myh1 Phenotypes

Phenotypes

XB-GENEPAGE-5835503

Gene Symbol: myh1 Gene Name: myosin, heavy chain 1, skeletal muscle, adult

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: myh1 assayed (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (30 sources): abnormal adipose tissue amount, abnormal anxiety-related response, abnormal bone mineralization, abnormal grip strength, abnormal lean body mass, abnormal locomotor activation, abnormal motor learning, abnormal response to new environment, abnormal skeletal muscle fiber type ratio, abnormal skeletal muscle morphology, abnormal sleep behavior, abnormal startle reflex, abnormal urine creatinine level, decreased anxiety-related response, decreased body length, decreased bone mineral content, decreased exploration in new environment, decreased fluid intake, decreased food intake, decreased grip strength, decreased lean body mass, decreased locomotor activity, decreased prepulse inhibition, decreased skeletal muscle mass, decreased startle reflex, decreased thigmotaxis, decreased urine creatinine level, decreased vertical activity, impaired skeletal muscle contractility, increased total body fat amount [+]

Monarch Ortholog Phenotypes

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

Mouse (30 sources): abnormal adipose tissue amount, abnormal anxiety-related response, abnormal bone mineralization, abnormal grip strength, abnormal lean body mass, abnormal locomotor activation, abnormal motor learning, abnormal response to new environment, abnormal skeletal muscle fiber type ratio, abnormal skeletal muscle morphology, [+]