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Symbol
Name
ID
Arl6
ADP-ribosylation factor-like 6
MGI:1927136
Phenotype annotations related to vision/eye
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Attenuation of retinal blood vessels
Astigmatism
Cataract
Pigmentary retinopathy
Bone spicule pigmentation of the retina
Retinal degeneration
Retinal dystrophy
Cone/cone-rod dystrophy
Rod-cone dystrophy
Hyperautofluorescent macular lesion
Hypertelorism
Abnormal electroretinogram
Strabismus
Nystagmus
Myopia
Color vision defect
Nyctalopia
Photophobia
Visual impairment
Reduced visual acuity
Blindness
Peripheral visual field loss
Glaucoma
Disease(s) Associated with ARL6
Bardet-Biedl syndrome
Bardet-Biedl syndrome 1
Bardet-Biedl syndrome 3
retinitis pigmentosa 55

Mouse Phenotypes
vision/eye phenotype
abnormal retina photoreceptor morphology
absent photoreceptor inner segment
disorganized photoreceptor inner segment
absent photoreceptor outer segment
abnormal retina neuronal layer morphology
abnormal retina outer nuclear layer morphology
Availability Mouse Genotype
Arl6tm1Vcs/Arl6tm1Vcs
Arl6tm2Vcs/Arl6tm2Vcs *

Contributing Projects:
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
04/30/2024
MGI 6.23
The Jackson Laboratory