OR2M3

olfactory receptor family 2 subfamily M member 3, the group of Olfactory receptors, family 2

Basic information

Region (hg38): 1:248197264-248212925

Previous symbols: [ "OR2M6", "OR2M3P" ]

Links

ENSG00000228198NCBI:127062HGNC:8269Uniprot:Q8NG83AlphaFoldGenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the OR2M3 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the OR2M3 gene is commonly pathogenic or not.

In the table, we include only reliable ClinVar variants with their consequences to MANE Select, Mane Plus Clinical transcripts, or transcripts with TSL equals 1. Click the count to view the source variants.

Warning: slight differences between displayed counts and the number of variants in ClinVar may occur, primarily due to (1) the application of a different transcript and/or consequence by our variant effect predictor or (2) differences in clinical significance: we classify Benign/Likely benign variants as Likely benign and Pathogenic/Likely pathogenic variants as Likely pathogenic.

Variant type Pathogenic Likely pathogenic VUS Likely benign Benign Sum
synonymous
0
missense
26
clinvar
4
clinvar
30
nonsense
0
start loss
0
frameshift
0
inframe indel
0
splice donor/acceptor (+/-2bp)
0
splice region
0
non coding
0
Total 0 0 26 4 0

Variants in OR2M3

This is a list of pathogenic ClinVar variants found in the OR2M3 region.

You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.

Position Type Phenotype Significance ClinVar
1-248203074-A-T not specified Likely benign (Feb 14, 2023)2458354
1-248203083-T-C not specified Uncertain significance (Feb 14, 2023)2458353
1-248203107-C-A not specified Uncertain significance (Jan 20, 2023)2465960
1-248203119-T-C not specified Uncertain significance (Jun 16, 2024)3302733
1-248203123-A-G not specified Uncertain significance (Dec 21, 2022)2241002
1-248203140-A-C not specified Uncertain significance (Oct 26, 2022)2217427
1-248203165-C-A not specified Uncertain significance (Mar 08, 2024)3205206
1-248203299-G-C not specified Uncertain significance (Jun 02, 2024)3302730
1-248203330-G-T not specified Uncertain significance (Apr 22, 2022)2239153
1-248203335-A-G not specified Uncertain significance (Sep 16, 2021)2249716
1-248203354-G-T not specified Uncertain significance (Sep 27, 2021)2362391
1-248203393-G-A not specified Uncertain significance (Dec 15, 2022)2335294
1-248203528-C-T not specified Uncertain significance (Mar 16, 2022)2391869
1-248203546-T-C not specified Uncertain significance (Mar 16, 2022)2278950
1-248203548-G-A not specified Uncertain significance (Dec 21, 2023)3205199
1-248203570-A-T not specified Uncertain significance (Jul 25, 2023)2613608
1-248203603-G-A not specified Uncertain significance (May 18, 2023)2548993
1-248203607-C-G not specified Uncertain significance (Jun 22, 2023)2605218
1-248203610-C-A not specified Uncertain significance (Jun 22, 2023)2605219
1-248203636-G-A not specified Likely benign (Aug 12, 2021)2243742
1-248203652-T-G not specified Uncertain significance (Jun 29, 2023)2607711
1-248203659-A-T not specified Uncertain significance (Oct 30, 2023)3205200
1-248203675-G-A not specified Uncertain significance (Jan 16, 2024)3205202
1-248203686-A-C not specified Likely benign (Jun 30, 2022)2299445
1-248203726-G-A not specified Uncertain significance (Dec 19, 2022)2336423

GnomAD

Source: gnomAD

GeneTypeBio TypeTranscript Coding Exons Length
OR2M3protein_codingprotein_codingENST00000456743 11061
pLI Probability
LOF Intolerant
pRec Probability
LOF Recessive
Individuals with
no LOFs
Individuals with
Homozygous LOFs
Individuals with
Heterozygous LOFs
Defined p
Z-Score Observed Expected Observed/Expected Mutation Rate Total Possible in Transcript
Missense-0.7341931661.160.000008832043
Missense in Polyphen2332.0530.71756514
Synonymous-1.057160.61.170.00000304645
Loss of Function

LoF frequencies by population

EthnicitySum of pLOFs p
African & African-American0.000.00
Ashkenazi Jewish
East Asian
Finnish
European (Non-Finnish)
Middle Eastern
South Asian
Other

dbNSFP

Source: dbNSFP

Function
FUNCTION: Odorant receptor. {ECO:0000305}.;
Pathway
Olfactory transduction - Homo sapiens (human);Olfactory receptor activity;Signaling by GPCR;Signal Transduction;Olfactory Signaling Pathway;G alpha (s) signalling events;GPCR downstream signalling (Consensus)

Intolerance Scores

loftool
0.769
rvis_EVS
1.49
rvis_percentile_EVS
95.35

Haploinsufficiency Scores

pHI
0.0931
hipred
N
hipred_score
0.112
ghis

Essentials

essential_gene_CRISPR
essential_gene_CRISPR2
essential_gene_gene_trap
N
gene_indispensability_pred
N
gene_indispensability_score
0.135

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium

Mouse Genome Informatics

Gene name
Olfr164
Phenotype

Gene ontology

Biological process
G protein-coupled receptor signaling pathway;detection of chemical stimulus involved in sensory perception of smell
Cellular component
plasma membrane;integral component of membrane
Molecular function
G protein-coupled receptor activity;olfactory receptor activity