OR56A1
Basic information
Region (hg38): 11:6019336-6034338
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 OR56A1 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 | 16 | 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 | 16 | 2 | 0 |
Variants in OR56A1
This is a list of pathogenic ClinVar variants found in the OR56A1 region.
You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.
Position | Type | Phenotype | Significance | ClinVar |
---|---|---|---|---|
11-6026784-T-G | not specified | Uncertain significance (Nov 27, 2023) | ||
11-6026804-C-G | not specified | Uncertain significance (Aug 13, 2021) | ||
11-6026809-T-G | not specified | Uncertain significance (Apr 05, 2023) | ||
11-6026986-G-A | not specified | Uncertain significance (Oct 27, 2022) | ||
11-6027005-T-C | not specified | Uncertain significance (Mar 07, 2024) | ||
11-6027095-T-G | not specified | Likely benign (Sep 26, 2023) | ||
11-6027097-C-T | not specified | Uncertain significance (Aug 02, 2021) | ||
11-6027142-T-G | not specified | Uncertain significance (Jan 19, 2024) | ||
11-6027178-C-T | not specified | Uncertain significance (Apr 07, 2022) | ||
11-6027233-G-A | not specified | Uncertain significance (Jun 11, 2024) | ||
11-6027260-C-A | not specified | Uncertain significance (Jan 24, 2023) | ||
11-6027343-G-A | not specified | Uncertain significance (Jan 10, 2022) | ||
11-6027386-G-T | not specified | Uncertain significance (Apr 13, 2023) | ||
11-6027389-G-A | not specified | Likely benign (Dec 14, 2022) | ||
11-6027449-G-A | not specified | Uncertain significance (Oct 22, 2021) | ||
11-6027455-C-T | not specified | Uncertain significance (Jun 11, 2024) | ||
11-6027472-A-G | not specified | Uncertain significance (Sep 16, 2021) | ||
11-6027506-A-C | not specified | Uncertain significance (Apr 07, 2022) | ||
11-6027553-G-T | not specified | Uncertain significance (Jan 08, 2024) | ||
11-6027626-A-G | not specified | Uncertain significance (Mar 29, 2023) | ||
11-6027668-T-C | not specified | Uncertain significance (Jun 11, 2024) |
GnomAD
Source:
Gene | Type | Bio Type | Transcript | Coding Exons | Length |
---|---|---|---|---|---|
OR56A1 | protein_coding | protein_coding | ENST00000316650 | 1 | 1071 |
pLI Probability LOF Intolerant | pRec Probability LOF Recessive | Individuals with no LOFs | Individuals with Homozygous LOFs | Individuals with Heterozygous LOFs | Defined | p |
---|---|---|---|---|---|---|
0.000560 | 0.484 | 0 | 0 | 0 | 0 | 0.00 |
Z-Score | Observed | Expected | Observed/Expected | Mutation Rate | Total Possible in Transcript | |
---|---|---|---|---|---|---|
Missense | -0.327 | 187 | 175 | 1.07 | 0.00000885 | 2072 |
Missense in Polyphen | 47 | 56.943 | 0.82539 | 752 | ||
Synonymous | -1.05 | 87 | 75.4 | 1.15 | 0.00000403 | 680 |
Loss of Function | 0.204 | 5 | 5.52 | 0.906 | 2.33e-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)
Recessive Scores
- pRec
- 0.0882
Intolerance Scores
- loftool
- 0.510
- rvis_EVS
- -0.69
- rvis_percentile_EVS
- 15.12
Haploinsufficiency Scores
- pHI
- 0.127
- hipred
- N
- hipred_score
- 0.146
- ghis
- 0.435
Essentials
- essential_gene_CRISPR
- essential_gene_CRISPR2
- N
- essential_gene_gene_trap
- N
- gene_indispensability_pred
- N
- gene_indispensability_score
- 0.00641
Gene Damage Prediction
All | Recessive | Dominant | |
---|---|---|---|
Mendelian | Medium | Medium | Medium |
Primary Immunodeficiency | Medium | Medium | Medium |
Cancer | Medium | Medium | Medium |
Gene ontology
- Biological process
- synaptic transmission, dopaminergic;adenylate cyclase-modulating G protein-coupled receptor signaling pathway;adenylate cyclase-inhibiting dopamine receptor signaling pathway;regulation of dopamine secretion;response to drug;behavioral response to cocaine;detection of chemical stimulus involved in sensory perception of smell;adenylate cyclase-activating adrenergic receptor signaling pathway
- Cellular component
- plasma membrane;integral component of plasma membrane
- Molecular function
- dopamine neurotransmitter receptor activity, coupled via Gi/Go;adrenergic receptor activity;olfactory receptor activity;dopamine binding