OR10R2

protein-coding

olfactory receptor family 10 subfamily R member 2, the group of Olfactory receptors, family 10

Gene summary

Olfactory receptors interact with odorant molecules in the nose, to initiate a neuronal response that triggers the perception of a smell. The olfactory receptor proteins are members of a large family of G-protein-coupled receptors (GPCR) arising from single coding-exon genes. Olfactory receptors share a 7-transmembrane domain structure with many neurotransmitter and hormone receptors and are responsible for the recognition and G protein-mediated transduction of odorant signals. The olfactory receptor gene family is the largest in the genome. [provided by RefSeq, Jul 2008]

MANE transcript

NM_001395749.1

Inheritance

—

ClinVar variants

U:37B:1

Top phenotype

—

gnomAD constraint

pLI —, LoF o/e 1.07

Max pathogenic AF

—

Genomic locus

chr1:158,472,220-158,480,936

External References & Databases

Transcript & Mutation Effects

hg38 • Region Span ~8.7 kb
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GenCC Phenotypes & Disease Associations

Curated gene-disease validity assertions and inheritance patterns

No GenCC data available for this gene.

ClinVar Associated Diseases & Phenotypes

Reported disease conditions connected to OR10R2 variants in ClinVar

2 Conditions Cataloged
not specifiedTotal: 40
not providedTotal: 1

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript NM_001395749.1. Only rare variants are included.

We include only reliable ClinVar variants with their consequences to MANE Select, MANE Plus Clinical transcripts, or transcripts with TSL equal to 1. Click a count to filter the variants table below.

Slight differences between displayed counts and ClinVar may occur due to a different transcript/consequence chosen by our variant effect predictor, or because we classify Benign/Likely benign as Likely benign and Pathogenic/Likely pathogenic as Likely pathogenic.

EffectPLPVUSLBBSum
synonymous
0
missense
36
clinvar
1
clinvar
37
nonsense
0
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
1
clinvar
1
Total00371038
Loading ClinVar variants...

Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 4 of 4 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_001395749.1RefSeqNP_001382678.12MANE Select
ENST00000641067.1EnsemblENSP00000493160.12MANE Select
NM_001004472.1RefSeqNP_001004472.11Standard
ENST00000641400.1EnsemblENSP00000493033.11Standard

Gene Ontology (GO) Annotations & Pathways

Biological processes, molecular functions, cellular components and pathways

Pathways ConsensusPathDB

  • Olfactory transduction - Homo sapiens (human)
  • Olfactory receptor activity
  • Signaling by GPCR
  • Signal Transduction
  • Olfactory Signaling Pathway

Biological Process

  • G protein-coupled receptor signaling pathway
  • detection of chemical stimulus involved in sensory perception of smell

Molecular Function

  • G protein-coupled receptor activity
  • olfactory receptor activity

Cellular Component

  • plasma membrane
  • integral component of membrane

gnomAD Constraint

Source: gnomAD

Gene type
protein_coding
Transcript type
protein_coding
Transcript
ENST00000368152
Coding exons
1
Length
1008
Individuals with no LoFs
0
Homozygous LoFs
0
Heterozygous LoFs
0
Defined
0
p
0.00
Z-ScoreObservedExpectedObserved/ExpectedMutation RateTotal Possible
Missense-0.6881951701.150.000007972179
Missense (PolyPhen)7455.2681.3389750
Synonymous-2.219369.61.340.00000365713
Loss of Function-0.14154.671.071.97e-775

Population LoF Frequency

PopulationCAFp-valueStatus
African00.0absent
Latino/Admixed American00.0absent
Ashkenazi Jewish00.0absent
East Asian00.0absent
Finnish00.0absent
European (Non-Finnish)00.0absent
South Asian00.0absent
Other00.0absent

dbNSFP Gene Annotations

Source: dbNSFP

Function
FUNCTION: Odorant receptor. {ECO:0000305}.;

Recessive Scores

pRec
0.0947

Intolerance Scores

LoFtool
0.516
RVIS EVS
1.84
RVIS percentile EVS
97.09

Essentials

Essential (CRISPR2)
N
Essential (gene trap)
N
Indispensability pred.
N
Indispensability score
0.112

Gene Damage Prediction

AllRecessiveDominant
MendelianHighHighHigh
Primary ImmunodeficiencyHighHighHigh
CancerHighHighHigh
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