Symbol Name ID |
Rab28
RAB28, member RAS oncogene family MGI:1917285 |
Darker colors indicate more annotations |
Human Phenotypes | Foveal hyperpigmentation |
Foveal atrophy |
Cone/cone-rod dystrophy |
High myopia |
Reduced visual acuity |
Central scotoma |
Disease(s) Associated with RAB28 | ||||||
cone-rod dystrophy 18 |
Mouse Phenotypes | long retina cone cell outer segment |
short photoreceptor outer segment |
abnormal retina cone cell outer segment morphology |
abnormal retina cone cell morphology |
retina cone cell degeneration |
abnormal retina pigmentation |
abnormal retina outer nuclear layer thickness |
increased susceptibility to age-related retinal degeneration |
decreased a-wave amplitude |
decreased b-wave amplitude |
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Availability | Mouse Genotype | ||||||||||
Rab28tm1d(EUCOMM)Hmgu/Rab28tm1d(EUCOMM)Hmgu | |||||||||||
Rab28tm1d(EUCOMM)Wtsi/Rab28tm1d(EUCOMM)Wtsi |
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 04/30/2024 MGI 6.23 |
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