Na(+)/citrate cotransporter isoform X1 [Homo sapiens]

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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.
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.
A novel homozygous SLC13A5 whole-gene deletion generated by Alu/Alu-mediated rearrangement in an Iraqi family with epileptic encephalopathy. [Am J Med Genet A. 2021]
A novel homozygous SLC13A5 whole-gene deletion generated by Alu/Alu-mediated rearrangement in an Iraqi family with epileptic encephalopathy.
Duan R, Saadi NW, Grochowski CM, Bhadila G, Faridoun A, Mitani T, Du H, Fatih JM, Jhangiani SN, Akdemir ZC, et al. Am J Med Genet A. 2021 Jul; 185(7):1972-1980. Epub 2021 Apr 2.

RefSeq mRNA
See reference mRNA sequence for the SLC13A5 gene (XM_011523795.4).
RefSeq protein isoforms
See 6 reference sequence protein isoforms for the SLC13A5 gene.

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Mus musculus inhibitor of CDK, cyclin A1 interacting protein 1 (Inca1), transcri...
Mus musculus inhibitor of CDK, cyclin A1 interacting protein 1 (Inca1), transcript variant 10, mRNA
gi|2469477126|ref|NM_001419094.1|

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