OR8G5

olfactory receptor family 8 subfamily G member 5, the group of Olfactory receptors, family 8

Basic information

Region (hg38): 11:124256376-124266224

Previous symbols: [ "OR8G5P", "OR8G6" ]

Links

ENSG00000255298NCBI:219865HGNC:19622Uniprot:Q8NG78AlphaFoldGenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the OR8G5 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the OR8G5 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
20
clinvar
1
clinvar
21
nonsense
0
start loss
0
frameshift
0
inframe indel
0
splice donor/acceptor (+/-2bp)
0
splice region
0
non coding
2
clinvar
2
Total 0 0 22 1 0

Variants in OR8G5

This is a list of pathogenic ClinVar variants found in the OR8G5 region.

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

Position Type Phenotype Significance ClinVar
11-124264855-T-C not specified Uncertain significance (Jun 21, 2023)2593538
11-124264867-A-G not specified Uncertain significance (Dec 20, 2023)3206748
11-124264939-C-T not specified Uncertain significance (Sep 27, 2024)3412246
11-124265035-A-G not specified Uncertain significance (Mar 31, 2024)3303429
11-124265040-G-A not specified Uncertain significance (Oct 12, 2021)2397278
11-124265071-C-T not specified Uncertain significance (Feb 08, 2023)2482346
11-124265091-C-A not specified Uncertain significance (Oct 20, 2021)2220734
11-124265100-A-G not specified Uncertain significance (Jul 19, 2023)2612563
11-124265166-C-G not specified Uncertain significance (Jan 19, 2024)3206747
11-124265167-C-G not specified Uncertain significance (Feb 23, 2023)2488471
11-124265226-A-T not specified Uncertain significance (Mar 26, 2024)3303428
11-124265240-C-A not specified Uncertain significance (Dec 14, 2024)3884367
11-124265281-C-A not specified Uncertain significance (Sep 26, 2024)3412245
11-124265295-G-A not specified Uncertain significance (Mar 27, 2023)2529979
11-124265301-G-A not specified Uncertain significance (Sep 06, 2022)2396296
11-124265370-G-A not specified Uncertain significance (Oct 16, 2023)3206749
11-124265409-A-G not specified Uncertain significance (Jan 16, 2024)3206750
11-124265471-T-A not specified Uncertain significance (Nov 24, 2024)3412244
11-124265497-G-C not specified Uncertain significance (Feb 03, 2025)3884369
11-124265511-A-G not specified Likely benign (Aug 21, 2023)2619935
11-124265584-A-G not specified Uncertain significance (Jan 27, 2022)2274507
11-124265595-A-G not specified Uncertain significance (Jan 19, 2024)3206751
11-124265677-C-T not specified Uncertain significance (Dec 27, 2023)3206752
11-124265704-T-A not specified Uncertain significance (Apr 01, 2024)3303427
11-124265742-G-A not specified Uncertain significance (Feb 08, 2025)3884368

GnomAD

Source: gnomAD

GeneTypeBio TypeTranscript Coding Exons Length
OR8G5protein_codingprotein_codingENST00000524943 11041
pLI Probability
LOF Intolerant
pRec Probability
LOF Recessive
Individuals with
no LOFs
Individuals with
Homozygous LOFs
Individuals with
Heterozygous LOFs
Defined p
0.01700.72900000.00
Z-Score Observed Expected Observed/Expected Mutation Rate Total Possible in Transcript
Missense-0.5411971771.110.000008852279
Missense in Polyphen5157.7790.88268838
Synonymous-2.119572.21.320.00000390699
Loss of Function0.73734.730.6342.02e-778

LoF frequencies by population

EthnicitySum of pLOFs p
African & African-American0.000.00
Ashkenazi Jewish0.000.00
East Asian0.000.00
Finnish0.000.00
European (Non-Finnish)0.000.00
Middle Eastern0.000.00
South Asian0.000.00
Other0.000.00

dbNSFP

Source: dbNSFP

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

Haploinsufficiency Scores

pHI
hipred
N
hipred_score
0.132
ghis

Gene Damage Prediction

AllRecessiveDominant
MendelianHighHighHigh
Primary ImmunodeficiencyHighHighHigh
CancerHighHighHigh

Mouse Genome Informatics

Gene name
Olfr935
Phenotype

Gene ontology

Biological process
G protein-coupled receptor signaling pathway;sensory perception of smell;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;odorant binding