|
Symbol Name ID |
Rom1
rod outer segment membrane protein 1 MGI:97998 |
| Darker colors indicate more annotations |
| Human Phenotypes | Attenuation of retinal blood vessels |
Chorioretinal atrophy |
Pigmentary retinopathy |
Rod-cone dystrophy |
Abnormal electroretinogram |
Nyctalopia |
Adult-onset night blindness |
Constriction of peripheral visual field |
| Disease(s) Associated with ROM1 | ||||||||
| retinitis pigmentosa 7 |
| Mouse Phenotypes | abnormal retina blood vessel morphology |
short photoreceptor outer segment |
abnormal retina rod cell outer segment morphology |
disorganized photoreceptor outer segment |
retina rod cell degeneration |
abnormal ocular fundus morphology |
abnormal retina morphology |
thin retina outer nuclear layer |
retina degeneration |
abnormal eye electrophysiology |
abnormal rod electrophysiology |
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| Availability | Mouse Genotype | |||||||||||
| Rom1Rgsc1156/Rom1Rgsc1156 | ||||||||||||
| Rom1tm1Mci/Rom1tm1Mci | ||||||||||||
| Rom1Rgsc1156/Rom1+ | ||||||||||||
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 04/23/2024 MGI 6.23 |
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