Mus musculus solute carrier family 26, member 5 (Slc26a5), transcript - Nucleotide

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The pathogenic roles of the p.R130S prestin variant in DFNB61 hearing loss. [J Physiol. 2024]
The pathogenic roles of the p.R130S prestin variant in DFNB61 hearing loss.
Takahashi S, Zhou Y, Cheatham MA, Homma K. J Physiol. 2024 Mar; 602(6):1199-1210. Epub 2024 Mar 3.
Epistatic genetic interactions between Insm1 and Ikzf2 during cochlear outer hair cell development. [Cell Rep. 2023]
Epistatic genetic interactions between Insm1 and Ikzf2 during cochlear outer hair cell development.
Li S, He S, Lu Y, Jia S, Liu Z. Cell Rep. 2023 May 30; 42(5):112504. Epub 2023 May 11.
Prestin's fast motor kinetics is essential for mammalian cochlear amplification. [Proc Natl Acad Sci U S A. 2023]
Prestin's fast motor kinetics is essential for mammalian cochlear amplification.
Takahashi S, Zhou Y, Kojima T, Cheatham MA, Homma K. Proc Natl Acad Sci U S A. 2023 Mar 14; 120(11):e2217891120. Epub 2023 Mar 9.

RefSeq alternative splicing
See 4 reference mRNA sequence splice variants for the Slc26a5 gene.
RefSeq protein product
See the reference protein sequence for prestin isoform 2 (NP_001276716.1).

Protein
Protein sequence from Nucleotide coding region
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Dryad Digital Repository [Dryad Digital Repository]
Dryad Digital Repository
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Ensembl
Ensembl [Ensembl]
Ensembl
Ensembl [Ensembl]
Ensembl
GenScript latest version of gene cDNA ORF Clone [GenScript latest version of g...]
GenScript latest version of gene cDNA ORF Clone
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UCSC Genome Browser [UCSC Genome Browser]
UCSC Genome Browser
Order SLC26A5 cDNA clone/Protein/Antibody/RNAi [OriGene]
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Nucleotide