OR1E2 (olfactory receptor family 1 subfamily E member 2) - Rat Genome Database
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Gene: OR1E2 (olfactory receptor family 1 subfamily E member 2) Homo sapiens
Analyze
Symbol: OR1E2
Name: olfactory receptor family 1 subfamily E member 2
RGD ID: 1347026
HGNC Page HGNC
Description: Predicted to have olfactory receptor activity. Predicted to be involved in sensory perception of chemical stimulus and signal transduction. Predicted to localize to integral component of plasma membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: olfactory receptor 17-93/17-135/17-136; olfactory receptor 1E2; olfactory receptor 1E4; olfactory receptor OR17-17; olfactory receptor OR17-3; olfactory receptor, family 1, subfamily E, member 2; olfactory receptor, family 1, subfamily E, member 4; olfactory receptor, family 1, subfamily E, member 7; OR17-135; OR17-136; OR17-93; OR1E4; OR1E7; OST529
RGD Orthologs
Mouse
Rat
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl173,432,870 - 3,433,841 (-)EnsemblGRCh38hg38GRCh38
GRCh38173,432,870 - 3,433,841 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37173,336,164 - 3,337,135 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36173,282,914 - 3,283,885 (-)NCBINCBI36hg18NCBI36
Build 34173,282,913 - 3,283,885NCBI
Celera173,349,902 - 3,350,873 (-)NCBI
Cytogenetic Map17p13.2NCBI
HuRef173,228,673 - 3,229,644 (-)NCBIHuRef
CHM1_1173,345,795 - 3,346,766 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Cellular Component

Molecular Function

References

References - curated
1. GOA_HUMAN data from the GO Consortium
2. RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:804088   PMID:8004088   PMID:9500546   PMID:10673334   PMID:12213199   PMID:12477932   PMID:14983052   PMID:15489334   PMID:21873635   PMID:22145905  


Genomics

Comparative Map Data
OR1E2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl173,432,870 - 3,433,841 (-)EnsemblGRCh38hg38GRCh38
GRCh38173,432,870 - 3,433,841 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37173,336,164 - 3,337,135 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36173,282,914 - 3,283,885 (-)NCBINCBI36hg18NCBI36
Build 34173,282,913 - 3,283,885NCBI
Celera173,349,902 - 3,350,873 (-)NCBI
Cytogenetic Map17p13.2NCBI
HuRef173,228,673 - 3,229,644 (-)NCBIHuRef
CHM1_1173,345,795 - 3,346,766 (-)NCBICHM1_1
Olfr376
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391173,262,072 - 73,266,530 (+)NCBIGRCm39mm39
GRCm381173,371,246 - 73,375,704 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1173,371,246 - 73,377,836 (+)EnsemblGRCm38mm10GRCm38
MGSCv371173,184,748 - 73,189,206 (+)NCBIGRCm37mm9NCBIm37
MGSCv361173,190,946 - 73,191,899 (+)NCBImm8
Celera1180,908,199 - 80,912,657 (+)NCBICelera
Cytogenetic Map11B4NCBI
Olr1501
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Rnor_6.01060,728,160 - 60,729,095 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1060,728,160 - 60,729,095 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01060,465,195 - 60,466,130 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41061,161,408 - 61,162,343 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11061,175,030 - 61,175,966 (+)NCBI
Celera1057,796,845 - 57,797,780 (+)NCBICelera
Cytogenetic Map10q24NCBI
LOC100517779
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.11249,543,859 - 49,548,236 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.21251,253,797 - 51,254,887 (+)NCBISscrofa10.2Sscrofa10.2susScr3
LOC103242153
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1162,945,702 - 2,947,679 (-)NCBI
ChlSab1.1 Ensembl162,946,477 - 2,947,421 (-)Ensembl
LOC101717240
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247866,124,859 - 6,127,071 (-)NCBI

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:32
Count of miRNA genes:32
Interacting mature miRNAs:32
Transcripts:ENST00000248384
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
Low 3 13 1 22 7 3 2 10 2
Below cutoff 335 254 116 18 111 7 651 353 863 23 357 117 11 192 478

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_003554 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC025125 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF087925 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF095725 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF399551 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC121105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC121106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK004235 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK004352 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CS248560 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KP290474 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KP290541 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U04686 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U76377 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U86241 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U86242 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000248384   ⟹   ENSP00000248384
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl173,432,870 - 3,433,841 (-)Ensembl
RefSeq Acc Id: NM_003554   ⟹   NP_003545
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38173,432,870 - 3,433,841 (-)NCBI
GRCh37173,336,164 - 3,337,135 (-)RGD
Build 36173,282,914 - 3,283,885 (-)NCBI Archive
Celera173,349,902 - 3,350,873 (-)RGD
HuRef173,228,673 - 3,229,644 (-)RGD
CHM1_1173,345,795 - 3,346,766 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_003545   ⟸   NM_003554
- UniProtKB: P47887 (UniProtKB/Swiss-Prot),   A0A126GW81 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000248384   ⟸   ENST00000248384
Protein Domains
G_PROTEIN_RECEP_F1_2


Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 17p13.3-13.2(chr17:2357067-4328426)x3 copy number gain See cases [RCV000052456] Chr17:2357067..4328426 [GRCh38]
Chr17:2260361..4231721 [GRCh37]
Chr17:2207111..4178470 [NCBI36]
Chr17:17p13.3-13.2		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:193307-5652222)x1 copy number loss See cases [RCV000053384] Chr17:193307..5652222 [GRCh38]
Chr17:45835..5555542 [GRCh37]
Chr17:43098..5496266 [NCBI36]
Chr17:17p13.3-13.2		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:198748-3436345)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053386]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053386]|See cases [RCV000053386] Chr17:198748..3436345 [GRCh38]
Chr17:50690..3339639 [GRCh37]
Chr17:48539..3286389 [NCBI36]
Chr17:17p13.3-13.2		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:2527510-3467165)x1 copy number loss See cases [RCV000053405] Chr17:2527510..3467165 [GRCh38]
Chr17:2430804..3370459 [GRCh37]
Chr17:2377554..3317209 [NCBI36]
Chr17:17p13.3-13.2		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:3036729-3684667)x3 copy number gain See cases [RCV000053972] Chr17:3036729..3684667 [GRCh38]
Chr17:2940023..3587961 [GRCh37]
Chr17:2886773..3534710 [NCBI36]
Chr17:17p13.3-13.2		 uncertain significance
GRCh38/hg38 17p13.3-13.2(chr17:3208843-3839780)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053973]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053973]|See cases [RCV000053973] Chr17:3208843..3839780 [GRCh38]
Chr17:3112137..3743074 [GRCh37]
Chr17:3058887..3689823 [NCBI36]
Chr17:17p13.3-13.2		 uncertain significance
GRCh38/hg38 17p13.3-13.2(chr17:2062380-5258340)x1 copy number loss See cases [RCV000133721] Chr17:2062380..5258340 [GRCh38]
Chr17:1965674..5161635 [GRCh37]
Chr17:1912424..5102359 [NCBI36]
Chr17:17p13.3-13.2		 pathogenic
GRCh38/hg38 17p13.3-13.1(chr17:162088-6959050)x1 copy number loss See cases [RCV000134135] Chr17:162088..6959050 [GRCh38]
Chr17:45835..6862369 [GRCh37]
Chr17:11879..6803093 [NCBI36]
Chr17:17p13.3-13.1		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:3155468-3543868)x1 copy number loss See cases [RCV000133921] Chr17:3155468..3543868 [GRCh38]
Chr17:3058762..3447162 [GRCh37]
Chr17:3005512..3393912 [NCBI36]
Chr17:17p13.3-13.2		 benign
GRCh38/hg38 17p13.3-13.1(chr17:198748-7491129)x3 copy number gain See cases [RCV000134970] Chr17:198748..7491129 [GRCh38]
Chr17:50690..7394448 [GRCh37]
Chr17:48539..7335172 [NCBI36]
Chr17:17p13.3-13.1		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:226472-3655099)x1 copy number loss See cases [RCV000135857] Chr17:226472..3655099 [GRCh38]
Chr17:396627..3558393 [GRCh37]
Chr17:76263..3505142 [NCBI36]
Chr17:17p13.3-13.2		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:1348488-3513273)x3 copy number gain See cases [RCV000137603] Chr17:1348488..3513273 [GRCh38]
Chr17:1251782..3416567 [GRCh37]
Chr17:1198532..3363317 [NCBI36]
Chr17:17p13.3-13.2		 likely pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:3102273-3667053)x3 copy number gain See cases [RCV000137331] Chr17:3102273..3667053 [GRCh38]
Chr17:3005567..3570347 [GRCh37]
Chr17:2952317..3517096 [NCBI36]
Chr17:17p13.3-13.2		 likely pathogenic|uncertain significance
GRCh38/hg38 17p13.3-13.1(chr17:162016-7697012)x1 copy number loss See cases [RCV000138214] Chr17:162016..7697012 [GRCh38]
Chr17:45835..7600330 [GRCh37]
Chr17:11807..7541055 [NCBI36]
Chr17:17p13.3-13.1		 pathogenic
GRCh38/hg38 17p13.3-12(chr17:162016-12343901)x3 copy number gain See cases [RCV000138531] Chr17:162016..12343901 [GRCh38]
Chr17:45835..12247218 [GRCh37]
Chr17:11807..12187943 [NCBI36]
Chr17:17p13.3-12		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:2062429-4141883)x3 copy number gain See cases [RCV000139738] Chr17:2062429..4141883 [GRCh38]
Chr17:1965723..4045177 [GRCh37]
Chr17:1912473..3991926 [NCBI36]
Chr17:17p13.3-13.2		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:150732-5935377)x1 copy number loss See cases [RCV000141658] Chr17:150732..5935377 [GRCh38]
Chr17:525..5838697 [GRCh37]
Chr17:525..5779421 [NCBI36]
Chr17:17p13.3-13.2		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:237248-4735533)x1 copy number loss See cases [RCV000141559] Chr17:237248..4735533 [GRCh38]
Chr17:396627..4638828 [GRCh37]
Chr17:87039..4585577 [NCBI36]
Chr17:17p13.3-13.2		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:198748-4265640)x1 copy number loss See cases [RCV000142440] Chr17:198748..4265640 [GRCh38]
Chr17:50690..4168935 [GRCh37]
Chr17:48539..4115684 [NCBI36]
Chr17:17p13.3-13.2		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:3168370-3862518)x3 copy number gain See cases [RCV000142062] Chr17:3168370..3862518 [GRCh38]
Chr17:3071664..3765812 [GRCh37]
Chr17:3018414..3712561 [NCBI36]
Chr17:17p13.3-13.2		 uncertain significance
