|
Symbol Name ID |
Pde6d
phosphodiesterase 6D, cGMP-specific, rod, delta MGI:1270843 |
| Darker colors indicate more annotations |
| Human Phenotypes | Retinal dysplasia |
Microphthalmia |
Coloboma |
Undetectable electroretinogram |
Oculomotor apraxia |
| Disease(s) Associated with PDE6D | |||||
| Joubert syndrome 22 |
| Mouse Phenotypes | decreased retina cone cell number |
short retina rod cell outer segment |
abnormal retina rod cell morphology |
thin retina outer nuclear layer |
retina degeneration |
abnormal eye electrophysiology |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
|
| Availability | Mouse Genotype | ||||||||
| Pde6dtm1.1Wbae/Pde6dtm1.1Wbae | |||||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/16/2024 MGI 6.23 |
|
|
|
||
Analysis Tools