lrit3 Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (67)

Interactants (0)

XB-GENEPAGE-6076512

Gene Symbol: lrit3 Gene Name: leucine-rich repeat, Ig-like and transmembrane domains 3

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: lrit3 assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (11 sources): Abnormal fundus morphology, Abnormal retinal morphology, Abnormality of macular pigmentation, Congenital stationary night blindness, High myopia, Myopia, Nyctalopia, Nystagmus, Optic disc hypoplasia, Reduced visual acuity, Strabismus [+]
Mouse (13 sources): abnormal cone electrophysiology, abnormal contextual conditioning behavior, abnormal epididymis morphology, abnormal retina neuronal layer morphology, abnormal rod electrophysiology, decreased b-wave amplitude, decreased red blood cell distribution width, decreased retina inner nuclear layer thickness, enlarged epididymis, impaired contextual conditioning behavior, increased a-wave amplitude, increased a-wave implicit time, increased b-wave implicit time [+]
View all ortholog results at Monarch