OR52I1 (olfactory receptor family 52 subfamily I member 1) - Rat Genome Database

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Gene: OR52I1 (olfactory receptor family 52 subfamily I member 1) Homo sapiens
Analyze
No known orthologs.
Symbol: OR52I1
Name: olfactory receptor family 52 subfamily I member 1
RGD ID: 1349331
HGNC Page HGNC:15220
Description: Predicted to enable olfactory receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway and detection of chemical stimulus involved in sensory perception of smell. Predicted to be located in membrane. Predicted to be active in plasma membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: olfactory receptor 52I1; olfactory receptor OR11-13; olfactory receptor, family 52, subfamily I, member 1; OR11-13
RGD Orthologs
Alliance Genes
More Info homologs ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38114,594,039 - 4,595,013 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl114,594,039 - 4,595,013 (+)EnsemblGRCh38hg38GRCh38
GRCh37114,615,269 - 4,616,243 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36114,571,845 - 4,572,819 (+)NCBINCBI36Build 36hg18NCBI36
Build 34114,571,844 - 4,572,819NCBI
Celera114,739,475 - 4,740,449 (+)NCBICelera
Cytogenetic Map11p15.4NCBI
HuRef114,273,694 - 4,274,668 (+)NCBIHuRef
CHM1_1114,615,203 - 4,616,177 (+)NCBICHM1_1
T2T-CHM13v2.0114,659,330 - 4,660,304 (+)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. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
Additional References at PubMed
PMID:12732197   PMID:14983052   PMID:19795399   PMID:21873635   PMID:33961781  


