OR6A2 (olfactory receptor family 6 subfamily A member 2) - Rat Genome Database

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Gene: OR6A2 (olfactory receptor family 6 subfamily A member 2) Homo sapiens
Analyze
Symbol: OR6A2
Name: olfactory receptor family 6 subfamily A member 2
RGD ID: 1605112
HGNC Page HGNC:15301
Description: Predicted to enable olfactory receptor activity. Predicted to be involved in 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: hI7 olfactory receptor; hP2 olfactory receptor; I7; MGC126538; MGC126540; olfactory receptor 11-55; olfactory receptor 6A1; olfactory receptor 6A2; olfactory receptor OR11-83; olfactory receptor, family 6, subfamily A, member 1; olfactory receptor, family 6, subfamily A, member 2 pseudogene; OR11-55; OR6A1; OR6A2P; seven transmembrane helix receptor
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
GRCh38116,791,736 - 6,799,689 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl116,791,736 - 6,799,689 (-)EnsemblGRCh38hg38GRCh38
GRCh37116,812,967 - 6,820,920 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36116,772,332 - 6,773,715 (-)NCBINCBI36Build 36hg18NCBI36
Celera116,934,849 - 6,936,232 (-)NCBICelera
Cytogenetic Map11p15.4NCBI
HuRef116,474,715 - 6,476,098 (-)NCBIHuRef
CHM1_1116,814,666 - 6,816,049 (-)NCBICHM1_1
T2T-CHM13v2.0116,850,158 - 6,858,111 (-)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
membrane  (IEA,NAS)
plasma membrane  (IBA,IEA)

Molecular Function

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:9787077   PMID:11416212   PMID:12477932   PMID:14983052   PMID:15489334   PMID:20608641   PMID:21873635   PMID:33961781   PMID:35025664   PMID:35283015  


Genomics

Comparative Map Data
OR6A2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38116,791,736 - 6,799,689 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl116,791,736 - 6,799,689 (-)EnsemblGRCh38hg38GRCh38
GRCh37116,812,967 - 6,820,920 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36116,772,332 - 6,773,715 (-)NCBINCBI36Build 36hg18NCBI36
Celera116,934,849 - 6,936,232 (-)NCBICelera
Cytogenetic Map11p15.4NCBI
HuRef116,474,715 - 6,476,098 (-)NCBIHuRef
CHM1_1116,814,666 - 6,816,049 (-)NCBICHM1_1
T2T-CHM13v2.0116,850,158 - 6,858,111 (-)NCBIT2T-CHM13v2.0
Or6a2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm397106,600,082 - 106,601,812 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl7106,594,606 - 106,605,279 (-)EnsemblGRCm39 Ensembl
GRCm387107,000,875 - 107,002,605 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl7106,995,399 - 107,006,072 (-)EnsemblGRCm38mm10GRCm38
MGSCv377114,144,389 - 114,146,119 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv367106,794,524 - 106,795,507 (-)NCBIMGSCv36mm8
Celera7107,026,760 - 107,028,491 (-)NCBICelera
Cytogenetic Map7E3NCBI
cM Map756.1NCBI
Or6a2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81170,239,077 - 170,240,060 (-)NCBIGRCr8
mRatBN7.21160,827,258 - 160,828,241 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1160,793,997 - 160,831,557 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1169,081,390 - 169,082,373 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01176,267,393 - 176,268,376 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01168,949,932 - 168,950,915 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01148,846,679 - 148,847,662 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1148,846,679 - 148,847,662 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0 Ensembl1171,059,028 - 171,060,011 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01155,149,851 - 155,150,834 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41164,256,455 - 164,257,438 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11164,351,931 - 164,352,915 (-)NCBI
Celera1158,741,544 - 158,742,527 (-)NCBICelera
Cytogenetic Map1q33NCBI
LOC102005030
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541422,706,291 - 22,707,274 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495541422,706,291 - 22,707,274 (-)NCBIChiLan1.0ChiLan1.0
LOC100974335
