SLC38A10

From Wikipedia, the free encyclopedia
Jump to: navigation, search
SLC38A10
Identifiers
Aliases SLC38A10, PP1744, solute carrier family 38 member 10
External IDs MGI: 1919305 HomoloGene: 41556 GeneCards: 124565
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001037984
NM_138570

RefSeq (protein)

NP_001033073.1
NP_612637.1

Location (UCSC) Chr 17: 81.25 – 81.3 Mb Chr 11: 120.1 – 120.15 Mb
PubMed search [1] [2]
Wikidata
View/Edit Human View/Edit Mouse

Sodium-coupled neutral amino acid transporter 10 also known as solute carrier family 38, member 10 is a protein that in humans is encoded by the SLC38A10 gene.[3]

Model organisms[edit]

Model organisms have been used in the study of SLC38A10 function. A conditional knockout mouse line, called Slc38a10tm1a(EUCOMM)Wtsi[12][13] 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.[14][15][16]

Male and female animals underwent a standardized phenotypic screen to determine the effects of deletion.[10][17] Twenty four tests were carried out on mutant mice and four significant abnormalities were observed.[10] Homozygous animals of both sex had decreased body weights, and DEXA analysis showed that this correlated with decreased bone mineral content and decreased body length. Indirect calorimetry analysis showed that males displayed increased oxygen consumption and energy expenditure, while clinical chemistry tests found that females had decreased circulating amylase levels and males had hypoalbuminemia and increased circulating creatinine levels.[10]

References[edit]

  1. ^ "Human PubMed Reference:". 
  2. ^ "Mouse PubMed Reference:". 
  3. ^ "Entrez Gene: solute carrier family 38, member 10". Retrieved 2011-08-30. 
  4. ^ "Body weight data for Slc38a10". Wellcome Trust Sanger Institute. 
  5. ^ "Indirect calorimetry data for Slc38a10". Wellcome Trust Sanger Institute. 
  6. ^ "DEXA data for Slc38a10". Wellcome Trust Sanger Institute. 
  7. ^ "Clinical chemistry data for Slc38a10". Wellcome Trust Sanger Institute. 
  8. ^ "Salmonella infection data for Slc38a10". Wellcome Trust Sanger Institute. 
  9. ^ "Citrobacter infection data for Slc38a10". Wellcome Trust Sanger Institute. 
  10. ^ a b c d 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. 
  11. ^ Mouse Resources Portal, Wellcome Trust Sanger Institute.
  12. ^ "International Knockout Mouse Consortium". 
  13. ^ "Mouse Genome Informatics". 
  14. ^ 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 (Jun 2011). "A conditional knockout resource for the genome-wide study of mouse gene function". Nature. 474 (7351): 337–42. doi:10.1038/nature10163. PMC 3572410free to read. PMID 21677750. 
  15. ^ Dolgin E (Jun 2011). "Mouse library set to be knockout". Nature. 474 (7351): 262–3. doi:10.1038/474262a. PMID 21677718. 
  16. ^ Collins FS, Rossant J, Wurst W (Jan 2007). "A mouse for all reasons". Cell. 128 (1): 9–13. doi:10.1016/j.cell.2006.12.018. PMID 17218247. 
  17. ^ van der Weyden L, White JK, Adams DJ, Logan DW (2011). "The mouse genetics toolkit: revealing function and mechanism". Genome Biology. 12 (6): 224. doi:10.1186/gb-2011-12-6-224. PMC 3218837free to read. PMID 21722353. 

Further reading[edit]