SLC41A3

From Wikipedia, the free encyclopedia
Jump to: navigation, search
SLC41A3
Identifiers
Aliases SLC41A3, SLC41A1-L2, solute carrier family 41 member 3
External IDs MGI: 1918949 HomoloGene: 23052 GeneCards: 54946
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001008485
NM_001008486
NM_001008487
NM_001164475
NM_017836

NM_001037493
NM_027868

RefSeq (protein)

NP_001008485.1
NP_001008486.1
NP_001008487.1
NP_001157947.1
NP_001008486.1

NP_001032570.1
NP_082144.2

Location (UCSC) Chr 3: 126.01 – 126.1 Mb Chr 6: 90.6 – 90.65 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

Solute carrier family 41, member 3 is a protein that in humans is encoded by the SLC41A3 gene.[1]

Model organisms[edit]

Model organisms have been used in the study of SLC41A3 function. A conditional knockout mouse line, called Slc41a3tm1a(KOMP)Wtsi[6][7] was generated as part of the International Knockout Mouse Consortium program — a high-throughput mutagenesis project to generate and distribute animal models of disease to interested scientists.[8][9][10]

Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion.[4][11] Twenty six tests were carried out on mutant mice and one significant abnormality was observed: homozygous mutants displayed abnormal locomotor coordination.[4]

References[edit]

  1. ^ "Entrez Gene: Solute carrier family 41, member 3". Retrieved 2011-09-28. 
  2. ^ "Salmonella infection data for Slc41a3". Wellcome Trust Sanger Institute. 
  3. ^ "Citrobacter infection data for Slc41a3". Wellcome Trust Sanger Institute. 
  4. ^ a b c Gerdin AK (2010). "The Sanger Mouse Genetics Programme: High throughput characterisation of knockout mice". Acta Ophthalmologica 88: 925–7. doi:10.1111/j.1755-3768.2010.4142.x. 
  5. ^ Mouse Resources Portal, Wellcome Trust Sanger Institute.
  6. ^ "International Knockout Mouse Consortium". 
  7. ^ "Mouse Genome Informatics". 
  8. ^ Skarnes, W. C.; Rosen, B.; West, A. P.; Koutsourakis, M.; Bushell, W.; Iyer, V.; Mujica, A. O.; Thomas, M.; Harrow, J.; Cox, T.; Jackson, D.; Severin, J.; Biggs, P.; Fu, J.; Nefedov, M.; De Jong, P. J.; Stewart, A. F.; Bradley, A. (2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature 474 (7351): 337–342. doi:10.1038/nature10163. PMC 3572410. PMID 21677750. 
  9. ^ Dolgin E (2011). "Mouse library set to be knockout". Nature 474 (7351): 262–3. doi:10.1038/474262a. PMID 21677718. 
  10. ^ Collins FS; Rossant J; Wurst W (2007). "A Mouse for All Reasons". Cell 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247. 
  11. ^ van der Weyden L; White JK; Adams DJ; Logan DW (2011). "The mouse genetics toolkit: revealing function and mechanism.". Genome Biol 12 (6): 224. doi:10.1186/gb-2011-12-6-224. PMC 3218837. PMID 21722353. 

Further reading[edit]

  • Wabakken, T.; Rian, E.; Kveine, M.; Aasheim, H. C. (2003). "The human solute carrier SLC41A1 belongs to a novel eukaryotic subfamily with homology to prokaryotic MgtE Mg2+ transporters". Biochemical and Biophysical Research Communications 306 (3): 718–724. doi:10.1016/S0006-291X(03)01030-1. PMID 12810078.