OR7E24

gene
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Also known as OR19-8HSHT2OR7E24Q

Summary

OR7E24 (olfactory receptor family 7 subfamily E member 24, HGNC:8396) is a protein-coding gene on chromosome 19p13.2, encoding Olfactory receptor 7E24 (Q6IFN5). Odorant receptor.

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.

Source: NCBI Gene 26648 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 63 total
  • MANE Select transcript: NM_001079935

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:8396
Approved symbolOR7E24
Nameolfactory receptor family 7 subfamily E member 24
Location19p13.2
Locus typegene with protein product
StatusApproved
AliasesOR19-8, HSHT2, OR7E24Q
Ensembl geneENSG00000237521
Ensembl biotypeprotein_coding
Entrez26648

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000456448, ENST00000641946

RefSeq mRNA: 2 — MANE Select: NM_001079935 NM_001079935, NM_001386108

CCDS: CCDS45955, CCDS92506

Canonical transcript exons

ENST00000456448 — 1 exons

ExonStartEnd
ENSE0000170165392509309252625

Expression profiles

Bgee: expression breadth broad, 16 present calls, max score 86.39.

Top tissues by expression

280 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
oocyteCL:000002386.39gold quality
secondary oocyteCL:000065585.41gold quality
frontal poleUBERON:000279565.12gold quality
middle frontal gyrusUBERON:000270264.80gold quality
paraflocculusUBERON:000535164.73gold quality
spermCL:000001963.79gold quality
male germ cellCL:000001562.83gold quality
endometrium epitheliumUBERON:000481161.13gold quality
cerebellar vermisUBERON:000472056.27gold quality
upper leg skinUBERON:000426256.17gold quality
pancreatic ductal cellCL:000207956.14silver quality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099154.38gold quality
cranial nerve IIUBERON:000094153.03gold quality
ileal mucosaUBERON:000033151.96silver quality
left testisUBERON:000453351.57gold quality
quadriceps femorisUBERON:000137751.29gold quality
right testisUBERON:000453451.25gold quality
Brodmann (1909) area 10UBERON:001354151.05gold quality
deltoidUBERON:000147651.01silver quality
epithelial cell of pancreasCL:000008350.53gold quality
testisUBERON:000047350.38gold quality
vastus lateralisUBERON:000137950.05gold quality
thymusUBERON:000237049.41gold quality
Brodmann (1909) area 46UBERON:000648349.30gold quality
blood vessel layerUBERON:000479749.29gold quality
metanephric glomerulusUBERON:000473649.21gold quality
cervix squamous epitheliumUBERON:000692249.20gold quality
hair follicleUBERON:000207349.18gold quality
olfactory bulbUBERON:000226448.92gold quality
choroid plexus epitheliumUBERON:000391148.89gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-ANND-3yes3.12

Regulation

Is transcription factor: no

Cross-species orthologs

14 orthologs

OrganismSymbolGene ID
mus_musculusOr7e174ENSMUSG00000044106
mus_musculusOr7e177ENSMUSG00000049028
mus_musculusOr7e173ENSMUSG00000050803
mus_musculusOr7e175ENSMUSG00000058491
mus_musculusOr7e176ENSMUSG00000066897
rattus_norvegicusENSRNOG00000066601
rattus_norvegicusOr7e176ENSRNOG00000070602
rattus_norvegicusOr7e174ENSRNOG00000071781
rattus_norvegicusOr7e173ENSRNOG00000071834
rattus_norvegicusENSRNOG00000074671
rattus_norvegicusOlr1177ENSRNOG00000079316
rattus_norvegicusOr7e173dENSRNOG00000080580
rattus_norvegicusENSRNOG00000089018
rattus_norvegicusOr7e176bENSRNOG00000090996

