Human sulfate transporter (DTD) mRNA, complete cds

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Pick Primers
Design and test primers for this sequence using Primer-BLAST.

Biallelic variants in SLC26A2 cause multiple epiphyseal dysplasia-4 by disturbing chondrocyte homeostasis. [Orphanet J Rare Dis. 2024]
Biallelic variants in SLC26A2 cause multiple epiphyseal dysplasia-4 by disturbing chondrocyte homeostasis.
Li S, Sheng Y, Wang X, Wang Q, Wang Y, Zhang Y, Wu C, Jiang X. Orphanet J Rare Dis. 2024 Jul 2; 19(1):245. Epub 2024 Jul 2.
Cooperative polarization of MCAM/CD146 and ERM family proteins in melanoma. [Mol Biol Cell. 2024]
Cooperative polarization of MCAM/CD146 and ERM family proteins in melanoma.
Miller SG, Hoh M, Ebmeier CC, Tay JW, Ahn NG. Mol Biol Cell. 2024 Mar 1; 35(3):ar31. Epub 2023 Dec 20.
Clinical and Genetic Characteristics of Multiple Epiphyseal Dysplasia Type 4. [Genes (Basel). 2022]
Clinical and Genetic Characteristics of Multiple Epiphyseal Dysplasia Type 4.
Markova T, Kenis V, Melchenko E, Alieva A, Nagornova T, Orlova A, Ogorodova N, Shchagina O, Polyakov A, Dadali E, et al. Genes (Basel). 2022 Aug 24; 13(9). Epub 2022 Aug 24.

RefSeq alternative splicing
See 3 reference mRNA sequence splice variants for the SLC26A2 gene.

Homo sapiens solute carrier family 26 member 2 (SLC26A2), RefSeqGene (LRG_684) o...
Homo sapiens solute carrier family 26 member 2 (SLC26A2), RefSeqGene (LRG_684) on chromosome 5
gi|427197665|ref|NG_007147.2||gnl|L G_684

Nucleotide

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide