Gene Gene information from NCBI Gene database.
Entrez ID 3361
Gene name 5-hydroxytryptamine receptor 5A
Gene symbol HTR5A
Synonyms (NCBI Gene)
5-HT5A
Chromosome 7
Chromosome location 7q36.2
Summary The neurotransmitter serotonin (5-hydroxytryptamine, 5-HT) has been implicated in a wide range of psychiatric conditions and also has vasoconstrictive and vasodilatory effects. The gene described in this record is a member of 5-hydroxytryptamine (serotoni
miRNA miRNA information provided by mirtarbase database.
41
miRTarBase ID miRNA Experiments Reference
MIRT1057302 hsa-miR-1224-5p CLIP-seq
MIRT1057303 hsa-miR-1304 CLIP-seq
MIRT1057304 hsa-miR-216a CLIP-seq
MIRT1057305 hsa-miR-216b CLIP-seq
MIRT1057306 hsa-miR-3120-5p CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
34
GO ID Ontology Definition Evidence Reference
GO:0001586 Function Gi/o-coupled serotonin receptor activity IDA 9865521, 35610220, 35835867
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 7988681
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601305 5300 ENSG00000157219
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P47898
Protein name 5-hydroxytryptamine receptor 5A (5-HT-5) (5-HT-5A) (5-HT5A) (Serotonin receptor 5A)
Protein function G-protein coupled receptor for 5-hydroxytryptamine (serotonin), a biogenic hormone that functions as a neurotransmitter, a hormone and a mitogen (PubMed:35610220, PubMed:35835867, PubMed:9865521). Also functions as a receptor for ergot alkaloid
PDB 7UM4 , 7UM5 , 7UM6 , 7UM7 , 7X5H
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 57 338 7 transmembrane receptor (rhodopsin family) Family
Sequence
Sequence length 357
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Calcium signaling pathway
Neuroactive ligand-receptor interaction
Serotonergic synapse
  Serotonin receptors
G alpha (i) signalling events
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
2
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Melanoma Benign rs149473122 RCV005902455
Prostate cancer Uncertain significance rs193920930 RCV000149304
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Autistic Disorder Associate 17203304
Glioma Associate 20388841
Intracranial Hypertension Stimulate 27487831
Neuroblastoma Associate 39217334