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Symbol
Name
ID

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

Phenotype annotations related to vision/eye

Darker colors indicate more annotations

Human Phenotypes	Blue sclerae	Hypertelorism	Proptosis	Strabismus	Ptosis
Disease(s) Associated with ROR2
autosomal recessive Robinow syndrome

Mouse Phenotypes		abnormal retina vasculature morphology	large orbits	cataract	persistence of hyaloid vascular system	ocular hypertelorism	entropion	abnormal vitreous body morphology	excessive tearing
Availability	Mouse Genotype	abnormal retina vasculature morphology	large orbits	cataract	persistence of hyaloid vascular system	ocular hypertelorism	entropion	abnormal vitreous body morphology	excessive tearing
	Ror2^tm1Anec/Ror2^tm1Anec
	Ror2^tm1Ymi/Ror2^tm1Ymi
	Ror2^em1(IMPC)Mbp/Ror2⁺

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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