Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3352
Gene name Gene Name - the full gene name approved by the HGNC.
5-hydroxytryptamine receptor 1D
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HTR1D
Synonyms (NCBI Gene) Gene synonyms aliases
5-HT1D, HT1DA, HTR1DA, HTRL, RDC4
Chromosome Chromosome number
1
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
1p36.12
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT019223 hsa-miR-335-5p Microarray 18185580
MIRT042672 hsa-miR-196b-5p CLASH 23622248
MIRT1057136 hsa-miR-128 CLIP-seq
MIRT1057137 hsa-miR-24 CLIP-seq
MIRT1057138 hsa-miR-2861 CLIP-seq
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0004993 Function G protein-coupled serotonin receptor activity IBA 21873635
GO:0004993 Function G protein-coupled serotonin receptor activity IMP 1652050
GO:0005886 Component Plasma membrane TAS
GO:0005887 Component Integral component of plasma membrane IBA 21873635
GO:0005887 Component Integral component of plasma membrane IDA 1652050
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
182133 5289 ENSG00000179546
Protein
UniProt ID P28221
Protein name 5-hydroxytryptamine receptor 1D (5-HT-1D) (5-HT1D) (Serotonin 1D alpha receptor) (5-HT-1D-alpha) (Serotonin receptor 1D)
Protein function G-protein coupled receptor for 5-hydroxytryptamine (serotonin) (PubMed:10452531, PubMed:1565658, PubMed:1652050, PubMed:33762731). Also functions as a receptor for ergot alkaloid derivatives, various anxiolytic and antidepressant drugs and other
PDB 7E32
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 55 356 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Detected in brain neocortex and caudate nucleus (at protein level). {ECO:0000269|PubMed:1828434}.
Sequence
Sequence length 377
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
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Autism Autistic Disorder rs121964908, rs62643608, rs181327458, rs797046134, rs869312704, rs1555013332, rs876657679, rs1057518999, rs1057518658, rs771827120, rs1555187899, rs773080572, rs753871454, rs1684130791, rs1684180699
View all (8 more)
19038234
Unknown
Disease term Disease name Evidence References Source
Mental depression Depressive disorder 21937687, 8018797 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Adrenocortical Carcinoma Associate 34220331
Agnosia Associate 38482990
Autistic Disorder Associate 17203304
Bipolar Disorder Associate 38482990
Breast Neoplasms Associate 39766808
Cognition Disorders Stimulate 38482990
Hashimoto Disease Associate 34493981
Hidradenitis Suppurativa Associate 39940809
Intellectual Disability Associate 38482990
Neoplasm Metastasis Associate 39766808