OR5T2 (olfactory receptor family 5 subfamily T member 2) - Rat Genome Database

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Gene: OR5T2 (olfactory receptor family 5 subfamily T member 2) Homo sapiens
Analyze
Symbol: OR5T2
Name: olfactory receptor family 5 subfamily T member 2
RGD ID: 1347254
HGNC Page HGNC:15296
Description: Predicted to enable odorant binding activity and olfactory receptor activity. Predicted to be involved in G protein-coupled receptor signaling pathway and sensory perception of smell. Predicted to be located in plasma membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: olfactory receptor 5T2; olfactory receptor OR11-177; olfactory receptor, family 5, subfamily T, member 2; OR11-177
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Pig
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
GRCh381156,231,282 - 56,234,255 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1156,231,282 - 56,234,255 (-)EnsemblGRCh38hg38GRCh38
GRCh371155,998,758 - 56,001,731 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361155,756,158 - 55,757,237 (-)NCBINCBI36Build 36hg18NCBI36
Build 341155,756,157 - 55,757,237NCBI
Celera1153,339,712 - 53,340,791 (-)NCBICelera
Cytogenetic Map11q12.1NCBI
HuRef1152,329,027 - 52,330,106 (-)NCBIHuRef
CHM1_11155,865,104 - 55,866,183 (-)NCBICHM1_1
T2T-CHM13v2.01156,169,635 - 56,172,608 (-)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

Biological Process

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
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:12477932   PMID:14983052   PMID:21873635  


Genomics

Comparative Map Data
OR5T2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381156,231,282 - 56,234,255 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1156,231,282 - 56,234,255 (-)EnsemblGRCh38hg38GRCh38
GRCh371155,998,758 - 56,001,731 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361155,756,158 - 55,757,237 (-)NCBINCBI36Build 36hg18NCBI36
Build 341155,756,157 - 55,757,237NCBI
Celera1153,339,712 - 53,340,791 (-)NCBICelera
Cytogenetic Map11q12.1NCBI
HuRef1152,329,027 - 52,330,106 (-)NCBIHuRef
CHM1_11155,865,104 - 55,866,183 (-)NCBICHM1_1
T2T-CHM13v2.01156,169,635 - 56,172,608 (-)NCBIT2T-CHM13v2.0
Or5t7
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39286,506,743 - 86,507,683 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl286,506,562 - 86,510,436 (-)EnsemblGRCm39 Ensembl
GRCm38286,676,399 - 86,677,339 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl286,676,218 - 86,680,092 (-)EnsemblGRCm38mm10GRCm38
MGSCv37286,516,556 - 86,517,488 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36286,477,238 - 86,478,170 (-)NCBIMGSCv36mm8
Celera288,272,545 - 88,273,477 (-)NCBICelera
Cytogenetic Map2DNCBI
cM Map249.86NCBI
Or5t16
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8392,553,938 - 92,554,873 (-)NCBIGRCr8
mRatBN7.2372,096,981 - 72,097,916 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl372,096,981 - 72,097,916 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx375,543,028 - 75,543,963 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0384,141,589 - 84,142,524 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0381,915,614 - 81,916,549 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0374,574,075 - 74,575,010 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl374,574,075 - 74,575,010 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0381,224,225 - 81,225,160 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4370,380,970 - 70,381,905 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1370,277,341 - 70,278,277 (-)NCBI
Celera371,411,631 - 71,412,566 (-)NCBICelera
Cytogenetic Map3q24NCBI
LOC100967935
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2957,385,785 - 57,389,527 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11158,401,304 - 58,405,050 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01151,470,275 - 51,471,819 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
OR5T2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11839,711,397 - 39,712,317 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1839,236,418 - 39,237,338 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01840,405,799 - 40,406,719 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1840,405,763 - 40,407,584 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11840,011,891 - 40,012,811 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01839,577,917 - 39,578,837 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01840,164,737 - 40,165,657 (-)NCBIUU_Cfam_GSD_1.0
LOC110259573
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1250,410,288 - 50,411,283 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1

