OR2T8 (olfactory receptor family 2 subfamily T member 8) - Rat Genome Database

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Gene: OR2T8 (olfactory receptor family 2 subfamily T member 8) Homo sapiens
Analyze
Symbol: OR2T8
Name: olfactory receptor family 2 subfamily T member 8
RGD ID: 1351258
HGNC Page HGNC:15020
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: olfactory receptor 2T8; olfactory receptor, family 2, subfamily T, member 8 pseudogene; OR2T8P
RGD Orthologs
Mouse
Rat
Pig
Green Monkey
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
GRCh381247,920,252 - 247,923,152 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1247,920,252 - 247,923,152 (+)EnsemblGRCh38hg38GRCh38
GRCh371248,083,554 - 248,086,454 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361246,150,943 - 246,151,881 (+)NCBINCBI36Build 36hg18NCBI36
Build 341244,410,360 - 244,411,299NCBI
Celera1221,369,888 - 221,370,826 (+)NCBICelera
Cytogenetic Map1q44NCBI
HuRef1218,467,794 - 218,468,732 (+)NCBIHuRef
CHM1_11249,356,635 - 249,357,573 (+)NCBICHM1_1
T2T-CHM13v2.01247,346,064 - 247,348,964 (+)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)
plasma membrane  (IBA,IEA)

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
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:21873635   PMID:32126975  


Genomics

Comparative Map Data
OR2T8
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381247,920,252 - 247,923,152 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1247,920,252 - 247,923,152 (+)EnsemblGRCh38hg38GRCh38
GRCh371248,083,554 - 248,086,454 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361246,150,943 - 246,151,881 (+)NCBINCBI36Build 36hg18NCBI36
Build 341244,410,360 - 244,411,299NCBI
Celera1221,369,888 - 221,370,826 (+)NCBICelera
Cytogenetic Map1q44NCBI
HuRef1218,467,794 - 218,468,732 (+)NCBIHuRef
CHM1_11249,356,635 - 249,357,573 (+)NCBICHM1_1
T2T-CHM13v2.01247,346,064 - 247,348,964 (+)NCBIT2T-CHM13v2.0
Or2t44
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391158,676,965 - 58,678,095 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1158,673,778 - 58,679,594 (+)EnsemblGRCm39 Ensembl
GRCm381158,786,139 - 58,787,269 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1158,782,952 - 58,788,768 (+)EnsemblGRCm38mm10GRCm38
MGSCv371158,599,641 - 58,600,771 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361158,602,431 - 58,603,423 (+)NCBIMGSCv36mm8
Celera1163,548,681 - 63,549,811 (+)NCBICelera
Cytogenetic Map11B1.3NCBI
cM Map1136.3NCBI
Or2t44
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81044,003,219 - 44,004,211 (+)NCBIGRCr8
mRatBN7.21043,503,630 - 43,504,622 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1043,499,669 - 43,507,890 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1048,205,003 - 48,205,995 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01047,695,344 - 47,696,336 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01043,198,956 - 43,199,948 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01044,730,354 - 44,731,346 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1044,730,354 - 44,731,346 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01044,490,659 - 44,491,651 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41045,016,068 - 45,017,060 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11045,029,690 - 45,030,683 (+)NCBI
Celera1042,780,249 - 42,781,241 (+)NCBICelera
Cytogenetic Map10q22NCBI
LOC100520723
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1253,090,259 - 53,091,233 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2256,217,017 - 56,217,991 (-)NCBISscrofa10.2Sscrofa10.2susScr3
LOC103230967
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12584,921,337 - 84,942,539 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_02366605587,366,779 - 87,371,460 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in OR2T8
19 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1q32.3-44(chr1:214023812-248918469)x3 copy number gain See cases [RCV000050981] Chr1:214023812..248918469 [GRCh38]
Chr1:214197155..249212668 [GRCh37]
