormal maxilla morphology |
abnormal premaxilla morphology |
short premaxilla |
short maxilla |
abnormal palatine bone morphology |
decreased palatine bone horizontal plate size |
abnormal craniofacial development |
abnormal palatal shelf fusion at midline |
short face |
bilateral cleft upper lip |
cleft secondary palate |
cleft palate |
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Availability | Mouse Genotype | |||||||||||||||||||
Wdr19twto/Wdr19twto |
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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