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Symbol
Name
ID

Wdr19
WD repeat domain 19
MGI:2443231

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Photophobia	Aplasia/Hypoplasia of the cerebellar vermis	Ataxia	Polydipsia	Intellectual disability	Intellectual disability, mild	Hyperreflexia	Global developmental delay
Disease(s) Associated with WDR19	Photophobia	Aplasia/Hypoplasia of the cerebellar vermis	Ataxia	Polydipsia	Intellectual disability	Intellectual disability, mild	Hyperreflexia	Global developmental delay
retinitis pigmentosa
Senior-Loken syndrome

Mouse Phenotypes		exencephaly
Availability	Mouse Genotype	exencephaly
	Wdr19^twto/Wdr19^twto

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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