Version 5.4
Mus musculus Protein: Slc41a1
Summary
InnateDB Protein IDBP-191499.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Slc41a1
Protein Name solute carrier family 41, member 1
Synonyms AI573938; B230315F01Rik;
Species Mus musculus
Ensembl Protein ENSMUSP00000083747
InnateDB Gene IDBG-191497 (Slc41a1)
Protein Structure
UniProt Annotation
Function Acts as a magnesium transporter that is responsive to magnesium balance. {ECO:0000250}.
Subcellular Localization Membrane {ECO:0000305}; Multi-pass membrane protein {ECO:0000305}.
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
Predicted by orthology
Total 1 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003674 molecular_function
GO:0008324 cation transmembrane transporter activity
Biological Process
GO:0006812 cation transport
GO:0008150 biological_process
Cellular Component
GO:0005575 cellular_component
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID MGI:2444823
InterPro IPR006667 SLC41 divalent cation transporters, integral membrane domain
PFAM PF01769
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8BJA2
PhosphoSite PhosphoSite-
TrEMBL
UniProt Splice Variant
Entrez Gene 98396
UniGene Mm.477647
RefSeq NP_776290
MGI ID
MGI Symbol Slc41a1
OMIM
CCDS CCDS15275
HPRD
IMGT
EMBL AK089802 BC096596 BC116280 BC116281
GenPept AAH96596 AAI16281 AAI16282 BAC40965

If you use InnateDB for your research, please cite the following publication:

Breuer et al., InnateDB: systems biology of innate immunity and beyond - recent updates and continuing curation. Nucl. Acids Res. (2013) 41 (D1) 

InnateDB is being developed jointly by the Brinkman Laboratory (Simon Fraser University, British Columbia, Canada), the Hancock Laboratory (University of British Columbia, Vancouver, British Columbia) and the Lynn EMBL Australia Group (South Australian Health & Medical Research Institute and Flinders University, Adelaide, Australia).

Funding is currently provided by Allergen and EMBL Australia. Previous funding has been provided by Genome Canada, the Foundation for the National Institutes of Health through the Grand Challenges in Global Health initiative and by Teagasc. InnateDB curated interactions are licensed under the Design Science License. All other data is licensed under the terms of the originating database. Contact: innatedb-mail@sfu.ca