| Monarch Ortholog Phenotypes
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Human (33 sources):
Abnormal electroretinogram,
Abnormal retinal vascular morphology,
Abnormal testis morphology,
Abnormality of fundus pigmentation,
Abnormality of retinal pigmentation,
Anteverted nares,
Attenuation of retinal blood vessels,
Atypical scarring of skin,
Blindness,
Bone spicule pigmentation of the retina,
Cataract,
Chorioretinal atrophy,
Conductive hearing impairment,
Constriction of peripheral visual field,
Glaucoma,
Hyperinsulinemia,
Hyperreflexia,
Hypogonadism,
Hypoplasia of penis,
Intellectual disability,
Keratoconus,
Nyctalopia,
Nystagmus,
Obesity,
Ophthalmoplegia,
Optic atrophy,
Photophobia,
Progressive night blindness,
Rod-cone dystrophy,
Sensorineural hearing impairment,
Type II diabetes mellitus,
Visual impairment,
Wide nasal bridge
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Mouse (24 sources):
abnormal cochlear hair cell stereociliary bundle morphology,
abnormal cochlear outer hair cell physiology,
abnormal cone electrophysiology,
abnormal distortion product otoacoustic emission,
abnormal eye electrophysiology,
abnormal photoreceptor inner segment morphology,
abnormal photoreceptor outer segment morphology,
abnormal photoreceptor outer segment size,
abnormal rod electrophysiology,
cochlear outer hair cell degeneration,
decreased a-wave amplitude,
decreased b-wave amplitude,
decreased inner hair cell stereocilia number,
decreased outer hair cell stereocilia number,
decreased retina inner nuclear layer thickness,
decreased total retina thickness,
increased or absent threshold for auditory brainstem response,
increased susceptibility to age-related hearing loss,
photoreceptor inner segment degeneration,
photoreceptor outer segment degeneration,
retina outer nuclear layer degeneration,
short cochlear hair cell stereocilia,
short photoreceptor outer segment,
thin retina outer nuclear layer
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View all ortholog results at Monarch
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