Symbol Name ID |
Arl3
ADP-ribosylation factor-like 3 MGI:1929699 |
Darker colors indicate more annotations |
Human Phenotypes | Cystoid macular edema |
Attenuation of retinal blood vessels |
Posterior subcapsular cataract |
Iris coloboma |
Bone spicule pigmentation of the retina |
Rod-cone dystrophy |
Asteroid hyalosis |
Vitreous floaters |
Strabismus |
Nystagmus |
Oculomotor apraxia |
Nyctalopia |
Reduced visual acuity |
Constriction of peripheral visual field |
Ptosis |
Disease(s) Associated with ARL3 | |||||||||||||||
Joubert syndrome | |||||||||||||||
retinitis pigmentosa 83 |
Mouse Phenotypes | abnormal photoreceptor connecting cilium morphology |
abnormal photoreceptor inner segment morphology |
abnormal photoreceptor outer segment morphology |
absent photoreceptor outer segment |
short photoreceptor outer segment |
abnormal retina rod cell outer segment morphology |
retina cone cell degeneration |
abnormal retina rod cell morphology |
retina rod cell degeneration |
abnormal retina morphology |
thin retina inner nuclear layer |
abnormal retina outer nuclear layer morphology |
retina outer nuclear layer degeneration |
decreased total retina thickness |
retina degeneration |
abnormal a-wave shape |
decreased a-wave amplitude |
decreased b-wave amplitude |
abnormal cone electrophysiology |
abnormal rod electrophysiology |
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Availability | Mouse Genotype | ||||||||||||||||||||
Arl3Gt(OST263303)Lex/Arl3Gt(OST263303)Lex | |||||||||||||||||||||
Tg(Rho-Arl3*Q71L)#Visu/0 | |||||||||||||||||||||
Arl3Gt(EUCJ0159b07)1.1Hmgu/Arl3Gt(EUCJ0159b07)1.1Hmgu Tg(Rho-icre)1Ck/0 (conditional) |
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Arl3Gt(EUCJ0159b07)1.1Hmgu/Arl3Gt(EUCJ0159b07)1.1Hmgu Tg(Six3-cre)69Frty/0 (conditional) |
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 04/16/2024 MGI 6.23 |
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