OR51G2

protein-coding

olfactory receptor family 51 subfamily G member 2, the group of Olfactory receptors, family 51

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_001005238.2

Inheritance

—

ClinVar variants

U:56B:5

Top phenotype

—

gnomAD constraint

pLI —, LoF o/e 0.75

Max pathogenic AF

—

Genomic locus

chr11:4,912,588-4,919,350

External References & Databases

Transcript & Mutation Effects

hg38 • Region Span ~6.8 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 OR51G2 variants in ClinVar

1 Conditions Cataloged
not specifiedTotal: 61

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript NM_001005238.2. 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
56
clinvar
5
clinvar
61
nonsense
0
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
0
Total00565061
Loading ClinVar variants...

Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 2 of 2 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_001005238.2RefSeqNP_001005238.11MANE Select
ENST00000641926.1EnsemblENSP00000493323.11MANE Select

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
ENST00000322013
Coding exons
1
Length
1023
Individuals with no LoFs
0
Homozygous LoFs
0
Heterozygous LoFs
0
Defined
0
p
0.00
Z-ScoreObservedExpectedObserved/ExpectedMutation RateTotal Possible
Missense-1.102251831.230.000009822043
Missense (PolyPhen)7065.0521.0761799
Synonymous-0.4547671.11.070.00000379680
Loss of Function0.54645.360.7463.22e-767

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
0.0842

Intolerance Scores

LoFtool
0.613
RVIS EVS
0.37
RVIS percentile EVS
75.43

Essentials

Essential (CRISPR2)
N
Essential (gene trap)
N
Indispensability pred.
N
Indispensability score
0.114

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium
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