Paralogs (130): OR1I1 (ENSG00000094661), OR12D3 (ENSG00000112462), OR7A10 (ENSG00000127515), OR7C2 (ENSG00000127529), OR7C1 (ENSG00000127530), OR1E2 (ENSG00000127780), OR1J1 (ENSG00000136834), OR1L4 (ENSG00000136939), OR4D1 (ENSG00000141194), OR4K1 (ENSG00000155249), OR3A3 (ENSG00000159961), OR7G1 (ENSG00000161807), OR1Q1 (ENSG00000165202), OR1K1 (ENSG00000165204), OR4K2 (ENSG00000165762), OR4D6 (ENSG00000166884), OR1F1 (ENSG00000168124), OR4K14 (ENSG00000169484), OR4K15 (ENSG00000169488), OR7G3 (ENSG00000170920), OR7G2 (ENSG00000170923), OR1M1 (ENSG00000170929), OR4D5 (ENSG00000171014), OR1L6 (ENSG00000171459), OR1L3 (ENSG00000171481), OR1L8 (ENSG00000171496), OR1N2 (ENSG00000171501), OR1N1 (ENSG00000171505), OR2AT4 (ENSG00000171561), OR1A1 (ENSG00000172146), OR1A2 (ENSG00000172150), OR4C11 (ENSG00000172188), OR4X2 (ENSG00000172208), OR4D9 (ENSG00000172742), OR10K1 (ENSG00000173285), OR1L1 (ENSG00000173679), OR7D4 (ENSG00000174667), OR4S2 (ENSG00000174982), OR4B1 (ENSG00000175619), OR4D11 (ENSG00000176200)

Protein

Protein identifiers

Olfactory receptor 7E24Q6IFN5 (reviewed: Q6IFN5)

Alternative names: Olfactory receptor OR19-14

All UniProt accessions (2): A0A2R8Y4Q1, Q6IFN5

UniProt curated annotations — full annotation on UniProt →

Function. Odorant receptor.

Subcellular location. Cell membrane.

Similarity. Belongs to the G-protein coupled receptor 1 family.

RefSeq proteins (2): NP_001073404, NP_001373037 (=MANE)

Domains & families (InterPro)

IDNameType
IPR000276GPCR_RhodpsnFamily
IPR000725Olfact_rcptFamily
IPR017452GPCR_Rhodpsn_7TMDomain

Pfam: PF13853

UniProt features (20 total): topological domain 8, transmembrane region 7, sequence variant 2, chain 1, glycosylation site 1, disulfide bond 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q6IFN5-F184.780.57

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Disulfide bonds (1): 115–207

Glycosylation sites (1): 23

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-9752946Expression and translocation of olfactory receptors

MSigDB gene sets: 36 (showing top): GOBP_SENSORY_PERCEPTION_OF_CHEMICAL_STIMULUS, KEGG_OLFACTORY_TRANSDUCTION, GOBP_DETECTION_OF_STIMULUS, GOBP_SENSORY_PERCEPTION, ACEVEDO_METHYLATED_IN_LIVER_CANCER_DN, MARSON_BOUND_BY_FOXP3_UNSTIMULATED, chr19p13, GOMF_OLFACTORY_RECEPTOR_ACTIVITY, GOMF_TRANSMEMBRANE_SIGNALING_RECEPTOR_ACTIVITY, GOMF_G_PROTEIN_COUPLED_RECEPTOR_ACTIVITY, HUTTMANN_B_CLL_POOR_SURVIVAL_UP, GOBP_SENSORY_PERCEPTION_OF_SMELL, GOBP_G_PROTEIN_COUPLED_RECEPTOR_SIGNALING_PATHWAY, GOBP_DETECTION_OF_STIMULUS_INVOLVED_IN_SENSORY_PERCEPTION, RAO_BOUND_BY_SALL4_ISOFORM_B

GO Biological Process (4): signal transduction (GO:0007165), G protein-coupled receptor signaling pathway (GO:0007186), sensory perception of smell (GO:0007608), detection of chemical stimulus involved in sensory perception of smell (GO:0050911)

GO Molecular Function (2): G protein-coupled receptor activity (GO:0004930), olfactory receptor activity (GO:0004984)

