SLC1A4

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Solute carrier family 1 (glutamate/neutral amino acid transporter), member 4
Identifiers
Symbol(s) SLC1A4; ASCT1; SATT
External IDs OMIM: 600229 MGI2135601 HomoloGene20655
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 6509 55963
Ensembl ENSG00000115902 ENSMUSG00000020142
Uniprot P43007 Q3US35
Refseq NM_003038 (mRNA)
NP_003029 (protein)
NM_018861 (mRNA)
NP_061349 (protein)
Location Chr 2: 65.07 - 65.1 Mb Chr 11: 20.2 - 20.23 Mb
Pubmed search [1] [2]

Solute carrier family 1 (glutamate/neutral amino acid transporter), member 4, also known as SLC1A4, is a human gene.[1]


[edit] See also

[edit] References

[edit] Further reading

  • Hofmann K, Düker M, Fink T, et al. (1995). "Human neutral amino acid transporter ASCT1: structure of the gene (SLC1A4) and localization to chromosome 2p13-p15.". Genomics 24 (1): 20–6. doi:10.1006/geno.1994.1577. PMID 7896285. 
  • Arriza JL, Kavanaugh MP, Fairman WA, et al. (1993). "Cloning and expression of a human neutral amino acid transporter with structural similarity to the glutamate transporter gene family.". J. Biol. Chem. 268 (21): 15329–32. PMID 8101838. 
  • Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". Gene 138 (1-2): 171–4. PMID 8125298. 
  • Shafqat S, Tamarappoo BK, Kilberg MS, et al. (1993). "Cloning and expression of a novel Na(+)-dependent neutral amino acid transporter structurally related to mammalian Na+/glutamate cotransporters.". J. Biol. Chem. 268 (21): 15351–5. PMID 8340364. 
  • Tamarappoo BK, McDonald KK, Kilberg MS (1996). "Expressed human hippocampal ASCT1 amino acid transporter exhibits a pH-dependent change in substrate specificity.". Biochim. Biophys. Acta 1279 (2): 131–6. PMID 8603078. 
  • Zerangue N, Kavanaugh MP (1996). "ASCT-1 is a neutral amino acid exchanger with chloride channel activity.". J. Biol. Chem. 271 (45): 27991–4. PMID 8910405. 
  • Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library.". Gene 200 (1-2): 149–56. PMID 9373149. 
  • Marin M, Tailor CS, Nouri A, Kabat D (2000). "Sodium-dependent neutral amino acid transporter type 1 is an auxiliary receptor for baboon endogenous retrovirus.". J. Virol. 74 (17): 8085–93. PMID 10933718. 
  • Younes M, Pathak M, Finnie D, et al. (2001). "Expression of the neutral amino acids transporter ASCT1 in esophageal carcinomas.". Anticancer Res. 20 (5C): 3775–9. PMID 11268453. 
  • Pinilla J, Barber A, Lostao MP (2002). "Active transport of alanine by the neutral amino-acid exchanger ASCT1.". Can. J. Physiol. Pharmacol. 79 (12): 1023–9. PMID 11824937. 
  • Lavillette D, Marin M, Ruggieri A, et al. (2002). "The envelope glycoprotein of human endogenous retrovirus type W uses a divergent family of amino acid transporters/cell surface receptors.". J. Virol. 76 (13): 6442–52. PMID 12050356. 
  • Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932. 
  • Marin M, Lavillette D, Kelly SM, Kabat D (2003). "N-linked glycosylation and sequence changes in a critical negative control region of the ASCT1 and ASCT2 neutral amino acid transporters determine their retroviral receptor functions.". J. Virol. 77 (5): 2936–45. PMID 12584318. 
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334. 
  • Hillier LW, Graves TA, Fulton RS, et al. (2005). "Generation and annotation of the DNA sequences of human chromosomes 2 and 4.". Nature 434 (7034): 724–31. doi:10.1038/nature03466. PMID 15815621. 
  • Chi A, Valencia JC, Hu ZZ, et al. (2007). "Proteomic and bioinformatic characterization of the biogenesis and function of melanosomes.". J. Proteome Res. 5 (11): 3135–44. doi:10.1021/pr060363j. PMID 17081065. 

This article incorporates text from the United States National Library of Medicine, which is in the public domain.