HTR1D
5-hydroxytryptamine receptor 1D
Also known as: 5-HT1D, 5HT1D_HUMAN, HT1DA, HTRL, RDC4
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P28221
- Gene
- HTR1D
- Ensembl
- ENSG00000179546
- Chromosome
- 1
- Canonical length
- 377 aa
- Protein class
- FDA approved drug targets, G-protein coupled receptors, Human disease related genes, Predicted membrane proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables Gi/o-coupled serotonin receptor activity and serotonin receptor activity. Involved in adenylate cyclase-inhibiting serotonin receptor signaling pathway and intestine smooth muscle contraction. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
377 residues, UniProt reviewed canonical sequence.
>P28221|HTR1D
1 MSPLNQSAEG LPQEASNRSL NATETSEAWD PRTLQALKIS LAVVLSVITL ATVLSNAFVL
61 TTILLTRKLH TPANYLIGSL ATTDLLVSIL VMPISIAYTI THTWNFGQIL CDIWLSSDIT
121 CCTASILHLC VIALDRYWAI TDALEYSKRR TAGHAATMIA IVWAISICIS IPPLFWRQAK
181 AQEEMSDCLV NTSQISYTIY STCGAFYIPS VLLIILYGRI YRAARNRILN PPSLYGKRFT
241 TAHLITGSAG SSLCSLNSSL HEGHSHSAGS PLFFNHVKIK LADSALERKR ISAARERKAT
301 KILGIILGAF IICWLPFFVV SLVLPICRDS CWIHPALFDF FTWLGYLNSL INPIIYTVFN
361 EEFRQAFQKI VPFRKASLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HTR1D can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Cell surface
- Secreted
- No
- Transmembrane segments
- 7
- Mean surface accessibility (rSASA)
- 0.38
- Highest tissue expression
- 8 nTPM
Expression across tissuesHPA
Tissue
- duodenum: 8 nTPM
- small intestine: 7.1 nTPM
- basal ganglia: 6.2 nTPM
- gallbladder: 1.3 nTPM
- hypothalamus: 0.7 nTPM
- amygdala: 0.5 nTPM
Single-cell type
- enterocytes: 10 nCPM
- prostatic club cells: 5.2 nCPM
- cholangiocytes: 4 nCPM
- early spermatids: 2.4 nCPM
- respiratory deuterosomal cells: 2.1 nCPM
- brain inhibitory neurons: 1.9 nCPM
Immune cell
- basophil: 0.2 nTPM
- neutrophil: 0.2 nTPM
- classical monocyte: 0.1 nTPM
- non-classical monocyte: 0.1 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- midbrain: 25 nTPM
- basal ganglia: 12 nTPM
- hypothalamus: 9.3 nTPM
- spinal cord: 4.7 nTPM
- pons: 4.2 nTPM
- thalamus: 4.2 nTPM
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 1.3
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.09
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway
- adenylate cyclase-inhibiting serotonin receptor signaling pathway
- chemical synaptic transmission
- G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger
- intestine smooth muscle contraction
- regulation of behavior
- regulation of locomotion
- vasoconstriction
Molecular functions
- G protein-coupled serotonin receptor activity
- Gi/o-coupled serotonin receptor activity
- neurotransmitter receptor activity
- serotonin receptor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads HTR1D as an antibody target. Whether an autoantibody or antibody against HTR1D could matter depends on whether native HTR1D is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HTR1D is annotated at the cell surface, where native HTR1D is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label HTR1D as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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