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XB-GENEPAGE-5877219
myo1d myosin ID
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: myo1d 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 (1 source): Abnormality of refraction |
| Mouse (9 sources): abnormal lean body mass, abnormal startle reflex, decreased bone mineral content, decreased startle reflex, digestive/alimentary phenotype, increased lean body mass, increased susceptibility to colitis induced morbidity/mortality, increased susceptibility to induced colitis, increased susceptibility to weight loss |
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View all ortholog results at Monarch |