Monarch Ortholog Phenotypes
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Human (33 sources):
Acute hepatic failure,
Ataxia,
Cerebellar atrophy,
Cerebellar vermis atrophy,
Distal lower limb muscle weakness,
Distal sensory impairment,
Dysmetric saccades,
Fever,
Frequent falls,
Gait ataxia,
Generalized limb muscle atrophy,
Global developmental delay,
Hepatic failure,
Hepatic fibrosis,
Hepatomegaly,
Hepatosplenomegaly,
Hyperreflexia,
Hyporeflexia,
Intellectual disability, mild,
Intention tremor,
Motor delay,
Optic atrophy,
Paresthesia,
Peripheral neuropathy,
Progressive cerebellar ataxia,
Saccadic smooth pursuit,
Sensorimotor neuropathy,
Somatic sensory dysfunction,
Spasticity,
Splenomegaly,
Stuttering,
Talipes equinovarus,
Tremor
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Mouse (38 sources):
abnormal Purkinje cell dendrite morphology,
abnormal Purkinje cell morphology,
abnormal axon morphology,
abnormal cerebellum vermis morphology,
abnormal innervation,
abnormal innervation pattern to muscle,
abnormal involuntary movement,
abnormal locomotor behavior,
abnormal locomotor coordination,
abnormal motor capabilities/coordination/movement,
abnormal motor nerve collateral sprouting,
abnormal muscle electrophysiology,
abnormal muscle regeneration,
abnormal myelin sheath morphology,
abnormal neuromuscular synapse morphology,
abnormal peripheral nervous system regeneration,
abnormal sciatic nerve morphology,
abnormal skeletal muscle fiber type ratio,
abnormal tail movements,
behavior/neurological phenotype,
decreased Purkinje cell number,
decreased body size,
decreased grip strength,
decreased motor neuron number,
decreased skeletal muscle fiber diameter,
decreased skeletal muscle mass,
hindlimb paralysis,
increased variability of skeletal muscle fiber size,
microgliosis,
muscle phenotype,
muscular atrophy,
nervous system phenotype,
peripheral nervous system degeneration,
premature death,
reduced fertility,
skeletal muscle fiber necrosis,
skeleton phenotype,
small myocardial fiber
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View all ortholog results at Monarch
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