adam9 ADAM metallopeptidase domain 9
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: adam9 assayed (1 source)|
|Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
|Human (6 sources): Abnormality of retinal pigmentation, Color vision defect, Cone/cone-rod dystrophy, Nyctalopia, Photophobia, Visual impairment|
|Mouse (10 sources): abnormal induced retina neovascularization, abnormal retina layer morphology, abnormal retina neuronal layer morphology, abnormal retina pigment epithelium morphology, decreased a-wave amplitude, decreased b-wave amplitude, decreased tumor growth/size, enhanced wound healing, increased keratinocyte migration, no abnormal phenotype detected|
View all ortholog results at Monarch