OR5H15

olfactory receptor family 5 subfamily H member 15, the group of Olfactory receptors, family 5

Basic information

Region (hg38): 3:98166696-98169774

Links

ENSG00000233412NCBI:403274HGNC:31287Uniprot:A6NDH6AlphaFoldGenCCjaxSfariGnomADPubmedClinVar

Phenotypes

GenCC

Source: genCC

No genCC data.

ClinVar

This is a list of variants' phenotypes submitted to ClinVar and linked to the OR5H15 gene.

Variants pathogenicity by type

Statistics on ClinVar variants can assist in determining whether a specific variant type in the OR5H15 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
22
clinvar
4
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 22 4 0

Variants in OR5H15

This is a list of pathogenic ClinVar variants found in the OR5H15 region.

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

Position Type Phenotype Significance ClinVar
3-98168716-C-A not specified Uncertain significance (Sep 27, 2022)2313909
3-98168781-T-C not specified Uncertain significance (May 29, 2024)3206230
3-98168797-T-C not specified Uncertain significance (Oct 03, 2022)2315876
3-98168814-A-G not specified Uncertain significance (Jun 10, 2024)3303203
3-98168908-A-G not specified Uncertain significance (Jun 07, 2023)2559188
3-98168934-C-T not specified Uncertain significance (Dec 28, 2023)3206222
3-98168985-G-C not specified Uncertain significance (Jul 19, 2023)2590638
3-98169013-C-T not specified Uncertain significance (Sep 27, 2022)2405380
3-98169019-G-C not specified Uncertain significance (Jul 13, 2021)2236743
3-98169034-G-A not specified Uncertain significance (Jul 11, 2023)2610316
3-98169063-C-T not specified Uncertain significance (Feb 11, 2022)2277091
3-98169109-C-T not specified Uncertain significance (Dec 28, 2022)2209779
3-98169156-A-C not specified Likely benign (Feb 09, 2023)2465004
3-98169179-A-T not specified Uncertain significance (Sep 25, 2023)3206223
3-98169207-A-G not specified Uncertain significance (Jan 03, 2024)3206224
3-98169220-T-C not specified Uncertain significance (Jan 30, 2024)3206225
3-98169288-C-G not specified Uncertain significance (Dec 14, 2023)3206226
3-98169297-T-C Likely benign (Feb 01, 2023)2653998
3-98169348-T-C not specified Uncertain significance (Jan 22, 2024)3206227
3-98169357-T-C not specified Likely benign (Dec 30, 2023)3206228
3-98169388-C-G not specified Uncertain significance (Jun 17, 2024)3303204
3-98169399-G-A not specified Likely benign (Sep 20, 2023)3206229
3-98169439-C-G not specified Uncertain significance (Jun 06, 2023)2520105
3-98169473-G-A not specified Uncertain significance (Jan 06, 2023)2465763
3-98169597-T-G not specified Uncertain significance (Apr 19, 2023)2526313

GnomAD

Source: gnomAD

GeneTypeBio TypeTranscript Coding Exons Length
OR5H15protein_codingprotein_codingENST00000356526 1942
pLI Probability
LOF Intolerant
pRec Probability
LOF Recessive
Individuals with
no LOFs
Individuals with
Homozygous LOFs
Individuals with
Heterozygous LOFs
Defined p
0.000008680.10000000.00
Z-Score Observed Expected Observed/Expected Mutation Rate Total Possible in Transcript
Missense-1.712201591.380.000007122013
Missense in Polyphen4035.4651.1279501
Synonymous-2.858456.71.480.00000252615
Loss of Function-1.6162.992.011.26e-741

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);Olfactory receptor activity (Consensus)

Intolerance Scores

loftool
0.964
rvis_EVS
1.98
rvis_percentile_EVS
97.61

Haploinsufficiency Scores

pHI
0.110
hipred
N
hipred_score
0.112
ghis

Essentials

essential_gene_CRISPR
essential_gene_CRISPR2
essential_gene_gene_trap
N
gene_indispensability_pred
N
gene_indispensability_score
0.00972

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium

Mouse Genome Informatics

Gene name
Olfr183
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