Homo sapiens solute carrier family 4 member 10 (SLC4A10), transcript v - Nucleotide

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Biallelic variants in SLC4A10 encoding a sodium-dependent bicarbonate transporter lead to a neurodevelopmental disorder. [Genet Med. 2024]
Biallelic variants in SLC4A10 encoding a sodium-dependent bicarbonate transporter lead to a neurodevelopmental disorder.
Maroofian R, Zamani M, Kaiyrzhanov R, Liebmann L, Karimiani EG, Vona B, Huebner AK, Calame DG, Misra VK, Sadeghian S, et al. Genet Med. 2024 Mar; 26(3):101034. Epub 2023 Dec 3.
SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission. [Brain. 2023]
SLC4A10 mutation causes a neurological disorder associated with impaired GABAergic transmission.
Fasham J, Huebner AK, Liebmann L, Khalaf-Nazzal R, Maroofian R, Kryeziu N, Wortmann SB, Leslie JS, Ubeyratna N, Mancini GMS, et al. Brain. 2023 Nov 2; 146(11):4547-4561.
Multilevel proteomics reveals host perturbations by SARS-CoV-2 and SARS-CoV. [Nature. 2021]
Multilevel proteomics reveals host perturbations by SARS-CoV-2 and SARS-CoV.
Stukalov A, Girault V, Grass V, Karayel O, Bergant V, Urban C, Haas DA, Huang Y, Oubraham L, Wang A, et al. Nature. 2021 Jun; 594(7862):246-252. Epub 2021 Apr 12.

RefSeq protein product
See the reference protein sequence for sodium-driven chloride bicarbonate exchanger isoform 11 (NP_001341376.1).

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Homo sapiens solute carrier family 4 member 10 (SLC4A10), transcript variant 11,...
Homo sapiens solute carrier family 4 member 10 (SLC4A10), transcript variant 11, mRNA
gi|1674985861|ref|NM_001354447.2|

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Nucleotide