PREDICTED: Homo sapiens solute carrier family 24 member 1 (SLC24A1), t - Nucleotide

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VIRMA mediates preferential m(6)A mRNA methylation in 3'UTR and near stop codon and associates with alternative polyadenylation. [Cell Discov. 2018]
VIRMA mediates preferential m(6)A mRNA methylation in 3'UTR and near stop codon and associates with alternative polyadenylation.
Yue Y, Liu J, Cui X, Cao J, Luo G, Zhang Z, Cheng T, Gao M, Shu X, Ma H, et al. Cell Discov. 2018; 4:10. Epub 2018 Feb 27.
Panel-Based Population Next-Generation Sequencing for Inherited Retinal Degenerations. [Sci Rep. 2016]
Panel-Based Population Next-Generation Sequencing for Inherited Retinal Degenerations.
Carrigan M, Duignan E, Malone CP, Stephenson K, Saad T, McDermott C, Green A, Keegan D, Humphries P, Kenna PF, et al. Sci Rep. 2016 Sep 14; 6:33248. Epub 2016 Sep 14.
Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness. [Clin Genet. 2016]
Next-generation sequencing confirms the implication of SLC24A1 in autosomal-recessive congenital stationary night blindness.
Neuillé M, Malaichamy S, Vadalà M, Michiels C, Condroyer C, Sachidanandam R, Srilekha S, Arokiasamy T, Letexier M, Démontant V, et al. Clin Genet. 2016 Jun; 89(6):690-9. Epub 2016 Mar 4.

RefSeq alternative splicing
See 52 reference mRNA sequence splice variants for the SLC24A1 gene.
RefSeq protein product
See the reference protein sequence for sodium/potassium/calcium exchanger 1 isoform X12 (XP_054235181.1).