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XB-GENEPAGE-942661
aldh3a2 aldehyde dehydrogenase 3 family member A2
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: aldh3a2 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 (34 sources): Abnormal dental enamel morphology, Abnormal pyramidal sign, Abnormality of retinal pigmentation, CNS demyelination, Corneal erosion, Dry skin, Dysarthria, Enamel hypoplasia, Erythema, Generalized hyperpigmentation, [+] |
Mouse (15 sources): abnormal epidermis stratum basale morphology, abnormal epidermis stratum granulosum morphology, abnormal epidermis stratum spinosum morphology, abnormal keratinocyte physiology, decreased aldehyde dehydrogenase activity, decreased erythrocyte cell number, decreased hemoglobin content, decreased locomotor activity, decreased mean corpuscular volume, decreased prepulse inhibition, [+] |
View all ortholog results at Monarch |