Homo sapiens solute carrier family 26 member 8 (SLC26A8), transcript v - Nucleotide

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The heterozygous mutations of SLC26A8 are not the main actors for male infertility. [Hum Mutat. 2022]
The heterozygous mutations of SLC26A8 are not the main actors for male infertility.
Liu M, Li J, Li Y, Jiang C, Xu W, Yang Y, Shen Y. Hum Mutat. 2022 May; 43(5):604-612. Epub 2022 Apr 7.
Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease. [Hum Mutat. 2022]
Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease.
Gao Y, Wu H, Xu Y, Shen Q, Xu C, Geng H, Lv M, Tan Q, Li K, Tang D, et al. Hum Mutat. 2022 Mar; 43(3):434-443. Epub 2021 Dec 30.
N-glycosylation and topology of the human SLC26 family of anion transport membrane proteins. [Am J Physiol Cell Physiol. 2014]
N-glycosylation and topology of the human SLC26 family of anion transport membrane proteins.
Li J, Xia F, Reithmeier RA. Am J Physiol Cell Physiol. 2014 May 15; 306(10):C943-60. Epub 2014 Mar 19.

RefSeq alternative splicing
See 7 reference mRNA sequence splice variants for the SLC26A8 gene.
RefSeq protein product
See the reference protein sequence for testis anion transporter 1 isoform a (NP_001180405.1).

Protein
Protein sequence from Nucleotide coding region
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txid627486[Organism:noexp] (9)
PopSet
Sequence 18272 from Patent EP1074617
Sequence 18272 from Patent EP1074617
gi|40038268|emb|AX883367.1||pat|EP| 17|18272

Nucleotide

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Nucleotide