SFR1
Swi5-dependent recombination DNA repair protein 1 homolog
Also known as: bA373N18.1, C10orf78, FLJ41960, MEI5, MEIR5, SFR1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q86XK3
- Gene
- SFR1
- Ensembl
- ENSG00000156384
- Chromosome
- 10
- Canonical length
- 245 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Nucleoli rim,Centrosome
OverviewNCBI Gene
Enables transcription coactivator activity. Involved in cellular response to estrogen stimulus; double-strand break repair via homologous recombination; and positive regulation of DNA-templated transcription. Located in centrosome; nucleolus; and nucleoplasm. Part of Swi5-Sfr1 complex. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
245 residues, UniProt reviewed canonical sequence.
>Q86XK3|SFR1
1 MAEGEKNQDF TFKMESPSDS AVVLPSTPQA SANPSSPYTN SSRKQPMSAT LRERLRKTRF
61 SFNSSYNVVK RLKVESEEND QTFSEKPASS TEENCLEFQE SFKHIDSEFE ENTNLKNTLK
121 NLNVCESQSL DSGSCSALQN EFVSEKLPKQ RLNAEKAKLV KQVQEKEDLL RRLKLVKMYR
181 SKNDLSQLQL LIKKWRSCSQ LLLYELQSAV SEENKKLSLT QLIDHYGLDD KLLHYNRSEE
241 EFIDVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SFR1 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)
- 0.59
- Highest tissue expression
- 17 nTPM
Expression across tissuesHPA
Tissue
- testis: 17 nTPM
- thymus: 11 nTPM
- spinal cord: 10 nTPM
- bone marrow: 9.4 nTPM
- lymph node: 8.4 nTPM
- ovary: 8.2 nTPM
Single-cell type
- early primary spermatocytes: 252 nCPM
- differentiating spermatogonia: 56 nCPM
- late primary spermatocytes: 55 nCPM
- oocytes: 37 nCPM
- schwann cells: 25 nCPM
- monocyte progenitors: 25 nCPM
Immune cell
- basophil: 24 nTPM
- naive CD4 T-cell: 22 nTPM
- naive B-cell: 19 nTPM
- naive CD8 T-cell: 18 nTPM
- classical monocyte: 17 nTPM
- memory B-cell: 17 nTPM
Brain region
- white matter: 19 nTPM
- basal ganglia: 13 nTPM
- medulla oblongata: 13 nTPM
- thalamus: 11 nTPM
- cerebellum: 11 nTPM
- pons: 11 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)
- 1.81
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.42
- DepMap mean gene effect
- -0.11
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cellular response to estrogen stimulus
- double-strand break repair via homologous recombination
- positive regulation of DNA-templated transcription
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- SFR1/Mei5 family
- Swi5-dependent recombination DNA repair protein 1 homolog
- Double-strand recombination repair protein
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SFR1 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 SFR1 as an antibody target. Whether an autoantibody or antibody against SFR1 could matter depends on whether native SFR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SFR1 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 SFR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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