SLC41A3

Solute carrier family 41, member 3 is a protein that in humans is encoded by the SLC41A3 gene.[5]

SLC41A3
Identifiers
AliasesSLC41A3, SLC41A1-L2, solute carrier family 41 member 3
External IDsOMIM: 610803 MGI: 1918949 HomoloGene: 23052 GeneCards: SLC41A3
Gene location (Human)
Chr.Chromosome 3 (human)[1]
Band3q21.2-q21.3Start126,006,355 bp[1]
End126,101,561 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

54946

71699

Ensembl

ENSG00000114544

ENSMUSG00000030089

UniProt

Q96GZ6

Q921R8

RefSeq (mRNA)

NM_001008485
NM_001008486
NM_001008487
NM_001164475
NM_017836

NM_001037493
NM_027868

RefSeq (protein)

NP_001032570
NP_082144

Location (UCSC)Chr 3: 126.01 – 126.1 MbChr 6: 90.6 – 90.65 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Model organisms

Model organisms have been used in the study of SLC41A3 function. A conditional knockout mouse line, called Slc41a3tm1a(KOMP)Wtsi[10][11] 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.[12][13][14]

Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion.[8][15] Twenty six tests were carried out on mutant mice and one significant abnormality was observed: homozygous mutants displayed abnormal locomotor coordination.[8]

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References
  1. GRCh38: Ensembl release 89: ENSG00000114544 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000030089 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: Solute carrier family 41, member 3". Retrieved 2011-09-28.
  6. "Salmonella infection data for Slc41a3". Wellcome Trust Sanger Institute.
  7. "Citrobacter infection data for Slc41a3". Wellcome Trust Sanger Institute.
  8. 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.
  9. Mouse Resources Portal, Wellcome Trust Sanger Institute.
  10. "International Knockout Mouse Consortium".
  11. "Mouse Genome Informatics".
  12. Skarnes WC, Rosen B, West AP, Koutsourakis M, Bushell W, Iyer V, Mujica AO, Thomas M, Harrow J, Cox T, Jackson D, Severin J, Biggs P, Fu J, Nefedov M, de Jong PJ, Stewart AF, Bradley A (June 2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature. 474 (7351): 337–42. doi:10.1038/nature10163. PMC 3572410. PMID 21677750.
  13. Dolgin E (June 2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–3. doi:10.1038/474262a. PMID 21677718.
  14. Collins FS, Rossant J, Wurst W (January 2007). "A mouse for all reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247.
  15. van der Weyden L, White JK, Adams DJ, Logan DW (June 2011). "The mouse genetics toolkit: revealing function and mechanism". Genome Biology. 12 (6): 224. doi:10.1186/gb-2011-12-6-224. PMC 3218837. PMID 21722353.

Further reading
  • Wabakken T, Rian E, Kveine M, Aasheim HC (July 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): 718–24. doi:10.1016/S0006-291X(03)01030-1. PMID 12810078.


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