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XB-GENEPAGE-955008
opn1lw opsin 1 (cone pigments), long-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.
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| Computed annotations: opn1lw 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 (14 sources): Abnormal electroretinogram, Abnormality of macular pigmentation, Abnormality of retinal pigmentation, Blue cone monochromacy, Color vision defect, Corneal dystrophy, Myopia, Nyctalopia, Nystagmus, Pendular nystagmus, [+] |
| Mouse (4 sources): decreased b-wave amplitude, decreased b-wave amplitude, decreased b-wave amplitude, decreased b-wave amplitude |
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View all ortholog results at Monarch |