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Symbol Name ID |
Ror1
receptor tyrosine kinase-like orphan receptor 1 MGI:1347520 |
| 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 cochlea coiling |
increased or absent threshold for auditory brainstem response |
decreased distortion product otoacoustic emission amplitude |
deafness |
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| Availability | Mouse Genotype | ||||||
| Ror1tm1Ymi/Ror1tm1Ymi | |||||||
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 04/16/2024 MGI 6.23 |
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