OR1I1 (olfactory receptor family 1 subfamily I member 1) - Rat Genome Database

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Gene: OR1I1 (olfactory receptor family 1 subfamily I member 1) Homo sapiens
Analyze
Symbol: OR1I1
Name: olfactory receptor family 1 subfamily I member 1
RGD ID: 1350140
HGNC Page HGNC:8207
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: olfactory receptor 19-20; olfactory receptor 1I1; olfactory receptor, family 1, subfamily I, member 1; OR19-20; OR1I1P; OR1I1Q
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
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
GRCh381915,082,211 - 15,092,970 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1915,082,211 - 15,092,970 (+)EnsemblGRCh38hg38GRCh38
GRCh371915,193,022 - 15,203,781 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361915,058,877 - 15,059,944 (+)NCBINCBI36Build 36hg18NCBI36
Build 341915,058,876 - 15,059,944NCBI
Celera1915,093,586 - 15,094,653 (+)NCBICelera
Cytogenetic Map19p13.12NCBI
HuRef1914,765,566 - 14,766,633 (+)NCBIHuRef
CHM1_11915,197,371 - 15,198,438 (+)NCBICHM1_1
T2T-CHM13v2.01915,207,150 - 15,217,911 (+)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)
plasma membrane  (IBA,IEA)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12213199   PMID:12477932   PMID:15057824   PMID:21873635   PMID:32126975   PMID:33660365  


Genomics

Comparative Map Data
OR1I1
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381915,082,211 - 15,092,970 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1915,082,211 - 15,092,970 (+)EnsemblGRCh38hg38GRCh38
GRCh371915,193,022 - 15,203,781 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361915,058,877 - 15,059,944 (+)NCBINCBI36Build 36hg18NCBI36
Build 341915,058,876 - 15,059,944NCBI
Celera1915,093,586 - 15,094,653 (+)NCBICelera
Cytogenetic Map19p13.12NCBI
HuRef1914,765,566 - 14,766,633 (+)NCBIHuRef
CHM1_11915,197,371 - 15,198,438 (+)NCBICHM1_1
T2T-CHM13v2.01915,207,150 - 15,217,911 (+)NCBIT2T-CHM13v2.0
Or1i2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391078,447,503 - 78,453,908 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1078,446,837 - 78,453,908 (-)EnsemblGRCm39 Ensembl
GRCm381078,611,669 - 78,618,074 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1078,611,003 - 78,618,074 (-)EnsemblGRCm38mm10GRCm38
MGSCv371078,074,414 - 78,080,819 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361078,014,827 - 78,015,768 (-)NCBIMGSCv36mm8
Celera1079,633,878 - 79,640,283 (-)NCBICelera
Cytogenetic Map10C1NCBI
cM Map1039.72NCBI
Or1i2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8711,636,515 - 11,637,456 (+)NCBIGRCr8
mRatBN7.2710,985,938 - 10,986,879 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl710,980,344 - 10,987,036 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx713,806,473 - 13,807,414 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0715,683,865 - 15,684,806 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0713,561,762 - 13,562,703 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0713,996,966 - 13,997,907 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl713,996,966 - 13,997,907 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0714,153,449 - 14,154,390 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4712,543,995 - 12,544,936 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1712,543,994 - 12,544,936 (+)NCBI
Celera79,103,332 - 9,104,273 (+)NCBICelera
Cytogenetic Map7q11NCBI
LOC102012872
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554958,171,204 - 8,172,145 (-)EnsemblChiLan1.0
ChiLan1.0NW_0049554958,171,204 - 8,172,145 (-)NCBIChiLan1.0ChiLan1.0
LOC134729652
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22019,998,913 - 19,999,953 (+)NCBINHGRI_mPanPan1-v2
