Homo sapiens solute carrier family 13 member 5 (SLC13A5), transcript v - Nucleotide

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Novel Homozygous Variants of SLC13A5 Expand the Functional Heterogeneity of a Homogeneous Syndrome of Early Infantile Epileptic Encephalopathy. [Pediatr Neurol. 2024]
Novel Homozygous Variants of SLC13A5 Expand the Functional Heterogeneity of a Homogeneous Syndrome of Early Infantile Epileptic Encephalopathy.
Alsemari A, Guzmán-Vega FJ, Meyer BF, Arold ST. Pediatr Neurol. 2024 Feb; 151:68-72. Epub 2023 Oct 19.
The citrate transporters SLC13A5 and SLC25A1 elicit different metabolic responses and phenotypes in the mouse. [Commun Biol. 2023]
The citrate transporters SLC13A5 and SLC25A1 elicit different metabolic responses and phenotypes in the mouse.
Fernandez-Fuente G, Overmyer KA, Lawton AJ, Kasza I, Shapiro SL, Gallego-Muñoz P, Coon JJ, Denu JM, Alexander CM, Puglielli L. Commun Biol. 2023 Sep 9; 6(1):926. Epub 2023 Sep 9.
NaCT/SLC13A5 facilitates citrate import and metabolism under nutrient-limited conditions. [Cell Rep. 2021]
NaCT/SLC13A5 facilitates citrate import and metabolism under nutrient-limited conditions.
Kumar A, Cordes T, Thalacker-Mercer AE, Pajor AM, Murphy AN, Metallo CM. Cell Rep. 2021 Sep 14; 36(11):109701.

RefSeq protein product
See the reference protein sequence for Na(+)/citrate cotransporter isoform d (NP_001271439.1).

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Protein sequence from Nucleotide coding region
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Homo sapiens solute carrier family 13 member 5 (SLC13A5), transcript variant 4, ...
Homo sapiens solute carrier family 13 member 5 (SLC13A5), transcript variant 4, mRNA
gi|1677482538|ref|NM_001284510.2|

Nucleotide

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Nucleotide