TGFBR3 (transforming growth factor beta receptor 3) - Rat Genome Database

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Gene: TGFBR3 (transforming growth factor beta receptor 3) Homo sapiens
Analyze
Symbol: TGFBR3
Name: transforming growth factor beta receptor 3
RGD ID: 736539
HGNC Page HGNC
Description: Exhibits several functions, including transforming growth factor beta binding activity; transforming growth factor beta receptor activity, type III; and type II transforming growth factor beta receptor binding activity. Involved in several processes, including response to gonadotropin; response to prostaglandin E; and transmembrane receptor protein serine/threonine kinase signaling pathway. Localizes to external side of plasma membrane; inhibin-betaglycan-ActRII complex; and receptor complex. Biomarker of endometrial adenocarcinoma.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: betaglycan; betaglycan proteoglycan; BGCAN; TGF-beta receptor type 3; TGF-beta receptor type III; TGFR-3; transforming growth factor beta receptor III; transforming growth factor beta receptor type 3; transforming growth factor, beta receptor 3
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
GRCh38.p13 Ensembl191,680,343 - 91,906,335 (-)EnsemblGRCh38hg38GRCh38
GRCh38191,680,343 - 91,906,002 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37192,145,900 - 92,371,559 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36191,920,575 - 92,124,243 (-)NCBINCBI36hg18NCBI36
Build 34191,860,007 - 92,063,676NCBI
Celera190,391,974 - 90,597,757 (-)NCBI
Cytogenetic Map1p22.1NCBI
HuRef190,263,929 - 90,491,182 (-)NCBIHuRef
CHM1_1192,261,010 - 92,486,411 (-)NCBICHM1_1
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
(-)-epigallocatechin 3-gallate  (EXP)
17beta-estradiol  (EXP,ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
2-hydroxypropanoic acid  (EXP)
3,4-methylenedioxymethamphetamine  (ISO)
4,4'-sulfonyldiphenol  (ISO)
4-hydroxyphenyl retinamide  (ISO)
4-vinylcyclohexene dioxide  (ISO)
5-aza-2'-deoxycytidine  (ISO)
5-fluorouracil  (EXP)
acetamide  (ISO)
aflatoxin B1  (EXP)
all-trans-retinoic acid  (ISO)
ammonium chloride  (ISO)
arsenous acid  (EXP)
azathioprine  (EXP)
benzene  (EXP)
benzo[a]pyrene  (EXP,ISO)
benzo[a]pyrene diol epoxide I  (EXP)
beta-naphthoflavone  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (ISO)
butan-1-ol  (EXP)
cadmium dichloride  (ISO)
carbon nanotube  (ISO)
choline  (ISO)
cisplatin  (ISO)
copper(II) sulfate  (EXP)
cyclosporin A  (EXP)
cytarabine  (EXP)
dexamethasone  (EXP,ISO)
diarsenic trioxide  (EXP)
diazepam  (EXP)
dicrotophos  (EXP)
doxorubicin  (EXP)
elemental selenium  (EXP)
endosulfan  (EXP,ISO)
enzyme inhibitor  (EXP)
ethanol  (EXP)
flavonoids  (ISO)
folic acid  (ISO)
fulvestrant  (ISO)
furan  (ISO)
genistein  (EXP)
hydroquinone  (EXP)
indometacin  (ISO)
L-methionine  (ISO)
lead diacetate  (ISO)
leflunomide  (EXP)
methylmercury chloride  (EXP)
methylseleninic acid  (EXP)
N-nitrosodiethylamine  (ISO)
nitrofen  (ISO)
ouabain  (EXP)
perfluorooctanoic acid  (EXP)
phenobarbital  (ISO)
picrotoxin  (ISO)
