F2RL2 (coagulation factor II thrombin receptor like 2) - Rat Genome Database

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Gene: F2RL2 (coagulation factor II thrombin receptor like 2) Homo sapiens
Analyze
Symbol: F2RL2
Name: coagulation factor II thrombin receptor like 2
RGD ID: 1348825
HGNC Page HGNC:3539
Description: Predicted to enable G protein-coupled receptor activity. Predicted to be involved in positive regulation of Rho protein signal transduction. Part of protein-containing complex.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: coagulation factor II (thrombin) receptor-like 2; Coagulation factor II receptor-like 2 (protease-actovated receptor 3); FLJ51933; PAR-3; PAR3; protease-activated receptor 3; proteinase-activated receptor 3; proteinase-activated receptor-3; thrombin receptor-like 2
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
GRCh38576,615,482 - 76,623,403 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl576,615,482 - 76,623,413 (-)EnsemblGRCh38hg38GRCh38
GRCh37575,911,307 - 75,919,228 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36575,947,063 - 75,954,996 (-)NCBINCBI36Build 36hg18NCBI36
Build 34575,947,063 - 75,954,996NCBI
Celera571,805,260 - 71,813,193 (-)NCBICelera
Cytogenetic Map5q13.3NCBI
HuRef571,119,015 - 71,126,968 (-)NCBIHuRef
CHM1_1575,344,295 - 75,352,247 (-)NCBICHM1_1
T2T-CHM13v2.0577,097,223 - 77,105,145 (-)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

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. Cross Talk Pathways Between Coagulation and Inflammation. Foley JH and Conway EM, Circ Res. 2016 Apr 29;118(9):1392-408. doi: 10.1161/CIRCRESAHA.116.306853.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. PID Annotation Import Pipeline Pipeline to import Pathway Interaction Database annotations from NCI into RGD
4. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
5. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:1851174   PMID:8290554   PMID:9087410   PMID:9614115   PMID:9618465   PMID:9639495   PMID:9716134   PMID:9722561   PMID:10079109   PMID:10409227   PMID:10477691   PMID:10766244  
PMID:10788464   PMID:11307827   PMID:11544528   PMID:11714832   PMID:12037136   PMID:12477932   PMID:12692840   PMID:12732212   PMID:12757837   PMID:12805069   PMID:12953056   PMID:14507634  
PMID:14515192   PMID:15254234   PMID:15489334   PMID:15504554   PMID:15582715   PMID:15850610   PMID:16046705   PMID:16102047   PMID:16458856   PMID:17057644   PMID:17347481   PMID:17376866  
PMID:17474147   PMID:18264801   PMID:18836030   PMID:19379695   PMID:19473969   PMID:19513616   PMID:19586901   PMID:19718071   PMID:19806263   PMID:19913121   PMID:20068591   PMID:20155436  
PMID:20390230   PMID:20442298   PMID:20454680   PMID:20628086   PMID:20930172   PMID:21596928   PMID:21873635   PMID:22541814   PMID:23333304   PMID:23739922   PMID:23788139   PMID:23921961  
PMID:24699825   PMID:25320242   PMID:26729042   PMID:26742564  


Genomics

Comparative Map Data
F2RL2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38576,615,482 - 76,623,403 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl576,615,482 - 76,623,413 (-)EnsemblGRCh38hg38GRCh38
GRCh37575,911,307 - 75,919,228 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36575,947,063 - 75,954,996 (-)NCBINCBI36Build 36hg18NCBI36
Build 34575,947,063 - 75,954,996NCBI
Celera571,805,260 - 71,813,193 (-)NCBICelera
Cytogenetic Map5q13.3NCBI
HuRef571,119,015 - 71,126,968 (-)NCBIHuRef
CHM1_1575,344,295 - 75,352,247 (-)NCBICHM1_1
T2T-CHM13v2.0577,097,223 - 77,105,145 (-)NCBIT2T-CHM13v2.0
F2rl2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391395,833,428 - 95,839,276 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1395,833,361 - 95,839,247 (+)EnsemblGRCm39 Ensembl
GRCm381395,696,920 - 95,702,768 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1395,696,853 - 95,702,739 (+)EnsemblGRCm38mm10GRCm38
MGSCv371396,466,875 - 96,472,723 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361396,797,656 - 96,803,438 (+)NCBIMGSCv36mm8
Celera1399,313,808 - 99,319,652 (+)NCBICelera
Cytogenetic Map13D1NCBI
cM Map1350.38NCBI
F2rl2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8228,706,766 - 28,711,808 (+)NCBIGRCr8
