|
Symbol Name ID |
Pcdh15
protocadherin 15 MGI:1891428 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Rod-cone dystrophy |
Visual impairment |
| Disease(s) Associated with PCDH15 | ||
| autosomal recessive nonsyndromic deafness 23 | ||
| Usher syndrome type 1D | ||
| Usher syndrome type 1F |
| Mouse Phenotypes | vision/eye phenotype |
thin retina outer nuclear layer |
abnormal electroretinogram waveform feature |
decreased a-wave amplitude |
decreased b-wave amplitude |
abnormal eye electrophysiology |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
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| Availability | Mouse Genotype | ||||||||
| Pcdh15av-5J/Pcdh15av-5J | |||||||||
| Pcdh15av-Jfb/Pcdh15av-Jfb | |||||||||
| Pcdh15em1Zma/Pcdh15em1Zma | * | ||||||||
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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