Homo sapiens solute carrier family 9 member A6 (SLC9A6), transcript va - Nucleotide

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Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability. [BMC Neurol. 2023]
Structural and functional implications of SLC13A3 and SLC9A6 mutations: an in silico approach to understanding intellectual disability.
Hussain SI, Muhammad N, Shah SUD, Fardous F, Khan SA, Khan N, Rehman AU, Siddique M, Wasan SA, Niaz R, et al. BMC Neurol. 2023 Oct 4; 23(1):353. Epub 2023 Oct 4.
Targeting NHE6 gene expression identifies lysosome and neurodevelopmental mechanisms in a haploid in vitro cell model. [Biol Open. 2023]
Targeting NHE6 gene expression identifies lysosome and neurodevelopmental mechanisms in a haploid in vitro cell model.
Wu Q, Ma L, Joesch-Cohen L, Schmidt M, Uzun EDG, Morrow EM. Biol Open. 2023 Nov 15; 12(11). Epub 2023 Nov 29.
Functional analysis of two SLC9A6 frameshift variants in lymphoblastoid cells from patients with Christianson syndrome. [CNS Neurosci Ther. 2023]
Functional analysis of two SLC9A6 frameshift variants in lymphoblastoid cells from patients with Christianson syndrome.
He H, Zhang H, Chen H, He F, Yin F, Stauber T, Zou X, Peng J. CNS Neurosci Ther. 2023 Dec; 29(12):4059-4069. Epub 2023 Jun 28.

RefSeq alternative splicing
See 12 reference mRNA sequence splice variants for the SLC9A6 gene.
RefSeq protein product
See the reference protein sequence for sodium/hydrogen exchanger 6 isoform c (NP_001171122.1).

Protein
Protein sequence from Nucleotide coding region
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Nucleotide