Seroatlas · Human Serome Atlas

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  LVRCRC

LocalizationUniProt · 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

Molecular functions

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.

Canonical record: https://seroatlas.com/gene/HTR1F. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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