Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3351
Gene name Gene Name - the full gene name approved by the HGNC.
5-hydroxytryptamine receptor 1B
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HTR1B
Synonyms (NCBI Gene) Gene synonyms aliases
5-HT-1B, 5-HT-1D-beta, 5-HT1B, 5-HT1DB, HTR1D2, HTR1DB, S12
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6q14.1
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this intronless gene is a G-protein coupled receptor for serotonin (5-hydroxytryptamine). Ligand binding activates second messengers that inhibit the activity of adenylate cyclase and manage the release of serotonin, dopamine, and a
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT002447 hsa-miR-96-5p Reporter assay 18283276
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001586 Function Gi/o-coupled serotonin receptor activity IDA 1348246
GO:0001586 Function Gi/o-coupled serotonin receptor activity IEA
GO:0001586 Function Gi/o-coupled serotonin receptor activity IMP 29925951
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0004993 Function G protein-coupled serotonin receptor activity IBA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
182131 5287 ENSG00000135312
Protein
UniProt ID P28222
Protein name 5-hydroxytryptamine receptor 1B (5-HT-1B) (5-HT1B) (S12) (Serotonin 1D beta receptor) (5-HT-1D-beta) (Serotonin receptor 1B)
Protein function G-protein coupled receptor for 5-hydroxytryptamine (serotonin) (PubMed:10452531, PubMed:1315531, PubMed:1328844, PubMed:1348246, PubMed:1351684, PubMed:1559993, PubMed:1565658, PubMed:1610347, PubMed:23519210, PubMed:23519215, PubMed:29925951, P
PDB 4IAQ , 4IAR , 5V54 , 6G79 , 7C61
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 66 369 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Detected in cerebral artery smooth muscle cells (at protein level). Detected in brain cortex, striatum, amygdala, medulla, hippocampus, caudate nucleus and putamen. {ECO:0000269|PubMed:1348246, ECO:0000269|PubMed:1351684, ECO:0000269|P
Sequence
Sequence length 390
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  cAMP signaling pathway
Neuroactive ligand-receptor interaction
Serotonergic synapse
Taste transduction
  Serotonin receptors
G alpha (i) signalling events
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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
Breast Cancer Postmenopausal breast cancer N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 32508318
Adrenocortical Carcinoma Associate 34220331
Alcoholism Associate 19736238, 22064162, 22550993
Anorexia Nervosa Associate 27579596
Anxiety Associate 27579596
Anxiety Disorders Associate 27579596
Attention Deficit Disorder with Hyperactivity Associate 16380908, 22841130
Autistic Disorder Associate 29904178
Bulimia Nervosa Associate 27579596
Conduct Disorder Associate 23457595, 25993020