|
XB-GENEPAGE-993051
opn1sw opsin 1 (cone pigments), short-wave-sensitive
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.
|
|---|
| Manual annotations: opn1sw assayed (1 source) |
| Computed annotations: opn1sw assayed (1 source) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
|
|---|
| Human (4 sources): Abnormal light-adapted electroretinogram, Color vision defect, Dyschromatopsia, Tritanomaly |
| Mouse (3 sources): abnormal cone electrophysiology, disorganized photoreceptor outer segment, vision/eye phenotype |
|
View all ortholog results at Monarch |