HTR1F
5-hydroxytryptamine receptor 1F
Also known as: 5-HT1F, 5HT1F_HUMAN, HTR1EL
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P30939
- Gene
- HTR1F
- Ensembl
- ENSG00000179097
- Chromosome
- 3
- Canonical length
- 366 aa
- Protein class
- FDA approved drug targets, G-protein coupled receptors, Predicted membrane proteins
OverviewNCBI Gene
Enables Gi/o-coupled serotonin receptor activity; serotonin binding activity; and serotonin receptor activity. Involved in adenylate cyclase-inhibiting serotonin receptor signaling pathway. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
366 residues, UniProt reviewed canonical sequence.
>P30939|HTR1F
1 MDFLNSSDQN LTSEELLNRM PSKILVSLTL SGLALMTTTI NSLVIAAIIV TRKLHHPANY
61 LICSLAVTDF LVAVLVMPFS IVYIVRESWI MGQVVCDIWL SVDITCCTCS ILHLSAIALD
121 RYRAITDAVE YARKRTPKHA GIMITIVWII SVFISMPPLF WRHQGTSRDD ECIIKHDHIV
181 STIYSTFGAF YIPLALILIL YYKIYRAAKT LYHKRQASRI AKEEVNGQVL LESGEKSTKS
241 VSTSYVLEKS LSDPSTDFDK IHSTVRSLRS EFKHEKSWRR QKISGTRERK AATTLGLILG
301 AFVICWLPFF VKELVVNVCD KCKISEEMSN FLAWLGYLNS LINPLIYTIF NEDFKKAFQK
361 LVRCRCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against HTR1F 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)
- 0.33
- Highest tissue expression
- 3.3 nTPM
Expression across tissuesHPA
Tissue
- retina: 3.3 nTPM
- placenta: 1.7 nTPM
- adipose tissue: 0.6 nTPM
- bone marrow: 0.6 nTPM
- spleen: 0.6 nTPM
- cerebral cortex: 0.5 nTPM
Single-cell type
- hematopoietic stem cells: 3,590 nCPM
- megakaryocyte-erythroid progenitors: 1,766 nCPM
- lactotrophs: 1,048 nCPM
- megakaryocyte progenitors: 693 nCPM
- thymocytes: 342 nCPM
- pericytes: 315 nCPM
Immune cell
- basophil: 0.7 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 6.5 nTPM
- white matter: 4.7 nTPM
- midbrain: 3.8 nTPM
- basal ganglia: 2.9 nTPM
- amygdala: 2.3 nTPM
- hippocampal formation: 1.9 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)
- 1.1
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.03
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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
Molecular functions
- G protein-coupled serotonin receptor activity
- Gi/o-coupled serotonin receptor activity
- neurotransmitter receptor activity
- serotonin binding
- serotonin receptor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads HTR1F as an antibody target. Whether an autoantibody or antibody against HTR1F could matter depends on whether native HTR1F is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
HTR1F is annotated at the cell surface, where native HTR1F 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 HTR1F as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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