OR7E24 (olfactory receptor family 7 subfamily E member 24) - Rat Genome Database

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Gene: OR7E24 (olfactory receptor family 7 subfamily E member 24) Homo sapiens
Analyze
Symbol: OR7E24
Name: olfactory receptor family 7 subfamily E member 24
RGD ID: 1351971
HGNC Page HGNC:8396
Description: Predicted to enable olfactory receptor activity. Predicted to be involved in signal transduction. Predicted to be located in membrane. Predicted to be active in plasma membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: HSHT2; olfactory receptor 7E24; olfactory receptor OR19-14; OR19-8; OR7E24P; OR7E24Q
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Pig
Alliance Genes
More Info more info ...
Related Pseudogenes: OR7E101P   OR7E106P   OR7E154P   OR7K1P  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38199,206,488 - 9,252,625 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl199,247,344 - 9,252,625 (+)EnsemblGRCh38hg38GRCh38
GRCh37199,358,020 - 9,363,301 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36199,222,720 - 9,223,739 (+)NCBINCBI36Build 36hg18NCBI36
Celera199,257,168 - 9,258,187 (+)NCBICelera
Cytogenetic Map19p13.2NCBI
HuRef198,943,482 - 8,944,501 (+)NCBIHuRef
CHM1_1199,361,410 - 9,362,429 (+)NCBICHM1_1
T2T-CHM13v2.0199,332,685 - 9,378,827 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
membrane  (IEA,NAS)
plasma membrane  (IBA,IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Autism  (IAGP)
References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:9268701   PMID:11385110   PMID:12213199   PMID:12477932   PMID:14983052   PMID:15057824   PMID:21873635   PMID:32126975   PMID:33961781   PMID:34373451  


Genomics

Comparative Map Data
OR7E24
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38199,206,488 - 9,252,625 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl199,247,344 - 9,252,625 (+)EnsemblGRCh38hg38GRCh38
GRCh37199,358,020 - 9,363,301 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36199,222,720 - 9,223,739 (+)NCBINCBI36Build 36hg18NCBI36
Celera199,257,168 - 9,258,187 (+)NCBICelera
Cytogenetic Map19p13.2NCBI
HuRef198,943,482 - 8,944,501 (+)NCBIHuRef
CHM1_1199,361,410 - 9,362,429 (+)NCBICHM1_1
T2T-CHM13v2.0199,332,685 - 9,378,827 (+)NCBIT2T-CHM13v2.0
Or7e178
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39920,223,391 - 20,247,389 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl920,223,448 - 20,247,390 (-)EnsemblGRCm39 Ensembl
GRCm38920,313,892 - 20,336,094 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl920,312,152 - 20,336,094 (-)EnsemblGRCm38mm10GRCm38
MGSCv37920,118,336 - 20,140,538 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36920,064,325 - 20,065,663 (-)NCBIMGSCv36mm8
Celera917,594,808 - 17,612,439 (-)NCBICelera
Cytogenetic Map9A3NCBI
cM Map97.52NCBI
Or7e177
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8826,979,464 - 26,980,484 (-)NCBIGRCr8
mRatBN7.2818,703,220 - 18,704,240 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl818,703,220 - 18,704,179 (-)EnsemblmRatBN7.2 Ensembl
Rnor_6.0820,993,731 - 20,994,711 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl820,993,743 - 20,994,660 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0821,066,271 - 21,067,239 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4819,119,217 - 19,120,170 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
Celera820,044,040 - 20,060,654 (-)NCBICelera
Cytogenetic Map8q13NCBI
LOC100973124
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22014,136,743 - 14,137,679 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11913,121,532 - 13,122,468 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0198,755,000 - 8,755,886 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1199,442,995 - 9,443,931 (+)NCBIpanpan1.1PanPan1.1panPan2
OR7E24
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12051,395,056 - 51,397,210 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2051,394,761 - 51,396,289 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2051,258,547 - 51,260,710 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02051,916,298 - 51,918,461 (+)NCBIROS_Cfam_1.0
UMICH_Zoey_3.12051,123,773 - 51,125,936 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02051,548,738 - 51,550,901 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02051,790,300 - 51,792,463 (+)NCBIUU_Cfam_GSD_1.0
LOC110259764
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1267,990,188 - 67,991,135 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1

Variants

.
Variants in OR7E24
35 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19p13.3-13.2(chr19:1972245-9648879)x3 copy number gain See cases [RCV000052879] Chr19:1972245..9648879 [GRCh38]
Chr19:1972244..9759555 [GRCh37]
Chr19:1923244..9620555 [NCBI36]
Chr19:19p13.3-13.2
pathogenic
GRCh38/hg38 19p13.2-13.13(chr19:8831147-13331227)x3 copy number gain See cases [RCV000052908] Chr19:8831147..13331227 [GRCh38]
Chr19:8941823..13442041 [GRCh37]
Chr19:8802823..13303041 [NCBI36]
Chr19:19p13.2-13.13
likely pathogenic
NM_001079935.1(OR7E24):c.179A>G (p.Asn60Ser) single nucleotide variant Malignant melanoma [RCV000063679] Chr19:9251222 [GRCh38]
Chr19:9361898 [GRCh37]
Chr19:9222898 [NCBI36]
Chr19:19p13.2
not provided
GRCh37/hg19 19p13.2(chr19:8661944-10104083)x1 copy number loss Ductal breast carcinoma [RCV000207085] Chr19:8661944..10104083 [GRCh37]
Chr19:19p13.2
uncertain significance
Single allele complex Ductal breast carcinoma [RCV000207119] Chr19:9001833..10085054 [GRCh37]
Chr19:19p13.2
likely pathogenic|uncertain significance
NM_001079935.2(OR7E24):c.989A>G (p.His330Arg) single nucleotide variant Inborn genetic diseases [RCV003270493] Chr19:9252032 [GRCh38]
Chr19:9362708 [GRCh37]
Chr19:19p13.2
uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19p13.3-13.2(chr19:3120160-9732820)x3 copy number gain not provided [RCV000684096] Chr19:3120160..9732820 [GRCh37]
Chr19:19p13.3-13.2
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
Single allele duplication Autism [RCV000754212] Chr19:7981357..10019383 [GRCh38]
Chr19:19p13.2
likely pathogenic
GRCh37/hg19 19p13.2(chr19:8905057-9606461)x1 copy number loss not provided [RCV000740030] Chr19:8905057..9606461 [GRCh37]
Chr19:19p13.2
likely benign
NM_001005191.3(OR7D4):c.511G>A (p.Gly171Ser) single nucleotide variant Inborn genetic diseases [RCV003249523] Chr19:9214327 [GRCh38]
Chr19:9325003 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.32dup (p.Leu12fs) duplication CIC-DUX Sarcoma [RCV000993818] Chr19:9251064..9251065 [GRCh38]
Chr19:9361740..9361741 [GRCh37]
Chr19:19p13.2
not provided
GRCh37/hg19 19p13.2(chr19:8518395-10053298)x3 copy number gain not provided [RCV001259373] Chr19:8518395..10053298 [GRCh37]
Chr19:19p13.2
uncertain significance
GRCh37/hg19 19p13.2(chr19:9245167-9465565)x3 copy number gain not provided [RCV001259371] Chr19:9245167..9465565 [GRCh37]
Chr19:19p13.2
likely benign
NM_001005191.3(OR7D4):c.924C>T (p.Ala308=) single nucleotide variant not provided [RCV000957878] Chr19:9213914 [GRCh38]
Chr19:9324590 [GRCh37]
Chr19:19p13.2
benign
NM_001005191.3(OR7D4):c.496T>C (p.Leu166=) single nucleotide variant not provided [RCV000957879] Chr19:9214342 [GRCh38]
Chr19:9325018 [GRCh37]
Chr19:19p13.2
likely benign
NM_001079935.2(OR7E24):c.895G>A (p.Val299Ile) single nucleotide variant Inborn genetic diseases [RCV002837060] Chr19:9251938 [GRCh38]
Chr19:9362614 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001005191.3(OR7D4):c.847C>G (p.Pro283Ala) single nucleotide variant Inborn genetic diseases [RCV003287724] Chr19:9213991 [GRCh38]
Chr19:9324667 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001005191.3(OR7D4):c.909A>T (p.Arg303Ser) single nucleotide variant Inborn genetic diseases [RCV002823204] Chr19:9213929 [GRCh38]
Chr19:9324605 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.764C>A (p.Ala255Asp) single nucleotide variant Inborn genetic diseases [RCV002784484] Chr19:9251807 [GRCh38]
Chr19:9362483 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.221A>C (p.His74Pro) single nucleotide variant Inborn genetic diseases [RCV002822841] Chr19:9251264 [GRCh38]
Chr19:9361940 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001005191.3(OR7D4):c.328A>G (p.Met110Val) single nucleotide variant Inborn genetic diseases [RCV002784688] Chr19:9214510 [GRCh38]
Chr19:9325186 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.284C>T (p.Thr95Met) single nucleotide variant Inborn genetic diseases [RCV002951659] Chr19:9251327 [GRCh38]
