0 sources retrieved · Most recent: April 2026 · Index updated 15 days ago
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2PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
plasma membraneolfactory receptor activityG protein-coupled receptor activitymembraneobesity due to melanocortin 4 receptor deficiencyCIDEC-related familial partial lipodystrophyBerardinelli-Seip congenital lipodystrophyFamilial partial lipodystrophy due to AKT2 mutations
AI summary not yet available. Showing NCBI Gene summary.
olfactory receptor family 4 subfamily M member 2B
⚠Limited data available — This gene has 0 indexed publications. Summary and analysis may be incomplete.
obesity due to melanocortin 4 receptor deficiencyOpen Targets
CIDEC-related familial partial lipodystrophyOpen Targets
Berardinelli-Seip congenital lipodystrophyOpen Targets
AKT2-related familial partial lipodystrophyOpen Targets
Familial partial lipodystrophy due to AKT2 mutationsOpen Targets
PPARG-related familial partial lipodystrophyOpen Targets
PLIN1-related familial partial lipodystrophyOpen Targets
congenital generalized lipodystrophy type 3Open Targets
Generalized congenital lipodystrophy with myopathyOpen Targets
LIPE-related familial partial lipodystrophyOpen Targets
morbid obesityOpen Targets
obesity due to CEP19 deficiencyOpen Targets
lipodystrophy, congenital generalized, type 5Open Targets
obesity due to prohormone convertase I deficiencyOpen Targets
obesity due to congenital leptin deficiencyOpen Targets
obesity due to leptin receptor gene deficiencyOpen Targets
galactokinase deficiencyOpen Targets
glycogen storage disease VIOpen Targets
hypoinsulinemic hypoglycemia and body hemihypertrophyOpen Targets
hyperinsulinism due to HNF1A deficiencyOpen Targets
No pathogenic variants reported on ClinVar for this gene.