OR4M2B — olfactory receptor family 4 subfamily M member 2B

2 sources retrieved · Most recent: April 2026 · Index updated 5 months ago

2PubMed Papers

#19,265 · top 99% of 19K genes

20Diseases

top 90%

0Drugs

0Pathogenic Variants

ReceptorExperimental GO EvidenceSwiss-Prot Reviewed

plasma membraneolfactory receptor activityG protein-coupled receptor activitymembraneBerardinelli-Seip congenital lipodystrophyPLIN1-related familial partial lipodystrophyPPARG-related familial partial lipodystrophyCIDEC-related familial partial lipodystrophy

AI Summary

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.

Disease Associations20

Berardinelli-Seip congenital lipodystrophyOpen Targets

0.05Suggestive

PLIN1-related familial partial lipodystrophyOpen Targets

0.05Suggestive

PPARG-related familial partial lipodystrophyOpen Targets

0.05Suggestive

CIDEC-related familial partial lipodystrophyOpen Targets

0.05Suggestive

MODYOpen Targets

0.05Suggestive

hypoinsulinemic hypoglycemia and body hemihypertrophyOpen Targets

0.05Suggestive

lipodystrophy, congenital generalized, type 5Open Targets

0.05Suggestive

autosomal dominant hyperinsulinism due to SUR1 deficiencyOpen Targets

0.05Suggestive

Generalized congenital lipodystrophy with myopathyOpen Targets

0.05Suggestive

hyperinsulinism due to INSR deficiencyOpen Targets

0.05Suggestive

obesity due to melanocortin 4 receptor deficiencyOpen Targets

0.05Suggestive

autosomal dominant hyperinsulinism due to Kir6.2 deficiencyOpen Targets

0.05Suggestive

hyperinsulinism due to glucokinase deficiencyOpen Targets

0.05Suggestive

obesity due to prohormone convertase I deficiencyOpen Targets

0.05Suggestive

hyperinsulinism-hyperammonemia syndromeOpen Targets

0.04Suggestive

familial partial lipodystrophy, Kobberling typeOpen Targets

0.04Suggestive

Familial partial lipodystrophy, Köbberling typeOpen Targets

0.04Suggestive

hyperinsulinism due to HNF1A deficiencyOpen Targets

0.04Suggestive

AKT2-related familial partial lipodystrophyOpen Targets

0.04Suggestive

Familial partial lipodystrophy due to AKT2 mutationsOpen Targets

0.04Suggestive

Pathogenic Variants

No pathogenic variants reported on ClinVar for this gene.

Tissue Expression6 tissues

Lung

Ovary

Bone Marrow

Heart

Liver

Brain

Loading gene record…

2 sources retrieved · Most recent: April 2026 · Index updated 5 months ago

2PubMed Papers

#19,265 · top 99% of 19K genes

20Diseases

top 90%

0Drugs

0Pathogenic Variants

ReceptorExperimental GO EvidenceSwiss-Prot Reviewed

AI Summary

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.

Disease Associations20

Berardinelli-Seip congenital lipodystrophyOpen Targets

0.05Suggestive

PLIN1-related familial partial lipodystrophyOpen Targets

0.05Suggestive

PPARG-related familial partial lipodystrophyOpen Targets

0.05Suggestive

CIDEC-related familial partial lipodystrophyOpen Targets

0.05Suggestive

MODYOpen Targets

0.05Suggestive

hypoinsulinemic hypoglycemia and body hemihypertrophyOpen Targets

0.05Suggestive

lipodystrophy, congenital generalized, type 5Open Targets

0.05Suggestive

autosomal dominant hyperinsulinism due to SUR1 deficiencyOpen Targets

0.05Suggestive

Generalized congenital lipodystrophy with myopathyOpen Targets

0.05Suggestive

hyperinsulinism due to INSR deficiencyOpen Targets

0.05Suggestive

obesity due to melanocortin 4 receptor deficiencyOpen Targets

0.05Suggestive

autosomal dominant hyperinsulinism due to Kir6.2 deficiencyOpen Targets

0.05Suggestive

hyperinsulinism due to glucokinase deficiencyOpen Targets

0.05Suggestive

obesity due to prohormone convertase I deficiencyOpen Targets

0.05Suggestive

hyperinsulinism-hyperammonemia syndromeOpen Targets

0.04Suggestive

familial partial lipodystrophy, Kobberling typeOpen Targets

0.04Suggestive

Familial partial lipodystrophy, Köbberling typeOpen Targets

0.04Suggestive

hyperinsulinism due to HNF1A deficiencyOpen Targets

0.04Suggestive

AKT2-related familial partial lipodystrophyOpen Targets

0.04Suggestive

Familial partial lipodystrophy due to AKT2 mutationsOpen Targets

0.04Suggestive

Pathogenic Variants

No pathogenic variants reported on ClinVar for this gene.

Tissue Expression6 tissues

Lung

Ovary

Bone Marrow

Heart

Liver

Brain