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Protein / target

Growth/differentiation factor 15

Encoded byGDF15Q99988Homo sapiensSwiss-Prot
Antibody-tractable
Druggability
UniProt loc high conf
4
Research papers

Protein at a glance

Biological role

Protein homodimerization

Strongest disease association

Hyperemesis Gravidarum

Via encoding gene GDF15 · Genetic evidence · score 0.70

Research activity

Emerging research

4 papers · latest 2025

Derived from structured UniProt, Open Targets and literature data on this page.

Protein profile

UniProt 2026_02

Canonical identity and biological annotation from UniProt.

Function overview

Hormone produced in response to various stresses to confer information about those stresses to the brain, and trigger an aversive response, characterized by nausea, vomiting, and/or loss of appetite.

View complete UniProt function annotation

Hormone produced in response to various stresses to confer information about those stresses to the brain, and trigger an aversive response, characterized by nausea, vomiting, and/or loss of appetite (PubMed:23468844, PubMed:24971956, PubMed:28846097, PubMed:28846098, PubMed:28846099, PubMed:28953886, PubMed:29046435, PubMed:30639358, PubMed:31875646, PubMed:33589633, PubMed:38092039). The aversive response is both required to reduce continuing exposure to those stresses at the time of exposure and to promote avoidance behavior in the future (PubMed:30639358, PubMed:33589633, PubMed:38092039). Acts by binding to its receptor, GFRAL, activating GFRAL-expressing neurons localized in the area postrema and nucleus tractus solitarius of the brainstem (PubMed:28846097, PubMed:28846098, PubMed:28846099, PubMed:28953886, PubMed:31535977). It then triggers the activation of neurons localized within the parabrachial nucleus and central amygdala, which constitutes part of the 'emergency circuit' that shapes responses to stressful conditions (PubMed:28953886). The GDF15-GFRAL signal induces expression of genes involved in metabolism, such as lipid metabolism in adipose tissues (PubMed:31402172). Required for avoidance behavior in response to food allergens: induced downstream of mast cell activation to promote aversion and minimize harmful effects of exposure to noxious substances (By similarity). In addition to suppress appetite, also promotes weight loss by enhancing energy expenditure in muscle: acts by increasing calcium futile cycling in muscle (By similarity). Contributes to the effect of metformin, an anti-diabetic drug, on appetite reduction and weight loss: produced in the kidney in response to metformin treatment, thereby activating the GDF15-GFRAL response, leading to reduced appetite and weight (PubMed:31875646, PubMed:37060902). The contribution of GDF15 to weight loss following metformin treatment is however limited and subject to discussion (PubMed:36001956). Produced in response to anticancer drugs, such as camptothecin or cisplatin, promoting nausea, vomiting and contributing to malnutrition (By similarity). Overproduced in many cancers, promoting anorexia in cancer (cachexia) (PubMed:32661391). Responsible for the risk of nausea and vomiting during pregnancy: high levels of GDF15 during pregnancy, mostly originating from the fetus, are associated with increased nausea and vomiting (PubMed:38092039). Maternal sensitivity to nausea is probably determined by pre-pregnancy exposure to GDF15, women with naturally high level of GDF15 being less susceptible to nausea than women with low levels of GDF15 before pregnancy (PubMed:38092039). Promotes metabolic adaptation in response to systemic inflammation caused by bacterial and viral infections in order to promote tissue tolerance and prevent tissue damage (PubMed:31402172). Required for tissue tolerance in response to myocardial infarction by acting as an inhibitor of leukocyte integring activation, thereby protecting against cardiac rupture (By similarity). Inhibits growth hormone signaling on hepatocytes (By similarity)

Subcellular location

Secreted
Domains and Gene Ontology detail (27)

Gene Ontology

  • Ccytoplasm
  • Cextracellular exosome
  • Cextracellular region
  • Cextracellular space
  • CGolgi apparatus
  • Cnucleus
  • Fcytokine activity
  • Fgrowth factor activity
  • Fhormone activity
  • Fprotein homodimerization activity
  • Pcell surface receptor protein serine/threonine kinase signaling pathway
  • Pcell-cell signaling

308 aa · 34 kDa

Biological roles

What this protein does, drawn together from its UniProt function, Gene Ontology terms and Reactome pathways.

