Monarch Ortholog Phenotypes
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Human (40 sources):
Cataract,
Chiari type I malformation,
Chorioretinal atrophy,
Edema,
Focal segmental glomerulosclerosis,
Gliosis,
Hearing impairment,
Horseshoe kidney,
Hyperextensible skin,
Intellectual disability,
Lens luxation,
Macular degeneration,
Macular hyperpigmentation,
Microphthalmia,
Morning glory anomaly,
Multicystic kidney dysplasia,
Myopia,
Nephrolithiasis,
Nephrotic syndrome,
Nystagmus,
Optic disc coloboma,
Optic nerve dysplasia,
Orbital cyst,
Proteinuria,
Renal cyst,
Renal dysplasia,
Renal hypoplasia,
Renal insufficiency,
Renal malrotation,
Retinal coloboma,
Retinal detachment,
Seizure,
Sensorineural hearing impairment,
Soft skin,
Stage 5 chronic kidney disease,
Strabismus,
Vesicoureteral reflux,
Visual impairment,
obsolete Joint hyperflexibility,
obsolete Joint laxity
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Mouse (96 sources):
Mullerian duct degeneration,
Wolffian duct degeneration,
abnormal axon extension,
abnormal brain commissure morphology,
abnormal brain development,
abnormal choroid plexus morphology,
abnormal cochlea morphology,
abnormal common crus morphology,
abnormal corpora quadrigemina morphology,
abnormal diencephalon morphology,
abnormal ear development,
abnormal endolymphatic duct morphology,
abnormal eye development,
abnormal intermediate mesoderm morphology,
abnormal kidney development,
abnormal kidney lobule morphology,
abnormal mesonephric mesenchyme morphology,
abnormal mesonephros morphology,
abnormal metanephric mesenchyme morphology,
abnormal midbrain-hindbrain boundary morphology,
abnormal nephrogenic zone morphology,
abnormal neural crest morphology,
abnormal optic fissure closure,
abnormal optic nerve innervation,
abnormal optic stalk morphology,
abnormal optic tract morphology,
abnormal organ of Corti morphology,
abnormal otolith organ morphology,
abnormal renal tubule morphology,
abnormal retina blood vessel morphology,
abnormal retina blood vessel pattern,
abnormal retina layer morphology,
abnormal retina nerve fiber layer morphology,
abnormal retina neuronal layer morphology,
abnormal retina pigment epithelium morphology,
abnormal retina vasculature morphology,
abnormal scala media morphology,
abnormal semicircular canal ampulla morphology,
abnormal stria vascularis morphology,
abnormal ureter development,
abnormal ureteric bud morphology,
abnormal vestibular saccular macula morphology,
abnormal vestibulocochlear ganglion morphology,
absent cerebellum,
absent cochlear ganglion,
absent cochlear nerve,
absent efferent ductules of testis,
absent epididymis,
absent metanephros,
absent midbrain-hindbrain boundary,
absent optic chiasm,
absent organ of Corti,
absent oviduct,
absent semicircular canal ampulla,
absent seminal vesicle,
absent tectum,
absent ureter,
absent ureteric bud,
absent uterine horn,
absent utricle,
absent vestibular saccule,
decreased renal glomerulus number,
decreased retina ganglion cell number,
delayed neural tube closure,
delayed optic fissure closure,
dilated endolymphatic duct,
dilated ureter,
double ureter,
duplex kidney,
ectopic ureteric bud,
endocrine/exocrine gland phenotype,
hearing/vestibular/ear phenotype,
impaired branching involved in ureteric bud morphogenesis,
incomplete rostral neuropore closure,
increased kidney apoptosis,
increased pancreatic beta cell mass,
increased pancreatic islet number,
kidney cortex hypoplasia,
kidney medulla cyst,
kidney medulla hypoplasia,
lethality throughout fetal growth and development, incomplete penetrance,
neonatal lethality, complete penetrance,
nervous system phenotype,
optic disk coloboma,
pancreatic islet hyperplasia,
perinatal lethality, complete penetrance,
postnatal lethality, incomplete penetrance,
rudimentary Mullerian ducts,
rudimentary Wolffian ducts,
short endolymphatic duct,
short scala media,
small endolymphatic duct,
small kidney,
small vestibular ganglion,
thin retina ganglion layer,
uveal coloboma
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View all ortholog results at Monarch
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