About   Help   FAQ
Symbol
Name
ID
Wdr19
WD repeat domain 19
MGI:2443231
Phenotype annotations related to craniofacial
Darker colors indicate more annotations
Human Phenotypes
Micrognathia
Mandibular prognathia
Craniofacial hyperostosis
Facial hyperostosis
Craniofacial osteosclerosis
Calvarial osteosclerosis
Macrocephaly
Frontal bossing
Sagittal craniosynostosis
Dolichocephaly
Scaphocephaly
Sclerosis of skull base
Coarse facial features
Facial palsy
Facial diplegia
Full cheeks
Everted lower lip vermilion
Smooth philtrum
Thin upper lip vermilion
Thin vermilion border
Broad alveolar ridges
Delayed eruption of permanent teeth
Hypoplasia of teeth
Misalignment of teeth
Widely spaced teeth
Bony paranasal bossing
Choanal stenosis
Concave nasal ridge
Depressed nasal bridge
Wide nasal bridge
Abnormality of the nasopharynx
Nasal obstruction
Telecanthus
Disease(s) Associated with WDR19
asphyxiating thoracic dystrophy 5
craniometaphyseal dysplasia

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
cleft upper lip
cleft secondary palate
cleft palate
Availability Mouse Genotype
Wdr19twto/Wdr19twto

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
06/11/2019
MGI 6.14
The Jackson Laboratory