Genomics

Variants

.
Variants in OR52I1
28 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11p15.4(chr11:3745061-7846057)x3 copy number gain See cases [RCV000053616] Chr11:3745061..7846057 [GRCh38]
Chr11:3766291..7867604 [GRCh37]
Chr11:3722867..7824180 [NCBI36]
Chr11:11p15.4		 pathogenic
GRCh38/hg38 11p15.5-13(chr11:202758-31726224)x3 copy number gain See cases [RCV000053613] Chr11:202758..31726224 [GRCh38]
Chr11:202758..31747772 [GRCh37]
Chr11:192758..31704348 [NCBI36]
Chr11:11p15.5-13		 pathogenic
NM_001005169.1(OR52I1):c.260G>A (p.Ser87Asn) single nucleotide variant Malignant melanoma [RCV000069364] Chr11:4594298 [GRCh38]
Chr11:4615528 [GRCh37]
Chr11:4572104 [NCBI36]
Chr11:11p15.4		 not provided
GRCh38/hg38 11p15.5-15.1(chr11:446754-18904742)x3 copy number gain See cases [RCV000133997] Chr11:446754..18904742 [GRCh38]
Chr11:446754..18926289 [GRCh37]
Chr11:436754..18882865 [NCBI36]
Chr11:11p15.5-15.1		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:61793-10727969)x3 copy number gain See cases [RCV000139987] Chr11:61793..10727969 [GRCh38]
Chr11:61793..10749516 [GRCh37]
Chr11:51793..10706092 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh38/hg38 11p15.5-15.4(chr11:196855-5321874)x3 copy number gain See cases [RCV000142890] Chr11:196855..5321874 [GRCh38]
Chr11:196855..5343104 [GRCh37]
Chr11:186855..5299680 [NCBI36]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.4(chr11:3898872-4853895)x1 copy number loss See cases [RCV000240109] Chr11:3898872..4853895 [GRCh37]
Chr11:11p15.4		 uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:193187-5291338)x3 copy number gain See cases [RCV000446036] Chr11:193187..5291338 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-6644927)x3 copy number gain See cases [RCV000449417] Chr11:230615..6644927 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.4(chr11:4387760-4840438)x3 copy number gain See cases [RCV000454235] Chr11:4387760..4840438 [GRCh37]
Chr11:11p15.4		 uncertain significance
GRCh37/hg19 11p15.4(chr11:4581868-4692979)x1 copy number loss See cases [RCV000446969] Chr11:4581868..4692979 [GRCh37]
Chr11:11p15.4		 likely benign
GRCh37/hg19 11p15.4(chr11:4371631-5253127) copy number gain Abnormal esophagus morphology [RCV000416780] Chr11:4371631..5253127 [GRCh37]
Chr11:11p15.4		 likely pathogenic
GRCh37/hg19 11p15.4(chr11:4364896-4926365)x3 copy number gain See cases [RCV000510292] Chr11:4364896..4926365 [GRCh37]
Chr11:11p15.4		 likely benign
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470) copy number gain See cases [RCV000511729] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.4(chr11:3629582-4677492)x3 copy number gain See cases [RCV000511398] Chr11:3629582..4677492 [GRCh37]
Chr11:11p15.4		 likely benign
GRCh37/hg19 11p15.5-12(chr11:230615-37698540)x3 copy number gain See cases [RCV000511561] Chr11:230615..37698540 [GRCh37]
Chr11:11p15.5-12		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-14.3(chr11:230615-25584362)x3 copy number gain See cases [RCV000512225] Chr11:230615..25584362 [GRCh37]
Chr11:11p15.5-14.3		 pathogenic
GRCh37/hg19 11p15.5-13(chr11:230615-31995219)x3 copy number gain See cases [RCV000512477] Chr11:230615..31995219 [GRCh37]
Chr11:11p15.5-13		 pathogenic
GRCh37/hg19 11p15.5-15.1(chr11:230615-17099213)x3 copy number gain not provided [RCV000683372] Chr11:230615..17099213 [GRCh37]
Chr11:11p15.5-15.1		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-9704511)x3 copy number gain not provided [RCV000683369] Chr11:230615..9704511 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:198510-134934063)x3 copy number gain not provided [RCV000737348] Chr11:198510..134934063 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
GRCh37/hg19 11p15.4(chr11:4533118-4639292)x1 copy number loss not provided [RCV000749918] Chr11:4533118..4639292 [GRCh37]
Chr11:11p15.4		 benign
GRCh37/hg19 11p15.4(chr11:4587253-4687238)x1 copy number loss not provided [RCV000749921] Chr11:4587253..4687238 [GRCh37]
Chr11:11p15.4		 benign
NM_001005169.1(OR52I1):c.240C>G (p.Ser80=) single nucleotide variant not provided [RCV000948383] Chr11:4594278 [GRCh38]
Chr11:4615508 [GRCh37]
Chr11:11p15.4		 benign
NM_001005169.1(OR52I1):c.241G>A (p.Val81Met) single nucleotide variant Inborn genetic diseases [RCV003246494] Chr11:4594279 [GRCh38]
Chr11:4615509 [GRCh37]
Chr11:11p15.4		 uncertain significance
GRCh37/hg19 11p15.5-15.3(chr11:193146-12643136) copy number gain Silver-Russell syndrome 1 [RCV000767567] Chr11:193146..12643136 [GRCh37]
Chr11:11p15.5-15.3		 pathogenic
GRCh37/hg19 11p15.5-13(chr11:235934-33826995)x3 copy number gain not provided [RCV001006372] Chr11:235934..33826995 [GRCh37]
Chr11:11p15.5-13		 pathogenic
GRCh37/hg19 11p15.4(chr11:4384773-4681230)x3 copy number gain not provided [RCV002472402] Chr11:4384773..4681230 [GRCh37]
Chr11:11p15.4		 uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:230616-8250724)x3 copy number gain not provided [RCV002472435] Chr11:230616..8250724 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.4(chr11:4388904-4639840)x3 copy number gain not provided [RCV001259588] Chr11:4388904..4639840 [GRCh37]
Chr11:11p15.4		 uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:210300-8664358)x3 copy number gain Silver-Russell syndrome 1 [RCV001263222] Chr11:210300..8664358 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-4851537)x3 copy number gain See cases [RCV001263059] Chr11:230615..4851537 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:10701-5080415)x2 copy number gain See cases [RCV001310286] Chr11:10701..5080415 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
