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Symbol
Name
ID
Ror2
receptor tyrosine kinase-like orphan receptor 2
MGI:1347521
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Chronic otitis media
Low-set ears
Low-set, posteriorly rotated ears
Posteriorly rotated ears
Hearing impairment
Disease(s) Associated with ROR2
autosomal recessive Robinow syndrome

Mouse Phenotypes
abnormal middle ear ossicle morphology
abnormal malleus morphology
abnormal cochlear hair cell morphology
abnormal cochlear outer hair cell morphology
abnormal organ of Corti morphology
abnormal tegmen tympani morphology
Availability Mouse Genotype
Ror2tm1Ymi/Ror2tm1Ymi

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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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory