OR1M1

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

Basic information

Region (hg38): 19:9087061-9095669

Links

ENSG00000170929NCBI:125963HGNC:8220Uniprot:Q8NGA1AlphaFoldGenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the OR1M1 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the OR1M1 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
clinvar
2
clinvar
26
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 0

Variants in OR1M1

This is a list of pathogenic ClinVar variants found in the OR1M1 region.

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

Position Type Phenotype Significance ClinVar
19-9093327-T-C not specified Uncertain significance (Jan 26, 2023)2479826
19-9093366-G-A not specified Uncertain significance (Aug 23, 2021)2256415
19-9093393-G-A not specified Uncertain significance (Oct 25, 2023)3204949
19-9093411-A-C not specified Uncertain significance (Oct 26, 2022)2278390
19-9093416-C-T not specified Uncertain significance (Dec 04, 2023)3204950
19-9093435-C-T not specified Uncertain significance (Mar 11, 2024)3204952
19-9093444-C-T not specified Uncertain significance (May 02, 2024)3302597
19-9093449-G-A not specified Uncertain significance (Jan 10, 2023)2463070
19-9093482-A-C not specified Uncertain significance (Aug 21, 2023)2619996
19-9093548-T-C not specified Uncertain significance (Aug 08, 2022)2395986
19-9093571-C-G not specified Uncertain significance (Mar 25, 2024)3302593
19-9093593-A-G not specified Likely benign (Aug 08, 2023)2616824
19-9093595-G-A not specified Uncertain significance (Oct 10, 2023)3204953
19-9093641-G-A not specified Likely benign (Jan 06, 2023)2474498
19-9093659-C-T not specified Uncertain significance (Nov 15, 2021)2384939
19-9093660-G-A not specified Uncertain significance (Mar 02, 2023)2470396
19-9093669-G-T not specified Uncertain significance (Jul 14, 2021)2236902
19-9093683-G-A not specified Uncertain significance (Dec 13, 2022)2359337
19-9093714-T-C not specified Uncertain significance (Feb 06, 2023)2472219
19-9093719-C-G not specified Uncertain significance (Nov 13, 2023)3204954
19-9093770-C-T not specified Uncertain significance (Sep 17, 2021)3204955
19-9093801-G-A not specified Uncertain significance (Dec 21, 2023)3204956
19-9093813-C-G not specified Uncertain significance (Feb 27, 2023)2489732
19-9093885-T-A not specified Uncertain significance (Jul 12, 2023)2611175
19-9093921-T-A not specified Uncertain significance (Apr 26, 2024)3302594

GnomAD

Source: gnomAD

GeneTypeBio TypeTranscript Coding Exons Length
OR1M1protein_codingprotein_codingENST00000429566 11035
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-1.042171781.220.00001012034
Missense in Polyphen9773.8551.3134878
Synonymous-0.7608677.51.110.00000500673
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)

Recessive Scores

pRec
0.0997

Intolerance Scores

loftool
0.834
rvis_EVS
0.71
rvis_percentile_EVS
85.68

Haploinsufficiency Scores

pHI
0.0858
hipred
N
hipred_score
0.170
ghis

Essentials

essential_gene_CRISPR
essential_gene_CRISPR2
N
essential_gene_gene_trap
N
gene_indispensability_pred
N
gene_indispensability_score
0.0622

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium

Mouse Genome Informatics

Gene name
Olfr24
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