GRCh37/hg19 11p15.5-15.4(chr11:230615-5525355)x3 copy number gain not provided [RCV001825269] Chr11:230615..5525355 [GRCh37]
Chr11:11p15.5-15.4		 not provided
GRCh37/hg19 11p15.5-14.2(chr11:230615-26881146)x3 copy number gain See cases [RCV002286351] Chr11:230615..26881146 [GRCh37]
Chr11:11p15.5-14.2		 pathogenic
NC_000011.10:g.(499700_4999400)_(5279346_5279697)del deletion Thalassemia, gamma-delta-beta [RCV000015529] Chr11:4999400..5279346 [GRCh38]
Chr11:11p15.5-15.4		 pathogenic
NM_001005169.1(OR52I1):c.314T>C (p.Met105Thr) single nucleotide variant Inborn genetic diseases [RCV002902733] Chr11:4594352 [GRCh38]
Chr11:4615582 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.181G>A (p.Glu61Lys) single nucleotide variant Inborn genetic diseases [RCV002907009] Chr11:4594219 [GRCh38]
Chr11:4615449 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.175C>T (p.Arg59Trp) single nucleotide variant Inborn genetic diseases [RCV002973343] Chr11:4594213 [GRCh38]
Chr11:4615443 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.436C>A (p.Leu146Met) single nucleotide variant Inborn genetic diseases [RCV002682468] Chr11:4594474 [GRCh38]
Chr11:4615704 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.658G>A (p.Ala220Thr) single nucleotide variant Inborn genetic diseases [RCV002945276] Chr11:4594696 [GRCh38]
Chr11:4615926 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.892G>C (p.Gly298Arg) single nucleotide variant Inborn genetic diseases [RCV002774262] Chr11:4594930 [GRCh38]
Chr11:4616160 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.166G>A (p.Asp56Asn) single nucleotide variant Inborn genetic diseases [RCV002973891] Chr11:4594204 [GRCh38]
Chr11:4615434 [GRCh37]
Chr11:11p15.4		 likely benign
NM_001005169.1(OR52I1):c.943T>G (p.Phe315Val) single nucleotide variant Inborn genetic diseases [RCV002759359] Chr11:4594981 [GRCh38]
Chr11:4616211 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.685G>C (p.Val229Leu) single nucleotide variant Inborn genetic diseases [RCV002912416] Chr11:4594723 [GRCh38]
Chr11:4615953 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.454G>A (p.Val152Ile) single nucleotide variant Inborn genetic diseases [RCV003000584] Chr11:4594492 [GRCh38]
Chr11:4615722 [GRCh37]
Chr11:11p15.4		 likely benign
NM_001005169.1(OR52I1):c.185C>T (p.Pro62Leu) single nucleotide variant Inborn genetic diseases [RCV002980281] Chr11:4594223 [GRCh38]
Chr11:4615453 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.938T>C (p.Met313Thr) single nucleotide variant Inborn genetic diseases [RCV002954651] Chr11:4594976 [GRCh38]
Chr11:4616206 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.68G>A (p.Gly23Glu) single nucleotide variant Inborn genetic diseases [RCV002931670] Chr11:4594106 [GRCh38]
Chr11:4615336 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.527A>G (p.Asn176Ser) single nucleotide variant Inborn genetic diseases [RCV002921390] Chr11:4594565 [GRCh38]
Chr11:4615795 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.134G>A (p.Gly45Glu) single nucleotide variant Inborn genetic diseases [RCV002769728] Chr11:4594172 [GRCh38]
Chr11:4615402 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.388A>T (p.Ile130Phe) single nucleotide variant Inborn genetic diseases [RCV002792367] Chr11:4594426 [GRCh38]
Chr11:4615656 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.176G>A (p.Arg59Gln) single nucleotide variant Inborn genetic diseases [RCV002961625] Chr11:4594214 [GRCh38]
Chr11:4615444 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.914T>G (p.Leu305Arg) single nucleotide variant Inborn genetic diseases [RCV002812559] Chr11:4594952 [GRCh38]
Chr11:4616182 [GRCh37]
Chr11:11p15.4		 likely benign
NM_001005169.1(OR52I1):c.802T>G (p.Leu268Val) single nucleotide variant Inborn genetic diseases [RCV003256042] Chr11:4594840 [GRCh38]
Chr11:4616070 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.164T>A (p.Met55Lys) single nucleotide variant Inborn genetic diseases [RCV003260079] Chr11:4594202 [GRCh38]
Chr11:4615432 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.897G>A (p.Met299Ile) single nucleotide variant Inborn genetic diseases [RCV003198014] Chr11:4594935 [GRCh38]
Chr11:4616165 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.533T>C (p.Val178Ala) single nucleotide variant Inborn genetic diseases [RCV003349949] Chr11:4594571 [GRCh38]
Chr11:4615801 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.449T>C (p.Met150Thr) single nucleotide variant Inborn genetic diseases [RCV003370152] Chr11:4594487 [GRCh38]
Chr11:4615717 [GRCh37]
Chr11:11p15.4		 uncertain significance
GRCh37/hg19 11p15.4(chr11:4376571-4623788)x3 copy number gain not provided [RCV003484830] Chr11:4376571..4623788 [GRCh37]
Chr11:11p15.4		 uncertain significance
GRCh37/hg19 11p15.5-15.4(chr11:230615-8821443)x3 copy number gain Russell-Silver syndrome [RCV003444025] Chr11:230615..8821443 [GRCh37]
Chr11:11p15.5-15.4		 pathogenic
NM_001005169.1(OR52I1):c.259A>C (p.Ser87Arg) single nucleotide variant Inborn genetic diseases [RCV003370429] Chr11:4594297 [GRCh38]
Chr11:4615527 [GRCh37]
Chr11:11p15.4		 uncertain significance
NM_001005169.1(OR52I1):c.515T>C (p.Phe172Ser) single nucleotide variant Inborn genetic diseases [RCV003349765] Chr11:4594553 [GRCh38]
Chr11:4615783 [GRCh37]
Chr11:11p15.4		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:160
Count of miRNA genes:80
Interacting mature miRNAs:80
Transcripts:ENST00000450052, ENST00000530443
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.

