OR2F2

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

Basic information

Region (hg38): 7:143935233-143936186

Links

ENSG00000221910 ∙ NCBI:135948 ∙ ∙ HGNC:8247 ∙ Uniprot:O95006 ∙ 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 OR2F2 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the OR2F2 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			18	3	1	22
nonsense						0
start loss						0
frameshift						0
inframe indel						0
splice donor/acceptor (+/-2bp)						0
splice region						0
non coding						0
Total	0	0	18	3	1

Variants in OR2F2

This is a list of pathogenic ClinVar variants found in the OR2F2 region.

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

Position	Type	Phenotype	Significance	ClinVar
7-143935283-A-C		not specified	Uncertain significance (Feb 10, 2022)
7-143935307-A-G		not specified	Uncertain significance (Jul 25, 2023)
7-143935359-T-G		not specified	Uncertain significance (Aug 02, 2023)
7-143935393-G-A		not specified	Uncertain significance (Jun 29, 2023)
7-143935409-G-A		not specified	Uncertain significance (Nov 11, 2024)
7-143935452-G-A		not specified	Uncertain significance (Jul 16, 2024)
7-143935503-G-T		not specified	Likely benign (Dec 02, 2024)
7-143935509-C-T		not specified	Uncertain significance (Apr 01, 2024)
7-143935572-C-T		not specified	Uncertain significance (Jul 16, 2024)
7-143935597-G-A		not specified	Uncertain significance (Nov 17, 2023)
7-143935630-C-T		not specified	Uncertain significance (Apr 22, 2022)
7-143935633-C-A		not specified	Uncertain significance (Jun 05, 2024)
7-143935660-G-A		not specified	Uncertain significance (Jun 29, 2023)
7-143935710-A-G		not specified	Uncertain significance (Feb 27, 2023)
7-143935744-A-G		not specified	Uncertain significance (Jan 26, 2022)
7-143935816-A-C		not specified	Uncertain significance (Oct 13, 2023)
7-143935816-A-G		not specified	Uncertain significance (Mar 14, 2023)
7-143935822-C-T		not specified	Likely benign (Sep 15, 2021)
7-143935824-G-A		not specified	Likely benign (Sep 15, 2021)
7-143935861-C-T		not specified	Uncertain significance (Apr 08, 2024)
7-143935864-T-C		not specified	Uncertain significance (Feb 03, 2022)
7-143935872-G-A		not specified	Uncertain significance (Apr 15, 2024)
7-143935891-G-A			Benign (Jul 13, 2018)
7-143935930-G-A		not specified	Uncertain significance (Jan 16, 2024)
7-143935989-G-A		not specified	Uncertain significance (Jun 11, 2021)

GnomAD

Source: gnomAD

Gene	Type	Bio Type	Transcript	Coding Exons	Length
OR2F2	protein_coding	protein_coding	ENST00000408955	1	1114

pLI Probability LOF Intolerant	pRec Probability LOF Recessive	Individuals with no LOFs	Individuals with Homozygous LOFs	Individuals with Heterozygous LOFs	Defined	p
0.0000293	0.347	0	0	0	0	0.00

	Z-Score	Observed	Expected	Observed/Expected	Mutation Rate	Total Possible in Transcript
Missense	-0.630	191	168	1.14	0.00000855	2043
Missense in Polyphen		40	48.442	0.82572		642
Synonymous	-0.769	82	73.6	1.11	0.00000393	696
Loss of Function	0.113	7	7.33	0.955	4.83e-7	75

LoF frequencies by population

Ethnicity	Sum of pLOFs	p
African & African-American	0.00	0.00
Ashkenazi Jewish	0.00	0.00
East Asian	0.00	0.00
Finnish	0.00	0.00
European (Non-Finnish)	0.00	0.00
Middle Eastern	0.00	0.00
South Asian	0.00	0.00
Other	0.00	0.00

dbNSFP

Source: dbNSFP

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

Intolerance Scores

• loftool: 0.579
• rvis_EVS: 0.62
• rvis_percentile_EVS: 83.36

Haploinsufficiency Scores

• hipred: N
• hipred_score: 0.112

Essentials

• essential_gene_CRISPR2: N
• essential_gene_gene_trap: N
• gene_indispensability_pred: N
• gene_indispensability_score: 0.164

Gene Damage Prediction

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

Mouse Genome Informatics

• Gene name: Olfr452

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