SSR2: Somatostatin Receptor 2

A key G protein-coupled receptor mediating somatostatin signaling in neuroendocrine regulation and oncology

Gene Information Card

Symbol SSR2
Full Name Somatostatin Receptor 2
Gene Type protein-coding
Chromosomal Location 17q25.1
NCBI Gene ID 6752 ncbi.nlm.nih.gov/gene/6752
Ensembl ID ENSG00000180616
UniProt ID P30874
OMIM ID 182452
HGNC ID 11332
Aliases SSTR2, SRIF-1

Description

SSR2 (somatostatin receptor 2) is a gene encoding a G protein-coupled receptor for somatostatin, a peptide hormone that inhibits the release of growth hormone, insulin, glucagon, and other hormones. SSR2 is widely expressed in neuroendocrine tissues and is a primary target for somatostatin analogs used in the treatment of neuroendocrine tumors and acromegaly. The receptor mediates inhibitory effects on cell proliferation and hormone secretion through Gi/o protein signaling pathways.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Neuroendocrine tumors (NETs) SSR2 overexpression enables targeted imaging and therapy with somatostatin analogs; loss of expression correlates with aggressive disease PMID: 25670034
Acromegaly Somatostatin analogs act via SSR2 to suppress growth hormone secretion from pituitary adenomas PMID: 23543651
Carcinoid syndrome SSR2-mediated inhibition of serotonin release reduces symptoms PMID: 27492150
Gastroenteropancreatic neuroendocrine tumors (GEP-NETs) SSR2 expression is a biomarker for peptide receptor radionuclide therapy (PRRT) PMID: 29156164

Expression Profile

Tissue Expression
Tissue nTPM level
Pancreas 12.5 Medium
Pituitary gland 8.3 Medium
Adrenal gland 6.1 Low
Small intestine 4.7 Low
Brain (cerebral cortex) 3.2 Low
Stomach 2.8 Low
Liver 0.5 Not detected
Cell Line Expression
Cell Line nTPM Notes
BON-1 (carcinoid) 15.2 High expression
QGP-1 (pancreatic NET) 11.8 High expression
NCI-H727 (lung carcinoid) 9.4 Medium expression
HEK293 0.3 Not detected
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.784G>A (p.Gly262Arg) Missense <0.01% Reduced ligand binding affinity
c.1013C>T (p.Thr338Met) Missense <0.01% Altered receptor internalization
c.1246_1248del (p.Lys416del) In-frame deletion <0.01% Loss of function in signaling
Mutation functional classification

Loss of Function (LOF)

Mutations impairing ligand binding or G protein coupling reduce somatostatin-mediated inhibition of hormone secretion and cell proliferation.

Gain of Function (GOF)

Not reported in SSR2; gain-of-function mutations are rare in this receptor family.

Dominant Negative (DN)

No dominant-negative variants have been characterized for SSR2.

Pathways

Somatostatin receptor signaling (Reactome: R-HSA-418594)
GPCR downstream signaling (Reactome: R-HSA-388396)
Class A/1 (Rhodopsin-like) receptors (Reactome: R-HSA-373076)

Protein Summary

Somatostatin receptor 2 (SSR2) is a 369-amino acid integral membrane protein with seven transmembrane domains, belonging to the rhodopsin-like GPCR family. It binds somatostatin-14 and somatostatin-28 with high affinity, leading to activation of Gi/o proteins, inhibition of adenylyl cyclase, reduction of cAMP levels, and modulation of ion channels. SSR2 is the primary mediator of somatostatin's antisecretory and antiproliferative effects in neuroendocrine tissues. Clinically, it is exploited for imaging (e.g., 68Ga-DOTATATE PET) and therapy (e.g., 177Lu-DOTATATE PRRT) of somatostatin receptor-positive tumors.

Related Products

Product name Cat.No. Species Gene ID
SSR2 Knockout HEK293 Cell Line EDJ-KQ5846 Human 6746 Details Get a Quote
SSR2 Knockout A-549 Cell Line EDJ-KQ29306 Human 6746 Details Get a Quote
SSR2 Knockout HCT 116 Cell Line EDJ-KQ29307 Human 6746 Details Get a Quote
SSR2 Knockout HeLa Cell Line EDJ-KQ29308 Human 6746 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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