Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3362
Gene name Gene Name - the full gene name approved by the HGNC.
5-hydroxytryptamine receptor 6
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HTR6
Synonyms (NCBI Gene) Gene synonyms aliases
5-HT6, 5-HT6R
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p36.13
Summary Summary of gene provided in NCBI Entrez Gene.
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 pathwa
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT2013104 hsa-miR-1182 CLIP-seq
MIRT2013105 hsa-miR-767-3p CLIP-seq
MIRT2013104 hsa-miR-1182 CLIP-seq
MIRT2245381 hsa-miR-1266 CLIP-seq
MIRT2245382 hsa-miR-4518 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0004969 Function Histamine receptor activity TAS 8522988
GO:0004993 Function G protein-coupled serotonin receptor activity IBA
GO:0004993 Function G protein-coupled serotonin receptor activity IDA 35714614, 36989299, 37327704
GO:0004993 Function G protein-coupled serotonin receptor activity IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
601109 5301 ENSG00000158748
Protein
UniProt ID P50406
Protein name 5-hydroxytryptamine receptor 6 (5-HT-6) (5-HT6) (Serotonin receptor 6)
Protein function G-protein coupled receptor for 5-hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a hormone and a mitogen (PubMed:35714614, PubMed:36989299, PubMed:37327704, PubMed:8522988). Also has a high affinity for tr
PDB 7XTB , 7YS6 , 8JLZ
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 43 320 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Expressed in several human brain regions, most prominently in the caudate nucleus. {ECO:0000269|PubMed:8522988}.
Sequence
Sequence length 440
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Calcium signaling pathway
cAMP signaling pathway
Neuroactive ligand-receptor interaction
Serotonergic synapse
  Serotonin receptors
G alpha (s) signalling events
ADORA2B mediated anti-inflammatory cytokines production
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Bipolar Disorder Bipolar I disorder N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Breast Neoplasms Inhibit 35359970
Migraine Disorders Associate 31587366
Pigmented Nodular Adrenocortical Disease Primary 1 Associate 31074783