mRatBN7.2226,972,054 - 26,977,098 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl226,972,054 - 26,977,098 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx234,011,700 - 34,016,699 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0232,111,806 - 32,116,807 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0226,928,439 - 26,933,433 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0226,240,385 - 26,245,533 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl226,240,385 - 26,245,533 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0245,371,780 - 45,376,928 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4226,073,852 - 26,078,618 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1225,994,220 - 25,998,987 (+)NCBI
Celera223,033,959 - 23,038,978 (+)NCBICelera
Cytogenetic Map2q12NCBI
F2rl2
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495542524,246,333 - 24,254,887 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495542524,246,333 - 24,254,887 (+)NCBIChiLan1.0ChiLan1.0
F2RL2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2438,681,399 - 38,689,370 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1536,835,029 - 36,842,961 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0538,680,372 - 38,688,509 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1539,297,424 - 39,305,370 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl539,297,424 - 39,305,370 (+)Ensemblpanpan1.1panPan2
F2RL2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1329,967,278 - 29,974,316 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl329,967,312 - 29,972,872 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha331,206,044 - 31,213,084 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0329,891,456 - 29,898,496 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl329,891,199 - 29,898,494 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1329,822,502 - 29,829,542 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0329,802,374 - 29,809,212 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0330,172,976 - 30,180,016 (+)NCBIUU_Cfam_GSD_1.0
F2rl2
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024407213190,515,607 - 190,522,114 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_004936549337,024 - 342,948 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_004936549336,871 - 342,992 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
F2RL2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl285,535,676 - 85,541,767 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1285,534,188 - 85,542,062 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2287,181,035 - 87,188,670 (+)NCBISscrofa10.2Sscrofa10.2susScr3
F2RL2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1470,887,979 - 70,895,419 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl470,886,113 - 70,895,113 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604919,720,145 - 19,727,047 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
F2rl2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248691,073,656 - 1,077,635 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248691,073,481 - 1,078,207 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in F2RL2
21 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5q13.3-22.1(chr5:74163186-110809453)x3 copy number gain See cases [RCV000051839] Chr5:74163186..110809453 [GRCh38]
Chr5:73459011..110145153 [GRCh37]
Chr5:73494767..110173052 [NCBI36]
Chr5:5q13.3-22.1		 pathogenic
NM_004101.3(F2RL2):c.421C>T (p.Leu141Phe) single nucleotide variant Malignant melanoma [RCV000066998] Chr5:76618286 [GRCh38]
Chr5:75914111 [GRCh37]
Chr5:75949867 [NCBI36]
Chr5:5q13.3		 not provided
NM_004101.3(F2RL2):c.252C>A (p.Thr84=) single nucleotide variant Malignant melanoma [RCV000066999] Chr5:76618455 [GRCh38]
Chr5:75914280 [GRCh37]
Chr5:75950036 [NCBI36]
Chr5:5q13.3		 not provided
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5q13.3(chr5:75792479-76012937)x1 copy number loss See cases [RCV000445841] Chr5:75792479..76012937 [GRCh37]
Chr5:5q13.3		 likely benign
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 copy number loss See cases [RCV000511978] Chr5:17628741..176575720 [GRCh37]
Chr5:5p15.1-q35.2		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5q13.3(chr5:75243653-75997611)x1 copy number loss not provided [RCV000682568] Chr5:75243653..75997611 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.160del (p.Ser54fs) deletion not provided [RCV000714769] Chr5:76618547 [GRCh38]
Chr5:75914372 [GRCh37]