potassium chromate  (EXP)
progesterone  (ISO)
rac-lactic acid  (EXP)
ramipril  (ISO)
resveratrol  (ISO)
rotenone  (ISO)
selenium atom  (EXP)
sirolimus  (ISO)
sodium arsenite  (ISO)
streptozocin  (ISO)
styrene  (EXP)
styrene oxide  (EXP)
sunitinib  (EXP)
tetrachloromethane  (ISO)
thapsigargin  (EXP)
thioacetamide  (ISO)
trichostatin A  (EXP)
triclosan  (EXP)
trimellitic anhydride  (ISO)
troglitazone  (ISO)
tunicamycin  (EXP)
valproic acid  (EXP,ISO)
vinclozolin  (ISO)
vincristine  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process
angiogenesis  (IBA)
animal organ regeneration  (IEA,ISO)
blastocyst development  (ISO)
blood vessel development  (ISO)
blood vessel remodeling  (ISO)
BMP signaling pathway  (IDA)
cardiac epithelial to mesenchymal transition  (IDA)
cardiac muscle cell proliferation  (ISS)
cell migration  (IBA,ISS)
collagen metabolic process  (ISO)
definitive erythrocyte differentiation  (ISS)
definitive hemopoiesis  (ISS)
epicardium-derived cardiac fibroblast cell development  (ISS)
epithelial to mesenchymal transition  (IBA,IDA)
heart morphogenesis  (ISS)
heart trabecula formation  (ISS)
heart trabecula morphogenesis  (ISS)
immune response  (IMP)
in utero embryonic development  (ISO)
intracellular signal transduction  (IMP)
liver development  (ISS)
muscular septum morphogenesis  (ISS)
negative regulation of apoptotic process involved in morphogenesis  (ISO)
negative regulation of cellular component movement  (IDA)
negative regulation of epithelial cell migration  (ISO)
negative regulation of epithelial cell proliferation  (ISS)
negative regulation of epithelial to mesenchymal transition  (ISO)
negative regulation of gene expression  (ISO)
negative regulation of transforming growth factor beta receptor signaling pathway  (IEA,ISO)
osteoblast differentiation  (ISO)
outflow tract morphogenesis  (ISS)
pathway-restricted SMAD protein phosphorylation  (IMP)
positive regulation of BMP signaling pathway  (ISO)
positive regulation of cardiac muscle cell proliferation  (ISS)
positive regulation of cell population proliferation  (ISO)
positive regulation of NF-kappaB transcription factor activity  (ISO)
positive regulation of transforming growth factor beta receptor signaling pathway  (IEA,ISO)
protein-containing complex assembly  (ISO)
regulation of ERK1 and ERK2 cascade  (ISS)
regulation of JNK cascade  (ISS)
regulation of protein binding  (IEA,ISO)
regulation of transforming growth factor beta receptor signaling pathway  (IBA)
response to follicle-stimulating hormone  (IDA)
response to hypoxia  (IEA,ISO)
response to luteinizing hormone  (IDA)
response to prostaglandin E  (IDA)
roof of mouth development  (ISO)
secondary palate development  (ISS)
transforming growth factor beta receptor complex assembly  (IEA,ISO)
transforming growth factor beta receptor signaling pathway  (IBA,IDA,IMP,ISS)
vasculogenesis  (IBA,ISO)
vasculogenesis involved in coronary vascular morphogenesis  (ISS)
ventricular cardiac muscle tissue morphogenesis  (ISS)
ventricular compact myocardium morphogenesis  (ISS)
ventricular septum morphogenesis  (ISS)

