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Symbol Name ID |
Fam161a
family with sequence similarity 161, member A MGI:1921123 |
| Darker colors indicate more annotations |
| Human Phenotypes | Optic disc pallor |
Bone spicule pigmentation of the retina |
Rod-cone dystrophy |
Nyctalopia |
Constriction of peripheral visual field |
| Disease(s) Associated with FAM161A | |||||
| retinitis pigmentosa 28 |
| Mouse Phenotypes | abnormal retina vasculature morphology |
abnormal retina blood vessel morphology |
abnormal photoreceptor connecting cilium morphology |
increased retina apoptosis |
abnormal retina photoreceptor morphology |
abnormal photoreceptor outer segment morphology |
disorganized photoreceptor outer segment |
retina photoreceptor degeneration |
abnormal optic disk morphology |
abnormal lens morphology |
abnormal retina morphology |
thin retina outer nuclear layer |
retina outer nuclear layer degeneration |
increased susceptibility to age-related retinal degeneration |
abnormal electroretinogram waveform feature |
increased a-wave implicit time |
increased b-wave implicit time |
decreased a-wave amplitude |
decreased b-wave amplitude |
abnormal vision |
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| Availability | Mouse Genotype | ||||||||||||||||||||
| Fam161aGt(462E7)Cmhd/Fam161aGt(462E7)Cmhd | |||||||||||||||||||||
| Fam161atm1b(KOMP)Wtsi/Fam161atm1b(KOMP)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 05/21/2024 MGI 6.23 |
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