sardh Phenotypes

Phenotypes

XB-GENEPAGE-6038612

Gene Symbol: sardh Gene Name: sarcosine dehydrogenase

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: sardh assayed (5 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (22 sources): Abnormality of movement, Ataxia, Bilateral tonic-clonic seizure, Congenital blindness, Dyslexia, Emotional lability, Global developmental delay, Hypersarcosinemia, Hypersarcosinuria, Hypertrophic cardiomyopathy, Infantile muscular hypotonia, Infantile sensorineural hearing impairment, Intellectual disability, mild, Loss of speech, Motor delay, Optic atrophy, Peroneal muscle weakness, Poor speech, Pulmonic stenosis, Sleep disturbance, Strabismus, Tetraparesis [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

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

Human (22 sources): Abnormality of movement, Ataxia, Bilateral tonic-clonic seizure, Congenital blindness, Dyslexia, Emotional lability, Global developmental delay, Hypersarcosinemia, Hypersarcosinuria, Hypertrophic cardiomyopathy, [+]