OR4K1

protein-coding

olfactory receptor family 4 subfamily K member 1, the group of Olfactory receptors, family 4

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_001004063.3

Inheritance

—

ClinVar variants

U:56B:2

Top phenotype

—

gnomAD constraint

pLI —, LoF o/e 1.61

Max pathogenic AF

—

Genomic locus

chr14:19,930,917-19,936,757

External References & Databases

Transcript & Mutation Effects

hg38 • Region Span ~5.8 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 OR4K1 variants in ClinVar

2 Conditions Cataloged
not specifiedTotal: 57
not providedTotal: 1

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript NM_001004063.3. 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
56
clinvar
1
clinvar
57
nonsense
0
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
0
Total00562058
Loading ClinVar variants...

Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 4 of 6 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_001004063.3RefSeqNP_001004063.21MANE Select
ENST00000641172.1EnsemblENSP00000493193.11MANE Select
ENST00000285600.4EnsemblENSP00000285600.31Standard
ENST00000641429.1EnsemblENSP00000493205.11Standard

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
ENST00000285600
Coding exons
1
Length
1076
Individuals with no LoFs
0
Homozygous LoFs
0
Heterozygous LoFs
0
Defined
0
p
0.00
Z-ScoreObservedExpectedObserved/ExpectedMutation RateTotal Possible
Missense-2.212351571.500.000007652005
Missense (PolyPhen)10257.4571.7752828
Synonymous-2.137857.51.360.00000288601
Loss of Function-1.3495.591.613.24e-778

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
0.0864

Intolerance Scores

LoFtool
0.841
RVIS EVS
1.38
RVIS percentile EVS
94.53

Essentials

Essential (CRISPR2)
N
Essential (gene trap)
N
Indispensability pred.
N
Indispensability score
0.0149

Gene Damage Prediction

AllRecessiveDominant
MendelianHighMediumHigh
Primary ImmunodeficiencyHighHighHigh
CancerHighHighHigh
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