About   Help   FAQ
Symbol
Name
ID
Wdr19
WD repeat domain 19
MGI:2443231
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Cataract
Retinal dystrophy
Rod-cone dystrophy
Optic atrophy
Papilledema
Hypertelorism
Hypermetropia
Myopia
Visual impairment
Progressive visual loss
Disease(s) Associated with WDR19
asphyxiating thoracic dystrophy 5
craniometaphyseal dysplasia
nephronophthisis 13

Mouse Phenotypes
anophthalmia
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
06/04/2019
MGI 6.14
The Jackson Laboratory