myo10 Phenotypes

Phenotypes

XB-GENEPAGE-1018817

Gene Symbol: myo10 Gene Name: myosin 10

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: myo10 assayed (5 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (28 sources): abnormal circulating alkaline phosphatase level, abnormal erythrocyte cell number, abnormal hematocrit, abnormal lens development, abnormal response to new environment, abnormal retina vasculature morphology, abnormal tail morphology, abnormal tail pigmentation, abnormal vascular branching morphogenesis, absent liver, behavior/neurological phenotype, belly spot, decreased body size, decreased circulating alkaline phosphatase level, decreased circulating iron level, decreased embryo size, decreased erythrocyte cell number, decreased hematocrit, decreased survivor rate, decreased tail pigmentation, failure of eyelid fusion, fused cornea and lens, fused phalanges, kinked tail, lethality during fetal growth through weaning, incomplete penetrance, no abnormal phenotype detected, persistence of hyaloid vascular system, white spotting [+]

Monarch Ortholog Phenotypes

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

Mouse (28 sources): abnormal circulating alkaline phosphatase level, abnormal erythrocyte cell number, abnormal hematocrit, abnormal lens development, abnormal response to new environment, abnormal retina vasculature morphology, abnormal tail morphology, abnormal tail pigmentation, abnormal vascular branching morphogenesis, absent liver, [+]