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Symbol
Name
ID

Ror2
receptor tyrosine kinase-like orphan receptor 2
MGI:1347521

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Intellectual disability	Global developmental delay
Disease(s) Associated with ROR2	Intellectual disability	Global developmental delay
autosomal recessive Robinow syndrome

Mouse Phenotypes		abnormal cochlear hair cell morphology	abnormal cochlear outer hair cell morphology
Availability	Mouse Genotype
	Ror2^tm1Ymi/Ror2^tm1Ymi

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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