OR5AN1
Basic information
Region (hg38): 11:59358895-59371714
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 OR5AN1 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 | 15 | 15 | ||||
nonsense | 0 | |||||
start loss | 0 | |||||
frameshift | 0 | |||||
inframe indel | 0 | |||||
splice donor/acceptor (+/-2bp) | 0 | |||||
splice region | 0 | |||||
non coding | 0 | |||||
Total | 0 | 0 | 15 | 0 | 0 |
Variants in OR5AN1
This is a list of pathogenic ClinVar variants found in the OR5AN1 region.
You can filter this list by clicking the number of variants in the Variants pathogenicity by type table.
Position | Type | Phenotype | Significance | ClinVar |
---|---|---|---|---|
11-59364475-A-G | not specified | Uncertain significance (Nov 29, 2021) | ||
11-59364514-C-T | not specified | Uncertain significance (Mar 21, 2023) | ||
11-59364540-C-A | not specified | Uncertain significance (Jan 30, 2024) | ||
11-59364615-G-C | not specified | Uncertain significance (Jul 26, 2024) | ||
11-59364634-C-T | not specified | Uncertain significance (Nov 08, 2024) | ||
11-59364778-C-T | not specified | Uncertain significance (Oct 24, 2023) | ||
11-59364814-T-C | not specified | Uncertain significance (May 17, 2023) | ||
11-59364861-T-C | not specified | Uncertain significance (Jul 13, 2021) | ||
11-59364937-A-G | not specified | Uncertain significance (Sep 10, 2024) | ||
11-59364960-C-G | not specified | Uncertain significance (Aug 08, 2023) | ||
11-59365017-A-C | not specified | Uncertain significance (Feb 23, 2023) | ||
11-59365017-A-T | not specified | Uncertain significance (Dec 16, 2023) | ||
11-59365036-C-G | not specified | Uncertain significance (Jul 02, 2024) | ||
11-59365050-G-A | not specified | Uncertain significance (Jul 05, 2024) | ||
11-59365108-T-C | not specified | Uncertain significance (Aug 16, 2021) | ||
11-59365114-A-T | not specified | Uncertain significance (Jun 10, 2024) | ||
11-59365134-A-G | not specified | Uncertain significance (Oct 06, 2024) | ||
11-59365162-G-C | not specified | Uncertain significance (May 26, 2024) | ||
11-59365164-T-G | not specified | Uncertain significance (Aug 04, 2023) | ||
11-59365219-C-G | not specified | Uncertain significance (Nov 24, 2024) | ||
11-59365293-T-C | not specified | Uncertain significance (Nov 27, 2024) | ||
11-59365364-A-T | not specified | Uncertain significance (Aug 12, 2022) | ||
11-59365366-A-G | not specified | Uncertain significance (Jun 06, 2022) | ||
11-59365381-G-C | not specified | Uncertain significance (Feb 05, 2024) |
GnomAD
Source:
Gene | Type | Bio Type | Transcript | Coding Exons | Length |
---|---|---|---|---|---|
OR5AN1 | protein_coding | protein_coding | ENST00000313940 | 1 | 1037 |
pLI Probability LOF Intolerant | pRec Probability LOF Recessive | Individuals with no LOFs | Individuals with Homozygous LOFs | Individuals with Heterozygous LOFs | Defined | p |
---|---|---|---|---|---|---|
0.0000593 | 0.284 | 0 | 0 | 0 | 0 | 0.00 |
Z-Score | Observed | Expected | Observed/Expected | Mutation Rate | Total Possible in Transcript | |
---|---|---|---|---|---|---|
Missense | -1.23 | 205 | 161 | 1.27 | 0.00000715 | 2038 |
Missense in Polyphen | 48 | 43.566 | 1.1018 | 611 | ||
Synonymous | -1.03 | 69 | 59.0 | 1.17 | 0.00000262 | 625 |
Loss of Function | -0.261 | 6 | 5.35 | 1.12 | 2.22e-7 | 84 |
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 involved in the detection of muscone, cyclopentadecanone, cyclopentadecanol, and omega-pentadecalactone (PubMed:24361078, PubMed:25901328). The activity of this receptor is mediated by G proteins which activate adenylyl cyclase (Probable). {ECO:0000269|PubMed:24361078, ECO:0000269|PubMed:25901328, 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
- 0.0948
Intolerance Scores
- loftool
- 0.764
- rvis_EVS
- 0.4
- rvis_percentile_EVS
- 76.15
Haploinsufficiency Scores
- pHI
- 0.0927
- hipred
- N
- hipred_score
- 0.112
- ghis
Essentials
- essential_gene_CRISPR
- essential_gene_CRISPR2
- N
- essential_gene_gene_trap
- N
- gene_indispensability_pred
- N
- gene_indispensability_score
- 0.325
Gene Damage Prediction
All | Recessive | Dominant | |
---|---|---|---|
Mendelian | Medium | Medium | Medium |
Primary Immunodeficiency | Medium | Medium | Medium |
Cancer | Medium | Medium | Medium |
Mouse Genome Informatics
- Gene name
- Olfr262
- Phenotype
Gene ontology
- Biological process
- G protein-coupled receptor signaling pathway;sensory perception of smell;detection of chemical stimulus involved in sensory perception;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