Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3355
Gene name Gene Name - the full gene name approved by the HGNC.
5-hydroxytryptamine receptor 1F
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HTR1F
Synonyms (NCBI Gene) Gene synonyms aliases
5-HT-1F, 5-HT1F, 5HT6, HTR1EL, MR77
Chromosome Chromosome number
3
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
3p11.2-p11.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT663891 hsa-miR-6823-5p HITS-CLIP 23824327
MIRT647681 hsa-miR-6887-3p HITS-CLIP 23824327
MIRT647680 hsa-miR-6832-3p HITS-CLIP 23824327
MIRT647679 hsa-miR-6734-3p HITS-CLIP 23824327
MIRT647678 hsa-miR-3667-3p HITS-CLIP 23824327
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 34239069
GO:0001586 Function Gi/o-coupled serotonin receptor activity IEA
GO:0004930 Function G protein-coupled receptor activity IEA
GO:0004993 Function G protein-coupled serotonin receptor activity IBA
GO:0004993 Function G protein-coupled serotonin receptor activity IDA 8380639
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
182134 5292 ENSG00000179097
Protein
UniProt ID P30939
Protein name 5-hydroxytryptamine receptor 1F (5-HT-1F) (5-HT1F) (Serotonin receptor 1F)
Protein function G-protein coupled receptor for 5-hydroxytryptamine (serotonin) (PubMed:21422162, PubMed:34239069, PubMed:8380639, PubMed:8384716). Also functions as a receptor for various alkaloids and psychoactive substances (PubMed:21422162, PubMed:8380639, P
PDB 7EXD
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 40 347 7 transmembrane receptor (rhodopsin family) Family
Sequence
Sequence length 366
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
Insomnia Insomnia, Insomnia (standard GWA) N/A N/A GWAS