Cellular Component

Molecular Pathway Annotations     Click to see Annotation Detail View
References

Additional References at PubMed
PMID:1319842   PMID:1333192   PMID:1657406   PMID:1657407   PMID:7852346   PMID:7935686   PMID:8106553   PMID:8125298   PMID:8530052   PMID:10092230   PMID:10207840   PMID:10746731  
PMID:10944857   PMID:11157754   PMID:11323414   PMID:11382746   PMID:11546783   PMID:12358857   PMID:12385827   PMID:12477932   PMID:12568406   PMID:12782414   PMID:12873459   PMID:12958365  
PMID:14557487   PMID:14585090   PMID:14976204   PMID:15009106   PMID:15489334   PMID:16344560   PMID:16502470   PMID:16613887   PMID:16621788   PMID:16710414   PMID:16886151   PMID:16982625  
PMID:17084394   PMID:17192875   PMID:17272393   PMID:17408468   PMID:17602227   PMID:17999987   PMID:18029348   PMID:18097622   PMID:18174230   PMID:18184661   PMID:18299279   PMID:18315732  
PMID:18397882   PMID:18398939   PMID:18845534   PMID:18931647   PMID:18978678   PMID:19056867   PMID:19131638   PMID:19164448   PMID:19199708   PMID:19249006   PMID:19299629   PMID:19322201  
PMID:19416857   PMID:19453261   PMID:19639191   PMID:19842711   PMID:19913121   PMID:20153821   PMID:20178540   PMID:20208565   PMID:20379614   PMID:20386084   PMID:20406198   PMID:20424473  
PMID:20548946   PMID:20587546   PMID:20628086   PMID:20634891   PMID:20677641   PMID:20734064   PMID:20856203   PMID:21186301   PMID:21261473   PMID:21297076   PMID:21307088   PMID:21411633  
PMID:21717526   PMID:21756058   PMID:21829018   PMID:21847367   PMID:21873635   PMID:22036907   PMID:22140272   PMID:22290546   PMID:22300218   PMID:22440163   PMID:22479366   PMID:22562249  
PMID:22927969   PMID:23092981   PMID:23209189   PMID:23226100   PMID:23322721   PMID:23376485   PMID:23387308   PMID:23835618   PMID:24124001   PMID:24216509   PMID:24347165   PMID:24551192  
PMID:24658685   PMID:24705316   PMID:24870032   PMID:24966170   PMID:24985072   PMID:25077702   PMID:25128652   PMID:25241763   PMID:25390077   PMID:25677673   PMID:25728212   PMID:25728278  
PMID:25861811   PMID:26186194   PMID:26190421   PMID:26205654   PMID:26383992   PMID:26531330   PMID:26548418   PMID:26882862   PMID:26980036   PMID:27628954   PMID:27784788   PMID:28514442  
PMID:28633389   PMID:29050936   PMID:29130787   PMID:29198452   PMID:29391598   PMID:29507755   PMID:29514796   PMID:29707897   PMID:30729664   PMID:31307515   PMID:31409900   PMID:31525642  
PMID:31786580   PMID:31922278   PMID:32281291   PMID:33146446   PMID:33410269  


Genomics

Comparative Map Data
TGFBR3
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl191,680,343 - 91,906,335 (-)EnsemblGRCh38hg38GRCh38
GRCh38191,680,343 - 91,906,002 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37192,145,900 - 92,371,559 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36191,920,575 - 92,124,243 (-)NCBINCBI36hg18NCBI36