Variants

.
Variants in OR5T2
31 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 11q11-12.1(chr11:55445689-57114783)x1 copy number loss See cases [RCV000050913] Chr11:55445689..57114783 [GRCh38]
Chr11:55213165..56882257 [GRCh37]
Chr11:54969741..56638833 [NCBI36]
Chr11:11q11-12.1		 benign
NM_001004746.1(OR5T2):c.965C>T (p.Pro322Leu) single nucleotide variant Malignant melanoma [RCV000069481] Chr11:56232221 [GRCh38]
Chr11:55999697 [GRCh37]
Chr11:55756273 [NCBI36]
Chr11:11q12.1		 not provided
Single allele deletion Intellectual disability [RCV001293382] Chr11:118359328..118372573 [GRCh37]
Chr11:11p15.3-q23.3		 pathogenic
GRCh38/hg38 11q12.1(chr11:56149822-56770518)x3 copy number gain See cases [RCV000134767] Chr11:56149822..56770518 [GRCh38]
Chr11:55917298..56537994 [GRCh37]
Chr11:55673874..56294570 [NCBI36]
Chr11:11q12.1		 benign
GRCh38/hg38 11q11-12.1(chr11:55316535-57539457)x3 copy number gain See cases [RCV000141200] Chr11:55316535..57539457 [GRCh38]
Chr11:55084011..57306930 [GRCh37]
Chr11:54840587..57063506 [NCBI36]
Chr11:11q11-12.1		 uncertain significance
GRCh38/hg38 11q11-12.1(chr11:55319519-58998777)x3 copy number gain See cases [RCV000142757] Chr11:55319519..58998777 [GRCh38]
Chr11:55086995..58766250 [GRCh37]
Chr11:54843571..58522826 [NCBI36]
Chr11:11q11-12.1		 pathogenic
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 11p15.5-q25(chr11:230616-134938470)x3 copy number gain See cases [RCV000510881] Chr11:230616..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
NM_001004746.4(OR5T2):c.721G>A (p.Ala241Thr) single nucleotide variant Inborn genetic diseases [RCV003270306] Chr11:56232342 [GRCh38]
Chr11:55999818 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.505G>T (p.Ala169Ser) single nucleotide variant Inborn genetic diseases [RCV003245321] Chr11:56232558 [GRCh38]
Chr11:56000034 [GRCh37]
Chr11:11q12.1		 likely benign
GRCh37/hg19 11p11.12-q12.1(chr11:51183548-56977098)x3 copy number gain See cases [RCV000512524] Chr11:51183548..56977098 [GRCh37]
Chr11:11p11.12-q12.1		 uncertain significance
GRCh37/hg19 11p11.12-q12.1(chr11:49313405-59008426)x3 copy number gain not provided [RCV000683370] Chr11:49313405..59008426 [GRCh37]
Chr11:11p11.12-q12.1		 uncertain significance
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 11q11-12.1(chr11:54697347-56021284)x3 copy number gain not provided [RCV000737528] Chr11:54697347..56021284 [GRCh37]
Chr11:11q11-12.1		 benign
GRCh37/hg19 11q11-12.1(chr11:54794237-56003589)x3 copy number gain not provided [RCV000737530] Chr11:54794237..56003589 [GRCh37]
Chr11:11q11-12.1		 benign
GRCh37/hg19 11p15.5-q25(chr11:70864-134938470)x3 copy number gain not provided [RCV000749874] Chr11:70864..134938470 [GRCh37]
Chr11:11p15.5-q25		 pathogenic
NM_001004746.4(OR5T2):c.821T>A (p.Ile274Lys) single nucleotide variant Inborn genetic diseases [RCV003245072] Chr11:56232242 [GRCh38]
Chr11:55999718 [GRCh37]
Chr11:11q12.1		 uncertain significance
Single allele duplication not provided [RCV000844966] Chr11:55033164..57518726 [GRCh37]
Chr11:11q11-12.1		 not provided
NM_001004746.4(OR5T2):c.169A>G (p.Met57Val) single nucleotide variant Inborn genetic diseases [RCV003247229] Chr11:56232894 [GRCh38]
Chr11:56000370 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.742A>G (p.Ile248Val) single nucleotide variant Inborn genetic diseases [RCV003273673] Chr11:56232321 [GRCh38]
Chr11:55999797 [GRCh37]
Chr11:11q12.1		 uncertain significance
GRCh37/hg19 11p11.12-q12.1(chr11:51164494-56879839)x3 copy number gain not provided [RCV001827812] Chr11:51164494..56879839 [GRCh37]
Chr11:11p11.12-q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.145A>G (p.Arg49Gly) single nucleotide variant Inborn genetic diseases [RCV003277523] Chr11:56232918 [GRCh38]
Chr11:56000394 [GRCh37]
Chr11:11q12.1		 likely benign
GRCh37/hg19 11p13-q25(chr11:32799481-134938470)x3 copy number gain MISSED ABORTION [RCV002282973] Chr11:32799481..134938470 [GRCh37]
Chr11:11p13-q25		 pathogenic
GRCh37/hg19 11p11.2-q12.2(chr11:51581311-54891247)x3 copy number gain See cases [RCV002286338] Chr11:51581311..54891247 [GRCh37]
Chr11:11p11.2-q12.2		 pathogenic
NM_001004746.4(OR5T2):c.467T>C (p.Ile156Thr) single nucleotide variant Inborn genetic diseases [RCV003282442] Chr11:56232596 [GRCh38]
