rd3 Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (93)

Interactants (9)

XB-GENEPAGE-1002199

Gene Symbol: rd3 Gene Name: retinal degeneration 3, GUCY2D regulator

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.
Computed annotations: rd3 assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (18 sources): Abnormal electroretinogram, Abnormality of macular pigmentation, Abnormality of neuronal migration, Abnormality of retinal pigmentation, Abnormality of the optic disc, Aplasia/Hypoplasia of the cerebellar vermis, Cataract, Congenital blindness, Encephalocele, Global developmental delay, Hearing impairment, Hemiplegia/hemiparesis, Hypotonia, Intellectual disability, Keratoconus, Nystagmus, Seizure, Severely reduced visual acuity [+]
Mouse (13 sources): abnormal eye electrophysiology, abnormal eye posterior chamber depth, abnormal mean corpuscular hemoglobin concentration, abnormal retina inner nuclear layer morphology, abnormal retina outer nuclear layer morphology, abnormal retina photoreceptor layer morphology, absent retina rod cells, decreased mean corpuscular hemoglobin, decreased mean corpuscular hemoglobin concentration, decreased total retina thickness, increased exploration in new environment, retina photoreceptor degeneration, thin retina outer nuclear layer [+]
View all ortholog results at Monarch