|
Symbol Name ID |
Myo7a
myosin VIIA MGI:104510 |
| Darker colors indicate more annotations |
| Human Phenotypes | Keratoconus |
Astigmatism |
Cataract |
Iris hypopigmentation |
Abnormal optic disc morphology |
Abnormality of retinal pigmentation |
Rod-cone dystrophy |
Abnormal electroretinogram |
Undetectable electroretinogram |
Nystagmus |
High hypermetropia |
Myopia |
Nyctalopia |
Visual impairment |
Blindness |
Severely reduced visual acuity |
Visual field defect |
Hemianopia |
Scotoma |
Visual loss |
Progressive visual loss |
| Disease(s) Associated with MYO7A | |||||||||||||||||||||
| Leber congenital amaurosis | |||||||||||||||||||||
| Usher syndrome | |||||||||||||||||||||
| Usher syndrome type 1 |
| Mouse Phenotypes | impaired pupillary reflex |
abnormal retina rod cell morphology |
retina rod cell degeneration |
abnormal retina pigment epithelium morphology |
persistence of hyaloid vascular system |
abnormal electroretinogram waveform feature |
decreased a-wave amplitude |
decreased b-wave amplitude |
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| Availability | Mouse Genotype | ||||||||
| Myo7apolka/Myo7apolka | |||||||||
| Myo7ash1-11J/Myo7ash1-11J | |||||||||
| Myo7atm1a(EUCOMM)Wtsi/Myo7atm1a(EUCOMM)Wtsi | |||||||||
| Myo7atm1b(EUCOMM)Wtsi/Myo7atm1b(EUCOMM)Wtsi | |||||||||
| Myo7atm1b(EUCOMM)Wtsi/Myo7a+ | |||||||||
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 05/28/2024 MGI 6.13 |
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