Chr5:5q13.3		 uncertain significance
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3		 pathogenic
GRCh37/hg19 5q13.3(chr5:75831037-75916434)x1 copy number loss not provided [RCV000744856] Chr5:75831037..75916434 [GRCh37]
Chr5:5q13.3		 benign
Single allele deletion Neurodevelopmental disorder [RCV000787436] Chr5:14685137..149511942 [GRCh37]
Chr5:5p15.2-q32		 uncertain significance
GRCh37/hg19 5q13.3(chr5:75795446-75932329)x1 copy number loss not provided [RCV000846125] Chr5:75795446..75932329 [GRCh37]
Chr5:5q13.3		 uncertain significance
GRCh37/hg19 5q13.3(chr5:75827808-75914307)x1 copy number loss not provided [RCV000847128] Chr5:75827808..75914307 [GRCh37]
Chr5:5q13.3		 uncertain significance
GRCh37/hg19 5q13.3(chr5:75827808-75913305)x1 copy number loss not provided [RCV000849260] Chr5:75827808..75913305 [GRCh37]
Chr5:5q13.3		 uncertain significance
GRCh37/hg19 5q13.2-15(chr5:72790061-97478870)x3 copy number gain not provided [RCV001005683] Chr5:72790061..97478870 [GRCh37]
Chr5:5q13.2-15		 pathogenic
GRCh37/hg19 5q13.3(chr5:75327560-76140898)x1 copy number loss not provided [RCV000848077] Chr5:75327560..76140898 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.877G>T (p.Asp293Tyr) single nucleotide variant Inborn genetic diseases [RCV003251858] Chr5:76617830 [GRCh38]
Chr5:75913655 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.554C>T (p.Ala185Val) single nucleotide variant Inborn genetic diseases [RCV002762620] Chr5:76618153 [GRCh38]
Chr5:75913978 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.1060G>A (p.Asp354Asn) single nucleotide variant Inborn genetic diseases [RCV002799648] Chr5:76617647 [GRCh38]
Chr5:75913472 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.173G>A (p.Gly58Asp) single nucleotide variant Inborn genetic diseases [RCV002981922] Chr5:76618534 [GRCh38]
Chr5:75914359 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.230A>G (p.His77Arg) single nucleotide variant Inborn genetic diseases [RCV002955661] Chr5:76618477 [GRCh38]
Chr5:75914302 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.784T>G (p.Tyr262Asp) single nucleotide variant Inborn genetic diseases [RCV002742149] Chr5:76617923 [GRCh38]
Chr5:75913748 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.205A>G (p.Lys69Glu) single nucleotide variant Inborn genetic diseases [RCV002892488] Chr5:76618502 [GRCh38]
Chr5:75914327 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.188C>T (p.Thr63Met) single nucleotide variant Inborn genetic diseases [RCV002703593] Chr5:76618519 [GRCh38]
Chr5:75914344 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.379T>C (p.Cys127Arg) single nucleotide variant Inborn genetic diseases [RCV002936402] Chr5:76618328 [GRCh38]
Chr5:75914153 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.134C>T (p.Pro45Leu) single nucleotide variant Inborn genetic diseases [RCV002680471] Chr5:76618573 [GRCh38]
Chr5:75914398 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.904G>A (p.Ala302Thr) single nucleotide variant Inborn genetic diseases [RCV003220126] Chr5:76617803 [GRCh38]
Chr5:75913628 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.503C>G (p.Ala168Gly) single nucleotide variant Inborn genetic diseases [RCV003219767] Chr5:76618204 [GRCh38]
Chr5:75914029 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.403C>G (p.Leu135Val) single nucleotide variant Inborn genetic diseases [RCV003191846] Chr5:76618304 [GRCh38]
Chr5:75914129 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.839A>G (p.Tyr280Cys) single nucleotide variant Inborn genetic diseases [RCV003219793] Chr5:76617868 [GRCh38]
Chr5:75913693 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.670T>C (p.Tyr224His) single nucleotide variant Inborn genetic diseases [RCV003308572] Chr5:76618037 [GRCh38]
Chr5:75913862 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.944C>T (p.Ala315Val) single nucleotide variant Inborn genetic diseases [RCV003263524] Chr5:76617763 [GRCh38]
Chr5:75913588 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.121C>T (p.Arg41Cys) single nucleotide variant Inborn genetic diseases [RCV003344677] Chr5:76618586 [GRCh38]
Chr5:75914411 [GRCh37]
Chr5:5q13.3		 uncertain significance
NM_004101.4(F2RL2):c.127G>A (p.Ala43Thr) single nucleotide variant Inborn genetic diseases [RCV003376053] Chr5:76618580 [GRCh38]
Chr5:75914405 [GRCh37]
