SLC7A4

From Wikipedia, the free encyclopedia
Solute carrier family 7 (orphan transporter), member 4
Identifiers
SymbolsSLC7A4; CAT-4; CAT4; HCAT3; VH
External IDsOMIM: 603752 MGI: 2146512 HomoloGene: 20883 ChEMBL: 5075 GeneCards: SLC7A4 Gene
RNA expression pattern
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez6545224022
EnsemblENSG00000099960ENSMUSG00000022756
UniProtO43246Q8BLQ7
RefSeq (mRNA)NM_004173NM_144852
RefSeq (protein)NP_004164NP_659101
Location (UCSC)Chr 22:
21.38 – 21.39 Mb
Chr 16:
17.57 – 17.58 Mb
PubMed search

Cationic amino acid transporter 4 is a protein that in humans is encoded by the SLC7A4 gene.[1][2][3]

See also

References

  1. Sperandeo MP, Borsani G, Incerti B, Zollo M, Rossi E, Zuffardi O, Castaldo P, Taglialatela M, Andria G, Sebastio G (Aug 1998). "The gene encoding a cationic amino acid transporter (SLC7A4) maps to the region deleted in the velocardiofacial syndrome". Genomics 49 (2): 230–6. doi:10.1006/geno.1998.5252. PMID 9598310. 
  2. Hammermann R, Brunn G, Racke K (Oct 2001). "Analysis of the genomic organization of the human cationic amino acid transporters CAT-1, CAT-2 and CAT-4". Amino Acids 21 (2): 211–9. doi:10.1007/s007260170029. PMID 11665818. 
  3. "Entrez Gene: SLC7A4 solute carrier family 7 (cationic amino acid transporter, y+ system), member 4". 

Further reading

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

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