OR51D1
Basic information
Region (hg38): 11:4637477-4643060
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 OR51D1 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 | 18 | ||||
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 | 0 | 0 |
Variants in OR51D1
This is a list of pathogenic ClinVar variants found in the OR51D1 region.
You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.
Position | Type | Phenotype | Significance | ClinVar |
---|---|---|---|---|
11-4639836-G-A | not specified | Uncertain significance (Apr 25, 2022) | ||
11-4639869-G-A | not specified | Uncertain significance (Aug 03, 2022) | ||
11-4639894-C-T | not specified | Uncertain significance (Jul 06, 2021) | ||
11-4639917-C-T | not specified | Uncertain significance (Jan 26, 2023) | ||
11-4639978-G-A | not specified | Uncertain significance (Oct 26, 2022) | ||
11-4639990-G-A | not specified | Uncertain significance (Oct 29, 2021) | ||
11-4640004-A-G | not specified | Uncertain significance (Mar 18, 2024) | ||
11-4640025-C-G | not specified | Uncertain significance (Jun 11, 2024) | ||
11-4640032-C-A | not specified | Uncertain significance (Dec 13, 2022) | ||
11-4640064-C-T | not specified | Uncertain significance (Dec 03, 2021) | ||
11-4640080-T-G | not specified | Uncertain significance (Jun 16, 2022) | ||
11-4640199-G-A | not specified | Uncertain significance (Nov 10, 2022) | ||
11-4640265-C-G | not specified | Uncertain significance (Mar 29, 2023) | ||
11-4640372-C-G | not specified | Uncertain significance (Sep 01, 2021) | ||
11-4640413-A-C | not specified | Uncertain significance (Oct 05, 2023) | ||
11-4640454-G-A | not specified | Uncertain significance (Dec 13, 2023) | ||
11-4640463-C-T | not specified | Uncertain significance (Feb 27, 2023) | ||
11-4640487-C-T | not specified | Uncertain significance (Sep 22, 2022) | ||
11-4640520-C-T | not specified | Uncertain significance (Apr 30, 2024) | ||
11-4640716-A-G | not specified | Uncertain significance (Feb 15, 2023) |
GnomAD
Source:
Gene | Type | Bio Type | Transcript | Coding Exons | Length |
---|---|---|---|---|---|
OR51D1 | protein_coding | protein_coding | ENST00000357605 | 1 | 1124 |
pLI Probability LOF Intolerant | pRec Probability LOF Recessive | Individuals with no LOFs | Individuals with Homozygous LOFs | Individuals with Heterozygous LOFs | Defined | p |
---|---|---|---|---|---|---|
0.00459 | 0.695 | 0 | 0 | 0 | 0 | 0.00 |
Z-Score | Observed | Expected | Observed/Expected | Mutation Rate | Total Possible in Transcript | |
---|---|---|---|---|---|---|
Missense | -1.19 | 215 | 171 | 1.26 | 0.00000856 | 2078 |
Missense in Polyphen | 72 | 60.459 | 1.1909 | 793 | ||
Synonymous | -1.35 | 86 | 71.5 | 1.20 | 0.00000353 | 727 |
Loss of Function | 0.681 | 4 | 5.76 | 0.694 | 3.35e-7 | 70 |
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. {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
- 0.810
- rvis_EVS
- 1.64
- rvis_percentile_EVS
- 96.13
Haploinsufficiency Scores
- pHI
- 0.254
- 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
- 0.0223
Gene Damage Prediction
All | Recessive | Dominant | |
---|---|---|---|
Mendelian | Medium | Medium | Medium |
Primary Immunodeficiency | Medium | Medium | Medium |
Cancer | Medium | Medium | Medium |
Mouse Genome Informatics
- Gene name
- Olfr557
- 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