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v299,234,603 - 9,332,485 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1119,193,057 - 9,362,922 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0116,924,625 - 6,930,405 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1116,612,202 - 6,613,379 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl116,612,202 - 6,613,185 (-)Ensemblpanpan1.1panPan2
OR6A2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12130,254,194 - 30,255,177 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2130,254,194 - 30,255,177 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2129,925,295 - 29,926,278 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02131,073,199 - 31,074,182 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2131,073,199 - 31,074,182 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12130,387,427 - 30,388,410 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02130,548,327 - 30,549,310 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02130,750,181 - 30,751,164 (-)NCBIUU_Cfam_GSD_1.0
LOC101975950
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494755,040,836 - 55,042,517 (+)NCBIHiC_Itri_2
SpeTri2.0NW_00493684145,223 - 46,348 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
LOC100738942
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl92,702,533 - 2,703,516 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.192,700,569 - 2,705,447 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.293,513,421 - 3,514,618 (-)NCBISscrofa10.2Sscrofa10.2susScr3
LOC103241237
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1158,032,819 - 58,036,267 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666038155,803,171 - 155,804,165 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
LOC101698941
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248178,578,482 - 8,579,465 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248178,578,482 - 8,579,465 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in OR6A2
21 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_003696.2(OR6A2):c.467G>A (p.Gly156Glu) single nucleotide variant Malignant melanoma [RCV000069645] Chr11:6795242 [GRCh38]
Chr11:6816473 [GRCh37]
Chr11:6773049 [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
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 11p15.5-12(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 11p15.5-15.3(chr11:193146-12643136) copy number gain Silver-Russell syndrome 1 [RCV000767567] Chr11:193146..12643136 [GRCh37]
Chr11:11p15.5-15.3
pathogenic
GRCh37/hg19 11p15.5-14.3(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 11p15.5-15.4(chr11:230615-9704511)x3 copy number gain not provided [RCV000683369] Chr11:230615..9704511 [GRCh37]
Chr11:11p15.5-15.4
pathogenic
GRCh37/hg19 11p15.5-15.1(chr11:230615-17099213)x3 copy number gain not provided [RCV000683372] Chr11:230615..17099213 [GRCh37]
Chr11:11p15.5-15.1
pathogenic
GRCh37/hg19 11p15.5-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(chr11:6754444-6982365)x1 copy number loss not provided [RCV000846230] Chr11:6754444..6982365 [GRCh37]
Chr11:11p15.4
uncertain significance
GRCh37/hg19 11p15.5-13(chr11:235934-33826995)x3 copy number gain not provided [RCV001006372] Chr11:235934..33826995 [GRCh37]
Chr11:11p15.5-13
pathogenic
NM_003696.3(OR6A2):c.668A>G (p.Tyr223Cys) single nucleotide variant Inborn genetic diseases [RCV003240248] Chr11:6795041 [GRCh38]
Chr11:6816272 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.650_651del (p.Ser217fs) microsatellite not provided [RCV000956903] Chr11:6795058..6795059 [GRCh38]
Chr11:6816289..6816290 [GRCh37]
Chr11:11p15.4
benign
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
NM_003696.3(OR6A2):c.447_456del (p.Met149fs) deletion not provided [RCV001811700] Chr11:6795253..6795262 [GRCh38]
Chr11:6816484..6816493 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.199A>G (p.Met67Val) single nucleotide variant not provided [RCV001812565] Chr11:6795510 [GRCh38]
Chr11:6816741 [GRCh37]
Chr11:11p15.4
uncertain significance
