Identity
HGNC
LOCATION
8p21.2
LOCUSID
ALIAS
HT015,MFRN,MFRN1,MSC,MSCP,PRO1278,PRO1584,PRO2217
FUSION GENES
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: 51312
MIM: 610387
HGNC: 29786
Ensembl: ENSG00000147454
Variants:
dbSNP: 51312
ClinVar: 51312
TCGA: ENSG00000147454
COSMIC: SLC25A37
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000147454 | ENST00000290075 | Q9NYZ2 |
| ENSG00000147454 | ENST00000417331 | F8W9Q7 |
| ENSG00000147454 | ENST00000519973 | Q9NYZ2 |
| ENSG00000147454 | ENST00000523930 | H0YAT5 |
Expression (GTEx)
Pathways
| Pathway | Source | External ID |
|---|---|---|
| Metabolism | REACTOME | R-HSA-1430728 |
| Mitochondrial iron-sulfur cluster biogenesis | REACTOME | R-HSA-1362409 |
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33686958 | 2021 | Identification of key genes in coronary artery disease: an integrative approach based on weighted gene co-expression network analysis and their correlation with immune infiltration. | 12 |
| 33686958 | 2021 | Identification of key genes in coronary artery disease: an integrative approach based on weighted gene co-expression network analysis and their correlation with immune infiltration. | 12 |
| 32810522 | 2020 | MiR-7 mediates mitochondrial impairment to trigger apoptosis and necroptosis in Rhabdomyosarcoma. | 14 |
| 32810522 | 2020 | MiR-7 mediates mitochondrial impairment to trigger apoptosis and necroptosis in Rhabdomyosarcoma. | 14 |
| 30391163 | 2019 | Strong correlation of ferrochelatase enzymatic activity with Mitoferrin-1 mRNA in lymphoblasts of patients with protoporphyria. | 5 |
| 30761871 | 2019 | The role of hepcidin, GDF15, and mitoferrin-1 in iron metabolism of polycythemia vera and essential thrombocytosis patients. | 2 |
| 30391163 | 2019 | Strong correlation of ferrochelatase enzymatic activity with Mitoferrin-1 mRNA in lymphoblasts of patients with protoporphyria. | 5 |
| 30761871 | 2019 | The role of hepcidin, GDF15, and mitoferrin-1 in iron metabolism of polycythemia vera and essential thrombocytosis patients. | 2 |
| 27643475 | 2016 | Identification of SLC25A37 as a major depressive disorder risk gene. | 18 |
| 27643475 | 2016 | Identification of SLC25A37 as a major depressive disorder risk gene. | 18 |
| 24854990 | 2015 | Distinct iron architecture in SF3B1-mutant myelodysplastic syndrome patients is linked to an SLC25A37 splice variant with a retained intron. | 34 |
| 24854990 | 2015 | Distinct iron architecture in SF3B1-mutant myelodysplastic syndrome patients is linked to an SLC25A37 splice variant with a retained intron. | 34 |
| 23266187 | 2013 | The mitochondrial transporter family SLC25: identification, properties and physiopathology. | 0 |
| 23266187 | 2013 | The mitochondrial transporter family SLC25: identification, properties and physiopathology. | 0 |
| 21627978 | 2011 | Abnormal mitoferrin-1 expression in patients with erythropoietic protoporphyria. | 28 |
Citation
Dessen P
SLC25A37 (solute carrier family 25 member 37)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/73357/slc25a37-(solute-carrier-family-25-member-37)