Markers in Region
SHGC-82187  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37114,608,546 - 4,608,843UniSTSGRCh37
GRCh37114,615,694 - 4,615,991UniSTSGRCh37
Build 36114,565,122 - 4,565,419RGDNCBI36
Celera114,732,752 - 4,733,049RGD
Celera114,739,900 - 4,740,197UniSTS
Cytogenetic Map11p15.4UniSTS
HuRef114,266,971 - 4,267,268UniSTS
HuRef114,274,119 - 4,274,416UniSTS
TNG Radiation Hybrid Map111976.0UniSTS
TNG Radiation Hybrid Map111979.0UniSTS
OR52I1__5885  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37114,615,767 - 4,616,333UniSTSGRCh37
Build 36114,572,343 - 4,572,909RGDNCBI36
Celera114,739,973 - 4,740,539RGD
HuRef114,274,192 - 4,274,758UniSTS


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 1 4 1 14 4 1 12 20 4 3
Below cutoff 646 752 494 136 684 67 719 411 1041 77 661 499 72 184 471 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000450052   ⟹   ENSP00000409094
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl114,593,750 - 4,595,013 (+)Ensembl
RefSeq Acc Id: ENST00000530443   ⟹   ENSP00000436453
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl114,594,039 - 4,595,013 (+)Ensembl
RefSeq Acc Id: NM_001005169   ⟹   NP_001005169
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38114,594,039 - 4,595,013 (+)NCBI
GRCh37114,615,269 - 4,616,243 (+)RGD
Build 36114,571,845 - 4,572,819 (+)NCBI Archive
Celera114,739,475 - 4,740,449 (+)RGD
HuRef114,273,694 - 4,274,668 (+)RGD
CHM1_1114,615,203 - 4,616,177 (+)NCBI
T2T-CHM13v2.0114,659,330 - 4,660,304 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001005169 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein BAC06007 (Get FASTA)   NCBI Sequence Viewer  
  CAJ56788 (Get FASTA)   NCBI Sequence Viewer  
  DAA04769 (Get FASTA)   NCBI Sequence Viewer  
  EAW68836 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000436453
  ENSP00000436453.1
GenBank Protein Q8NGK6 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_001005169   ⟸   NM_001005169
- UniProtKB: Q6IF91 (UniProtKB/Swiss-Prot),   Q8NGK6 (UniProtKB/Swiss-Prot),   A0A126GWB9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000409094   ⟸   ENST00000450052
RefSeq Acc Id: ENSP00000436453   ⟸   ENST00000530443
Protein Domains
G-protein coupled receptors family 1 profile

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8NGK6-F1-model_v2 AlphaFold Q8NGK6 1-324 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:15220 AgrOrtholog
COSMIC OR52I1 COSMIC
Ensembl Genes ENSG00000232268 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000530443 ENTREZGENE
  ENST00000530443.4 UniProtKB/Swiss-Prot
Gene3D-CATH Rhodopsin 7-helix transmembrane proteins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000232268 GTEx
HGNC ID HGNC:15220 ENTREZGENE
Human Proteome Map OR52I1 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:390037 UniProtKB/Swiss-Prot
NCBI Gene 390037 ENTREZGENE
PANTHER OLFACTORY RECEPTOR 52I1-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OLFACTORY RECEPTOR 56B1-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam 7tm_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA32412 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 A0A126GWB9 ENTREZGENE, UniProtKB/TrEMBL
  O52I1_HUMAN UniProtKB/Swiss-Prot
  Q6IF91 ENTREZGENE
  Q8NGK6 ENTREZGENE
UniProt Secondary Q6IF91 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-15 OR52I1  olfactory receptor family 52 subfamily I member 1  OR52I1  olfactory receptor, family 52, subfamily I, member 1  Symbol and/or name change 5135510 APPROVED