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Symbol Name ID |
Pde6d
phosphodiesterase 6D, cGMP-specific, rod, delta MGI:1270843 |
| Darker colors indicate more annotations |
| Human Phenotypes | Oculomotor apraxia |
Temporal cortical atrophy |
Hypoplasia of the corpus callosum |
Agenesis of cerebellar vermis |
Molar tooth sign on MRI |
Global developmental delay |
| 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 |
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| 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) |
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last database update 04/16/2024 MGI 6.23 |
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