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Symbol
Name
ID

Wdr37
WD repeat domain 37
MGI:1920393

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Secondary microcephaly
Disease(s) Associated with WDR37	Secondary microcephaly
neurooculocardiogenitourinary syndrome

Mouse Phenotypes		abnormal spine curvature	kyphosis	fusion of vertebral arches	vertebral fusion	increased bone mineral content
Availability	Mouse Genotype
	Wdr37^{tm1a(KOMP)Wtsi}/Wdr37^{tm1a(KOMP)Wtsi}

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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