OR1I1
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12047,037,917 - 47,038,873 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2047,037,917 - 47,146,610 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2046,888,653 - 46,889,609 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02047,530,991 - 47,531,947 (-)NCBIROS_Cfam_1.0
UMICH_Zoey_3.12046,762,423 - 46,763,379 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02047,181,614 - 47,182,570 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02047,452,759 - 47,453,715 (-)NCBIUU_Cfam_GSD_1.0
LOC101977308
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405118205,818,354 - 205,819,322 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365965,367,493 - 5,368,434 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365965,367,493 - 5,368,693 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
LOC100523537
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl262,470,357 - 62,471,298 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1262,470,108 - 62,471,575 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2262,031,244 - 62,032,482 (-)NCBISscrofa10.2Sscrofa10.2susScr3
LOC103234061
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1613,682,193 - 13,683,939 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl613,682,583 - 13,683,647 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660745,844,972 - 5,846,239 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
LOC101705676
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046249012,175,915 - 2,176,856 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046249012,175,915 - 2,177,027 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in OR1I1
16 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19p13.12-q11(chr19:13974677-27839676)x3 copy number gain See cases [RCV000052912] Chr19:13974677..27839676 [GRCh38]
Chr19:14085489..28330584 [GRCh37]
Chr19:13946489..33022424 [NCBI36]
Chr19:19p13.12-q11		 pathogenic
GRCh38/hg38 19p13.12(chr19:14477761-15133653)x3 copy number gain See cases [RCV000133793] Chr19:14477761..15133653 [GRCh38]
Chr19:14588573..15244464 [GRCh37]
Chr19:14449573..15105464 [NCBI36]
Chr19:19p13.12		 uncertain significance
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3 copy number gain See cases [RCV000133888] Chr19:11227942..44626354 [GRCh38]
Chr19:11338618..45129651 [GRCh37]
Chr19:11199618..49821491 [NCBI36]
Chr19:19p13.2-q13.31		 pathogenic
GRCh38/hg38 19p13.12-13.11(chr19:14154962-16914313)x1 copy number loss See cases [RCV000134176] Chr19:14154962..16914313 [GRCh38]
Chr19:14265774..17025123 [GRCh37]
Chr19:14126774..16886123 [NCBI36]
Chr19:19p13.12-13.11		 pathogenic
GRCh38/hg38 19p13.13-13.12(chr19:13533925-15371089)x1 copy number loss See cases [RCV000136502] Chr19:13533925..15371089 [GRCh38]
Chr19:13644739..15481900 [GRCh37]
Chr19:13505739..15342900 [NCBI36]
Chr19:19p13.13-13.12		 pathogenic
GRCh38/hg38 19p13.12(chr19:14406909-15410770)x1 copy number loss See cases [RCV000136896] Chr19:14406909..15410770 [GRCh38]
Chr19:14517721..15521581 [GRCh37]
Chr19:14378721..15382581 [NCBI36]
Chr19:19p13.12		 uncertain significance
GRCh37/hg19 19p13.12-13.11(chr19:14124666-16431349)x1 copy number loss See cases [RCV000448818] Chr19:14124666..16431349 [GRCh37]
Chr19:19p13.12-13.11		 pathogenic
GRCh37/hg19 19p13.12-13.11(chr19:14883158-16788770)x1 copy number loss See cases [RCV000511367] Chr19:14883158..16788770 [GRCh37]
Chr19:19p13.12-13.11		 pathogenic
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
NM_001004713.2(OR1I1):c.364C>T (p.Arg122Cys) single nucleotide variant Inborn genetic diseases [RCV003292059] Chr19:15087429 [GRCh38]
Chr19:15198240 [GRCh37]