Chr1:212263778..247179291 [NCBI36]
Chr1:1q32.3-44		 pathogenic
GRCh38/hg38 1q41-44(chr1:223347693-248918469)x3 copy number gain See cases [RCV000050581] Chr1:223347693..248918469 [GRCh38]
Chr1:223521035..249212668 [GRCh37]
Chr1:221587658..247179291 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q44(chr1:247682931-248609256)x3 copy number gain See cases [RCV000051191] Chr1:247682931..248609256 [GRCh38]
Chr1:247846233..248772557 [GRCh37]
Chr1:245912856..246839180 [NCBI36]
Chr1:1q44		 benign
GRCh38/hg38 1q41-44(chr1:221902539-248918469)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051875]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051875]|See cases [RCV000051875] Chr1:221902539..248918469 [GRCh38]
Chr1:222075881..249212668 [GRCh37]
Chr1:220142504..247179291 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q41-44(chr1:223828500-248891309)x3 copy number gain See cases [RCV000051878] Chr1:223828500..248891309 [GRCh38]
Chr1:224016202..249185508 [GRCh37]
Chr1:222082825..247152131 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q41-44(chr1:223887780-248891309)x3 copy number gain See cases [RCV000051880] Chr1:223887780..248891309 [GRCh38]
Chr1:224075482..249185508 [GRCh37]
Chr1:222142105..247152131 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q42.11-44(chr1:224096488-248918469)x3 copy number gain See cases [RCV000051882] Chr1:224096488..248918469 [GRCh38]
Chr1:224284190..249212668 [GRCh37]
Chr1:222350813..247179291 [NCBI36]
Chr1:1q42.11-44		 pathogenic
GRCh38/hg38 1q32.2-44(chr1:209646207-248931113)x3 copy number gain See cases [RCV000051861] Chr1:209646207..248931113 [GRCh38]
Chr1:209819552..249225312 [GRCh37]
Chr1:207886175..247191935 [NCBI36]
Chr1:1q32.2-44		 pathogenic
GRCh38/hg38 1q42.3-44(chr1:236237049-248918469)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051883]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051883]|See cases [RCV000051883] Chr1:236237049..248918469 [GRCh38]
Chr1:236400349..249212668 [GRCh37]
Chr1:234466972..247179291 [NCBI36]
Chr1:1q42.3-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:239657468-248918610)x3 copy number gain See cases [RCV000051886] Chr1:239657468..248918610 [GRCh38]
Chr1:239820768..249212809 [GRCh37]
Chr1:237887391..247179432 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:240244444-248891309)x3 copy number gain See cases [RCV000051888] Chr1:240244444..248891309 [GRCh38]
Chr1:240407744..249185508 [GRCh37]
Chr1:238474367..247152131 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:242828731-248891309)x3 copy number gain See cases [RCV000053504] Chr1:242828731..248891309 [GRCh38]
Chr1:242992033..249185508 [GRCh37]
Chr1:241058656..247152131 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:243055227-248918469)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053506]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053506]|See cases [RCV000053506] Chr1:243055227..248918469 [GRCh38]
Chr1:243218529..249212668 [GRCh37]
Chr1:241285152..247179291 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q44(chr1:245584222-248918610)x1 copy number loss See cases [RCV000054067] Chr1:245584222..248918610 [GRCh38]
Chr1:245747524..249212809 [GRCh37]
Chr1:243814147..247179432 [NCBI36]
Chr1:1q44		 pathogenic
GRCh38/hg38 1q44(chr1:246386899-248918469)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054068]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054068]|See cases [RCV000054068] Chr1:246386899..248918469 [GRCh38]
Chr1:246550201..249212668 [GRCh37]
Chr1:244616824..247179291 [NCBI36]
Chr1:1q44		 pathogenic
GRCh38/hg38 1q44(chr1:247092432-248918469)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054069]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054069]|See cases [RCV000054069] Chr1:247092432..248918469 [GRCh38]
Chr1:247255734..249212668 [GRCh37]
Chr1:245322357..247179291 [NCBI36]
Chr1:1q44		 pathogenic
GRCh38/hg38 1q42.2-44(chr1:232097468-248918610)x1 copy number loss See cases [RCV000053985] Chr1:232097468..248918610 [GRCh38]
Chr1:232233214..249212809 [GRCh37]