Chr5:5q13.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:983
Count of miRNA genes:480
Interacting mature miRNAs:519
Transcripts:ENST00000296641, ENST00000504899
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
F2RL2_622  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37575,912,737 - 75,913,474UniSTSGRCh37
Build 36575,948,493 - 75,949,230RGDNCBI36
Celera571,806,690 - 71,807,427RGD
HuRef571,120,445 - 71,121,182UniSTS
STS-N26732  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37575,911,358 - 75,911,550UniSTSGRCh37
Build 36575,947,114 - 75,947,306RGDNCBI36
Celera571,805,311 - 71,805,503RGD
Cytogenetic Map5q13.3UniSTS
Cytogenetic Map5q13UniSTS
HuRef571,119,066 - 71,119,258UniSTS
GeneMap99-GB4 RH Map5370.41UniSTS
NCBI RH Map5351.2UniSTS
D11S3114  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map5q23.3UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map15q11.2-q21.3UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map11p15UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map2q12.1UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map17p13.1UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map11q14.2UniSTS
Cytogenetic Map1q23.1UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map18q12.1-q21.1UniSTS
Cytogenetic Map2q37UniSTS
Cytogenetic Map20q11.21UniSTS
Cytogenetic Map6p21.32UniSTS
Cytogenetic Map10q26.3UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map14q12UniSTS
Cytogenetic Map8p11.22UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map2q21.1UniSTS
Cytogenetic Map6q27UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map9q21.12UniSTS
Cytogenetic Map7p22.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map10q24.31UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p31.1UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map3q13.31UniSTS
Cytogenetic Map6q13UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map1q21.3UniSTS
Cytogenetic Map1q22UniSTS
Cytogenetic Map1p36UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map7q22UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map19p13.1-p12UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map5q23.1UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1q25UniSTS
Cytogenetic Map1q21.2UniSTS
Cytogenetic Map12q22UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map21q22.11UniSTS
Cytogenetic Map3q23UniSTS
Cytogenetic Map6p21.3UniSTS
Cytogenetic Map2q12.3UniSTS
Cytogenetic Map12p13.31UniSTS
Cytogenetic Map8p11.2UniSTS
Cytogenetic Map7q21.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map5q35.3UniSTS
Cytogenetic Map5p13UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map5p12UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map12q21.1UniSTS
Cytogenetic Map16q12.1UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic MapXq13.2UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map14q24UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map7p22.3UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map22q11.1UniSTS
Cytogenetic Map22q13UniSTS
Cytogenetic Map11q13.1-q13.2UniSTS
Cytogenetic Map7p22UniSTS
Cytogenetic Map1p32-p31UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map7q21-q22UniSTS
Cytogenetic Map11p15.5UniSTS
Cytogenetic Map12p13.1UniSTS
Cytogenetic Map8p22UniSTS
Cytogenetic Map3q25.33UniSTS
Cytogenetic Map10q23.31UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map2q33.2UniSTS
Cytogenetic Map1p35-p34.3UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map5q35.2UniSTS
Cytogenetic Map10q22.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map3q12.3UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map12p12.2-p11.2UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2q14.3UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11p15.3UniSTS
Cytogenetic Map1p36.11-p34.2UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map6q22.31UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map5q31.3UniSTS
Cytogenetic Map11q14UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map3p14.3UniSTS
Cytogenetic Map12p13.2UniSTS
Cytogenetic Map6p21.2UniSTS
Cytogenetic Map10q11.1-q24UniSTS
Cytogenetic Map1p36.31UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic MapXp11.22UniSTS
Cytogenetic Map10p15.1UniSTS
Cytogenetic MapXq24UniSTS
Cytogenetic Map7p22.1UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic MapXq21.1UniSTS
Cytogenetic Map15q22UniSTS
