Monarch Ortholog Phenotypes
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Human (13 sources):
Agenesis of corpus callosum,
Aplasia/Hypoplasia of the corpus callosum,
Cerebral cortical atrophy,
EEG abnormality,
Global developmental delay,
Hemiparesis,
Intellectual disability,
Porencephalic cyst,
Schizencephaly,
Seizure,
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Mouse (53 sources):
abnormal Ammon gyrus morphology,
abnormal axon extension,
abnormal cerebral cortex morphology,
abnormal cerebral hemisphere morphology,
abnormal cochlea morphology,
abnormal cochlear inner hair cell morphology,
abnormal hippocampal fimbria morphology,
abnormal incudomalleolar joint morphology,
abnormal incudostapedial joint morphology,
abnormal incus long process morphology,
abnormal incus morphology,
abnormal kidney development,
abnormal malleus morphology,
abnormal metanephric mesenchyme morphology,
abnormal metanephric ureteric bud development,
abnormal middle ear ossicle morphology,
abnormal pallium development,
abnormal primary sex determination,
abnormal stapes head morphology,
abnormal ureteric bud tip morphology,
absent dentate gyrus,
absent efferent ductules of testis,
absent epididymis,
absent incus,
absent incus lenticular process,
absent internal female genitalia,
absent internal male genitalia,
absent Mullerian ducts,
absent oviduct,
absent pinna reflex,
absent seminal vesicle,
absent testes,
absent ureter,
agonadal,
cardiovascular system phenotype,
conductive hearing loss,
deafness,
decreased anterior commissure size,
decreased cochlear nerve compound action potential,
decreased corpus callosum size,
decreased hippocampal fornix size,
gonadal ridge hypoplasia,
impaired branching involved in ureteric bud morphogenesis,
increased cochlear inner hair cell number,
increased cochlear nerve compound action potential,
increased cochlear outer hair cell number,
increased metanephric mesenchyme apoptosis,
neonatal lethality, complete penetrance,
sensorineural hearing loss,
small kidney,
small olfactory bulb,
syndromic hearing loss,
Wolffian duct degeneration
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View all ortholog results at Monarch
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