Chr1:230299837..247179432 [NCBI36]
Chr1:1q42.2-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:237041745-248918469)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053989]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053989]|See cases [RCV000053989] Chr1:237041745..248918469 [GRCh38]
Chr1:237205045..249212668 [GRCh37]
Chr1:235271668..247179291 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:238061020-248918469)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053991]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053991]|See cases [RCV000053991] Chr1:238061020..248918469 [GRCh38]
Chr1:238224320..249212668 [GRCh37]
Chr1:236290943..247179291 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:239496961-248918469)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053993]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053993]|See cases [RCV000053993] Chr1:239496961..248918469 [GRCh38]
Chr1:239660261..249212668 [GRCh37]
Chr1:237726884..247179291 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:239558430-248918469)x1 copy number loss See cases [RCV000054023] Chr1:239558430..248918469 [GRCh38]
Chr1:239721730..249212668 [GRCh37]
Chr1:237788353..247179291 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:239629868-248924593)x1 copy number loss See cases [RCV000054024] Chr1:239629868..248924593 [GRCh38]
Chr1:239793168..249218792 [GRCh37]
Chr1:237859791..247185415 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:241047422-248924593)x1 copy number loss See cases [RCV000054025] Chr1:241047422..248924593 [GRCh38]
Chr1:241210722..249218792 [GRCh37]
Chr1:239277345..247185415 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:241757249-248891309)x1 copy number loss See cases [RCV000054028] Chr1:241757249..248891309 [GRCh38]
Chr1:241920551..249185508 [GRCh37]
Chr1:239987174..247152131 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:242076868-248918469)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054029]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000054029]|See cases [RCV000054029] Chr1:242076868..248918469 [GRCh38]
Chr1:242240170..249212668 [GRCh37]
Chr1:240306793..247179291 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q44(chr1:243786629-248918469)x1 copy number loss See cases [RCV000054061] Chr1:243786629..248918469 [GRCh38]
Chr1:243949931..249212668 [GRCh37]
Chr1:242016554..247179291 [NCBI36]
Chr1:1q44		 pathogenic
GRCh38/hg38 1q44(chr1:244498870-248918610)x1 copy number loss See cases [RCV000054064] Chr1:244498870..248918610 [GRCh38]
Chr1:244662172..249212809 [GRCh37]
Chr1:242728795..247179432 [NCBI36]
Chr1:1q44		 pathogenic
GRCh37/hg19 1q42.2-44(chr1:233012994-249206918)x1 copy number loss See cases [RCV002292708] Chr1:233012994..249206918 [GRCh37]
Chr1:1q42.2-44		 pathogenic
GRCh38/hg38 1q44(chr1:245312815-248918469)x3 copy number gain See cases [RCV000133864] Chr1:245312815..248918469 [GRCh38]
Chr1:245476117..249212668 [GRCh37]
Chr1:243542740..247179291 [NCBI36]
Chr1:1q44		 pathogenic
GRCh38/hg38 1q44(chr1:247613108-248093562)x3 copy number gain See cases [RCV000133783] Chr1:247613108..248093562 [GRCh38]
Chr1:247776410..248256864 [GRCh37]
Chr1:245843033..246323487 [NCBI36]
Chr1:1q44		 benign
GRCh38/hg38 1q43-44(chr1:238753749-248918467)x1 copy number loss See cases [RCV000134751] Chr1:238753749..248918467 [GRCh38]
Chr1:238917049..249212666 [GRCh37]
Chr1:236983672..247179289 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:238351121-248918469)x1 copy number loss See cases [RCV000134172] Chr1:238351121..248918469 [GRCh38]
Chr1:238514421..249212668 [GRCh37]
Chr1:236581044..247179291 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q32.2-44(chr1:209963625-248918469)x3 copy number gain See cases [RCV000134979] Chr1:209963625..248918469 [GRCh38]
Chr1:210136970..249212668 [GRCh37]
Chr1:208203593..247179291 [NCBI36]
Chr1:1q32.2-44		 pathogenic
GRCh38/hg38 1q41-44(chr1:223815147-248918469)x3 copy number gain See cases [RCV000135839] Chr1:223815147..248918469 [GRCh38]
Chr1:224002849..249212668 [GRCh37]
Chr1:222069472..247179291 [NCBI36]
