Homo sapiens solute carrier family 25 member 38 (SLC25A38), RefSeqGene - Nucleotide

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SLC25A38 as a novel biomarker for metastasis and clinical outcome in uveal melanoma. [Cell Death Dis. 2022]
SLC25A38 as a novel biomarker for metastasis and clinical outcome in uveal melanoma.
Fan Z, Duan J, Luo P, Shao L, Chen Q, Tan X, Zhang L, Xu X. Cell Death Dis. 2022 Apr 11; 13(4):330. Epub 2022 Apr 11.
SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature. [Hum Mutat. 2021]
SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature.
Heeney MM, Berhe S, Campagna DR, Oved JH, Kurre P, Shaw PJ, Teo J, Shanap MA, Hassab HM, Glader BE, et al. Hum Mutat. 2021 Nov; 42(11):1367-1383. Epub 2021 Aug 5.
Clinical characterization and hematopoietic stem cell transplant outcomes for congenital sideroblastic anemia caused by a novel pathogenic variant in SLC25A38. [Pediatr Blood Cancer. 2020]
Clinical characterization and hematopoietic stem cell transplant outcomes for congenital sideroblastic anemia caused by a novel pathogenic variant in SLC25A38.
Uminski K, Houston DS, Hartley JN, Liu J, Cuvelier GDE, Israels SJ. Pediatr Blood Cancer. 2020 Oct; 67(10):e28623. Epub 2020 Aug 13.

RefSeq alternative splicing
See 9 reference mRNA sequence splice variants for the SLC25A38 gene.

Protein
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RNA
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Nucleotide