Chr19:9362003 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001005191.3(OR7D4):c.925G>A (p.Asp309Asn) single nucleotide variant Inborn genetic diseases [RCV003006776] Chr19:9213913 [GRCh38]
Chr19:9324589 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001005191.3(OR7D4):c.170C>G (p.Thr57Ser) single nucleotide variant Inborn genetic diseases [RCV002931552] Chr19:9214668 [GRCh38]
Chr19:9325344 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001005191.3(OR7D4):c.617T>A (p.Leu206Gln) single nucleotide variant Inborn genetic diseases [RCV002982056] Chr19:9214221 [GRCh38]
Chr19:9324897 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.431T>C (p.Ile144Thr) single nucleotide variant Inborn genetic diseases [RCV002954580] Chr19:9251474 [GRCh38]
Chr19:9362150 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.589T>C (p.Cys197Arg) single nucleotide variant Inborn genetic diseases [RCV002698131] Chr19:9251632 [GRCh38]
Chr19:9362308 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.623C>A (p.Ser208Tyr) single nucleotide variant Inborn genetic diseases [RCV002742383] Chr19:9251666 [GRCh38]
Chr19:9362342 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.769T>C (p.Ser257Pro) single nucleotide variant Inborn genetic diseases [RCV002787140] Chr19:9251812 [GRCh38]
Chr19:9362488 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001005191.3(OR7D4):c.95T>C (p.Leu32Pro) single nucleotide variant Inborn genetic diseases [RCV002648407] Chr19:9214743 [GRCh38]
Chr19:9325419 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.19C>A (p.Leu7Ile) single nucleotide variant Inborn genetic diseases [RCV002813366] Chr19:9251062 [GRCh38]
Chr19:9361738 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.83C>T (p.Ser28Leu) single nucleotide variant Inborn genetic diseases [RCV002672380] Chr19:9251126 [GRCh38]
Chr19:9361802 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001005191.3(OR7D4):c.718A>C (p.Thr240Pro) single nucleotide variant Inborn genetic diseases [RCV002714731] Chr19:9214120 [GRCh38]
Chr19:9324796 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.364T>C (p.Phe122Leu) single nucleotide variant Inborn genetic diseases [RCV002717447] Chr19:9251407 [GRCh38]
Chr19:9362083 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001005191.3(OR7D4):c.247G>A (p.Val83Met) single nucleotide variant Inborn genetic diseases [RCV002809669] Chr19:9214591 [GRCh38]
Chr19:9325267 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.872T>C (p.Val291Ala) single nucleotide variant Inborn genetic diseases [RCV002832073] Chr19:9251915 [GRCh38]
Chr19:9362591 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001005191.3(OR7D4):c.598T>A (p.Tyr200Asn) single nucleotide variant Inborn genetic diseases [RCV002674671] Chr19:9214240 [GRCh38]
Chr19:9324916 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.553A>C (p.Thr185Pro) single nucleotide variant Inborn genetic diseases [RCV002832624] Chr19:9251596 [GRCh38]
Chr19:9362272 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001005191.3(OR7D4):c.224C>G (p.Ser75Cys) single nucleotide variant Inborn genetic diseases [RCV002719018] Chr19:9214614 [GRCh38]
Chr19:9325290 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.782C>T (p.Ser261Phe) single nucleotide variant Inborn genetic diseases [RCV002808841] Chr19:9251825 [GRCh38]
Chr19:9362501 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.139G>T (p.Gly47Trp) single nucleotide variant Inborn genetic diseases [RCV002679664] Chr19:9251182 [GRCh38]
Chr19:9361858 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001005191.3(OR7D4):c.418C>T (p.Leu140Phe) single nucleotide variant Inborn genetic diseases [RCV003177878] Chr19:9214420 [GRCh38]
Chr19:9325096 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001005191.3(OR7D4):c.803C>T (p.Ser268Phe) single nucleotide variant Inborn genetic diseases [RCV003180557] Chr19:9214035 [GRCh38]