Chr1:1q41-44		 pathogenic
GRCh38/hg38 1q44(chr1:244582123-248918469)x1 copy number loss See cases [RCV000135611] Chr1:244582123..248918469 [GRCh38]
Chr1:244745425..249212668 [GRCh37]
Chr1:242812048..247179291 [NCBI36]
Chr1:1q44		 pathogenic
GRCh38/hg38 1q44(chr1:247798967-248521608)x3 copy number gain See cases [RCV000136496] Chr1:247798967..248521608 [GRCh38]
Chr1:247962269..248684909 [GRCh37]
Chr1:246028892..246751532 [NCBI36]
Chr1:1q44		 benign
GRCh38/hg38 1q44(chr1:247682929-248093696)x3 copy number gain See cases [RCV000136013] Chr1:247682929..248093696 [GRCh38]
Chr1:247846231..248256998 [GRCh37]
Chr1:245912854..246323621 [NCBI36]
Chr1:1q44		 benign
GRCh38/hg38 1q44(chr1:247682931-248093562)x3 copy number gain See cases [RCV000137046] Chr1:247682931..248093562 [GRCh38]
Chr1:247846233..248256864 [GRCh37]
Chr1:245912856..246323487 [NCBI36]
Chr1:1q44		 benign
GRCh38/hg38 1q42.13-44(chr1:229022909-248918469)x3 copy number gain See cases [RCV000136666] Chr1:229022909..248918469 [GRCh38]
Chr1:229158656..249212668 [GRCh37]
Chr1:227225279..247179291 [NCBI36]
Chr1:1q42.13-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:236556082-248918469)x1 copy number loss See cases [RCV000137554] Chr1:236556082..248918469 [GRCh38]
Chr1:236719382..249212668 [GRCh37]
Chr1:234786005..247179291 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:242932576-248864636)x4 copy number gain See cases [RCV000137155] Chr1:242932576..248864636 [GRCh38]
Chr1:243095878..249158835 [GRCh37]
Chr1:241162501..247125458 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:240465122-248918469)x1 copy number loss See cases [RCV000137260] Chr1:240465122..248918469 [GRCh38]
Chr1:240628422..249212668 [GRCh37]
Chr1:238695045..247179291 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q44(chr1:247389261-248472496)x3 copy number gain See cases [RCV000137367] Chr1:247389261..248472496 [GRCh38]
Chr1:247552563..248635797 [GRCh37]
Chr1:245619186..246702420 [NCBI36]
Chr1:1q44		 likely benign
GRCh38/hg38 1q44(chr1:247798967-248376495)x1 copy number loss See cases [RCV000138075] Chr1:247798967..248376495 [GRCh38]
Chr1:247962269..248539796 [GRCh37]
Chr1:246028892..246606419 [NCBI36]
Chr1:1q44		 likely benign
GRCh38/hg38 1q42.11-44(chr1:224022862-248918469)x3 copy number gain See cases [RCV000137769] Chr1:224022862..248918469 [GRCh38]
Chr1:224210564..249212668 [GRCh37]
Chr1:222277187..247179291 [NCBI36]
Chr1:1q42.11-44		 pathogenic
GRCh38/hg38 1q44(chr1:247613235-248521590)x3 copy number gain See cases [RCV000138760] Chr1:247613235..248521590 [GRCh38]
Chr1:247776537..248684891 [GRCh37]
Chr1:245843160..246751514 [NCBI36]
Chr1:1q44		 benign
GRCh38/hg38 1q44(chr1:247682929-248521590)x3 copy number gain See cases [RCV000139219] Chr1:247682929..248521590 [GRCh38]
Chr1:247846231..248684891 [GRCh37]
Chr1:245912854..246751514 [NCBI36]
Chr1:1q44		 benign
GRCh38/hg38 1q44(chr1:247682929-248622297)x3 copy number gain See cases [RCV000138963] Chr1:247682929..248622297 [GRCh38]
Chr1:247846231..248785598 [GRCh37]
Chr1:245912854..246852221 [NCBI36]
Chr1:1q44		 benign
GRCh38/hg38 1q43-44(chr1:242045279-248930485)x1 copy number loss See cases [RCV000139889] Chr1:242045279..248930485 [GRCh38]
Chr1:242208581..249224684 [GRCh37]
Chr1:240275204..247191307 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:238033575-248924534)x1 copy number loss See cases [RCV000140039] Chr1:238033575..248924534 [GRCh38]
Chr1:238196875..249218733 [GRCh37]
Chr1:236263498..247185356 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q44(chr1:247671583-248317448)x3 copy number gain See cases [RCV000141216] Chr1:247671583..248317448 [GRCh38]
Chr1:247834885..248480750 [GRCh37]
Chr1:245901508..246547373 [NCBI36]
Chr1:1q44		 benign
GRCh38/hg38 1q42.12-44(chr1:225438480-248787200)x3 copy number gain See cases [RCV000142448] Chr1:225438480..248787200 [GRCh38]
Chr1:225626182..249060210 [GRCh37]
Chr1:223692805..247048022 [NCBI36]
Chr1:1q42.12-44		 pathogenic
GRCh38/hg38 1q44(chr1:247716624-248114768)x3 copy number gain See cases [RCV000142608] Chr1:247716624..248114768 [GRCh38]
