OR10G8

olfactory receptor family 10 subfamily G member 8, the group of Olfactory receptors, family 10

Basic information

Region (hg38): 11:124026798-124030634

Links

ENSG00000234560 ∙ NCBI:219869 ∙ ∙ HGNC:14845 ∙ Uniprot:Q8NGN5 ∙ 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 OR10G8 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the OR10G8 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				2		2
missense			22	6		28
nonsense						0
start loss						0
frameshift						0
inframe indel						0
splice donor/acceptor (+/-2bp)						0
splice region						0
non coding						0
Total	0	0	22	8	0

Variants in OR10G8

This is a list of pathogenic ClinVar variants found in the OR10G8 region.

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

Position	Type	Phenotype	Significance	ClinVar
11-124029626-T-A		not specified	Likely benign (Jun 02, 2023)
11-124029632-G-A		not specified	Likely benign (Aug 17, 2022)
11-124029665-C-T		not specified	Uncertain significance (Aug 27, 2024)
11-124029681-C-G		not specified	Uncertain significance (Aug 03, 2022)
11-124029681-C-T		not specified	Uncertain significance (Dec 06, 2024)
11-124029684-T-C		not specified	Uncertain significance (May 30, 2024)
11-124029689-G-A		not specified	Likely benign (Nov 10, 2024)
11-124029690-C-T		not specified	Uncertain significance (Mar 16, 2022)
11-124029693-C-T		not specified	Uncertain significance (Sep 17, 2021)
11-124029694-C-A			Likely benign (Jun 01, 2023)
11-124029783-A-G		not specified	Uncertain significance (Feb 27, 2024)
11-124029792-T-C		not specified	Uncertain significance (Oct 12, 2022)
11-124029817-G-C			Likely benign (Jun 01, 2023)
11-124029849-T-C		not specified	Uncertain significance (Mar 30, 2024)
11-124029877-C-G		not specified	Uncertain significance (Apr 13, 2022)
11-124029894-T-C		not specified	Uncertain significance (Jul 16, 2024)
11-124029978-G-A		not specified	Likely benign (Jan 07, 2022)
11-124030005-C-G		not specified	Uncertain significance (Sep 20, 2023)
11-124030005-C-T		not specified	Uncertain significance (Apr 11, 2023)
11-124030006-G-A		not specified	Likely benign (Apr 08, 2024)
11-124030012-G-C		not specified	Uncertain significance (Aug 30, 2024)
11-124030021-C-A		not specified	Likely benign (Feb 21, 2024)
11-124030023-T-C		not specified	Uncertain significance (Sep 11, 2024)
11-124030035-G-A		not specified	Uncertain significance (May 01, 2022)
11-124030058-A-G		not specified	Likely benign (Apr 30, 2024)

GnomAD

Source: gnomAD

Gene	Type	Bio Type	Transcript	Coding Exons	Length
OR10G8	protein_coding	protein_coding	ENST00000431524	1	1045

pLI Probability LOF Intolerant	pRec Probability LOF Recessive	Individuals with no LOFs	Individuals with Homozygous LOFs	Individuals with Heterozygous LOFs	Defined	p
0.0169	0.728	0	0	0	0	0.00

	Z-Score	Observed	Expected	Observed/Expected	Mutation Rate	Total Possible in Transcript
Missense	-1.01	207	170	1.22	0.00000964	1995
Missense in Polyphen		69	57.437	1.2013		767
Synonymous	-1.26	89	75.1	1.19	0.00000475	676
Loss of Function	0.733	3	4.72	0.636	2.05e-7	66

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;Signaling by GPCR;Signal Transduction;Olfactory Signaling Pathway;G alpha (s) signalling events;GPCR downstream signalling (Consensus)

Recessive Scores

• pRec: 0.0830

Intolerance Scores

• loftool: 0.455
• rvis_EVS: 0.8
• rvis_percentile_EVS: 87.54

Haploinsufficiency Scores

• pHI: 0.0644
• hipred: N
• hipred_score: 0.158

Essentials

• essential_gene_CRISPR2: N
• essential_gene_gene_trap: N
• gene_indispensability_pred: N
• gene_indispensability_score: 0.0672

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