OR2M2

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

Basic information

Region (hg38): 1:248174821-248181067

Links

ENSG00000198601 ∙ NCBI:391194 ∙ ∙ HGNC:8268 ∙ Uniprot:Q96R28 ∙ AlphaFold ∙ GenCC ∙ jax ∙ Sfari ∙ GnomAD ∙ Pubmed ∙ ClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the OR2M2 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the OR2M2 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			24	2	3	29
nonsense						0
start loss						0
frameshift						0
inframe indel						0
splice donor/acceptor (+/-2bp)						0
splice region						0
non coding						0
Total	0	0	24	2	3

Variants in OR2M2

This is a list of pathogenic ClinVar variants found in the OR2M2 region.

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

Position	Type	Phenotype	Significance	ClinVar
1-248180057-C-A		not specified	Uncertain significance (Feb 26, 2024)
1-248180059-C-T		not specified	Uncertain significance (Oct 10, 2023)
1-248180087-C-CT		EBV-positive nodal T- and NK-cell lymphoma	Likely benign (-)
1-248180094-G-T		not specified	Uncertain significance (Sep 27, 2021)
1-248180185-C-G		not specified	Uncertain significance (Jul 14, 2021)
1-248180245-C-G			Benign (Jun 07, 2017)
1-248180298-A-G		not specified	Likely benign (Aug 16, 2022)
1-248180331-G-A		not specified	Uncertain significance (May 17, 2023)
1-248180415-A-C		not specified	Uncertain significance (Jun 13, 2023)
1-248180503-A-C		not specified	Uncertain significance (Jun 02, 2023)
1-248180508-G-T		not specified	Uncertain significance (Jun 07, 2023)
1-248180512-A-G		not specified	Uncertain significance (Aug 28, 2023)
1-248180525-A-C		not specified	Likely benign (Jun 11, 2021)
1-248180551-G-A		not specified	Uncertain significance (Dec 05, 2022)
1-248180553-A-G		not specified	Uncertain significance (Dec 21, 2023)
1-248180595-A-G		not specified	Uncertain significance (Dec 27, 2023)
1-248180603-G-T		not specified	Uncertain significance (Dec 06, 2021)
1-248180686-G-A		not specified	Uncertain significance (Apr 04, 2024)
1-248180688-T-C			Benign (Oct 13, 2017)
1-248180689-G-A			Benign (Aug 03, 2017)
1-248180707-G-C		not specified	Uncertain significance (Sep 17, 2021)
1-248180718-C-T		not specified	Uncertain significance (Dec 08, 2023)
1-248180730-G-A		not specified	Uncertain significance (Oct 12, 2022)
1-248180790-A-G		not specified	Uncertain significance (Dec 21, 2023)
1-248180791-C-G		not specified	Uncertain significance (May 15, 2024)

GnomAD

Source: gnomAD

Gene	Type	Bio Type	Transcript	Coding Exons	Length
OR2M2	protein_coding	protein_coding	ENST00000359682	1	1044

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	-1.35	233	182	1.28	0.00000943	2285
Missense in Polyphen		49	40.565	1.2079		636
Synonymous	-0.520	72	66.6	1.08	0.00000332	701
Loss of Function

LoF frequencies by population

Ethnicity	Sum of pLOFs	p
African & African-American	0.00	0.00
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: 0.873
• rvis_EVS: 1.13
• rvis_percentile_EVS: 92.26

Haploinsufficiency Scores

• pHI: 0.0811
• hipred: N
• hipred_score: 0.112

Essentials

• essential_gene_gene_trap: N
• gene_indispensability_pred: N
• gene_indispensability_score: 0.114

Gene Damage Prediction

	All	Recessive	Dominant
Mendelian	Medium	Medium	Medium
Primary Immunodeficiency	Medium	Medium	Medium
Cancer	Medium	Medium	Medium

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