Build 34191,860,007 - 92,063,676NCBI
Celera190,391,974 - 90,597,757 (-)NCBI
Cytogenetic Map1p22.1NCBI
HuRef190,263,929 - 90,491,182 (-)NCBIHuRef
CHM1_1192,261,010 - 92,486,411 (-)NCBICHM1_1
Tgfbr3
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm395107,254,433 - 107,437,495 (-)NCBIGRCm39mm39
GRCm39 Ensembl5107,254,436 - 107,437,495 (-)Ensembl
GRCm385107,106,567 - 107,289,629 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl5107,106,570 - 107,289,629 (-)EnsemblGRCm38mm10GRCm38
MGSCv375107,535,589 - 107,718,614 (-)NCBIGRCm37mm9NCBIm37
MGSCv365107,346,872 - 107,529,822 (-)NCBImm8
Celera5104,218,970 - 104,402,013 (-)NCBICelera
Cytogenetic Map5E5NCBI
Tgfbr3
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.2142,489,397 - 2,665,383 (+)NCBI
Rnor_6.0 Ensembl143,506,339 - 3,682,545 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.0143,506,416 - 3,680,508 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.0143,509,601 - 3,683,814 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4143,051,039 - 3,240,286 (+)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.1143,051,038 - 3,240,286 (+)NCBI
Celera142,505,821 - 2,679,576 (+)NCBICelera
Cytogenetic Map14p22NCBI
Tgfbr3
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554232,573,795 - 2,765,772 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554232,573,851 - 2,765,353 (+)NCBIChiLan1.0ChiLan1.0
TGFBR3
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.1193,080,452 - 93,285,587 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl193,080,452 - 93,285,587 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v0194,337,275 - 94,539,229 (-)NCBIMhudiblu_PPA_v0panPan3
TGFBR3
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1657,025,096 - 57,220,240 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl657,025,112 - 57,217,121 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha659,730,730 - 59,925,446 (+)NCBI
ROS_Cfam_1.0657,407,397 - 57,602,731 (+)NCBI
UMICH_Zoey_3.1657,084,907 - 57,279,569 (+)NCBI
UNSW_CanFamBas_1.0657,060,369 - 57,254,710 (+)NCBI
UU_Cfam_GSD_1.0657,523,587 - 57,718,361 (+)NCBI
Tgfbr3
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405058101,608,922 - 101,793,829 (-)NCBI
SpeTri2.0NW_0049365377,154,125 - 7,340,218 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TGFBR3
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl4125,101,190 - 125,316,796 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.14125,109,939 - 125,310,788 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.24136,671,290 - 136,820,333 (+)NCBISscrofa10.2Sscrofa10.2susScr3
TGFBR3
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12041,353,182 - 41,565,357 (+)NCBI
ChlSab1.1 Ensembl2041,353,325 - 41,565,343 (+)Ensembl
Vero_WHO_p1.0NW_02366603376,431,842 - 76,637,238 (-)NCBI
Tgfbr3
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_0046247425,871,155 - 6,080,773 (+)NCBI

