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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,
  • D22S675,
  • solute carrier family 5 (sodium/glucose cotransporter), member 1,
  • SGLT1,
  • NM_000343,
  • SGLT1,
  • D22S675,
  • OTTHUMG00000030768,
  • HGNC:11036,
  • uc003amc.4,
  • sodium/glucose cotransporter 1,
  • NAGT
  • identifiers:
  • 6523,
  • ENSG00000100170,
  • SLC5A1

Genome feature

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


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

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]

Homology

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Interactions

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Expression

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

Gene Ontology

Gene --> GO terms.

 

Other

919 SN Ps

5 Cross References

20 Data Sets

9 Homologues

0 Located Features

97 Rna Seq Results