mag Phenotypes

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Phenotypes

Gene Literature (34)

Nucleotides (141)

Interactants (206)

XB-GENEPAGE-6462483

Gene Symbol: mag Gene Name: myelin associated glycoprotein

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: mag assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (30 sources): Abnormal pyramidal sign, Areflexia of lower limbs, Astigmatism, Babinski sign, Cerebellar atrophy, Cognitive impairment, Corpus callosum atrophy, Distal lower limb amyotrophy, Dysmetria, Generalized hypotonia, Glaucoma, Global developmental delay, Hypermetropia, Hyporeflexia, Hyporeflexia of lower limbs, Hypotonia, Impaired vibratory sensation, Intellectual disability, Neonatal hypotonia, Nystagmus, Optic atrophy, Peripheral neuropathy, Reduced visual acuity, Spastic dysarthria, Spastic paraparesis, Spastic paraplegia, Spasticity, Temporal optic disc pallor, Titubation, Ventriculomegaly [+]
Mouse (20 sources): abnormal Schwann cell morphology, abnormal axon morphology, abnormal coping response, abnormal grooming behavior, abnormal myelin sheath morphology, abnormal sleep behavior, abnormal startle reflex, convulsive seizures, decreased aggression towards mice, decreased circulating glucose level, decreased coping response, decreased locomotor activity, decreased prepulse inhibition, decreased startle reflex, increased B cell proliferation, increased bone mineral content, increased grip strength, increased lean body mass, nervous system phenotype, tomacula [+]
View all ortholog results at Monarch