Chr11:56000072 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.395T>C (p.Val132Ala) single nucleotide variant Inborn genetic diseases [RCV002749102] Chr11:56232668 [GRCh38]
Chr11:56000144 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.928A>T (p.Asn310Tyr) single nucleotide variant Inborn genetic diseases [RCV002688522] Chr11:56232135 [GRCh38]
Chr11:55999611 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.19G>T (p.Val7Phe) single nucleotide variant Inborn genetic diseases [RCV002911436] Chr11:56233044 [GRCh38]
Chr11:56000520 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.944A>C (p.His315Pro) single nucleotide variant Inborn genetic diseases [RCV002665468] Chr11:56232119 [GRCh38]
Chr11:55999595 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.131T>C (p.Ile44Thr) single nucleotide variant Inborn genetic diseases [RCV002743656] Chr11:56232932 [GRCh38]
Chr11:56000408 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.434C>A (p.Ala145Asp) single nucleotide variant Inborn genetic diseases [RCV002743011] Chr11:56232629 [GRCh38]
Chr11:56000105 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.852T>A (p.Asn284Lys) single nucleotide variant Inborn genetic diseases [RCV002986640] Chr11:56232211 [GRCh38]
Chr11:55999687 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.431A>C (p.Asn144Thr) single nucleotide variant Inborn genetic diseases [RCV002955747] Chr11:56232632 [GRCh38]
Chr11:56000108 [GRCh37]
Chr11:11q12.1		 likely benign
NM_001004746.4(OR5T2):c.164A>G (p.Lys55Arg) single nucleotide variant Inborn genetic diseases [RCV002813798] Chr11:56232899 [GRCh38]
Chr11:56000375 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.434C>T (p.Ala145Val) single nucleotide variant Inborn genetic diseases [RCV002812654] Chr11:56232629 [GRCh38]
Chr11:56000105 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.-12C>A single nucleotide variant Inborn genetic diseases [RCV002936403] Chr11:56233074 [GRCh38]
Chr11:56000550 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.626T>C (p.Ile209Thr) single nucleotide variant Inborn genetic diseases [RCV002669176] Chr11:56232437 [GRCh38]
Chr11:55999913 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.503G>A (p.Gly168Glu) single nucleotide variant Inborn genetic diseases [RCV002965003] Chr11:56232560 [GRCh38]
Chr11:56000036 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.382C>T (p.Leu128Phe) single nucleotide variant Inborn genetic diseases [RCV002724089] Chr11:56232681 [GRCh38]
Chr11:56000157 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.875A>G (p.Asn292Ser) single nucleotide variant Inborn genetic diseases [RCV003196918] Chr11:56232188 [GRCh38]
Chr11:55999664 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.865A>G (p.Ser289Gly) single nucleotide variant Inborn genetic diseases [RCV003201310] Chr11:56232198 [GRCh38]
Chr11:55999674 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.38A>G (p.Lys13Arg) single nucleotide variant Inborn genetic diseases [RCV003173607] Chr11:56233025 [GRCh38]
Chr11:56000501 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.149A>T (p.Asp50Val) single nucleotide variant Inborn genetic diseases [RCV003211477] Chr11:56232914 [GRCh38]
Chr11:56000390 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.739T>C (p.Ser247Pro) single nucleotide variant Inborn genetic diseases [RCV003191230] Chr11:56232324 [GRCh38]
Chr11:55999800 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.812T>C (p.Ile271Thr) single nucleotide variant Inborn genetic diseases [RCV003357391] Chr11:56232251 [GRCh38]
Chr11:55999727 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.515T>A (p.Ile172Asn) single nucleotide variant Inborn genetic diseases [RCV003345670] Chr11:56232548 [GRCh38]
Chr11:56000024 [GRCh37]
Chr11:11q12.1		 uncertain significance
NM_001004746.4(OR5T2):c.909T>G (p.Phe303Leu) single nucleotide variant Inborn genetic diseases [RCV003372472] Chr11:56232154 [GRCh38]
Chr11:55999630 [GRCh37]
Chr11:11q12.1		 uncertain significance
GRCh37/hg19 11p11.12-q13.1(chr11:50398499-63924462)x3 copy number gain not specified [RCV003986918] Chr11:50398499..63924462 [GRCh37]
Chr11:11p11.12-q13.1		 likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:131
Count of miRNA genes:130
Interacting mature miRNAs:131
Transcripts:ENST00000313264
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 1 8 2
Below cutoff 43 38 19 9 35 8 67 35 67 7 262 26 1 12 34

