mme Phenotypes

Phenotypes

XB-GENEPAGE-1011097

Gene Symbol: mme Gene Name: membrane metalloendopeptidase

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (32 sources): Areflexia, Ataxia, Cerebellar atrophy, Cerebellar vermis atrophy, Cogwheel rigidity, Decreased number of large peripheral myelinated nerve fibers, Distal amyotrophy, Distal lower limb muscle weakness, Distal sensory impairment, Distal upper limb muscle weakness, Dysarthria, Foot dorsiflexor weakness, Gait ataxia, Glomerular deposits, Glomerulonephritis, Hypometric saccades, Hyporeflexia, Limb ataxia, Limb pain, Nephrotic syndrome, Nystagmus, Pain, Pectus carinatum, Peripheral axonal neuropathy, Pes cavus, Pregnancy exposure, Progressive cerebellar ataxia, Renal insufficiency, Rigidity, Sensorimotor neuropathy, Tremor, Unsteady gait [+]
Mouse (9 sources): abnormal axon morphology, abnormal internode morphology, behavior/neurological phenotype, decreased heart weight, dermatitis, diffuse hepatic necrosis, increased myelin sheath thickness, increased susceptibility to type I hypersensitivity reaction, skin edema
View all ortholog results at Monarch