SFRP2 (Secreted Frizzled Related Protein 2)

A Wnt signaling modulator involved in development, fibrosis, and cancer

Gene Information Card

Symbol SFRP2
Full Name Secreted Frizzled Related Protein 2
Gene Type Protein coding
Chromosomal Location 4q31.3
NCBI Gene ID 6423 ncbi.nlm.nih.gov/gene/6423
Ensembl ID ENSG00000145423
UniProt ID Q96HF1
OMIM ID 604156
HGNC ID 10777
Aliases FRP-2, SARP2, SDF-5

Description

SFRP2 encodes a member of the secreted frizzled-related protein (SFRP) family, which functions as a modulator of Wnt signaling. The protein contains a cysteine-rich domain homologous to the Wnt-binding site of frizzled receptors, allowing it to bind Wnt ligands and inhibit canonical and non-canonical Wnt pathways. SFRP2 plays roles in embryonic development, tissue homeostasis, and is implicated in fibrosis and tumorigenesis through epigenetic silencing or aberrant expression.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Colorectal cancer Promoter hypermethylation silences SFRP2, leading to constitutive Wnt activation and tumor progression ClinVar, COSMIC
Breast cancer Reduced SFRP2 expression correlates with poor prognosis; re-expression inhibits Wnt signaling and cell proliferation NCBI Gene, OMIM
Pulmonary fibrosis SFRP2 promotes fibroblast activation and extracellular matrix deposition via non-canonical Wnt signaling NCBI Gene, PubMed
Osteoarthritis SFRP2 dysregulation alters Wnt/β-catenin signaling in chondrocytes, contributing to cartilage degradation OMIM, PubMed

Expression Profile

Tissue Expression
Tissue nTPM level
Heart 12.3 Medium
Lung 8.7 Low
Liver 5.1 Low
Kidney 15.6 Medium
Breast 20.4 Medium
Colon 25.8 High
Prostate 18.2 Medium
Ovary 22.1 High
Cell Line Expression
Cell Line nTPM Notes
MCF7 (breast cancer) 45.2 High expression
HCT116 (colorectal cancer) 38.7 High expression
A549 (lung cancer) 12.1 Low expression
HEK293 (embryonic kidney) 30.5 Medium expression
HepG2 (liver cancer) 8.3 Low expression
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1A>G (p.Met1?) Missense <0.1% Loss of start codon; likely loss of function
c.202C>T (p.Arg68Trp) Missense <0.1% Unknown significance; reported in COSMIC
c.454G>A (p.Gly152Ser) Missense <0.1% Unknown significance; reported in COSMIC
Promoter hypermethylation Epigenetic Frequent in colorectal cancer Transcriptional silencing; loss of tumor suppressor function
Mutation functional classification

Loss of Function (LOF)

Promoter hypermethylation and rare missense variants (e.g., p.Met1?) reduce or abolish SFRP2 expression or function, leading to unchecked Wnt signaling.

Gain of Function (GOF)

No well-characterized gain-of-function mutations reported in SFRP2.

Dominant Negative (DN)

No evidence of dominant-negative mutations in SFRP2.

Pathways

Wnt signaling pathway (KEGG: hsa04310)
Regulation of Wnt-mediated beta-catenin signaling (Reactome: R-HSA-4641262)
Signaling by WNT (Reactome: R-HSA-195721)

Protein Summary

SFRP2 is a 295-amino-acid secreted protein containing a signal peptide and a cysteine-rich domain (CRD) that binds Wnt ligands. It acts as a decoy receptor, preventing Wnt from interacting with frizzled receptors and thereby inhibiting both canonical (β-catenin-dependent) and non-canonical Wnt signaling. The protein is involved in developmental processes, tissue remodeling, and is frequently epigenetically silenced in cancers, where its loss contributes to tumor progression. SFRP2 also promotes fibrosis in lung and kidney tissues through alternative Wnt pathways.

Related Products

Product name Cat.No. Species Gene ID
SFRP2 Knockout HEK293 Cell Line EDJ-KQ117 Human 6423 Details Get a Quote
SFRP2 Knockout HeLa Cell Line EDJ-KQ54447 Human 6423 Details Get a Quote
SFRP2 Knockout A-549 Cell Line EDJ-KQ62937 Human 6423 Details Get a Quote
SFRP2 Knockout HCT 116 Cell Line EDJ-KQ71407 Human 6423 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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