spg21 Phenotypes

XB-GENEPAGE-978834

Gene Symbol: spg21 Gene Name: SPG21, maspardin

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: spg21 assayed (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (26 sources): Abnormal cerebellum morphology, Abnormality of extrapyramidal motor function, Abnormality of peripheral nerve conduction, Abnormal pyramidal sign, Akinetic mutism, Apraxia, Babinski sign, Dementia, Dysarthria, Dysgraphia, Dysphagia, Frontotemporal cerebral atrophy, Gait disturbance, Global developmental delay, Hyperreflexia, Hypoplasia of the corpus callosum, Lower limb muscle weakness, Mental deterioration, Motor delay, obsolete Difficulty walking, Peripheral neuropathy, Personality disorder, Primitive reflex, Spasticity, Spastic paraparesis, Spastic paraplegia [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Human (26 sources): Abnormal cerebellum morphology, Abnormality of extrapyramidal motor function, Abnormality of peripheral nerve conduction, Abnormal pyramidal sign, Akinetic mutism, Apraxia, Babinski sign, Dementia, Dysarthria, Dysgraphia, [+]