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000313264   ⟹   ENSP00000323688
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1156,232,014 - 56,233,261 (-)Ensembl
RefSeq Acc Id: ENST00000641661   ⟹   ENSP00000493233
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1156,231,282 - 56,234,255 (-)Ensembl
RefSeq Acc Id: NM_001004746   ⟹   NP_001004746
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381156,231,282 - 56,234,255 (-)NCBI
GRCh371155,999,582 - 56,000,661 (-)RGD
Build 361155,756,158 - 55,757,237 (-)NCBI Archive
Celera1153,339,712 - 53,340,791 (-)RGD
HuRef1152,329,027 - 52,330,106 (-)RGD
CHM1_11155,865,104 - 55,866,183 (-)NCBI
T2T-CHM13v2.01156,169,635 - 56,172,608 (-)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_001004746   ⟸   NM_001004746
- UniProtKB: Q8NGG2 (UniProtKB/Swiss-Prot),   Q6IFC8 (UniProtKB/Swiss-Prot),   B9EGX5 (UniProtKB/Swiss-Prot),   A0A286YF86 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000323688   ⟸   ENST00000313264
RefSeq Acc Id: ENSP00000493233   ⟸   ENST00000641661
Protein Domains
G-protein coupled receptors family 1 profile

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q8NGG2-F1-model_v2 AlphaFold Q8NGG2 1-359 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:15296 AgrOrtholog
COSMIC OR5T2 COSMIC
Ensembl Genes ENSG00000181718 Ensembl, ENTREZGENE, UniProtKB/TrEMBL
  ENSG00000262851 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000573647.2 UniProtKB/Swiss-Prot
  ENST00000641661 ENTREZGENE
  ENST00000641661.1 UniProtKB/TrEMBL
Gene3D-CATH Rhodopsin 7-helix transmembrane proteins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000181718 GTEx
  ENSG00000262851 GTEx
HGNC ID HGNC:15296 ENTREZGENE
Human Proteome Map OR5T2 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:219464 UniProtKB/Swiss-Prot
NCBI Gene 219464 ENTREZGENE
PANTHER OLFACTORY RECEPTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OLFACTORY RECEPTOR 5T2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam 7tm_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA32567 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 A0A126GVS3_HUMAN UniProtKB/TrEMBL
  A0A126GW02_HUMAN UniProtKB/TrEMBL
  A0A286YF86 ENTREZGENE, UniProtKB/TrEMBL
  B9EGX5 ENTREZGENE
  OR5T2_HUMAN UniProtKB/Swiss-Prot
  Q6IFC8 ENTREZGENE
  Q8NGG2 ENTREZGENE
UniProt Secondary B9EGX5 UniProtKB/Swiss-Prot
  Q6IFC8 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-15 OR5T2  olfactory receptor family 5 subfamily T member 2  OR5T2  olfactory receptor, family 5, subfamily T, member 2  Symbol and/or name change 5135510 APPROVED