Chr19:9324711 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.691G>A (p.Gly231Arg) single nucleotide variant Inborn genetic diseases [RCV003263458] Chr19:9251734 [GRCh38]
Chr19:9362410 [GRCh37]
Chr19:19p13.2
uncertain significance
NM_001079935.2(OR7E24):c.986C>G (p.Ser329Cys) single nucleotide variant Inborn genetic diseases [RCV003359520] Chr19:9252029 [GRCh38]
Chr19:9362705 [GRCh37]
Chr19:19p13.2
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:229
Count of miRNA genes:222
Interacting mature miRNAs:229
Transcripts:ENST00000456448
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 2
Low 1 2 1 370 1
Below cutoff 212 274 137 32 190 23 399 172 309 19 155 154 11 121 260 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001079935 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001386108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438594 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438595 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438596 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438597 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047438598 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320515 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320516 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320517 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320518 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054320519 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC006271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC011464 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF399400 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC146920 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK004227 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KP290367 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  Y10529 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000456448   ⟹   ENSP00000387523
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl199,250,930 - 9,252,625 (+)Ensembl
RefSeq Acc Id: ENST00000641946   ⟹   ENSP00000494223
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl199,247,344 - 9,252,625 (+)Ensembl
RefSeq Acc Id: NM_001079935   ⟹   NP_001073404
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38199,250,930 - 9,252,625 (+)NCBI
GRCh37199,361,720 - 9,362,739 (+)RGD
Build 36199,222,720 - 9,223,739 (+)NCBI Archive
Celera199,257,168 - 9,258,187 (+)RGD
HuRef198,943,482 - 8,944,501 (+)ENTREZGENE
CHM1_1199,361,410 - 9,362,429 (+)NCBI
T2T-CHM13v2.0199,377,132 - 9,378,827 (+)NCBI
Sequence:
RefSeq Acc Id: NM_001386108   ⟹   NP_001373037
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38199,247,344 - 9,252,625 (+)NCBI
T2T-CHM13v2.0199,373,546 - 9,378,827 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047438594   ⟹   XP_047294550
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38199,206,488 - 9,252,477 (+)NCBI
RefSeq Acc Id: XM_047438595   ⟹   XP_047294551
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38199,250,022 - 9,252,477 (+)NCBI
RefSeq Acc Id: XM_047438596   ⟹   XP_047294552
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38199,213,175 - 9,252,477 (+)NCBI
RefSeq Acc Id: XM_047438597   ⟹   XP_047294553
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38199,206,488 - 9,252,477 (+)NCBI
RefSeq Acc Id: XM_047438598   ⟹   XP_047294554
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38199,213,175 - 9,252,477 (+)NCBI
RefSeq Acc Id: XM_054320515   ⟹   XP_054176490
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0199,332,685 - 9,378,679 (+)NCBI
RefSeq Acc Id: XM_054320516   ⟹   XP_054176491
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0199,376,224 - 9,378,679 (+)NCBI
RefSeq Acc Id: XM_054320517   ⟹   XP_054176492
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0199,339,372 - 9,378,679 (+)NCBI