Oncogenic signallingUniProtLipid & lipoprotein metabolismGOImmune signallingUniProt · GOKinase signallingGO
View supporting evidence

Oncogenic signalling

  • ·Hormone produced in response to various stresses to confer information about those stres…

Lipid & lipoprotein metabolism

  • ·positive regulation of fatty acid oxidation

Immune signalling

  • ·Hormone produced in response to various stresses to confer information about those stres…
  • ·cytokine activity

Kinase signalling

  • ·cell surface receptor protein serine/threonine kinase signaling pathway
  • ·positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction

Concepts derived from UniProt GO Reactome — each badge above shows which sources supported that role.

Translational evidence

Open Targets 26

Why this target matters therapeutically, strongest evidence first. Disease associations are gene-level (via the gene that encodes this protein) and open into the full confidence synthesis; the development universe, tractability and safety annotations are target-level, from Open Targets.

Strongest disease associations · via encoding gene GDF15

Gene-level evidence surfaced through the gene GDF15that encodes this protein — not a direct protein–disease relationship. Ranked by Forefront's causal-directness weighting, so genetically- and clinically-evidenced diseases lead over ones that merely share the literature.

Hyperemesis Gravidarum
0.71Moderately supported

Genetic evidence dominant · Open Targets 0.58

Coffee consumption
0.68Moderately supported

Genetic evidence dominant · Open Targets 0.41

Obesity disorder
0.30Limited support

Literature evidence dominant · Open Targets 0.13

Obesity due to melanocortin 4 receptor deficiency
0.26Preliminary

Literature evidence dominant · Open Targets 0.13 · no direct causal or clinical evidence

Central Nervous System Neoplasms
0.21Preliminary

Literature evidence dominant · Open Targets 0.12 · no direct causal or clinical evidence

View evidence synthesis (5)
Hyperemesis GravidarumModerately supported
0.71
agreement 0.570.85
Genetic97%Literature3%Genetic literaturedup

Open Targets aggregate 0.58 · 2 independent evidence families · 1 not counted as duplicate

Coffee consumptionModerately supported
0.68
agreement 0.560.80
Genetic100%

Open Targets aggregate 0.41 · 1 independent evidence family

Obesity disorderLimited support
0.30
agreement 0.180.42
Literature43%Animal model33%Genetic24%

Open Targets aggregate 0.13 · 3 independent evidence families

Obesity due to melanocortin 4 receptor deficiencyPreliminary
0.26
agreement 0.080.44
Literature51%Animal model49%

Open Targets aggregate 0.13 · 2 independent evidence families · no direct causal or clinical evidence

Central Nervous System NeoplasmsPreliminary
0.21
agreement 0.020.40
Literature62%RNA expression38%

Open Targets aggregate 0.12 · 2 independent evidence families · no direct causal or clinical evidence

The evidence agreement range shows how closely the independent evidence families agree — it is not a statistical confidence interval, and nothing here is fitted to outcome data. Derived from Open Targets evidence types under Forefront weighting; the per-type scores above show the calculation.

Show all associations
Hyperemesis Gravidarum0.58
Coffee consumption0.41
Obesity disorder0.13
Obesity due to melanocortin 4 receptor deficiency0.13
Central Nervous System Neoplasms0.12
Neoplasms0.12
Glioblastoma0.12

Tractability

AntibodiesEmerging

Feasibility evidence (uniprot loc high conf and go cc high conf) — no clinical-stage drug of this modality recorded.

Protein degradersEmerging

Feasibility evidence (database ubiquitination and half-life data) — no clinical-stage drug of this modality recorded.

View underlying tractability evidence (5)
AB · UniProt loc high confAB · GO CC high confAB · UniProt SigP or TMHMMPR · Database UbiquitinationPR · Half-life Data

Raw Open Targets tractability assessment buckets, by modality.

Research activity

4 papers · to 2025

Papers linked directly to this protein. This is the protein's own literature — descriptor-derived papers are kept separate below.

Most cited

Recent

Europe PMC papers linked directly to this protein.