Chr1:247879926..248278070 [GRCh37]
Chr1:245946549..246344693 [NCBI36]
Chr1:1q44		 benign
GRCh38/hg38 1q44(chr1:247404783-248472496)x3 copy number gain See cases [RCV000142763] Chr1:247404783..248472496 [GRCh38]
Chr1:247568085..248635797 [GRCh37]
Chr1:245634708..246702420 [NCBI36]
Chr1:1q44		 likely benign|uncertain significance
GRCh38/hg38 1q43-44(chr1:237643281-248918469)x1 copy number loss See cases [RCV000142518] Chr1:237643281..248918469 [GRCh38]
Chr1:237806581..249212668 [GRCh37]
Chr1:235873204..247179291 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:238192880-248930485)x1 copy number loss See cases [RCV000143374] Chr1:238192880..248930485 [GRCh38]
Chr1:238356180..249224684 [GRCh37]
Chr1:236422803..247191307 [NCBI36]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q32.2-44(chr1:207346642-248930485)x3 copy number gain See cases [RCV000143727] Chr1:207346642..248930485 [GRCh38]
Chr1:207519987..249224684 [GRCh37]
Chr1:205586610..247191307 [NCBI36]
Chr1:1q32.2-44		 pathogenic
GRCh37/hg19 1q43-44(chr1:242324398-249224684)x4 copy number gain See cases [RCV000511337] Chr1:242324398..249224684 [GRCh37]
Chr1:1q43-44		 likely pathogenic
GRCh37/hg19 1q42.2-44(chr1:234050864-249213059)x3 copy number gain See cases [RCV000240034] Chr1:234050864..249213059 [GRCh37]
Chr1:1q42.2-44		 pathogenic
GRCh37/hg19 1q43-44(chr1:243103401-249119318)x1 copy number loss See cases [RCV000240522] Chr1:243103401..249119318 [GRCh37]
Chr1:1q43-44		 pathogenic
GRCh37/hg19 1q31.3-44(chr1:195483439-249213000)x3 copy number gain See cases [RCV000449172] Chr1:195483439..249213000 [GRCh37]
Chr1:1q31.3-44		 pathogenic
GRCh37/hg19 1q42.3-44(chr1:236515525-249224684)x3 copy number gain See cases [RCV000449458] Chr1:236515525..249224684 [GRCh37]
Chr1:1q42.3-44		 pathogenic
GRCh37/hg19 1q41-44(chr1:214697099-249224684)x3 copy number gain See cases [RCV000449210] Chr1:214697099..249224684 [GRCh37]
Chr1:1q41-44		 pathogenic
GRCh37/hg19 1q42.2-44(chr1:231670870-249213000)x3 copy number gain See cases [RCV000447654] Chr1:231670870..249213000 [GRCh37]
Chr1:1q42.2-44		 pathogenic
GRCh37/hg19 1q43-44(chr1:237233879-249206548)x1 copy number loss See cases [RCV000447669] Chr1:237233879..249206548 [GRCh37]
Chr1:1q43-44		 pathogenic
GRCh37/hg19 1q43-44(chr1:239781260-249224684)x3 copy number gain See cases [RCV000447584] Chr1:239781260..249224684 [GRCh37]
Chr1:1q43-44		 pathogenic
GRCh37/hg19 1q42.3-44(chr1:235374095-249224684)x1 copy number loss See cases [RCV000447426] Chr1:235374095..249224684 [GRCh37]
Chr1:1q42.3-44		 pathogenic
GRCh37/hg19 1q44(chr1:247962269-248260734)x3 copy number gain See cases [RCV000445751] Chr1:247962269..248260734 [GRCh37]
Chr1:1q44		 benign
GRCh37/hg19 1q43-44(chr1:241601964-249224684)x1 copy number loss See cases [RCV000448028] Chr1:241601964..249224684 [GRCh37]
Chr1:1q43-44		 pathogenic
GRCh37/hg19 1q43-44(chr1:242656460-249213000)x3 copy number gain See cases [RCV000448507] Chr1:242656460..249213000 [GRCh37]
Chr1:1q43-44		 pathogenic
GRCh37/hg19 1q42.3-44(chr1:235797384-249224684)x1 copy number loss See cases [RCV000510546] Chr1:235797384..249224684 [GRCh37]
Chr1:1q42.3-44		 pathogenic
GRCh37/hg19 1q44(chr1:244197791-249224684)x4 copy number gain See cases [RCV000510563] Chr1:244197791..249224684 [GRCh37]
Chr1:1q44		 likely pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1q42.11-44(chr1:224105294-249224684)x3 copy number gain See cases [RCV000510981] Chr1:224105294..249224684 [GRCh37]
Chr1:1q42.11-44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1q44(chr1:245341153-249212429) copy number loss not provided [RCV000767543] Chr1:245341153..249212429 [GRCh37]
Chr1:1q44		 likely pathogenic
GRCh37/hg19 1q44(chr1:246753355-249224684)x3 copy number gain See cases [RCV000512337] Chr1:246753355..249224684 [GRCh37]
Chr1:1q44		 uncertain significance
GRCh37/hg19 1q41-44(chr1:218252551-249224684)x3 copy number gain not provided [RCV000684700] Chr1:218252551..249224684 [GRCh37]
Chr1:1q41-44		 pathogenic
GRCh37/hg19 1q42.13-44(chr1:228529973-249181598)x3 copy number gain not provided [RCV000684707] Chr1:228529973..249181598 [GRCh37]
