Gene Gene information from NCBI Gene database.
Entrez ID 6423
Gene name Secreted frizzled related protein 2
Gene symbol SFRP2
Synonyms (NCBI Gene)
FRP-2SARP1SDF-5
Chromosome 4
Chromosome location 4q31.3
Summary 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 p
miRNA miRNA information provided by mirtarbase database.
128
miRTarBase ID miRNA Experiments Reference
MIRT003607 hsa-miR-29a-3p Luciferase reporter assayqRT-PCRWestern blot 20551325
MIRT006749 hsa-miR-218-5p Luciferase reporter assay 21501592
MIRT006749 hsa-miR-218-5p Luciferase reporter assay 21501592
MIRT006749 hsa-miR-218-5p Luciferase reporter assay 21501592
MIRT006749 hsa-miR-218-5p Luciferase reporter assay 23060446
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
101
GO ID Ontology Definition Evidence Reference
GO:0001558 Process Regulation of cell growth IEA
GO:0001569 Process Branching involved in blood vessel morphogenesis IEA
GO:0001569 Process Branching involved in blood vessel morphogenesis ISS
GO:0001756 Process Somitogenesis IEA
GO:0001843 Process Neural tube closure IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
604157 10777 ENSG00000145423
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q96HF1
Protein name Secreted frizzled-related protein 2 (FRP-2) (sFRP-2) (Secreted apoptosis-related protein 1) (SARP-1)
Protein function Soluble frizzled-related proteins (sFRPS) function as modulators of Wnt signaling through direct interaction with Wnts. They have a role in regulating cell growth and differentiation in specific cell types. SFRP2 may be important for eye retinal
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01392 Fz 40 150 Fz domain Domain
PF01759 NTR 187 285 UNC-6/NTR/C345C module Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in adipose tissue, heart, brain, skeletal muscle, pancreas, thymus, prostate, testis, ovary, small intestine and colon. Highest levels in adipose tissue, small intestine and colon. {ECO:0000269|PubMed:9391078, ECO:0000269|Pub
Sequence
Sequence length 295
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Wnt signaling pathway  
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Anophthalmia-microphthalmia syndrome Conflicting classifications of pathogenicity rs770485715 RCV000207374
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
ACTH Secreting Pituitary Adenoma Inhibit 29620167
Adenocarcinoma Associate 19513747, 26482433
Adenocarcinoma Inhibit 37999144
Adenocarcinoma Mucinous Associate 20686305
Adenoma Inhibit 17131472
Adenoma Associate 17352030, 19700653, 21154739, 25432628, 25759530, 27896617, 28753106, 29620167, 30578081, 34477243
Alopecia Associate 35862273
Alzheimer Disease Associate 26482433
Astrocytoma Associate 32647207
Breast Neoplasms Associate 18283316, 18403594, 18990230, 19513569, 22026417