Symbol Name ID |
Dhdds
dehydrodolichyl diphosphate synthase MGI:1914672 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Cystoid macular edema |
Rod-cone dystrophy |
Nyctalopia |
Reduced visual acuity |
Constriction of peripheral visual field |
Disease(s) Associated with DHDDS | |||||
retinitis pigmentosa 59 |
Mouse Phenotypes | vision/eye phenotype |
increased retina vascular tortuosity |
retina microaneurysm |
decreased retina photoreceptor cell number |
abnormal photoreceptor outer segment morphology |
abnormal retina pigment epithelium morphology |
retina pigment epithelium atrophy |
abnormal retina morphology |
thin retina outer nuclear layer |
decreased total retina thickness |
retina gliosis |
decreased a-wave amplitude |
decreased b-wave amplitude |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
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Availability | Mouse Genotype | |||||||||||||||
Dhddsem1Sjpi/Dhddsem1Sjpi | * | |||||||||||||||
Dhddstm1.1Sjpi/Dhddstm1.1Sjpi Tg(BEST1-rtTA,tetO-cre)1Yzl/0 (conditional) |
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Dhddstm1.1Sjpi/Dhdds+ Tg(BEST1-rtTA,tetO-cre)1Yzl/0 (conditional) |
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 09/03/2024 MGI 6.24 |
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