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Gene : SLC5A1 Homo sapiens

Name  ? solute carrier family 5 member 1 Cytological Location  22q12.3
Brief Description  solute carrier family 5 member 1
Description  This gene encodes a member of the sodium-dependent glucose transporter (SGLT) family. The encoded integral membrane protein is the primary mediator of dietary glucose and galactose uptake from the intestinal lumen. Mutations in this gene have been associated with glucose-galactose malabsorption. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
  • synonyms:
  • SLC5A1,
  • NAGT,
  • SGLT1,
  • D22S675,
  • OTTHUMG00000030768,
  • solute carrier family 5 (sodium/glucose cotransporter), member 1,
  • SGLT1,
  • NAGT,
  • HGNC:11036,
  • NM_000343,
  • uc003amc.4,
  • D22S675,
  • sodium/glucose cotransporter 1
  • identifiers:
  • 6523,
  • ENSG00000100170,
  • SLC5A1

Genome feature

Region: gene ? Length: 69980  
Location: 22:32043050-32113029 Cyto location: 22q12.3

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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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1 Diseases

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

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



919 SN Ps

5 Cross References

20 Data Sets

9 Homologues

0 Located Features

97 Rna Seq Results