OR7G1

olfactory receptor family 7 subfamily G member 1, the group of Olfactory receptors, family 7

Basic information

Region (hg38): 19:9114828-9115763

Previous symbols: [ "OR7G1P" ]

Links

ENSG00000161807NCBI:125962HGNC:8465Uniprot:Q8NGA0AlphaFoldGenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the OR7G1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the OR7G1 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
clinvar
1
clinvar
19
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 1 0

Variants in OR7G1

This is a list of pathogenic ClinVar variants found in the OR7G1 region.

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

Position Type Phenotype Significance ClinVar
19-9114872-T-G not specified Uncertain significance (Dec 13, 2023)3206669
19-9114919-G-C not specified Uncertain significance (Jan 10, 2023)2455158
19-9114926-C-T not specified Uncertain significance (Dec 17, 2021)2267776
19-9114935-T-A not specified Uncertain significance (Feb 21, 2024)3206668
19-9114935-T-C not specified Uncertain significance (Jun 13, 2024)3303401
19-9114955-A-G not specified Uncertain significance (Dec 18, 2023)3206667
19-9114958-C-T not specified Uncertain significance (Jun 22, 2023)2595775
19-9114974-C-G not specified Uncertain significance (May 05, 2023)2544218
19-9114998-A-G not specified Likely benign (Sep 23, 2023)3206666
19-9115001-C-G not specified Uncertain significance (May 08, 2023)2545178
19-9115032-G-C not specified Uncertain significance (Jun 13, 2024)3303400
19-9115075-G-A not specified Uncertain significance (Sep 25, 2023)3206665
19-9115091-C-A not specified Uncertain significance (Mar 28, 2024)3303398
19-9115120-A-T not specified Uncertain significance (Apr 12, 2024)3303399
19-9115138-A-T not specified Uncertain significance (Dec 07, 2021)2266016
19-9115307-T-G not specified Uncertain significance (May 17, 2023)2547766
19-9115351-A-T not specified Uncertain significance (Dec 28, 2023)3206664
19-9115388-T-C not specified Uncertain significance (Dec 02, 2022)2332310
19-9115571-T-C not specified Uncertain significance (May 17, 2023)2518025
19-9115589-T-A not specified Uncertain significance (Aug 02, 2021)2240780
19-9115606-G-A not specified Uncertain significance (Aug 10, 2021)2242611
19-9115660-T-C not specified Uncertain significance (Jul 05, 2023)2598120
19-9115677-G-T not specified Uncertain significance (Mar 14, 2023)2457799

GnomAD

Source: gnomAD

GeneTypeBio TypeTranscript Coding Exons Length
OR7G1protein_codingprotein_codingENST00000541538 11166
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-0.4451781621.100.000007562037
Missense in Polyphen6052.2391.1486708
Synonymous-0.7127163.81.110.00000316650
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
0.675
rvis_EVS
1.64
rvis_percentile_EVS
96.11

Haploinsufficiency Scores

pHI
0.0674
hipred
N
hipred_score
0.112
ghis

Essentials

essential_gene_CRISPR
essential_gene_CRISPR2
essential_gene_gene_trap
gene_indispensability_pred
N
gene_indispensability_score
0.0399

Gene Damage Prediction

AllRecessiveDominant
MendelianHighHighHigh
Primary ImmunodeficiencyHighHighHigh
CancerHighHighHigh

Mouse Genome Informatics

Gene name
Olfr854
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