Chr19:19p13.12		 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-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
GRCh37/hg19 19p13.12(chr19:14368330-15712368)x1 copy number loss not provided [RCV001007034] Chr19:14368330..15712368 [GRCh37]
Chr19:19p13.12		 pathogenic
NM_001004713.2(OR1I1):c.659G>A (p.Arg220His) single nucleotide variant not provided [RCV000957923] Chr19:15087724 [GRCh38]
Chr19:15198535 [GRCh37]
Chr19:19p13.12		 benign
GRCh37/hg19 19p13.12-12(chr19:14286624-20956753)x3 copy number gain not provided [RCV001259370] Chr19:14286624..20956753 [GRCh37]
Chr19:19p13.12-12		 pathogenic
GRCh37/hg19 19p13.12(chr19:15184922-15582812) copy number gain not specified [RCV002052676] Chr19:15184922..15582812 [GRCh37]
Chr19:19p13.12		 uncertain significance
GRCh37/hg19 19p13.12-13.11(chr19:14124666-16431349) copy number loss not specified [RCV002052675] Chr19:14124666..16431349 [GRCh37]
Chr19:19p13.12-13.11		 pathogenic
NC_000019.9:g.(?_14847048)_(17394124_?)del deletion not provided [RCV003116664] Chr19:14847048..17394124 [GRCh37]
Chr19:19p13.12-13.11		 uncertain significance
NM_001004713.2(OR1I1):c.1024C>T (p.Pro342Ser) single nucleotide variant Inborn genetic diseases [RCV002860710] Chr19:15088089 [GRCh38]
Chr19:15198900 [GRCh37]
Chr19:19p13.12		 uncertain significance
NM_001004713.2(OR1I1):c.838G>A (p.Val280Met) single nucleotide variant Inborn genetic diseases [RCV002687284] Chr19:15087903 [GRCh38]
Chr19:15198714 [GRCh37]
Chr19:19p13.12		 uncertain significance
NM_001004713.2(OR1I1):c.118A>C (p.Ile40Leu) single nucleotide variant Inborn genetic diseases [RCV002865171] Chr19:15087183 [GRCh38]
Chr19:15197994 [GRCh37]
Chr19:19p13.12		 uncertain significance
NM_001004713.2(OR1I1):c.370G>A (p.Val124Met) single nucleotide variant Inborn genetic diseases [RCV002661134] Chr19:15087435 [GRCh38]
Chr19:15198246 [GRCh37]
Chr19:19p13.12		 uncertain significance
NM_001004713.2(OR1I1):c.360C>G (p.Ile120Met) single nucleotide variant Inborn genetic diseases [RCV002693464] Chr19:15087425 [GRCh38]
Chr19:15198236 [GRCh37]
Chr19:19p13.12		 uncertain significance
NM_001004713.2(OR1I1):c.195C>G (p.Asn65Lys) single nucleotide variant Inborn genetic diseases [RCV002910335] Chr19:15087260 [GRCh38]
Chr19:15198071 [GRCh37]
Chr19:19p13.12		 uncertain significance
NM_001004713.2(OR1I1):c.391C>T (p.Arg131Cys) single nucleotide variant Inborn genetic diseases [RCV002739450] Chr19:15087456 [GRCh38]
Chr19:15198267 [GRCh37]
Chr19:19p13.12		 uncertain significance
NM_001004713.2(OR1I1):c.166C>T (p.His56Tyr) single nucleotide variant Inborn genetic diseases [RCV002787123] Chr19:15087231 [GRCh38]
Chr19:15198042 [GRCh37]
Chr19:19p13.12		 uncertain significance
NM_001004713.2(OR1I1):c.395A>G (p.Tyr132Cys) single nucleotide variant Inborn genetic diseases [RCV002930674] Chr19:15087460 [GRCh38]
Chr19:15198271 [GRCh37]
Chr19:19p13.12		 uncertain significance
NM_001004713.2(OR1I1):c.509C>T (p.Ala170Val) single nucleotide variant Inborn genetic diseases [RCV002897915] Chr19:15087574 [GRCh38]
Chr19:15198385 [GRCh37]
Chr19:19p13.12		 uncertain significance
NM_001004713.2(OR1I1):c.354G>A (p.Met118Ile) single nucleotide variant Inborn genetic diseases [RCV003203616] Chr19:15087419 [GRCh38]
Chr19:15198230 [GRCh37]
Chr19:19p13.12		 uncertain significance
NM_001004713.2(OR1I1):c.239A>T (p.Lys80Met) single nucleotide variant Inborn genetic diseases [RCV003200189] Chr19:15087304 [GRCh38]
Chr19:15198115 [GRCh37]
Chr19:19p13.12		 uncertain significance
GRCh38/hg38 19p13.12-13.11(chr19:15014099-16261691) copy number loss Chromosome 19p13.13 deletion syndrome [RCV003223562] Chr19:15014099..16261691 [GRCh38]
Chr19:19p13.12-13.11		 pathogenic|uncertain significance
