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Gene : SLC29A1 Homo sapiens

Name  ? solute carrier family 29 member 1 (Augustine blood group) Cytological Location  6p21.1
Brief Description  solute carrier family 29 member 1 (Augustine blood group)
Description  This gene is a member of the equilibrative nucleoside transporter family. The gene encodes a transmembrane glycoprotein that localizes to the plasma and mitochondrial membranes and mediates the cellular uptake of nucleosides from the surrounding medium. The protein is categorized as an equilibrative (as opposed to concentrative) transporter that is sensitive to inhibition by nitrobenzylthioinosine (NBMPR). Nucleoside transporters are required for nucleotide synthesis in cells that lack de novo nucleoside synthesis pathways, and are also necessary for the uptake of cytotoxic nucleosides used for cancer and viral chemotherapies. Multiple alternatively spliced variants, encoding the same protein, have been found for this gene. [provided by RefSeq, Jul 2008]
  • synonyms:
  • OTTHUMG00000014759,
  • uc003owv.1,
  • NM_001078175,
  • U81375,
  • HGNC:11003,
  • solute carrier family 29 (equilibrative nucleoside transporter), member 1,
  • ENT1,
  • ENT1,
  • SLC29A1
  • identifiers:
  • 2030,
  • ENSG00000112759,
  • SLC29A1

Genome feature

Region: gene ? Length: 14558  
Location: 6:44219587-44234144 Cyto location: 6p21.1

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0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene Ontology

Gene --> GO terms.



472 SN Ps

5 Cross References

17 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results