OR10A4
Basic information
Region (hg38): 11:6876625-6877619
Previous symbols: [ "OR10A4P" ]
Links
Phenotypes
GenCC
Source:
ClinVar
This is a list of variants' phenotypes submitted to
Variants pathogenicity by type
Statistics on ClinVar variants can assist in determining whether a specific variant type in the OR10A4 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 | 14 | 16 | ||||
nonsense | 0 | |||||
start loss | 0 | |||||
frameshift | 0 | |||||
inframe indel | 0 | |||||
splice donor/acceptor (+/-2bp) | 0 | |||||
splice region | 0 | |||||
non coding | 0 | |||||
Total | 0 | 0 | 14 | 0 | 2 |
Variants in OR10A4
This is a list of pathogenic ClinVar variants found in the OR10A4 region.
You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.
Position | Type | Phenotype | Significance | ClinVar |
---|---|---|---|---|
11-6876685-T-C | not specified | Uncertain significance (Jun 17, 2024) | ||
11-6876759-G-A | not specified | Uncertain significance (Feb 07, 2023) | ||
11-6876958-T-C | not specified | Uncertain significance (Jan 10, 2022) | ||
11-6877119-A-G | not specified | Uncertain significance (Jun 05, 2023) | ||
11-6877181-C-G | not specified | Uncertain significance (Jan 23, 2024) | ||
11-6877204-T-C | not specified | Uncertain significance (Dec 17, 2023) | ||
11-6877272-C-G | not specified | Uncertain significance (Dec 27, 2023) | ||
11-6877273-T-A | not specified | Uncertain significance (Apr 23, 2024) | ||
11-6877283-C-A | not specified | Uncertain significance (Jan 30, 2024) | ||
11-6877325-C-G | not specified | Uncertain significance (Nov 01, 2022) | ||
11-6877383-C-T | Benign (Jun 01, 2018) | |||
11-6877395-T-C | not specified | Uncertain significance (Jan 09, 2024) | ||
11-6877473-T-C | not specified | Uncertain significance (Mar 28, 2024) | ||
11-6877513-T-G | not specified | Uncertain significance (Jan 23, 2023) | ||
11-6877522-G-C | not specified | Uncertain significance (Mar 30, 2024) | ||
11-6877540-T-C | not specified | Uncertain significance (Feb 28, 2023) | ||
11-6877545-G-C | not specified | Uncertain significance (Jul 05, 2022) | ||
11-6877558-G-A | Benign (Apr 04, 2018) | |||
11-6877573-C-A | not specified | Uncertain significance (Jul 30, 2023) | ||
11-6877590-C-G | not specified | Uncertain significance (Jan 04, 2022) |
GnomAD
Source:
Gene | Type | Bio Type | Transcript | Coding Exons | Length |
---|---|---|---|---|---|
OR10A4 | protein_coding | protein_coding | ENST00000379829 | 1 | 995 |
pLI Probability LOF Intolerant | pRec Probability LOF Recessive | Individuals with no LOFs | Individuals with Homozygous LOFs | Individuals with Heterozygous LOFs | Defined | p |
---|---|---|---|---|---|---|
0.0000168 | 0.263 | 0 | 0 | 0 | 0 | 0.00 |
Z-Score | Observed | Expected | Observed/Expected | Mutation Rate | Total Possible in Transcript | |
---|---|---|---|---|---|---|
Missense | -1.19 | 206 | 163 | 1.26 | 0.00000791 | 2046 |
Missense in Polyphen | 59 | 47.082 | 1.2531 | 712 | ||
Synonymous | -0.568 | 74 | 68.0 | 1.09 | 0.00000345 | 679 |
Loss of Function | -0.149 | 7 | 6.59 | 1.06 | 3.65e-7 | 79 |
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:
- Function
- FUNCTION: Odorant receptor (Potential). May be involved in taste perception. {ECO:0000305}.;
- Pathway
- Olfactory transduction - Homo sapiens (human);Olfactory receptor activity;GPCRs, Class A Rhodopsin-like;Signaling by GPCR;Signal Transduction;Olfactory Signaling Pathway;G alpha (s) signalling events;GPCR downstream signalling
(Consensus)
Recessive Scores
- pRec
- 0.169
Intolerance Scores
- loftool
- 0.751
- rvis_EVS
- 2.02
- rvis_percentile_EVS
- 97.71
Haploinsufficiency Scores
- pHI
- 0.315
- 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
- 0.0820
Gene Damage Prediction
All | Recessive | Dominant | |
---|---|---|---|
Mendelian | High | Medium | High |
Primary Immunodeficiency | High | High | High |
Cancer | High | High | High |
Mouse Genome Informatics
- Gene name
- Olfr17
- Phenotype
- respiratory system phenotype; nervous system phenotype (the observable morphological and physiological characteristics of the extensive, intricate network of electochemical structures in the body that is comprised of the brain, spinal cord, nerves, ganglia and parts of the receptor organs that are manifested through development and lifespan); growth/size/body region phenotype; taste/olfaction phenotype; craniofacial phenotype; cellular phenotype;
Gene ontology
- Biological process
- G protein-coupled receptor signaling pathway;axon guidance;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