Monarch Ortholog Phenotypes
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Human (41 sources):
Areflexia,
Arrhythmia,
Axonal degeneration,
Axonal degeneration/regeneration,
Axonal regeneration,
Basal lamina onion bulb formation,
CNS hypomyelination,
Decreased motor nerve conduction velocity,
Decreased nerve conduction velocity,
Decreased number of large peripheral myelinated nerve fibers,
Decreased number of peripheral myelinated nerve fibers,
Distal amyotrophy,
Distal muscle weakness,
Distal sensory impairment,
EMG: neuropathic changes,
Flexion contracture,
Foot dorsiflexor weakness,
Gait disturbance,
Hammertoe,
Hand muscle atrophy,
Hypertrophic nerve changes,
Hyporeflexia,
Inability to walk by childhood/adolescence,
Kyphoscoliosis,
Limb muscle weakness,
Motor delay,
Neuropathic spinal arthropathy,
Onion bulb formation,
Peripheral axonal degeneration,
Peripheral demyelination,
Peripheral hypomyelination,
Peripheral neuropathy,
Pes cavus,
Proximal muscle weakness,
Scoliosis,
Skeletal muscle atrophy,
Split hand,
Steppage gait,
Talipes equinovarus,
Ulnar claw,
Vocal cord paresis
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Mouse (23 sources):
abnormal action potential,
abnormal axonal transport,
abnormal axon extension,
abnormal calcium ion homeostasis,
abnormal dorsal root ganglion morphology,
abnormal endoplasmic reticulum morphology,
abnormal epididymis morphology,
abnormal neurite morphology,
abnormal neuromuscular synapse morphology,
abnormal seminal vesicle morphology,
abnormal thymus morphology,
cellular phenotype,
chromatolysis,
enlarged epididymis,
increased mitochondrial DNA content,
increased mitochondrial size,
limb grasping,
nervous system phenotype,
oxidative stress,
short stride length,
small adrenal glands,
small superior vagus ganglion,
small thymus
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View all ortholog results at Monarch
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