slc26a5 Phenotypes

Phenotypes

XB-GENEPAGE-1000031

Gene Symbol: slc26a5 Gene Name: solute carrier family 26 member 5

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: slc26a5 assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (24 sources): abnormal Claudius cell morphology, abnormal cochlear outer hair cell electromotility, abnormal cochlear outer hair cell morphology, abnormal cochlear outer hair cell physiology, abnormal distortion product otoacoustic emission, abnormal otoacoustic response, absent cochlear microphonics, absent cochlear outer hair cell electromotility, absent distortion product otoacoustic emissions, cochlear ganglion degeneration, cochlear hair cell degeneration, cochlear inner hair cell degeneration, cochlear outer hair cell degeneration, deafness, decreased cochlear microphonics, decreased cochlear nerve compound action potential, decreased cochlear outer hair cell electromotility, decreased cochlear outer hair cell number, degeneration of organ of Corti supporting cells, hearing/vestibular/ear phenotype, increased cochlear nerve compound action potential, increased or absent threshold for auditory brainstem response, organ of Corti degeneration, short cochlear outer hair cells [+]

Monarch Ortholog Phenotypes

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

Mouse (24 sources): abnormal Claudius cell morphology, abnormal cochlear outer hair cell electromotility, abnormal cochlear outer hair cell morphology, abnormal cochlear outer hair cell physiology, abnormal distortion product otoacoustic emission, abnormal otoacoustic response, absent cochlear microphonics, absent cochlear outer hair cell electromotility, absent distortion product otoacoustic emissions, cochlear ganglion degeneration, [+]