cldn11 Phenotypes

Phenotypes

XB-GENEPAGE-959935

Gene Symbol: cldn11 Gene Name: claudin 11 (oligodendrocyte transmembrane protein)

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: cldn11 assayed (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (15 sources): abnormal Sertoli cell barrier morphology, abnormal auditory brainstem response waveform shape, abnormal distortion product otoacoustic emission, abnormal grip strength, abnormal myelin sheath morphology, abnormal seminiferous tubule morphology, abnormal startle reflex, abnormal stria vascularis morphology, absent strial basal cell tight junctions, cochlear outer hair cell degeneration, deafness, decreased endocochlear potential, increased or absent threshold for auditory brainstem response, increased startle reflex, nervous system phenotype [+]

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Mouse (15 sources): abnormal Sertoli cell barrier morphology, abnormal auditory brainstem response waveform shape, abnormal distortion product otoacoustic emission, abnormal grip strength, abnormal myelin sheath morphology, abnormal seminiferous tubule morphology, abnormal startle reflex, abnormal stria vascularis morphology, absent strial basal cell tight junctions, cochlear outer hair cell degeneration, [+]