slc24a5 Phenotypes

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Phenotypes

Gene Literature (2)

Nucleotides (96)

Interactants (24)

XB-GENEPAGE-853668

Gene Symbol: slc24a5 Gene Name: solute carrier family 24 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: slc24a5 assayed (4 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (11 sources): Abnormal foveal morphology on macular OCT, Abnormal fundus morphology, Abnormal hair morphology, Abnormal iris pigmentation, Aplasia/Hypoplasia of the macula, Generalized hypopigmentation, Hypoplasia of the fovea, Nystagmus, Photophobia, Reduced visual acuity, Visual impairment [+]
Mouse (15 sources): abnormal ciliary body pigmentation, abnormal dermal pigmentation, abnormal ear pigmentation, abnormal epidermal pigmentation, abnormal fasting circulating glucose level, abnormal grip strength, abnormal hair shaft melanin granule morphology, abnormal hair shaft melanin granule shape, abnormal iris transillumination, abnormal melanosome morphology, abnormal prepulse inhibition, abnormal retina pigment epithelium morphology, decreased fasting circulating glucose level, decreased prepulse inhibition, increased grip strength [+]
View all ortholog results at Monarch