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Symbol Name ID |
Myrf
myelin regulatory factor MGI:2684944 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal choroid morphology |
Abnormality of retinal pigmentation |
Microphthalmia |
Strabismus |
High hypermetropia |
Glaucoma |
| Disease(s) Associated with MYRF | ||||||
| nanophthalmos |
| Mouse Phenotypes | decreased retina cone cell number |
short photoreceptor inner segment |
short photoreceptor outer segment |
abnormal optic nerve morphology |
abnormal retina pigmentation |
retina pigment epithelium atrophy |
thin retina outer nuclear layer |
decreased total retina thickness |
retina degeneration |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
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| Availability | Mouse Genotype | |||||||||||
| Myrftm1Barr/Myrftm1Barr Olig2tm2(TVA,cre)Rth/Olig2+ (conditional) |
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| Myrftm1Barr/Myrftm1Barr Tg(rx3-icre)1Mjam/0 (conditional) |
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| Myrftm1Barr/Myrf+ Tg(rx3-icre)1Mjam/0 (conditional) |
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| Myrftm1Barr/Myrftm1.1Barr Tg(rx3-icre)1Mjam/0 (conditional) |
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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 06/04/2024 MGI 6.13 |
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