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: 254428
MIM: 610801
HGNC: 19429
Ensembl: ENSG00000133065
Variants:
dbSNP: 254428
ClinVar: 254428
TCGA: ENSG00000133065
COSMIC: SLC41A1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000133065 | ENST00000367137 | Q8IVJ1 |
| ENSG00000133065 | ENST00000367137 | B2RMP2 |
Expression (GTEx)
Pathways
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 35163527 | 2022 | Alzheimer's Disease-Associated SNP rs708727 in SLC41A1 May Increase Risk for Parkinson's Disease: Report from Enlarged Slovak Study. | 3 |
| 35163527 | 2022 | Alzheimer's Disease-Associated SNP rs708727 in SLC41A1 May Increase Risk for Parkinson's Disease: Report from Enlarged Slovak Study. | 3 |
| 28222767 | 2017 | Knockdown of SLC41A1 magnesium transporter promotes mineralization and attenuates magnesium inhibition during osteogenesis of mesenchymal stromal cells. | 12 |
| 28222767 | 2017 | Knockdown of SLC41A1 magnesium transporter promotes mineralization and attenuates magnesium inhibition during osteogenesis of mesenchymal stromal cells. | 12 |
| 27612022 | 2016 | Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population. | 7 |
| 27612022 | 2016 | Genetic Analysis of the ZNF512B, SLC41A1, and ALDH2 Polymorphisms in Parkinson's Disease in the Iranian Population. | 7 |
| 26308152 | 2015 | Genetic analysis of SLC41A1 in Chinese Parkinson's disease patients. | 9 |
| 26355001 | 2015 | Insulin Modulates the Na+/Mg2+ Exchanger SLC41A1 and Influences Mg2+ Efflux from Intracellular Stores in Transgenic HEK293 Cells. | 14 |
| 26308152 | 2015 | Genetic analysis of SLC41A1 in Chinese Parkinson's disease patients. | 9 |
| 26355001 | 2015 | Insulin Modulates the Na+/Mg2+ Exchanger SLC41A1 and Influences Mg2+ Efflux from Intracellular Stores in Transgenic HEK293 Cells. | 14 |
| 24661466 | 2014 | Variant R244H in Na+/Mg2+ exchanger SLC41A1 in Taiwanese Parkinson's disease is associated with loss of Mg2+ efflux function. | 8 |
| 24661466 | 2014 | Variant R244H in Na+/Mg2+ exchanger SLC41A1 in Taiwanese Parkinson's disease is associated with loss of Mg2+ efflux function. | 8 |
| 23661805 | 2013 | Mutation of the Mg2+ transporter SLC41A1 results in a nephronophthisis-like phenotype. | 28 |
| 23823179 | 2013 | Nature of SLC41A1 complexes: report on the split-ubiquitin yeast two hybrid assay. | 2 |
| 23844728 | 2013 | SLC41A1 is the only magnesium responsive gene significantly overexpressed in placentas of preeclamptic women. | 8 |
Citation
Dessen P
SLC41A1 (solute carrier family 41 member 1)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/73440/slc41a1-(solute-carrier-family-41-member-1)