Cytogenetic Map6p25UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic MapXq12-q13UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map7q31UniSTS
Cytogenetic Map7q31.1-q31.3UniSTS
Cytogenetic Map11q13.4UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic MapXq13.1-q21.1UniSTS
Cytogenetic Map20pter-q12UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map12q13.11-q14.3UniSTS
Cytogenetic Map2q32.1UniSTS
Cytogenetic Map15q21-q22UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map20q11.22-q11.23UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map4q21.22UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map9p24.1UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map3q13.33UniSTS
Cytogenetic Map8q11.2UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic Map1q41-q42.2UniSTS
Cytogenetic Map11q22-q23UniSTS
Cytogenetic Map12q23-q24.1UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map6p12.3UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map15q26.3UniSTS
Cytogenetic Map15q13.1UniSTS
Cytogenetic MapXq13.1UniSTS
Cytogenetic Map10q11.21UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map3p21UniSTS
Cytogenetic Map15q11-q13UniSTS
Cytogenetic Map13q12-q14UniSTS
Cytogenetic Map18q21.1UniSTS
Cytogenetic Map9p23UniSTS
Cytogenetic Map7p12.3UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map2q37.2UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map10q11.22UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.31UniSTS
Cytogenetic Map14q32.2UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map5q11.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map7q32.1UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map10q24UniSTS
Cytogenetic MapXq28UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map15q11.2UniSTS
Cytogenetic Map13q32.3UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map12q24.33UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic Map5q12.1UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map17q21.1UniSTS
Cytogenetic Map8q23.1UniSTS
Cytogenetic Map10p12.31UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic MapXq21UniSTS
Cytogenetic Map6p12UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic Map19qUniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map22q12.3-q13.1UniSTS
Cytogenetic Map1q25.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map5p13.1UniSTS
Cytogenetic Map9q21.11UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map1q24.2UniSTS
Cytogenetic Map2q34UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map14q21.2UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map5p13.3UniSTS
Cytogenetic Map1q42.3UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map6p21.31UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map9q34.1UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map18q12.1UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map9p22.3UniSTS
Cytogenetic Map8q21.11UniSTS
Cytogenetic Map6p22.3UniSTS
Cytogenetic Map5q32UniSTS
Cytogenetic Map4p12UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map19q11UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map14q22.1UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map12q13.11UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map2q36.1UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map17q21.32UniSTS
Cytogenetic Map16q23.1UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map1p32.2-p32.1UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map21q22.2UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map4q13.2UniSTS
Cytogenetic Map4q31.23UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map14q24.2UniSTS


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 visual system adipose tissue appendage entire extraembryonic component
High 1
Medium 221 19 22 36 9 15 75 120 40 22 32 56 23 2 20
Low 1981 1425 727 385 330 249 2540 982 1019 169 555 822 142 1 304 1669 2
Below cutoff 168 1435 956 192 1179 192 1351 731 2139 198 810 666 8 880 753

