aipl1 Phenotypes

Phenotypes

XB-GENEPAGE-921759

Gene Symbol: aipl1 Gene Name: aryl hydrocarbon receptor interacting protein like 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (25 sources): Abnormal electroretinogram, Abnormality of neuronal migration, Abnormality of retinal pigmentation, Abnormality of the optic disc, Aplasia/Hypoplasia of the cerebellar vermis, Attenuation of retinal blood vessels, Blindness, Cataract, Cone/cone-rod dystrophy, Encephalocele, Global developmental delay, Hearing impairment, Hemiplegia/hemiparesis, Hypotonia, Intellectual disability, Keratoconus, Macular atrophy, Nyctalopia, Nystagmus, Optic disc pallor, Pendular nystagmus, Reduced visual acuity, Seizure, Severely reduced visual acuity, Undetectable light- and dark-adapted electroretinogram [+]
Mouse (17 sources): abnormal Muller cell morphology, abnormal electroretinogram waveform feature, abnormal eye electrophysiology, abnormal photoreceptor inner segment morphology, abnormal photoreceptor outer segment morphology, abnormal retina bipolar cell morphology, abnormal retina cone cell morphology, abnormal retina neuronal layer morphology, abnormal retina outer plexiform layer morphology, abnormal retina photoreceptor morphology, abnormal rod electrophysiology, absent visual evoked potential, decreased retina cone cell number, decreased retina photoreceptor cell number, retina photoreceptor degeneration, retina rod cell degeneration, thin retina outer nuclear layer [+]
View all ortholog results at Monarch