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Symbol Name ID |
Ildr1
immunoglobulin-like domain containing receptor 1 MGI:2146574 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Sensorineural hearing impairment |
| Disease(s) Associated with ILDR1 | |
| autosomal recessive nonsyndromic deafness 42 |
| Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal inner ear morphology |
abnormal cochlear hair cell morphology |
abnormal inner hair cell stereociliary bundle morphology |
abnormal outer hair cell stereociliary bundle morphology |
cochlear inner hair cell degeneration |
cochlear outer hair cell degeneration |
abnormal organ of Corti morphology |
abnormal tunnel of Corti morphology |
absent tunnel of Corti |
organ of Corti degeneration |
abnormal endocochlear potential |
increased or absent threshold for auditory brainstem response |
absent distortion product otoacoustic emissions |
deafness |
sensorineural hearing loss |
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| Availability | Mouse Genotype | ||||||||||||||||
| Ildr1Gt(D178D03)Wrst/Ildr1Gt(D178D03)Wrst | |||||||||||||||||
| Ildr1tm1(KOMP)Wtsi/Ildr1tm1(KOMP)Wtsi | * | ||||||||||||||||
| Ildr1tm1.1Lwa/Ildr1tm1.1Lwa | |||||||||||||||||
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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