nipa1 Phenotypes

Phenotypes

XB-GENEPAGE-961418

Gene Symbol: nipa1 Gene Name: NIPA magnesium transporter 1

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: nipa1 assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (23 sources): Babinski sign, Bilateral tonic-clonic seizure, Clonus, Degeneration of the lateral corticospinal tracts, Gait disturbance, Hyperreflexia, Impaired vibration sensation in the lower limbs, Impaired vibratory sensation, Limitation of movement at ankles, Limited hip movement, Lower limb hyperreflexia, Lower limb muscle weakness, Lower limb spasticity, Pes cavus, Postural tremor, Seizure, Skeletal muscle atrophy, Spastic gait, Spastic paraplegia, Tremor, Urinary bladder sphincter dysfunction, Urinary incontinence, Urinary urgency [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

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

Human (23 sources): Babinski sign, Bilateral tonic-clonic seizure, Clonus, Degeneration of the lateral corticospinal tracts, Gait disturbance, Hyperreflexia, Impaired vibration sensation in the lower limbs, Impaired vibratory sensation, Limitation of movement at ankles, Limited hip movement, [+]