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Symbol Name ID |
P2rx2
purinergic receptor P2X, ligand-gated ion channel, 2 MGI:2665170 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Progressive sensorineural hearing impairment |
Tinnitus |
| Disease(s) Associated with P2RX2 | ||
| autosomal dominant nonsyndromic deafness 41 |
| Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal cochlear inner hair cell morphology |
abnormal inner hair cell synaptic ribbon morphology |
increased or absent threshold for auditory brainstem response |
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| Availability | Mouse Genotype | ||||
| P2rx2em1Xzl/P2rx2+ | * | ||||
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 04/23/2024 MGI 6.23 |
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