GO Cellular Component (2): plasma membrane (GO:0005886), membrane (GO:0016020)

Reactome top-level categories

Rollup of top-1 pathways:

CategoryPathways
Olfactory Signaling Pathway1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
transmembrane signaling receptor activity2
cell communication1
cellular process1
signaling1
regulation of cellular process1
cellular response to stimulus1
G protein-coupled receptor activity1
signal transduction1
sensory perception of chemical stimulus1
sensory perception of smell1
detection of chemical stimulus involved in sensory perception1
G protein-coupled receptor signaling pathway1
detection of chemical stimulus involved in sensory perception of smell1
membrane1
cell periphery1
cellular anatomical structure1

Protein interactions and networks

STRING

212 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
OR7E24EXOC3L4Q17RC7562
OR7E24MYO15BQ96JP2499
OR7E24SPACA6W5XKT8480
OR7E24TMEM184CQ9NVA4460
OR7E24GPSM1Q86YR5407
OR7E24CCDC178Q5BJE1397
OR7E24LRTM3Q8NDH2392
OR7E24CNGA2Q16280331
OR7E24GNG8Q9UK08322
OR7E24ASTE1Q2TB18322
OR7E24TMC5Q6UXY8320
OR7E24GBP6Q6ZN66319
OR7E24USF3Q68DE3314
OR7E24ANO2Q9NQ90306
OR7E24SPOUT1Q5T280300

IntAct

7 interactions, top by confidence:

ABTypeScore
OR7E24ACTA2psi-mi:“MI:0915”(physical association)0.400
OR7E24ECE1psi-mi:“MI:0915”(physical association)0.370
ECE1OR7E24psi-mi:“MI:0915”(physical association)0.370

BioGRID (2): ACTA2 (Affinity Capture-MS), OR7E24 (Negative Genetic)

ESM2 similar proteins: A6ND48, A6NFC9, B2RN74, O43869, O60412, O60431, P23265, P31388, P34987, P47883, P47884, P47887, P58170, Q0VAX9, Q5JRS4, Q60894, Q6IFN5, Q7Z3T1, Q8NG78, Q8NG84, Q8NG94, Q8NG99, Q8NGC0, Q8NGC1, Q8NGC5, Q8NGE7, Q8NGG2, Q8NGG3, Q8NGN1, Q8NGN2, Q8NGR1, Q8NGR2, Q8NGR6, Q8NGT2, Q8NGW1, Q8NGW6, Q8NGZ2, Q8NGZ5, Q8NH06, Q8NH07

Diamond homologs: A4D2G3, A6ND48, A6NL26, O43749, O60412, O76099, P0C7N5, P0DMU2, P0DN82, P23265, P23266, P23269, P23272, P23273, P23274, P30953, P30955, P34984, P34985, P34986, P35896, P47887, P47890, P58173, P58181, P58182, P70526, Q0VAX9, Q13606, Q13607, Q15617, Q15619, Q60893, Q6IFN5, Q6UXT6, Q7TQQ0, Q7TRF3, Q8N127, Q8NG98, Q8NGA6

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

63 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance59
Likely benign3
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

293 predictions. Top by Δscore:

