Gene

HTR6

Species
Homo sapiens
Symbol
HTR6
Name
5-hydroxytryptamine receptor 6
Synonyms
  • 5-HT-6
  • 5-HT6
Biotype
protein coding gene
Automated Description
Enables G protein-coupled serotonin receptor activity and serotonin receptor activity. Involved in adenylate cyclase-activating serotonin receptor signaling pathway and positive regulation of TOR signaling. Is active in plasma membrane. Implicated in Alzheimer's disease.
RGD Description
This gene encodes a protein that belongs to the seven-transmembrane G protein-coupled receptor family of proteins. The encoded protein couples with the Gs alpha subunit and stimulates adenylate cyclase to activate the cyclic AMP-dependent signaling pathway. This receptor is thought to regulate cholinergic neuronal transmission in the brain. Several antidepressants and antipsychotic drugs have a high affinity for this receptor. [provided by RefSeq, Aug 2013]
Cross References
Additional Information
Literature

Orthology

Gene tree
PANTHER:PTHR24247
Links to orthology data in JBrowse by filter level: Stringent,  Moderate,  No filter,  Best and Best Reverse

Paralogy

Function - GO Annotations

Pathways

No data available

Phenotypes

Primary Sources
None
Other Sources
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Annotation details
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    Disease Associations

    Cases where the expected disease association was NOT found
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    Alleles and Variants

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      Transgenic Alleles

      Species
      (carrying the transgene)
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      Transgenic construct
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        Models

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          Sequence Feature Viewer

          Genome location
          Assembly version
          GRCh38
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          Data currently unavailable; sequence viewer under construction

          Sequence Details

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          Expression

          Primary Sources
          None
          Other Sources
          Cell color indicative of annotation volume; red slash indicates species lacks structure or developmental stage.

          Molecular Interactions

          HTR6 molecule type
          Interactor gene
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            Genetic Interactions

            HTR6 role
            HTR6 genetic perturbation
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