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XB-GENEPAGE-1004101
myo5a myosin VA
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.
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Computed annotations: myo5a assayed (2 sources) |
Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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Human (42 sources): Abnormal cerebellar vermis morphology, Abnormality of movement, Abnormality of the optic nerve, Accumulation of melanosomes in melanocytes, Aplasia/Hypoplasia of the macula, Ataxia, Cerebellar hypoplasia, Cerebral calcification, Cerebral cortical atrophy, Cerebral cortical hemiatrophy, [+] |
Mouse (38 sources): abnormal Purkinje cell dendrite morphology, abnormal ear pigmentation, abnormal epidermal melanocyte morphology, abnormal epidermal pigmentation, abnormal eye blink conditioning behavior, abnormal foot pigmentation, abnormal hair cycle, abnormal hair follicle melanin granule morphology, abnormal hair follicle melanocyte morphology, abnormal involuntary movement, [+] |
View all ortholog results at Monarch |