GRCh38/hg38 17p13.3-12(chr17:150732-14764202)x3 copy number gain See cases [RCV000142236] Chr17:150732..14764202 [GRCh38]
Chr17:525..14667519 [GRCh37]
Chr17:525..14608244 [NCBI36]
Chr17:17p13.3-12		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:2922729-3436438)x3 copy number gain See cases [RCV000142895] Chr17:2922729..3436438 [GRCh38]
Chr17:2826023..3339732 [GRCh37]
Chr17:2772773..3286482 [NCBI36]
Chr17:17p13.3-13.2		 pathogenic
GRCh38/hg38 17p13.3-13.2(chr17:3187406-3880628)x3 copy number gain See cases [RCV000142793] Chr17:3187406..3880628 [GRCh38]
Chr17:3090700..3783922 [GRCh37]
Chr17:3037450..3730671 [NCBI36]
Chr17:17p13.3-13.2		 uncertain significance
GRCh38/hg38 17p13.3-13.2(chr17:3168370-3852982)x3 copy number gain See cases [RCV000143610] Chr17:3168370..3852982 [GRCh38]
Chr17:3071664..3756276 [GRCh37]
Chr17:3018414..3703025 [NCBI36]
Chr17:17p13.3-13.2		 likely benign|uncertain significance
GRCh37/hg19 17p13.3-13.2(chr17:919381-4046915)x3 copy number gain See cases [RCV000240175] Chr17:919381..4046915 [GRCh37]
Chr17:17p13.3-13.2		 pathogenic
GRCh37/hg19 17p13.3-13.2(chr17:1751557-5378509)x1 copy number loss See cases [RCV000445994] Chr17:1751557..5378509 [GRCh37]
Chr17:17p13.3-13.2		 pathogenic
GRCh37/hg19 17p13.3-13.1(chr17:1113102-6742486) copy number gain See cases [RCV000445679] Chr17:1113102..6742486 [GRCh37]
Chr17:17p13.3-13.1		 pathogenic
GRCh37/hg19 17p13.3-13.2(chr17:48858-3379400)x1 copy number loss See cases [RCV000448506] Chr17:48858..3379400 [GRCh37]
Chr17:17p13.3-13.2		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938) copy number gain See cases [RCV000511439] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-13.2(chr17:525-3825428)x1 copy number loss See cases [RCV000511508] Chr17:525..3825428 [GRCh37]
Chr17:17p13.3-13.2		 pathogenic
GRCh37/hg19 17p13.3-12(chr17:525-15027737)x3 copy number gain See cases [RCV000511786] Chr17:525..15027737 [GRCh37]
Chr17:17p13.3-12		 pathogenic
GRCh37/hg19 17p13.3-13.2(chr17:1922768-3429136)x3 copy number gain See cases [RCV000511855] Chr17:1922768..3429136 [GRCh37]
Chr17:17p13.3-13.2		 likely pathogenic
GRCh37/hg19 17p13.3-13.2(chr17:2339561-3447162) copy number loss Lissencephaly [RCV000626516] Chr17:2339561..3447162 [GRCh37]
Chr17:17p13.3-13.2		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3 copy number gain See cases [RCV000512441] Chr17:526..81041938 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-13.2(chr17:525-4151421)x3 copy number gain See cases [RCV000512413] Chr17:525..4151421 [GRCh37]
Chr17:17p13.3-13.2		 pathogenic
GRCh37/hg19 17p13.3-13.2(chr17:2944083-3429136)x3 copy number gain not provided [RCV000683878] Chr17:2944083..3429136 [GRCh37]
Chr17:17p13.3-13.2		 uncertain significance
GRCh37/hg19 17p13.3-12(chr17:525-11186432)x3 copy number gain not provided [RCV000683866] Chr17:525..11186432 [GRCh37]
Chr17:17p13.3-12		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:12344-81057996)x3 copy number gain not provided [RCV000739325] Chr17:12344..81057996 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:8547-81060040)x3 copy number gain not provided [RCV000739324] Chr17:8547..81060040 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-q25.3(chr17:7214-81058310)x3 copy number gain not provided [RCV000739320] Chr17:7214..81058310 [GRCh37]
Chr17:17p13.3-q25.3		 pathogenic
GRCh37/hg19 17p13.3-13.2(chr17:7214-3871323)x1 copy number loss not provided [RCV000739319] Chr17:7214..3871323 [GRCh37]
Chr17:17p13.3-13.2		 pathogenic
GRCh37/hg19 17p13.3-13.2(chr17:3293338-3372179)x3 copy number gain not provided [RCV000739373] Chr17:3293338..3372179 [GRCh37]
Chr17:17p13.3-13.2		 benign
GRCh37/hg19 17p13.2(chr17:3336162-4918458)x1 copy number loss not provided [RCV000739374] Chr17:3336162..4918458 [GRCh37]
Chr17:17p13.2		 likely pathogenic
GRCh37/hg19 17p13.3-13.2(chr17:2050166-4315506)x1 copy number loss not provided [RCV000751897] Chr17:2050166..4315506 [GRCh37]
Chr17:17p13.3-13.2		 pathogenic
GRCh37/hg19 17p13.3-13.2(chr17:47546-6287620) copy number gain Chromosome 17p13.3, telomeric, duplication syndrome [RCV000767586] Chr17:47546..6287620 [GRCh37]
Chr17:17p13.3-13.2		 pathogenic
GRCh37/hg19 17p13.3-13.2(chr17:3288124-3441645)x1 copy number loss not provided [RCV000849665] Chr17:3288124..3441645 [GRCh37]
Chr17:17p13.3-13.2		 uncertain significance
GRCh37/hg19 17p13.3-13.2(chr17:3160211-3424544)x3 copy number gain not provided [RCV000846629] Chr17:3160211..3424544 [GRCh37]
Chr17:17p13.3-13.2		 uncertain significance
GRCh37/hg19 17p13.3-13.2(chr17:8547-5627408)x1 copy number loss See cases [RCV001007429] Chr17:8547..5627408 [GRCh37]
Chr17:17p13.3-13.2		 pathogenic
GRCh37/hg19 17p13.3-13.2(chr17:3146183-3646235)x3 copy number gain not provided [RCV001006859] Chr17:3146183..3646235 [GRCh37]
Chr17:17p13.3-13.2		 likely benign

