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Symbol
Name
ID
Wdr19
WD repeat domain 19
MGI:2443231
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Facial palsy
Facial diplegia
Disease(s) Associated with WDR19
craniometaphyseal dysplasia

Mouse Phenotypes
abnormal myotome development
abnormal dermomyotome development
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
06/18/2019
MGI 6.14
The Jackson Laboratory