Rattus norvegicus mRNA for sulfate transporter, complete cds

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Dysplastic spondylolysis is caused by mutations in the diastrophic dysplasia sulfate transporter gene. [Proc Natl Acad Sci U S A. 2015]
Dysplastic spondylolysis is caused by mutations in the diastrophic dysplasia sulfate transporter gene.
Cai T, Yang L, Cai W, Guo S, Yu P, Li J, Hu X, Yan M, Shao Q, Jin Y, et al. Proc Natl Acad Sci U S A. 2015 Jun 30; 112(26):8064-9. Epub 2015 Jun 15.
SLC26A2 disease spectrum in Sweden - high frequency of recessive multiple epiphyseal dysplasia (rMED). [Clin Genet. 2015]
SLC26A2 disease spectrum in Sweden - high frequency of recessive multiple epiphyseal dysplasia (rMED).
Mäkitie O, Geiberger S, Horemuzova E, Hagenäs L, Moström E, Nordenskjöld M, Grigelioniene G, Nordgren A. Clin Genet. 2015 Mar; 87(3):273-8. Epub 2014 Apr 1.
In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine. [Proteomics. 2013]
In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.
Principe S, Jones EE, Kim Y, Sinha A, Nyalwidhe JO, Brooks J, Semmes OJ, Troyer DA, Lance RS, Kislinger T, et al. Proteomics. 2013 May; 13(10-11):1667-1671. Epub 2013 Apr 23.

RefSeq alternative splicing
See 7 reference mRNA sequence splice variants for the Slc26a2 gene.

Homo sapiens cDNA: FLJ21425 fis, clone COL04162
Homo sapiens cDNA: FLJ21425 fis, clone COL04162
gi|10437520|dbj|AK025078.1|

Nucleotide

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Nucleotide