GRCh37/hg19 11p15.4(chr11:6502523-7248333)x3 copy number gain not provided [RCV001836564] Chr11:6502523..7248333 [GRCh37]
Chr11:11p15.4
uncertain significance
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
NM_003696.3(OR6A2):c.560C>G (p.Ser187Cys) single nucleotide variant Inborn genetic diseases [RCV002991037] Chr11:6795149 [GRCh38]
Chr11:6816380 [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
NM_003696.3(OR6A2):c.370G>T (p.Ala124Ser) single nucleotide variant Inborn genetic diseases [RCV002754370] Chr11:6795339 [GRCh38]
Chr11:6816570 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.251C>T (p.Ala84Val) single nucleotide variant Inborn genetic diseases [RCV002817156] Chr11:6795458 [GRCh38]
Chr11:6816689 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.590T>G (p.Met197Arg) single nucleotide variant Inborn genetic diseases [RCV002688327] Chr11:6795119 [GRCh38]
Chr11:6816350 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.387G>A (p.Met129Ile) single nucleotide variant Inborn genetic diseases [RCV002821146] Chr11:6795322 [GRCh38]
Chr11:6816553 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.793G>T (p.Ala265Ser) single nucleotide variant Inborn genetic diseases [RCV002924431] Chr11:6794916 [GRCh38]
Chr11:6816147 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.622G>A (p.Ala208Thr) single nucleotide variant Inborn genetic diseases [RCV002764921] Chr11:6795087 [GRCh38]
Chr11:6816318 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.262G>C (p.Gly88Arg) single nucleotide variant Inborn genetic diseases [RCV002854318] Chr11:6795447 [GRCh38]
Chr11:6816678 [GRCh37]
Chr11:11p15.4
likely benign
NM_003696.3(OR6A2):c.893G>A (p.Arg298His) single nucleotide variant Inborn genetic diseases [RCV002699194] Chr11:6794816 [GRCh38]
Chr11:6816047 [GRCh37]
Chr11:11p15.4
likely benign
NM_003696.3(OR6A2):c.392T>C (p.Ile131Thr) single nucleotide variant Inborn genetic diseases [RCV002669736] Chr11:6795317 [GRCh38]
Chr11:6816548 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.445A>G (p.Met149Val) single nucleotide variant Inborn genetic diseases [RCV002934335] Chr11:6795264 [GRCh38]
Chr11:6816495 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.845T>C (p.Leu282Pro) single nucleotide variant Inborn genetic diseases [RCV003219850] Chr11:6794864 [GRCh38]
Chr11:6816095 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.791A>T (p.Tyr264Phe) single nucleotide variant Inborn genetic diseases [RCV003283783] Chr11:6794918 [GRCh38]
Chr11:6816149 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.904G>A (p.Val302Ile) single nucleotide variant Inborn genetic diseases [RCV003188431] Chr11:6794805 [GRCh38]
Chr11:6816036 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.856A>G (p.Ile286Val) single nucleotide variant Inborn genetic diseases [RCV003192996] Chr11:6794853 [GRCh38]
Chr11:6816084 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.542A>G (p.His181Arg) single nucleotide variant Inborn genetic diseases [RCV003219676] Chr11:6795167 [GRCh38]
Chr11:6816398 [GRCh37]
Chr11:11p15.4
uncertain significance
NM_003696.3(OR6A2):c.385A>G (p.Met129Val) single nucleotide variant Inborn genetic diseases [RCV003345499] Chr11:6795324 [GRCh38]
Chr11:6816555 [GRCh37]
Chr11:11p15.4
likely benign
NM_003696.3(OR6A2):c.166C>T (p.Leu56Phe) single nucleotide variant Inborn genetic diseases [RCV003367063] Chr11:6795543 [GRCh38]
Chr11:6816774 [GRCh37]
Chr11:11p15.4
uncertain significance
GRCh37/hg19 11p15.4(chr11:6801941-7136661)x3 copy number gain not provided [RCV003484831] Chr11:6801941..7136661 [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
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:129
Count of miRNA genes:127
Interacting mature miRNAs:128
Transcripts:ENST00000332601
Prediction methods:Microtar, 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
OR6A2__5928  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37116,815,579 - 6,816,196UniSTSGRCh37
Build 36116,772,155 - 6,772,772RGDNCBI36
Celera116,934,672 - 6,935,289RGD
HuRef116,474,538 - 6,475,155UniSTS
