myo10.2 Phenotypes

Phenotypes

XB-GENEPAGE-5995372

Gene Symbol: myo10.2 Gene Name: myosin 10, gene 2

Anatomical Phenotypes Phenotypes manually curated with terms from the Xenopus phenotype ontology covering anatomical, gene ontology, and neurobehavioral phenotypes.
abnormally localised mitotic spindle in epithelial cell (5 sources), increased size of the mitotic spindle (1 source)

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: myo10.2 assayed (4 sources)

Experiments (Reagents) These are short form descriptions of experiments using reagents targeting the gene of interest.
Xla Wt + myo10.2 MO (3 sources), Xla Wt + GFP-myo10.2 (1 source), Xla Wt + GFP-myo10.2del_1-2241 (1 source), Xla Wt + GFP-myo10.2del_2697-7764 (1 source)

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, [+]