OR7C2

protein-coding

olfactory receptor family 7 subfamily C member 2, the group of Olfactory receptors, family 7

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]

Previous symbols:
  • OR7C3

MANE transcript

NM_012377.1

Inheritance

—

ClinVar variants

U:42B:1

Top phenotype

—

gnomAD constraint

pLI —, LoF o/e 8.35

Max pathogenic AF

—

Genomic locus

chr19:14,941,489-14,942,448

External References & Databases

Transcript & Mutation Effects

hg38 • Region Span ~1.0 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 OR7C2 variants in ClinVar

2 Conditions Cataloged
not specifiedTotal: 42
not providedTotal: 1

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript NM_012377.1. 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
1
clinvar
1
missense
42
clinvar
42
nonsense
0
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
0
Total00421043
Loading ClinVar variants...

Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 2 of 2 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_012377.1RefSeqNP_036509.11MANE Select
ENST00000248072.3EnsemblENSP00000248072.31MANE Select

Gene Ontology (GO) Annotations & Pathways

Biological processes, molecular functions, cellular components and pathways

Pathways ConsensusPathDB

  • Olfactory transduction - Homo sapiens (human)
  • Olfactory receptor activity
  • GPCRs, Class A Rhodopsin-like
  • Signaling by GPCR
  • Signal Transduction

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
ENST00000248072
Coding exons
1
Length
960
Individuals with no LoFs
0
Homozygous LoFs
0
Heterozygous LoFs
0
Defined
0
p
0.00
Z-ScoreObservedExpectedObserved/ExpectedMutation RateTotal Possible
Missense-0.2931831721.060.000008722082
Missense (PolyPhen)5051.7040.96705699
Synonymous0.7156572.80.8930.00000392689
Loss of Function-2.3610.1208.355.19e-91

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
0.0970

Intolerance Scores

LoFtool
0.745
RVIS EVS
0.6
RVIS percentile EVS
82.74

Essentials

Essential (CRISPR2)
N
Essential (gene trap)
N
Indispensability pred.
N
Indispensability score
0.0552

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium
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