meox2 Phenotypes

Phenotypes

XB-GENEPAGE-852817

Gene Symbol: meox2 Gene Name: mesenchyme homeobox 2

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: meox2 assayed (6 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (16 sources): abnormal gastrocnemius morphology, abnormal limb morphology, abnormal limb posture, abnormal muscle development, abnormal myogenesis, abnormal skeletal muscle morphology, decreased skeletal muscle mass, decreased survivor rate, increased variability of skeletal muscle fiber size, joint contracture, limb grasping, muscle phenotype, postnatal lethality, incomplete penetrance, skeleton phenotype, thin myocardium, thin myometrium [+]

Monarch Ortholog Phenotypes

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

Mouse (16 sources): abnormal gastrocnemius morphology, abnormal limb morphology, abnormal limb posture, abnormal muscle development, abnormal myogenesis, abnormal skeletal muscle morphology, decreased skeletal muscle mass, decreased survivor rate, increased variability of skeletal muscle fiber size, joint contracture, [+]