Position Markers
D1S1588  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37192,214,251 - 92,214,382UniSTSGRCh37
Build 36191,986,839 - 91,986,970RGDNCBI36
Celera190,460,313 - 90,460,444RGD
Cytogenetic Map1p33-p32UniSTS
HuRef190,332,191 - 90,332,319UniSTS
Marshfield Genetic Map1125.51RGD
Marshfield Genetic Map1125.51UniSTS
deCODE Assembly Map1116.15UniSTS
Stanford-G3 RH Map14496.0UniSTS
Whitehead-RH Map1262.1UniSTS
NCBI RH Map1643.6UniSTS
SHGC-75157  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37192,145,963 - 92,146,162UniSTSGRCh37
Build 36191,918,551 - 91,918,750RGDNCBI36
Celera190,392,037 - 90,392,236RGD
Cytogenetic Map1p33-p32UniSTS
HuRef190,263,992 - 90,264,191UniSTS
TNG Radiation Hybrid Map142667.0UniSTS
GeneMap99-GB4 RH Map1263.37UniSTS
NCBI RH Map1647.2UniSTS
D1S3441  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37192,148,049 - 92,148,386UniSTSGRCh37
Build 36191,920,637 - 91,920,974RGDNCBI36
Celera190,394,123 - 90,394,460RGD
Cytogenetic Map1p33-p32UniSTS
HuRef190,266,078 - 90,266,415UniSTS
Whitehead-YAC Contig Map1 UniSTS
SHGC-30223  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37192,148,009 - 92,148,135UniSTSGRCh37
Build 36191,920,597 - 91,920,723RGDNCBI36
Celera190,394,083 - 90,394,209RGD
Cytogenetic Map1p33-p32UniSTS
HuRef190,266,038 - 90,266,164UniSTS
GeneMap99-GB4 RH Map1259.83UniSTS
GeneMap99-GB4 RH Map1261.45UniSTS
Whitehead-RH Map1262.2UniSTS
GeneMap99-G3 RH Map14452.0UniSTS
G59838  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37192,148,132 - 92,148,379UniSTSGRCh37
Build 36191,920,720 - 91,920,967RGDNCBI36
Celera190,394,206 - 90,394,453RGD
Cytogenetic Map1p33-p32UniSTS
HuRef190,266,161 - 90,266,408UniSTS
TNG Radiation Hybrid Map142700.0UniSTS
SHGC-148101  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37192,151,202 - 92,151,460UniSTSGRCh37
Build 36191,923,790 - 91,924,048RGDNCBI36
Celera190,397,276 - 90,397,534RGD
Cytogenetic Map1p33-p32UniSTS
HuRef190,269,231 - 90,269,489UniSTS
TNG Radiation Hybrid Map142680.0UniSTS
SHGC-75166  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37192,277,472 - 92,277,621UniSTSGRCh37
Build 36192,050,060 - 92,050,209RGDNCBI36
Celera190,523,525 - 90,523,674RGD
Cytogenetic Map1p33-p32UniSTS
HuRef190,397,141 - 90,397,290UniSTS
TNG Radiation Hybrid Map142587.0UniSTS
GeneMap99-GB4 RH Map1265.25UniSTS
Whitehead-RH Map1263.4UniSTS
NCBI RH Map1647.8UniSTS
SHGC-58228  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37192,151,822 - 92,152,025UniSTSGRCh37
Build 36191,924,410 - 91,924,613RGDNCBI36
Celera190,397,896 - 90,398,099RGD
Cytogenetic Map1p33-p32UniSTS
HuRef190,269,851 - 90,270,054UniSTS
TNG Radiation Hybrid Map142700.0UniSTS
D1S3573  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37192,148,015 - 92,148,114UniSTSGRCh37
Build 36191,920,603 - 91,920,702RGDNCBI36
Celera190,394,089 - 90,394,188RGD
Cytogenetic Map1p33-p32UniSTS
HuRef190,266,044 - 90,266,143UniSTS
TNG Radiation Hybrid Map142680.0UniSTS
Stanford-G3 RH Map14486.0UniSTS
NCBI RH Map1650.2UniSTS
GeneMap99-G3 RH Map14442.0UniSTS
AL009304  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37192,278,831 - 92,278,910UniSTSGRCh37
Build 36192,051,419 - 92,051,498RGDNCBI36
Celera190,524,884 - 90,524,963RGD
Cytogenetic Map1p33-p32UniSTS
HuRef190,398,500 - 90,398,579UniSTS
RH68993  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37192,148,113 - 92,148,240UniSTSGRCh37
Build 36191,920,701 - 91,920,828RGDNCBI36
Celera190,394,187 - 90,394,314RGD
Cytogenetic Map1p33-p32UniSTS
HuRef190,266,142 - 90,266,269UniSTS
GeneMap99-GB4 RH Map1257.67UniSTS
NCBI RH Map1632.9UniSTS
TGFBR3_3871  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37192,147,990 - 92,148,896UniSTSGRCh37
Build 36191,920,578 - 91,921,484RGDNCBI36
Celera190,394,064 - 90,394,970RGD
HuRef190,266,019 - 90,266,925UniSTS