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_053128 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001256566 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_004101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC026725 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF053124 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF374726 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298585 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK312848 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL048674 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC093648 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC093650 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC095499 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BM989640 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX537386 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DC419029 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  U92971 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000296641   ⟹   ENSP00000296641
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl576,615,482 - 76,623,403 (-)Ensembl
RefSeq Acc Id: ENST00000504899   ⟹   ENSP00000426703
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl576,617,373 - 76,623,413 (-)Ensembl
RefSeq Acc Id: NM_001256566   ⟹   NP_001243495
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38576,615,482 - 76,623,403 (-)NCBI
GRCh37575,911,307 - 75,919,259 (-)NCBI
HuRef571,119,015 - 71,126,968 (-)NCBI
CHM1_1575,344,295 - 75,352,226 (-)NCBI
T2T-CHM13v2.0577,097,223 - 77,105,145 (-)NCBI
Sequence:
RefSeq Acc Id: NM_004101   ⟹   NP_004092
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38576,615,482 - 76,623,403 (-)NCBI
GRCh37575,911,307 - 75,919,259 (-)NCBI
Build 36575,947,063 - 75,954,996 (-)NCBI Archive
HuRef571,119,015 - 71,126,968 (-)NCBI
CHM1_1575,344,295 - 75,352,247 (-)NCBI
T2T-CHM13v2.0577,097,223 - 77,105,145 (-)NCBI
Sequence:
Reference Protein Sequences
RefSeq Acc Id: NP_004092   ⟸   NM_004101
- Peptide Label: isoform 1 precursor
- UniProtKB: Q52M68 (UniProtKB/Swiss-Prot),   B4DQ13 (UniProtKB/Swiss-Prot),   B2R754 (UniProtKB/Swiss-Prot),   Q7Z3W3 (UniProtKB/Swiss-Prot),   O00254 (UniProtKB/Swiss-Prot),   Q4VBN6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001243495   ⟸   NM_001256566
- Peptide Label: isoform 2
- UniProtKB: Q4VBN6 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000426703   ⟸   ENST00000504899
RefSeq Acc Id: ENSP00000296641   ⟸   ENST00000296641
Protein Domains
G-protein coupled receptors family 1 profile

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O00254-F1-model_v2 AlphaFold O00254 1-374 view protein structure

Promoters
RGD ID:6869916
Promoter ID:EPDNEW_H8123
Type:initiation region
Name:F2RL2_1
Description:coagulation factor II thrombin receptor like 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H8126  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38576,623,379 - 76,623,439EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:3539 AgrOrtholog
COSMIC F2RL2 COSMIC
Ensembl Genes ENSG00000164220 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000296641 ENTREZGENE
  ENST00000296641.5 UniProtKB/Swiss-Prot
  ENST00000504899 ENTREZGENE
  ENST00000504899.1 UniProtKB/Swiss-Prot
Gene3D-CATH Rhodopsin 7-helix transmembrane proteins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000164220 GTEx
HGNC ID HGNC:3539 ENTREZGENE
Human Proteome Map F2RL2 Human Proteome Map
InterPro GPCR_Rhodpsn UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  GPCR_Rhodpsn_7TM UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Prot_act_rcpt_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Protea_act_rcpt UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:2151 UniProtKB/Swiss-Prot
NCBI Gene 2151 ENTREZGENE
OMIM 601919 OMIM
PANTHER G-PROTEIN COUPLED RECEPTOR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEINASE-ACTIVATED RECEPTOR 3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam 7tm_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA27948 PharmGKB
PRINTS GPCRRHODOPSN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEASEAR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTEASEAR3 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 B2R754 ENTREZGENE
  B4DQ13 ENTREZGENE
  O00254 ENTREZGENE, UniProtKB/Swiss-Prot
  Q4VBN6 ENTREZGENE, UniProtKB/TrEMBL
  Q52M68 ENTREZGENE
  Q7Z3W3 ENTREZGENE
UniProt Secondary B2R754 UniProtKB/Swiss-Prot
  B4DQ13 UniProtKB/Swiss-Prot
  Q52M68 UniProtKB/Swiss-Prot
  Q7Z3W3 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-01-26 F2RL2  coagulation factor II thrombin receptor like 2    coagulation factor II (thrombin) receptor-like 2  Symbol and/or name change 5135510 APPROVED