LRFN3
Leucine-rich repeat and fibronectin type-III domain-containing protein 3
Also known as: FIGLER1, LRFN3_HUMAN, MGC2656, SALM4
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9BTN0
- Gene
- LRFN3
- Ensembl
- ENSG00000126243
- Chromosome
- 19
- Canonical length
- 628 aa
- Protein class
- Predicted membrane proteins
OverviewNCBI Gene
Predicted to be involved in regulation of presynapse assembly; regulation of synaptic membrane adhesion; and synaptic membrane adhesion. Predicted to be located in plasma membrane. Predicted to be active in cell surface; glutamatergic synapse; and synaptic membrane. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
628 residues, UniProt reviewed canonical sequence.
>Q9BTN0|LRFN3
1 MAILPLLLCL LPLAPASSPP QSATPSPCPR RCRCQTQSLP LSVLCPGAGL LFVPPSLDRR
61 AAELRLADNF IASVRRRDLA NMTGLLHLSL SRNTIRHVAA GAFADLRALR ALHLDGNRLT
121 SLGEGQLRGL VNLRHLILSN NQLAALAAGA LDDCAETLED LDLSYNNLEQ LPWEALGRLG
181 NVNTLGLDHN LLASVPAGAF SRLHKLARLD MTSNRLTTIP PDPLFSRLPL LARPRGSPAS
241 ALVLAFGGNP LHCNCELVWL RRLAREDDLE ACASPPALGG RYFWAVGEEE FVCEPPVVTH
301 RSPPLAVPAG RPAALRCRAV GDPEPRVRWV SPQGRLLGNS SRARAFPNGT LELLVTEPGD
361 GGIFTCIAAN AAGEATAAVE LTVGPPPPPQ LANSTSCDPP RDGDPDALTP PSAASASAKV
421 ADTGPPTDRG VQVTEHGATA ALVQWPDQRP IPGIRMYQIQ YNSSADDILV YRMIPAESRS
481 FLLTDLASGR TYDLCVLAVY EDSATGLTAT RPVGCARFST EPALRPCGAP HAPFLGGTMI
541 IALGGVIVAS VLVFIFVLLM RYKVHGGQPP GKAKIPAPVS SVCSQTNGAL GPTPTPAPPA
601 PEPAALRAHT VVQLDCEPWG PGHEPVGPLocalizationUniProt · AlphaFold · HPA
Whether an antibody against LRFN3 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
- 1
- Mean surface accessibility (rSASA)
- 0.4
- Highest tissue expression
- 9.4 nTPM
Expression across tissuesHPA
Tissue
- pituitary gland: 9.4 nTPM
- cerebral cortex: 9 nTPM
- ovary: 8.5 nTPM
- blood vessel: 8.2 nTPM
- endometrium: 7.9 nTPM
- cervix: 6.9 nTPM
Single-cell type
- hepatic stellate cells: 19 nCPM
- pancreatic islet cells: 10 nCPM
- alveolar cells type 1: 8.5 nCPM
- prostatic club cells: 8.2 nCPM
- foveolar cells: 8 nCPM
- salivary duct cells: 7.8 nCPM
Immune cell
- gdT-cell: 0.5 nTPM
- MAIT T-cell: 0.5 nTPM
- memory CD8 T-cell: 0.5 nTPM
- memory CD4 T-cell: 0.4 nTPM
- naive CD4 T-cell: 0.3 nTPM
- T-reg: 0.3 nTPM
Brain region
- cerebral cortex: 25 nTPM
- cerebellum: 22 nTPM
- hippocampal formation: 21 nTPM
- amygdala: 21 nTPM
- basal ganglia: 18 nTPM
- thalamus: 18 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)
- 0.27
- gnomAD pLI
- 0.97
- gnomAD missense Z
- 2.24
- DepMap mean gene effect
- -0.05
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 7% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Cysteine-rich flanking region, C-terminal
- Leucine-rich repeat
- Leucine-rich repeat, typical subtype
- Immunoglobulin subtype 2
- Immunoglobulin domain subtype
- Fibronectin type III
- Immunoglobulin-like domain
- Immunoglobulin I-set
- Immunoglobulin-like fold
- Leucine-rich repeat domain superfamily
- Fibronectin type III superfamily
- Immunoglobulin-like domain superfamily
- Leucine-rich repeat and fibronectin type-III domain-containing
- Fibronectin type III domain
- Immunoglobulin I-set domain
- Leucine rich repeat
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads LRFN3 as an antibody target. Whether an autoantibody or antibody against LRFN3 could matter depends on whether native LRFN3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
LRFN3 is annotated at the cell surface, where native LRFN3 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 LRFN3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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