SFRP2
Secreted frizzled-related protein 2
Also known as: FRP-2, SARP1, SDF-5, SFRP2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96HF1
- Gene
- SFRP2
- Ensembl
- ENSG00000145423
- Chromosome
- 4
- Canonical length
- 295 aa
- Protein class
- Predicted secreted proteins
- Subcellular location
- Intermediate filaments
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
This gene encodes a member of the SFRP family that contains a cysteine-rich domain homologous to the putative Wnt-binding site of Frizzled proteins. SFRPs act as soluble modulators of Wnt signaling. Methylation of this gene is a potential marker for the presence of colorectal cancer. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
295 residues, UniProt reviewed canonical sequence.
>Q96HF1|SFRP2
1 MLQGPGSLLL LFLASHCCLG SARGLFLFGQ PDFSYKRSNC KPIPANLQLC HGIEYQNMRL
61 PNLLGHETMK EVLEQAGAWI PLVMKQCHPD TKKFLCSLFA PVCLDDLDET IQPCHSLCVQ
121 VKDRCAPVMS AFGFPWPDML ECDRFPQDND LCIPLASSDH LLPATEEAPK VCEACKNKND
181 DDNDIMETLC KNDFALKIKV KEITYINRDT KIILETKSKT IYKLNGVSER DLKKSVLWLK
241 DSLQCTCEEM NDINAPYLVM GQKQGGELVI TSVKRWQKGQ REFKRISRSI RKLQCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SFRP2 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)
- 0.35
- Highest tissue expression
- 342 nTPM
Expression across tissuesHPA
Tissue
- blood vessel: 342 nTPM
- gallbladder: 299 nTPM
- urinary bladder: 287 nTPM
- esophagus: 200 nTPM
- adipose tissue: 176 nTPM
- breast: 145 nTPM
Single-cell type
- fibroblasts: 702 nCPM
- pituicytes/fscs: 61 nCPM
- pituitary stem cells: 60 nCPM
- fibro-adipogenic progenitors: 25 nCPM
- decidual stromal cells: 19 nCPM
- mucous neck cells: 16 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
- hypothalamus: 31 nTPM
- hippocampal formation: 28 nTPM
- white matter: 28 nTPM
- choroid plexus: 27 nTPM
- amygdala: 12 nTPM
- pons: 12 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)
- 1.06
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.31
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- none
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
- BMP signaling pathway
- branching involved in blood vessel morphogenesis
- canonical Wnt signaling pathway
- cardiac left ventricle morphogenesis
- cardiac muscle cell apoptotic process
- cell-cell signaling
- cellular response to X-ray
- chondrocyte development
- collagen fibril organization
- convergent extension involved in axis elongation
- digestive tract morphogenesis
- embryonic digit morphogenesis
- hematopoietic stem cell proliferation
- male gonad development
- mesodermal cell fate specification
- negative regulation of BMP signaling pathway
- negative regulation of canonical Wnt signaling pathway
- negative regulation of cardiac muscle cell apoptotic process
- negative regulation of cell growth
- negative regulation of cell migration
- negative regulation of cell population proliferation
- negative regulation of DNA-templated transcription
- negative regulation of epithelial cell proliferation
- negative regulation of epithelial to mesenchymal transition
- negative regulation of extrinsic apoptotic signaling pathway via death domain receptors
- negative regulation of gene expression
- negative regulation of intrinsic apoptotic signaling pathway in response to DNA damage
- negative regulation of mesodermal cell fate specification
- negative regulation of peptidyl-tyrosine phosphorylation
- negative regulation of Wnt signaling pathway
- neural tube closure
- non-canonical Wnt signaling pathway
- outflow tract morphogenesis
- positive regulation of angiogenesis
- positive regulation of apoptotic process
- positive regulation of canonical Wnt signaling pathway
- positive regulation of cell adhesion mediated by integrin
- positive regulation of cell growth
- positive regulation of cell population proliferation
- positive regulation of fat cell differentiation
- positive regulation of osteoblast differentiation
- positive regulation of transcription by RNA polymerase II
- post-anal tail morphogenesis
- regulation of establishment of planar polarity
- regulation of midbrain dopaminergic neuron differentiation
- regulation of neuron projection development
- regulation of stem cell division
- response to nutrient
- response to xenobiotic stimulus
- sclerotome development
- stem cell fate specification
- Wnt signaling pathway involved in somitogenesis
- negative regulation of dermatome development
Molecular functions
- endopeptidase activator activity
- fibronectin binding
- integrin binding
- receptor ligand activity
- Wnt-protein binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SFRP2 as an antibody target. Whether an autoantibody or antibody against SFRP2 could matter depends on whether native SFRP2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SFRP2 is annotated as secreted, so native SFRP2 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 SFRP2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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