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Symbol
Name
ID
Ror1
receptor tyrosine kinase-like orphan receptor 1
MGI:1347520
Phenotype annotations related to hearing/vestibular/ear
Darker colors indicate more annotations
Human Phenotypes
Congenital sensorineural hearing impairment
Disease(s) Associated with ROR1
autosomal recessive nonsyndromic deafness 108

Mouse Phenotypes
abnormal cochlea morphology
abnormal cochlear hair cell morphology
decreased cochlear coiling
increased or absent threshold for auditory brainstem response
abnormal distortion product otoacoustic emission
deafness
Availability Mouse Genotype
Ror1tm1Ymi/Ror1tm1Ymi

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
10/08/2019
MGI 6.14
The Jackson Laboratory