Olfr2  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37116,816,275 - 6,816,777UniSTSGRCh37
Celera116,935,368 - 6,935,870UniSTS
HuRef116,475,234 - 6,475,736UniSTS
UniSTS:485547  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37116,815,858 - 6,817,014UniSTSGRCh37
Celera116,934,951 - 6,936,107UniSTS
HuRef116,474,817 - 6,475,973UniSTS


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 1 1
Low 1 1 3 5 3 5 74 2 1 2
Below cutoff 618 528 466 126 369 58 706 283 1025 76 698 545 69 183 474 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_003696 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB065822 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC002555 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC087280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF065870 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF321237 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF399472 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC101489 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC101491 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK004427 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK004533 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK004672 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK004705 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BK004735 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471064 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068267 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KP290513 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000332601   ⟹   ENSP00000330384
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl116,794,525 - 6,795,897 (-)Ensembl
RefSeq Acc Id: ENST00000641196   ⟹   ENSP00000492990
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl116,791,736 - 6,799,689 (-)Ensembl
RefSeq Acc Id: NM_003696   ⟹   NP_003687
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38116,791,736 - 6,799,689 (-)NCBI
GRCh37116,815,756 - 6,817,139 (-)RGD
Build 36116,772,332 - 6,773,715 (-)NCBI Archive
Celera116,934,849 - 6,936,232 (-)RGD
HuRef116,474,715 - 6,476,098 (-)RGD
CHM1_1116,814,666 - 6,816,049 (-)NCBI
T2T-CHM13v2.0116,850,158 - 6,858,111 (-)NCBI
Sequence:
RefSeq Acc Id: NP_003687   ⟸   NM_003696
- UniProtKB: Q6IF35 (UniProtKB/Swiss-Prot),   Q3MJC7 (UniProtKB/Swiss-Prot),   Q9H206 (UniProtKB/Swiss-Prot),   O95222 (UniProtKB/Swiss-Prot),   A0A126GW91 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000330384   ⟸   ENST00000332601
RefSeq Acc Id: ENSP00000492990   ⟸   ENST00000641196
Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O95222-F1-model_v2 AlphaFold O95222 1-327 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:15301 AgrOrtholog
COSMIC OR6A2 COSMIC
Ensembl Genes ENSG00000184933 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000641196 ENTREZGENE
  ENST00000641196.1 UniProtKB/Swiss-Prot
Gene3D-CATH Rhodopsin 7-helix transmembrane proteins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000184933 GTEx
HGNC ID HGNC:15301 ENTREZGENE
Human Proteome Map OR6A2 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:8590 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 8590 ENTREZGENE
OMIM 608495 OMIM
PANTHER G-PROTEIN COUPLED RECEPTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OLFACTORY RECEPTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam 7tm_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA32574 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 A0A126GW91 ENTREZGENE, UniProtKB/TrEMBL
  O95222 ENTREZGENE, UniProtKB/Swiss-Prot
  Q3MJC7 ENTREZGENE
  Q6IF35 ENTREZGENE
  Q9H206 ENTREZGENE
UniProt Secondary Q3MJC7 UniProtKB/Swiss-Prot
  Q6IF35 UniProtKB/Swiss-Prot
  Q9H206 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-15 OR6A2  olfactory receptor family 6 subfamily A member 2    olfactory receptor, family 6, subfamily A, member 2  Symbol and/or name change 5135510 APPROVED
2011-09-01 OR6A2  olfactory receptor, family 6, subfamily A, member 2  OR6A2  olfactory receptor, family 6, subfamily A, member 2  Symbol and/or name change 5135510 APPROVED