2 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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10PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
plasma membranesignal transductionolfactory receptor activitysensory perception of chemical stimulusLynch syndromeLynch syndrome 2colorectal cancer, susceptibility to, 3colorectal cancer, hereditary nonpolyposis, type 6
OR1E2 encodes an olfactory receptor protein functioning as a G-protein coupled signaling receptor. Based on limited published evidence, OR1E2 is involved in odorant detection and sensory perception of chemical stimuli through plasma membrane-localized receptor activity. Molecular docking studies suggest OR1E2 binds aroma compounds including δ-decalactone and 2-acetylpyrrole with binding affinity ≤-5.0 kcal/mol 1, implicating its role in human aroma perception. OR1E2 peptides were detected in plasma proteomics studies 2, though functional significance in non-olfactory contexts remains unclear.
1
OR1E2 binds aroma compounds δ-decalactone and 2-acetylpyrrole with favorable binding affinity, suggesting a role in aroma perception
PMID: 404284862
OR1E2 peptides detected in plasma proteomics analysis comparing breast cancer to control samples
PMID: 31889940⚠Limited data available — This gene has 2 indexed publications. Summary and analysis may be incomplete.
Lynch syndromeOpen Targets
colorectal cancer, susceptibility to, 3Open Targets
Lynch syndrome 2Open Targets
colorectal cancer, hereditary nonpolyposis, type 6Open Targets
Meckel's diverticulumOpen Targets
Familial adenomatous polyposisOpen Targets
familial adenomatous polyposis 2Open Targets
AXIN2-related attenuated familial adenomatous polyposisOpen Targets
inflammatory bowel diseaseOpen Targets
hereditary mixed polyposis syndromeOpen Targets
inflammatory bowel disease 13Open Targets
inflammatory bowel disease 19Open Targets
Testicular regression syndromeOpen Targets
46,XX ovotesticular disorder of sex developmentOpen Targets
Congenital malabsorptive diarrhea due to paucity of enteroendocrine cellsOpen Targets
Genetic intractable diarrhea of infancyOpen Targets
Lynch syndrome 8Open Targets
IntussusceptionOpen Targets
chronic intestinal pseudoobstructionOpen Targets
inflammatory bowel disease 30Open Targets
No pathogenic variants reported on ClinVar for this gene.