Chr1:1q42.13-44		 pathogenic
GRCh37/hg19 1q43-44(chr1:241051170-249224684)x1 copy number loss not provided [RCV000684716] Chr1:241051170..249224684 [GRCh37]
Chr1:1q43-44		 pathogenic
GRCh37/hg19 1q44(chr1:244797639-249224684)x1 copy number loss not provided [RCV000684725] Chr1:244797639..249224684 [GRCh37]
Chr1:1q44		 pathogenic
GRCh37/hg19 1q44(chr1:247846257-249224684)x1 copy number loss not provided [RCV000684732] Chr1:247846257..249224684 [GRCh37]
Chr1:1q44		 uncertain significance
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1q42.2-44(chr1:232232335-249218992)x3 copy number gain not provided [RCV000749394] Chr1:232232335..249218992 [GRCh37]
Chr1:1q42.2-44		 pathogenic
GRCh37/hg19 1q44(chr1:247710624-248142049)x1 copy number loss not provided [RCV000736952] Chr1:247710624..248142049 [GRCh37]
Chr1:1q44		 benign
GRCh37/hg19 1q44(chr1:247828797-248266555)x3 copy number gain not provided [RCV000736953] Chr1:247828797..248266555 [GRCh37]
Chr1:1q44		 benign
GRCh37/hg19 1q44(chr1:247828797-248286356)x3 copy number gain not provided [RCV000736954] Chr1:247828797..248286356 [GRCh37]
Chr1:1q44		 benign
GRCh37/hg19 1q44(chr1:247828797-248290903)x3 copy number gain not provided [RCV000736955] Chr1:247828797..248290903 [GRCh37]
Chr1:1q44		 benign
GRCh37/hg19 1q44(chr1:247828797-248322479)x3 copy number gain not provided [RCV000736956] Chr1:247828797..248322479 [GRCh37]
Chr1:1q44		 benign
GRCh37/hg19 1q44(chr1:247828797-248795852)x3 copy number gain not provided [RCV000736957] Chr1:247828797..248795852 [GRCh37]
Chr1:1q44		 benign
GRCh37/hg19 1q44(chr1:247896549-248131388)x3 copy number gain not provided [RCV000736958] Chr1:247896549..248131388 [GRCh37]
Chr1:1q44		 benign
GRCh37/hg19 1q44(chr1:248071583-248843314)x3 copy number gain not provided [RCV000749443] Chr1:248071583..248843314 [GRCh37]
Chr1:1q44		 benign
GRCh37/hg19 1q43-44(chr1:238669293-249224684)x3 copy number gain not provided [RCV000849904] Chr1:238669293..249224684 [GRCh37]
Chr1:1q43-44		 pathogenic
Single allele deletion Neurodevelopmental disorder [RCV000787401] Chr1:247846701..248592414 [GRCh37]
Chr1:1q44		 uncertain significance
GRCh37/hg19 1q44(chr1:246565044-249224684)x1 copy number loss not provided [RCV000848153] Chr1:246565044..249224684 [GRCh37]
Chr1:1q44		 pathogenic
GRCh37/hg19 1q44(chr1:244379481-249224684)x1 copy number loss not provided [RCV000845861] Chr1:244379481..249224684 [GRCh37]
Chr1:1q44		 pathogenic
GRCh37/hg19 1q32.2-44(chr1:210152794-249218992)x3 copy number gain See cases [RCV001194578] Chr1:210152794..249218992 [GRCh37]
Chr1:1q32.2-44		 pathogenic
GRCh37/hg19 1q44(chr1:247576587-248688602)x4 copy number gain not provided [RCV000849147] Chr1:247576587..248688602 [GRCh37]
Chr1:1q44		 uncertain significance
GRCh37/hg19 1q25.3-44(chr1:182388773-249111240)x3 copy number gain not provided [RCV000845852] Chr1:182388773..249111240 [GRCh37]
Chr1:1q25.3-44		 pathogenic
GRCh37/hg19 1q42.3-44(chr1:235582580-249224684)x3 copy number gain not provided [RCV000846184] Chr1:235582580..249224684 [GRCh37]
Chr1:1q42.3-44		 pathogenic
GRCh37/hg19 1q43-44(chr1:243258050-249224684)x3 copy number gain not provided [RCV002472628] Chr1:243258050..249224684 [GRCh37]
Chr1:1q43-44		 pathogenic
GRCh37/hg19 1q32.1-44(chr1:204045948-249218992)x3 copy number gain See cases [RCV001007407] Chr1:204045948..249218992 [GRCh37]
Chr1:1q32.1-44		 pathogenic
GRCh37/hg19 1q44(chr1:246853199-249181899)x1 copy number loss not provided [RCV001259601] Chr1:246853199..249181899 [GRCh37]
Chr1:1q44		 likely pathogenic
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44		 uncertain significance
GRCh37/hg19 1q44(chr1:246820858-249213969)x3 copy number gain not provided [RCV001795835] Chr1:246820858..249213969 [GRCh37]
Chr1:1q44		 uncertain significance
GRCh37/hg19 1q44(chr1:248049805-248844899)x1 copy number loss not provided [RCV001832879] Chr1:248049805..248844899 [GRCh37]
Chr1:1q44		 likely benign
GRCh37/hg19 1q44(chr1:246850401-249205263)x3 copy number gain See cases [RCV002292210] Chr1:246850401..249205263 [GRCh37]
Chr1:1q44		 pathogenic