VariantEffectΔscore
19:9250962:G:GTdonor_gain0.8700
19:9250961:GGGT:Gdonor_gain0.7100
19:9250973:C:CGdonor_gain0.7100
19:9250976:T:Gdonor_gain0.6200
19:9251422:T:Gacceptor_gain0.6100
19:9250973:C:Gdonor_gain0.5900
19:9251080:AAAAG:Aacceptor_gain0.5800
19:9251330:TCCCC:Tdonor_gain0.5600
19:9250962:G:Tdonor_gain0.5400
19:9251084:GGT:Gacceptor_gain0.5400
19:9251426:T:Gacceptor_gain0.5400
19:9251215:C:CGdonor_gain0.5300
19:9251900:CCAG:Cacceptor_loss0.5300
19:9251901:CA:Cacceptor_loss0.5300
19:9251902:A:Cacceptor_loss0.5300
19:9251903:GGA:Gacceptor_loss0.5300
19:9251080:A:AGacceptor_gain0.5200
19:9251209:ACG:Adonor_gain0.5200
19:9251895:A:AGacceptor_loss0.5200
19:9251896:T:Gacceptor_loss0.5200
19:9251892:A:AGacceptor_loss0.5100
19:9251893:C:Gacceptor_loss0.5100
19:9251992:A:Gdonor_gain0.5100
19:9250981:A:Gdonor_gain0.5000
19:9251081:A:Gacceptor_gain0.4900
19:9251083:A:AGacceptor_gain0.4900
19:9251084:G:GGacceptor_gain0.4900
19:9251421:AT:Aacceptor_gain0.4900
19:9250967:A:Gdonor_gain0.4800
19:9250977:G:GGdonor_gain0.4700

AlphaMissense

2245 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
19:9251131:T:CF30L0.887
19:9251133:C:AF30L0.887
19:9251133:C:GF30L0.887
19:9251848:T:CF269L0.854
19:9251850:T:AF269L0.854
19:9251850:T:GF269L0.854
19:9251551:A:CS170R0.830
19:9251553:T:AS170R0.830
19:9251553:T:GS170R0.830
19:9251464:T:CF141L0.815
19:9251466:T:AF141L0.815
19:9251466:T:GF141L0.815
19:9251451:G:AM136I0.810
19:9251451:G:CM136I0.810
19:9251451:G:TM136I0.810
19:9251959:T:CF306L0.788
19:9251961:C:AF306L0.788
19:9251961:C:GF306L0.788
19:9251809:T:CF256L0.780
19:9251811:C:AF256L0.780
19:9251811:C:GF256L0.780
19:9251188:T:CF49L0.778
19:9251190:C:AF49L0.778
19:9251190:C:GF49L0.778
19:9251626:T:CF195L0.771
19:9251628:C:AF195L0.771
19:9251628:C:GF195L0.771
19:9251223:C:AN60K0.767
19:9251223:C:GN60K0.767
19:9251462:G:CR140P0.763

dbSNP variants (sampled 300 via entrez): RS1000046280 (19:9231787 A>G), RS1000158473 (19:9241502 A>C), RS1000162779 (19:9215690 T>C), RS1000185343 (19:9209656 T>A), RS1000239318 (19:9225549 G>T), RS1000311394 (19:9225311 A>G), RS1000343010 (19:9249200 A>G), RS1000380054 (19:9242608 C>A), RS1000445685 (19:9242904 TTC>T), RS1000476084 (19:9243503 C>T), RS1000518761 (19:9220454 A>G), RS1000552878 (19:9225497 TAAAA>T,TAAA,TAAAAA), RS1000622302 (19:9221070 C>A,G,T), RS1000683558 (19:9248930 C>G,T), RS1000692714 (19:9221456 T>A)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (1): CIC-rearranged sarcoma (MONDO:0956989)

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

3 total (human), top 3 by PubMed support.

ChemicalActions (top 5)PubMed papers
Arsenicaffects methylation1
Tretinoindecreases expression1
Aflatoxin B1increases methylation1

Clinical trials (associated diseases)

3 trials via MONDO — disease-level, not drug-specific.

TrialPhaseStatusTitle
NCT02389244PHASE2ACTIVE_NOT_RECRUITINGA Phase II Study Evaluating Efficacy and Safety of Regorafenib in Patients With Metastatic Bone Sarcomas
NCT06414434PHASE1ACTIVE_NOT_RECRUITINGBTX-A51 in Patients With Liposarcoma or CIC-rearranged Sarcoma
NCT06820957PHASE2/PHASE3ACTIVE_NOT_RECRUITINGTesting a New Combination of Anti-cancer Drugs in Patients Newly Diagnosed With Ewing Sarcoma Who Have Cancer That Has Spread to Other Parts of the Body
  • Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): CIC-rearranged sarcoma