RFLNB
Refilin-B
Also known as: Cfm1, FAM101B, MGC45871, RefilinB, RFLB_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8N5W9
- Gene
- RFLNB
- Ensembl
- ENSG00000183688
- Chromosome
- 17
- Canonical length
- 214 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Actin filaments,Cytosol
OverviewNCBI Gene
Enables filamin binding activity. Predicted to be involved in several processes, including actin filament bundle organization; negative regulation of bone mineralization involved in bone maturation; and negative regulation of chondrocyte development. Predicted to act upstream of or within actin cytoskeleton organization and epithelial to mesenchymal transition. Predicted to be located in actin cytoskeleton and cytoplasm. Predicted to be active in actin filament bundle. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
214 residues, UniProt reviewed canonical sequence.
>Q8N5W9|RFLNB
1 MVGRLSLQDV PELVDAKKKG DGVLDSPDSG LPPSPSPSHW GLAAGGGGGE RAAAPGTLEP
61 DAAAATPAAP SPASLPLAPG CALRLCPLSF GEGVEFDPLP PKEVRYTSLV KYDSERHFID
121 DVQLPLGLAV ASCSQTVTCV PNGTWRNYKA EVRFEPRHRP TRFLSTTIVY PKYPKAVYTT
181 TLDYNCRKTL RRFLSSVELE AAELPGSDDL SDECLocalizationUniProt · AlphaFold · HPA
Whether an antibody against RFLNB 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.61
- Highest tissue expression
- 74 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 74 nTPM
- adipose tissue: 19 nTPM
- thymus: 16 nTPM
- breast: 15 nTPM
- colon: 13 nTPM
- heart muscle: 13 nTPM
Single-cell type
- choroid plexus epithelial cells: 18 nCPM
- podocytes: 11 nCPM
- neutrophil progenitors: 10 nCPM
- neutrophils: 5.5 nCPM
- ependymal cells: 5 nCPM
- megakaryocyte progenitors: 3.9 nCPM
Immune cell
- basophil: 202 nTPM
- eosinophil: 81 nTPM
- neutrophil: 36 nTPM
- naive CD4 T-cell: 9.7 nTPM
- plasmacytoid DC: 9.1 nTPM
- naive CD8 T-cell: 8.7 nTPM
Brain region
- choroid plexus: 21 nTPM
- hippocampal formation: 5.6 nTPM
- cerebral cortex: 4.7 nTPM
- spinal cord: 4.4 nTPM
- medulla oblongata: 4.2 nTPM
- basal ganglia: 4.1 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)
- 1.27
- gnomAD pLI
- 0.27
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
- actin filament bundle organization
- epithelial to mesenchymal transition
- negative regulation of bone mineralization involved in bone maturation
- negative regulation of chondrocyte development
- skeletal system morphogenesis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of RFLNB 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 RFLNB as an antibody target. Whether an autoantibody or antibody against RFLNB could matter depends on whether native RFLNB is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
RFLNB is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label RFLNB as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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