PREDICTED: Homo sapiens solute carrier family 4 member 11 (SLC4A11), t - Nucleotide

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Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells. [PLoS One. 2024]
Investigation of the functional impact of CHED- and FECD4-associated SLC4A11 mutations in human corneal endothelial cells.
Chung DD, Chen AC, Choo CH, Zhang W, Williams D, Griffis CG, Bonezzi P, Jatavallabhula K, Sampath AP, Aldave AJ. PLoS One. 2024; 19(1):e0296928. Epub 2024 Jan 22.
Structural insights into the conformational changes of BTR1/SLC4A11 in complex with PIP(2). [Nat Commun. 2023]
Structural insights into the conformational changes of BTR1/SLC4A11 in complex with PIP(2).
Lu Y, Zuo P, Chen H, Shan H, Wang W, Dai Z, Xu H, Chen Y, Liang L, Ding D, et al. Nat Commun. 2023 Oct 3; 14(1):6157. Epub 2023 Oct 3.
Pathogenicity and Function Analysis of Two Novel SLC4A11 Variants in Patients With Congenital Hereditary Endothelial Dystrophy. [Transl Vis Sci Technol. 2023]
Pathogenicity and Function Analysis of Two Novel SLC4A11 Variants in Patients With Congenital Hereditary Endothelial Dystrophy.
Zhen T, Li Y, Guo Q, Yao S, You Y, Lei B. Transl Vis Sci Technol. 2023 Oct 3; 12(10):1.

RefSeq alternative splicing
See 26 reference mRNA sequence splice variants for the SLC4A11 gene.
RefSeq protein product
See the reference protein sequence for solute carrier family 4 member 11 isoform X4 (XP_016883583.1).

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Nucleotide