GRCh37/hg19 1q31.3-44(chr1:197867914-249224684)x3 copy number gain See cases [RCV002287837] Chr1:197867914..249224684 [GRCh37]
Chr1:1q31.3-44		 pathogenic
GRCh37/hg19 1q43-44(chr1:239910960-249224684)x1 copy number loss not provided [RCV002474504] Chr1:239910960..249224684 [GRCh37]
Chr1:1q43-44		 pathogenic
Single allele deletion Developmental and epileptic encephalopathy, 54 [RCV002481171] Chr1:242045197..249212668 [GRCh37]
Chr1:1q43-44		 likely pathogenic
GRCh37/hg19 1q41-44(chr1:223972939-249224684)x3 copy number gain not provided [RCV002475745] Chr1:223972939..249224684 [GRCh37]
Chr1:1q41-44		 pathogenic
NM_001005522.2(OR2T8):c.136C>A (p.Leu46Met) single nucleotide variant Inborn genetic diseases [RCV002887857] Chr1:247921153 [GRCh38]
Chr1:248084455 [GRCh37]
Chr1:1q44		 uncertain significance
NM_001005522.2(OR2T8):c.442C>T (p.Leu148Phe) single nucleotide variant Inborn genetic diseases [RCV002705161] Chr1:247921459 [GRCh38]
Chr1:248084761 [GRCh37]
Chr1:1q44		 likely benign
NM_001005522.2(OR2T8):c.488G>T (p.Ser163Ile) single nucleotide variant Inborn genetic diseases [RCV002705196] Chr1:247921505 [GRCh38]
Chr1:248084807 [GRCh37]
Chr1:1q44		 uncertain significance
NM_001005522.2(OR2T8):c.365C>T (p.Ala122Val) single nucleotide variant Inborn genetic diseases [RCV002853584] Chr1:247921382 [GRCh38]
Chr1:248084684 [GRCh37]
Chr1:1q44		 likely benign
NM_001005522.2(OR2T8):c.679C>T (p.Arg227Cys) single nucleotide variant Inborn genetic diseases [RCV002915482] Chr1:247921696 [GRCh38]
Chr1:248084998 [GRCh37]
Chr1:1q44		 uncertain significance
NM_001005522.2(OR2T8):c.97G>A (p.Val33Ile) single nucleotide variant Inborn genetic diseases [RCV002697092] Chr1:247921114 [GRCh38]
Chr1:248084416 [GRCh37]
Chr1:1q44		 uncertain significance
NM_001005522.2(OR2T8):c.229C>T (p.Pro77Ser) single nucleotide variant Inborn genetic diseases [RCV002742440] Chr1:247921246 [GRCh38]
Chr1:248084548 [GRCh37]
Chr1:1q44		 uncertain significance
NM_001005522.2(OR2T8):c.833T>C (p.Met278Thr) single nucleotide variant Inborn genetic diseases [RCV002709284] Chr1:247921850 [GRCh38]
Chr1:248085152 [GRCh37]
Chr1:1q44		 uncertain significance
NM_001005522.2(OR2T8):c.717C>G (p.Cys239Trp) single nucleotide variant Inborn genetic diseases [RCV002769234] Chr1:247921734 [GRCh38]
Chr1:248085036 [GRCh37]
Chr1:1q44		 uncertain significance
NM_001005522.2(OR2T8):c.298T>A (p.Phe100Ile) single nucleotide variant Inborn genetic diseases [RCV002896698] Chr1:247921315 [GRCh38]
Chr1:248084617 [GRCh37]
Chr1:1q44		 uncertain significance
NM_001005522.2(OR2T8):c.146G>C (p.Trp49Ser) single nucleotide variant Inborn genetic diseases [RCV003206536] Chr1:247921163 [GRCh38]
Chr1:248084465 [GRCh37]
Chr1:1q44		 uncertain significance
NM_001005522.2(OR2T8):c.691G>A (p.Ala231Thr) single nucleotide variant Inborn genetic diseases [RCV003203568] Chr1:247921708 [GRCh38]
Chr1:248085010 [GRCh37]
Chr1:1q44		 uncertain significance
GRCh37/hg19 1q44(chr1:245704069-249212562)x1 copy number loss not provided [RCV003222664] Chr1:245704069..249212562 [GRCh37]
Chr1:1q44		 pathogenic
NM_001005522.2(OR2T8):c.37C>G (p.Leu13Val) single nucleotide variant Inborn genetic diseases [RCV003200359] Chr1:247921054 [GRCh38]
Chr1:248084356 [GRCh37]
Chr1:1q44		 uncertain significance
GRCh38/hg38 1q43-44(chr1:243221458-248919110)x1 copy number loss Intellectual disability, autosomal dominant 22 [RCV003327711] Chr1:243221458..248919110 [GRCh38]
Chr1:1q43-44		 pathogenic
GRCh38/hg38 1q43-44(chr1:239907336-248919110)x1 copy number loss Intellectual disability, autosomal dominant 22 [RCV003333897] Chr1:239907336..248919110 [GRCh38]
Chr1:1q43-44		 pathogenic
NM_001005522.2(OR2T8):c.274C>T (p.Arg92Cys) single nucleotide variant Inborn genetic diseases [RCV003344416] Chr1:247921291 [GRCh38]
Chr1:248084593 [GRCh37]
Chr1:1q44		 uncertain significance
NM_001005522.2(OR2T8):c.694C>T (p.Arg232Cys) single nucleotide variant Inborn genetic diseases [RCV003349480] Chr1:247921711 [GRCh38]
Chr1:248085013 [GRCh37]
Chr1:1q44		 uncertain significance
GRCh37/hg19 1q42.13-44(chr1:229373250-249206595)x3 copy number gain not provided [RCV003484052] Chr1:229373250..249206595 [GRCh37]