RefSeq Acc Id: XM_054320518   ⟹   XP_054176493
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0199,332,685 - 9,378,679 (+)NCBI
RefSeq Acc Id: XM_054320519   ⟹   XP_054176494
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0199,339,372 - 9,378,679 (+)NCBI
RefSeq Acc Id: NP_001073404   ⟸   NM_001079935
- Peptide Label: isoform 1
- UniProtKB: B9EJD9 (UniProtKB/Swiss-Prot),   Q9UPJ1 (UniProtKB/Swiss-Prot),   Q6IFN5 (UniProtKB/Swiss-Prot),   A0A126GVS1 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000387523   ⟸   ENST00000456448
RefSeq Acc Id: ENSP00000494223   ⟸   ENST00000641946
RefSeq Acc Id: NP_001373037   ⟸   NM_001386108
- Peptide Label: isoform 2
- UniProtKB: A0A2R8Y4Q1 (UniProtKB/TrEMBL),   A0A126GVS1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294553   ⟸   XM_047438597
- Peptide Label: isoform X3
- UniProtKB: O43789 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294550   ⟸   XM_047438594
- Peptide Label: isoform X1
- UniProtKB: A0A126GVS1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294552   ⟸   XM_047438596
- Peptide Label: isoform X3
- UniProtKB: O43789 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294554   ⟸   XM_047438598
- Peptide Label: isoform X3
- UniProtKB: O43789 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_047294551   ⟸   XM_047438595
- Peptide Label: isoform X2
- UniProtKB: A0A126GVS1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176493   ⟸   XM_054320518
- Peptide Label: isoform X3
- UniProtKB: O43789 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176490   ⟸   XM_054320515
- Peptide Label: isoform X1
- UniProtKB: A0A126GVS1 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176492   ⟸   XM_054320517
- Peptide Label: isoform X3
- UniProtKB: O43789 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176494   ⟸   XM_054320519
- Peptide Label: isoform X3
- UniProtKB: O43789 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054176491   ⟸   XM_054320516
- Peptide Label: isoform X2
- UniProtKB: A0A126GVS1 (UniProtKB/TrEMBL)
Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q6IFN5-F1-model_v2 AlphaFold Q6IFN5 1-339 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:8396 AgrOrtholog
COSMIC OR7E24 COSMIC
Ensembl Genes ENSG00000237521 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000456448 ENTREZGENE
  ENST00000456448.3 UniProtKB/Swiss-Prot
  ENST00000641946 ENTREZGENE
  ENST00000641946.1 UniProtKB/TrEMBL
Gene3D-CATH Rhodopsin 7-helix transmembrane proteins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000237521 GTEx
HGNC ID HGNC:8396 ENTREZGENE
Human Proteome Map OR7E24 Human Proteome Map
InterPro GPCR_Rhodpsn UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_Rhodpsn_7TM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Olfact_rcpt UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:26648 UniProtKB/Swiss-Prot
NCBI Gene 26648 ENTREZGENE
PANTHER OLFACTORY RECEPTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OLFACTORY RECEPTOR 7E24 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam 7tm_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA32675 PharmGKB
PRINTS GPCRRHODOPSN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OLFACTORYR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE G_PROTEIN_RECEP_F1_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Family A G protein-coupled receptor-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A126GVS1 ENTREZGENE, UniProtKB/TrEMBL
  A0A2R8Y4Q1 ENTREZGENE, UniProtKB/TrEMBL
  B9EJD9 ENTREZGENE
  O43789 ENTREZGENE, UniProtKB/TrEMBL
  O7E24_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
  Q9UPJ1 ENTREZGENE
UniProt Secondary B9EJD9 UniProtKB/Swiss-Prot
  Q9UPJ1 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-15 OR7E24  olfactory receptor family 7 subfamily E member 24  OR7E24  olfactory receptor, family 7, subfamily E, member 24  Symbol and/or name change 5135510 APPROVED