Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 54977
MIM: 610819
HGNC: 26054
Ensembl: ENSG00000144659
Variants:
dbSNP: 54977
ClinVar: 54977
TCGA: ENSG00000144659
COSMIC: SLC25A38
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35411037 | 2022 | SLC25A38 as a novel biomarker for metastasis and clinical outcome in uveal melanoma. | 3 |
| 35411037 | 2022 | SLC25A38 as a novel biomarker for metastasis and clinical outcome in uveal melanoma. | 3 |
| 32605921 | 2021 | Novel frameshift variant (c.409dupG) in SLC25A38 is a common cause of congenital sideroblastic anaemia in the Indian subcontinent. | 2 |
| 34298585 | 2021 | SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature. | 7 |
| 32605921 | 2021 | Novel frameshift variant (c.409dupG) in SLC25A38 is a common cause of congenital sideroblastic anaemia in the Indian subcontinent. | 2 |
| 34298585 | 2021 | SLC25A38 congenital sideroblastic anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature. | 7 |
| 31155012 | 2020 | Dentate gyrus volume deficit in schizophrenia. | 16 |
| 32790119 | 2020 | Clinical characterization and hematopoietic stem cell transplant outcomes for congenital sideroblastic anemia caused by a novel pathogenic variant in SLC25A38. | 4 |
| 31155012 | 2020 | Dentate gyrus volume deficit in schizophrenia. | 16 |
| 32790119 | 2020 | Clinical characterization and hematopoietic stem cell transplant outcomes for congenital sideroblastic anemia caused by a novel pathogenic variant in SLC25A38. | 4 |
| 29499877 | 2018 | Novel mutations in mitochondrial carrier family gene SLC25A38, causing congenital sideroblastic anemia in Iranian families, identified by whole exome sequencing. | 3 |
| 29499877 | 2018 | Novel mutations in mitochondrial carrier family gene SLC25A38, causing congenital sideroblastic anemia in Iranian families, identified by whole exome sequencing. | 3 |
| 28772256 | 2017 | Non syndromic childhood onset congenital sideroblastic anemia: A report of 13 patients identified with an ALAS2 or SLC25A38 mutation. | 6 |
| 28772256 | 2017 | Non syndromic childhood onset congenital sideroblastic anemia: A report of 13 patients identified with an ALAS2 or SLC25A38 mutation. | 6 |
| 26813789 | 2016 | Appoptosin interacts with mitochondrial outer-membrane fusion proteins and regulates mitochondrial morphology. | 15 |
Citation
Dessen P
SLC25A38 (solute carrier family 25 member 38)
Atlas Genet Cytogenet Oncol Haematol. 2017-01-01
Online version: http://atlasgeneticsoncology.org/gene/56709/slc25a38-(solute-carrier-family-25-member-38)
