Symbol Name ID |
Ror2
receptor tyrosine kinase-like orphan receptor 2 MGI:1347521 |
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 | ||||||||
Ror2tm1Anec/Ror2tm1Anec | |||||||||
Ror2tm1Ymi/Ror2tm1Ymi | |||||||||
Ror2em1(IMPC)Mbp/Ror2+ |
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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last database update 08/02/2024 MGI 6.24 |
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