ERFE
Erythroferrone
Also known as: C1QTNF15, CTRP15, ERFE_HUMAN, FAM132B, FLJ37034
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q4G0M1
- Gene
- ERFE
- Ensembl
- ENSG00000178752
- Chromosome
- 2
- Canonical length
- 354 aa
- Protein class
- Predicted intracellular proteins, Predicted secreted proteins
- Secretome location
- Secreted to blood
- Quaternary structure
- Homodimer
OverviewNCBI Gene
Enables molecular sequestering activity. Involved in negative regulation of BMP signaling pathway. Predicted to be located in extracellular region. Predicted to be active in extracellular space. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
354 residues, UniProt reviewed canonical sequence.
>Q4G0M1|ERFE
1 MAPARRPAGA RLLLVYAGLL AAAAAGLGSP EPGAPSRSRA RREPPPGNEL PRGPGESRAG
61 PAARPPEPTA ERAHSVDPRD AWMLFVRQSD KGVNGKKRSR GKAKKLKFGL PGPPGPPGPQ
121 GPPGPIIPPE ALLKEFQLLL KGAVRQRERA EPEPCTCGPA GPVAASLAPV SATAGEDDDD
181 VVGDVLALLA APLAPGPRAP RVEAAFLCRL RRDALVERRA LHELGVYYLP DAEGAFRRGP
241 GLNLTSGQYR APVAGFYALA ATLHVALGEP PRRGPPRPRD HLRLLICIQS RCQRNASLEA
301 IMGLESSSEL FTISVNGVLY LQMGQWTSVF LDNASGCSLT VRSGSHFSAV LLGVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ERFE 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.52
- Highest tissue expression
- 23 nTPM
Expression across tissuesHPA
Tissue
- thyroid gland: 23 nTPM
- skeletal muscle: 14 nTPM
- testis: 12 nTPM
- cerebellum: 9.2 nTPM
- kidney: 7 nTPM
- cerebral cortex: 4 nTPM
Single-cell type
- late primary spermatocytes: 68 nCPM
- early spermatids: 52 nCPM
- myosatellite cells: 26 nCPM
- late spermatids: 10 nCPM
- erythrocytes: 7 nCPM
- endometrial luminal cells: 4.8 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 5.8 nTPM
- basal ganglia: 4.5 nTPM
- cerebral cortex: 4.4 nTPM
- hippocampal formation: 3.2 nTPM
- amygdala: 2.4 nTPM
- thalamus: 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)
- 1.28
- gnomAD pLI
- 0
OntologyGO
Biological processes
- establishment of localization in cell
- fatty acid transport
- intracellular iron ion homeostasis
- negative regulation of apoptotic process
- negative regulation of autophagy
- negative regulation of BMP signaling pathway
- negative regulation of gluconeogenesis
- negative regulation of osteoblast differentiation
- negative regulation of osteoclast differentiation
- positive regulation of D-glucose import
- positive regulation of insulin receptor signaling pathway
- positive regulation of phosphatidylinositol 3-kinase/protein kinase B signal transduction
- regulation of fatty acid metabolic process
- positive regulation of fatty acid transport
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of ERFE in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ERFE as an antibody target. Whether an autoantibody or antibody against ERFE could matter depends on whether native ERFE is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ERFE is annotated as secreted, so native ERFE circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label ERFE as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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