NM_001004713.2(OR1I1):c.281T>C (p.Phe94Ser) single nucleotide variant Inborn genetic diseases [RCV003282700] Chr19:15087346 [GRCh38]
Chr19:15198157 [GRCh37]
Chr19:19p13.12		 uncertain significance
GRCh37/hg19 19p13.12-13.11(chr19:14888106-17360864)x3 copy number gain not provided [RCV003485195] Chr19:14888106..17360864 [GRCh37]
Chr19:19p13.12-13.11		 uncertain significance
GRCh37/hg19 19p13.13-13.11(chr19:13970692-18139376)x3 copy number gain not specified [RCV003986122] Chr19:13970692..18139376 [GRCh37]
Chr19:19p13.13-13.11		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:139
Count of miRNA genes:136
Interacting mature miRNAs:139
Transcripts:ENST00000209540
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
High
Medium
Low 2 4 2
Below cutoff 211 326 154 38 166 23 516 184 332 10 233 162 15 137 342

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000209540   ⟹   ENSP00000209540
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1915,086,980 - 15,088,221 (+)Ensembl
RefSeq Acc Id: ENST00000641398   ⟹   ENSP00000493393
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1915,082,211 - 15,092,970 (+)Ensembl
RefSeq Acc Id: NM_001004713   ⟹   NP_001004713
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381915,082,211 - 15,092,970 (+)NCBI
GRCh371915,197,877 - 15,198,944 (+)RGD
Build 361915,058,877 - 15,059,944 (+)NCBI Archive
Celera1915,093,586 - 15,094,653 (+)RGD
HuRef1914,765,566 - 14,766,633 (+)RGD
CHM1_11915,197,371 - 15,198,438 (+)NCBI
T2T-CHM13v2.01915,207,150 - 15,217,911 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001004713 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAC18915 (Get FASTA)   NCBI Sequence Viewer  
  AAI40931 (Get FASTA)   NCBI Sequence Viewer  
  AAK95033 (Get FASTA)   NCBI Sequence Viewer  
  ALI87655 (Get FASTA)   NCBI Sequence Viewer  
  EAW84460 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000209540.2
  ENSP00000493393
  ENSP00000493393.1
GenBank Protein O60431 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001004713   ⟸   NM_001004713
- UniProtKB: B2RU23 (UniProtKB/Swiss-Prot),   Q96R92 (UniProtKB/Swiss-Prot),   O60431 (UniProtKB/Swiss-Prot),   A0A126GW67 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000209540   ⟸   ENST00000209540
RefSeq Acc Id: ENSP00000493393   ⟸   ENST00000641398
Protein Domains
G-protein coupled receptors family 1 profile

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O60431-F1-model_v2 AlphaFold O60431 1-355 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:8207 AgrOrtholog
COSMIC OR1I1 COSMIC
Ensembl Genes ENSG00000094661 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000209540.2 UniProtKB/Swiss-Prot
  ENST00000641398 ENTREZGENE
  ENST00000641398.1 UniProtKB/Swiss-Prot
Gene3D-CATH Rhodopsin 7-helix transmembrane proteins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000094661 GTEx
HGNC ID HGNC:8207 ENTREZGENE
Human Proteome Map OR1I1 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:126370 UniProtKB/Swiss-Prot
NCBI Gene 126370 ENTREZGENE
PANTHER OLFACTORY RECEPTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OLFACTORY RECEPTOR 1I1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam 7tm_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA32078 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
Superfamily-SCOP Family A G protein-coupled receptor-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A126GW67 ENTREZGENE, UniProtKB/TrEMBL
  B2RU23 ENTREZGENE
  O60431 ENTREZGENE, UniProtKB/Swiss-Prot
  Q96R92 ENTREZGENE
UniProt Secondary B2RU23 UniProtKB/Swiss-Prot
  Q96R92 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-15 OR1I1  olfactory receptor family 1 subfamily I member 1  OR1I1  olfactory receptor, family 1, subfamily I, member 1  Symbol and/or name change 5135510 APPROVED