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Symbol
Name
ID
Wdr19
WD repeat domain 19
MGI:2443231
Phenotype annotations related to skeleton
Darker colors indicate more annotations
Human Phenotypes
Frontal bossing
Sagittal craniosynostosis
Broad long bone diaphyses
Short distal phalanx of finger
Broad distal phalanx of finger
Broad phalanx of the toes
Brachydactyly
Cutaneous finger syndactyly
Short foot
Metaphyseal widening
Acetabular spurs
Rhizomelia
Joint hypermobility
Cone-shaped epiphysis
Short iliac bones
Hip dysplasia
Thoracic dysplasia
Pectus excavatum
Narrow chest
Abnormality of bone mineral density
Disease(s) Associated with WDR19
asphyxiating thoracic dystrophy 5
cranioectodermal dysplasia 4
Senior-Loken syndrome

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
polyphalangy
absent tibia
abnormal sternum ossification
split sternum
abnormal rib morphology
rib bifurcation
rib fusion
short ribs
abnormal spine curvature
abnormal vertebrae morphology
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)
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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory