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Gene : SLC6A2 Homo sapiens

Name  ? solute carrier family 6 member 2 Cytological Location  16q12.2
Brief Description  solute carrier family 6 member 2
description  This gene encodes a member of the sodium:neurotransmitter symporter family. This member is a multi-pass membrane protein, which is responsible for reuptake of norepinephrine into presynaptic nerve terminals and is a regulator of norepinephrine homeostasis. Mutations in this gene cause orthostatic intolerance, a syndrome characterized by lightheadedness, fatigue, altered mentation and syncope. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.[provided by RefSeq, Feb 2010]
  • synonyms:
  • NAT1,
  • SLC6A5,
  • OTTHUMG00000133208,
  • NAT1,
  • solute carrier family 6 (neurotransmitter transporter), member 2,
  • NET,
  • norepinephrine transporter,
  • uc002eig.3,
  • NET1,
  • NET,
  • HGNC:11048,
  • solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2,
  • NET1,
  • NM_001043,
  • SLC6A5,
  • SLC6A2
  • identifiers:
  • 6530,
  • ENSG00000103546,
  • SLC6A2

Genome feature

Region: gene ? Length: 50563  
Location: 16:55655630-55706192 Cyto location: 16q12.2

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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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551 SN Ps

5 Cross References

19 Data Sets

24 Homologues

0 Located Features

90 Rna Seq Results