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:8190 AgrOrtholog
COSMIC OR1E2 COSMIC
Ensembl Genes ENSG00000127780 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Protein ENSP00000248384 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000248384 ENTREZGENE, UniProtKB/Swiss-Prot
GTEx ENSG00000127780 GTEx
HGNC ID HGNC:8190 ENTREZGENE
Human Proteome Map OR1E2 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:8388 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 8388 ENTREZGENE
Pfam 7tm_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA32063 PharmGKB
PRINTS GPCRRHODOPSN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OLFACTORYR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE G_PROTEIN_RECEP_F1_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  G_PROTEIN_RECEP_F1_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A126GW63_HUMAN UniProtKB/TrEMBL
  A0A126GW81 ENTREZGENE, UniProtKB/TrEMBL
  OR1E2_HUMAN UniProtKB/Swiss-Prot, ENTREZGENE
UniProt Secondary O43877 UniProtKB/Swiss-Prot
  O95632 UniProtKB/Swiss-Prot
  Q0VAD5 UniProtKB/Swiss-Prot
  Q0VAD6 UniProtKB/Swiss-Prot
  Q9UL13 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-15 OR1E2  olfactory receptor family 1 subfamily E member 2    olfactory receptor, family 1, subfamily E, member 2  Symbol and/or name change 5135510 APPROVED
2011-09-01 OR1E2  olfactory receptor, family 1, subfamily E, member 2  OR1E2  olfactory receptor, family 1, subfamily E, member 2  Symbol and/or name change 5135510 APPROVED