Chr1:1q42.13-44		 pathogenic
GRCh37/hg19 1q44(chr1:246983973-249224684)x1 copy number loss not provided [RCV003484177] Chr1:246983973..249224684 [GRCh37]
Chr1:1q44		 uncertain significance
GRCh37/hg19 1q44(chr1:247755802-248142441)x1 copy number loss not provided [RCV003484199] Chr1:247755802..248142441 [GRCh37]
Chr1:1q44		 uncertain significance
NM_001005522.2(OR2T8):c.93T>C (p.Ser31=) single nucleotide variant not provided [RCV003417162] Chr1:247921110 [GRCh38]
Chr1:248084412 [GRCh37]
Chr1:1q44		 likely benign
NM_001005522.2(OR2T8):c.85G>C (p.Val29Leu) single nucleotide variant not provided [RCV003415117] Chr1:247921102 [GRCh38]
Chr1:248084404 [GRCh37]
Chr1:1q44		 likely benign
NM_001005522.2(OR2T8):c.91A>G (p.Ser31Gly) single nucleotide variant not provided [RCV003415118] Chr1:247921108 [GRCh38]
Chr1:248084410 [GRCh37]
Chr1:1q44		 likely benign
NM_001005522.2(OR2T8):c.92G>C (p.Ser31Thr) single nucleotide variant not provided [RCV003415119] Chr1:247921109 [GRCh38]
Chr1:248084411 [GRCh37]
Chr1:1q44		 likely benign
GRCh37/hg19 1q43-44(chr1:238681812-249224684)x3 copy number gain not specified [RCV003986862] Chr1:238681812..249224684 [GRCh37]
Chr1:1q43-44		 likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:96
Count of miRNA genes:95
Interacting mature miRNAs:95
Transcripts:ENST00000319968
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 2 2 2 2 3
Low 15 42 648 8 91 8 381 13 622 4 428 675 1 3 356
Below cutoff 1173 902 401 134 851 62 1565 486 2178 95 535 445 75 664 775 1

Sequence


Reference Sequences
RefSeq Acc Id: ENST00000319968   ⟹   ENSP00000326225
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,921,018 - 247,921,956 (+)Ensembl
RefSeq Acc Id: ENST00000641945   ⟹   ENSP00000493286
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1247,920,252 - 247,923,152 (+)Ensembl
RefSeq Acc Id: NM_001005522   ⟹   NP_001005522
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381247,920,252 - 247,923,152 (+)NCBI
GRCh371248,080,963 - 248,085,258 (+)NCBI
Build 361246,150,943 - 246,151,881 (+)NCBI Archive
Celera1221,369,888 - 221,370,826 (+)RGD
HuRef1218,467,794 - 218,468,732 (+)RGD
CHM1_11249,356,635 - 249,357,573 (+)NCBI
T2T-CHM13v2.01247,346,064 - 247,348,964 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001005522 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein A6NH00 (Get FASTA)   NCBI Sequence Viewer  
  ALI87751 (Get FASTA)   NCBI Sequence Viewer  
  EAW77208 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000493286
  ENSP00000493286.1
Reference Protein Sequences
RefSeq Acc Id: NP_001005522   ⟸   NM_001005522
- UniProtKB: A6NH00 (UniProtKB/Swiss-Prot),   A0A126GWC5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000493286   ⟸   ENST00000641945
RefSeq Acc Id: ENSP00000326225   ⟸   ENST00000319968
Protein Domains
G-protein coupled receptors family 1 profile

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-A6NH00-F1-model_v2 AlphaFold A6NH00 1-312 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:15020 AgrOrtholog
COSMIC OR2T8 COSMIC
Ensembl Genes ENSG00000177462 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000641945 ENTREZGENE
  ENST00000641945.2 UniProtKB/Swiss-Prot
Gene3D-CATH Rhodopsin 7-helix transmembrane proteins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000177462 GTEx
HGNC ID HGNC:15020 ENTREZGENE
Human Proteome Map OR2T8 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:343172 UniProtKB/Swiss-Prot
NCBI Gene 343172 ENTREZGENE
PANTHER OLFACTORY RECEPTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  OLFACTORY RECEPTOR 2T33-RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam 7tm_4 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA32208 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 A0A126GWC5 ENTREZGENE, UniProtKB/TrEMBL
  A6NH00 ENTREZGENE, UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-15 OR2T8  olfactory receptor family 2 subfamily T member 8  OR2T8  olfactory receptor, family 2, subfamily T, member 8  Symbol and/or name change 5135510 APPROVED