miRNA Target Status

Confirmed Target Of
miRNA GeneMature miRNAMethod NameResult TypeData TypeSupport TypePMID
MIR21hsa-miR-21-5pMirtarbaseexternal_infoMicroarrayFunctional MTI (Weak)19253296
MIR21hsa-miR-21-5pMirecordsexternal_infoNANA11829576

Predicted Target Of
Summary Value
Count of predictions:6794
Count of miRNA genes:1326
Interacting mature miRNAs:1740
Transcripts:ENST00000212355, ENST00000370399, ENST00000417833, ENST00000465892, ENST00000468996, ENST00000470600, ENST00000525962, ENST00000529608, ENST00000532540, ENST00000533089, ENST00000533370
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
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 visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 1968 1624 1159 252 561 98 3485 1166 809 233 1011 1302 156 1204 2167 4
Low 465 1134 562 369 1036 364 869 1025 2872 181 446 295 15 1 621 2 2
Below cutoff 6 233 5 3 347 3 2 5 49 5 3 16 3

Sequence

Nucleotide Sequences
RefSeq Transcripts NG_027757 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001195683 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001195684 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_003243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_036634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_006710867 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC099334 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC114486 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI090023 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ251961 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ251962 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK225799 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK291345 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL162263 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL390780 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL445992 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY796304 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC099914 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC126116 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC136295 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC143869 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX090279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CA406273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471097 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA724452 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA854401 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA862176 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB224305 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DR002506 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  HG764816 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  L07594 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC624783 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC624784 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC624785 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC624786 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC624787 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  LC624788 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000212355   ⟹   ENSP00000212355
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl191,680,343 - 91,886,151 (-)Ensembl
RefSeq Acc Id: ENST00000370399   ⟹   ENSP00000359426
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl191,682,426 - 91,906,335 (-)Ensembl
RefSeq Acc Id: ENST00000417833   ⟹   ENSP00000395975
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl191,797,427 - 91,886,122 (-)Ensembl
RefSeq Acc Id: ENST00000465892   ⟹   ENSP00000432638
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl191,683,729 - 91,886,109 (-)Ensembl
RefSeq Acc Id: ENST00000468996
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl191,727,777 - 91,766,432 (-)Ensembl
RefSeq Acc Id: ENST00000470600
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl191,695,490 - 91,712,363 (-)Ensembl
RefSeq Acc Id: ENST00000525962   ⟹   ENSP00000436127
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl191,682,430 - 91,861,593 (-)Ensembl
RefSeq Acc Id: ENST00000529608
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl191,719,893 - 91,727,918 (-)Ensembl
RefSeq Acc Id: ENST00000532540   ⟹   ENSP00000434994
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl191,682,647 - 91,885,932 (-)Ensembl
RefSeq Acc Id: ENST00000533089   ⟹   ENSP00000433477
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl191,680,343 - 91,862,046 (-)Ensembl
RefSeq Acc Id: ENST00000533370
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl191,863,839 - 91,886,151 (-)Ensembl
RefSeq Acc Id: NM_001195683   ⟹   NP_001182612
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38191,680,343 - 91,886,151 (-)NCBI
GRCh37192,145,900 - 92,371,559 (-)ENTREZGENE
HuRef190,263,929 - 90,491,182 (-)ENTREZGENE
CHM1_1192,261,010 - 92,466,689 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001195684   ⟹   NP_001182613
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38191,680,343 - 91,906,002 (-)NCBI
GRCh37192,145,900 - 92,371,559 (-)ENTREZGENE
HuRef190,263,929 - 90,491,182 (-)ENTREZGENE
CHM1_1192,261,010 - 92,486,411 (-)NCBI
Sequence:
RefSeq Acc Id: NM_003243   ⟹   NP_003234
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38191,680,343 - 91,886,151 (-)NCBI
GRCh37192,145,900 - 92,371,559 (-)ENTREZGENE
Build 36191,920,575 - 92,124,243 (-)NCBI Archive
HuRef190,263,929 - 90,491,182 (-)ENTREZGENE
CHM1_1192,261,010 - 92,466,689 (-)NCBI
Sequence:
RefSeq Acc Id: NR_036634
RefSeq Status: REVIEWED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38191,680,343 - 91,886,151 (-)NCBI
GRCh37192,145,900 - 92,371,559 (-)ENTREZGENE
HuRef190,263,929 - 90,491,182 (-)ENTREZGENE
CHM1_1192,261,010 - 92,466,689 (-)NCBI
Sequence:
RefSeq Acc Id: XM_006710867   ⟹   XP_006710930
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38191,682,716 - 91,886,150 (-)NCBI
Sequence:
Reference Sequences
RefSeq Acc Id: NP_001182613   ⟸   NM_001195684
- Peptide Label: isoform b precursor
- UniProtKB: Q03167 (UniProtKB/Swiss-Prot),   A0A0A8KWK3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001182612   ⟸   NM_001195683
- Peptide Label: isoform b precursor
- UniProtKB: Q03167 (UniProtKB/Swiss-Prot),   A0A0A8KWK3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_003234   ⟸   NM_003243
- Peptide Label: isoform a precursor
- UniProtKB: Q03167 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_006710930   ⟸   XM_006710867
- Peptide Label: isoform X1
- UniProtKB: Q03167 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000359426   ⟸   ENST00000370399
RefSeq Acc Id: ENSP00000432638   ⟸   ENST00000465892
RefSeq Acc Id: ENSP00000434994   ⟸   ENST00000532540
RefSeq Acc Id: ENSP00000433477   ⟸   ENST00000533089
RefSeq Acc Id: ENSP00000395975   ⟸   ENST00000417833
RefSeq Acc Id: ENSP00000436127   ⟸   ENST00000525962
RefSeq Acc Id: ENSP00000212355   ⟸   ENST00000212355
Protein Domains
ZP

Promoters
RGD ID:6856194
Promoter ID:EPDNEW_H1262
Type:initiation region
Name:TGFBR3_3
Description:transforming growth factor beta receptor 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1263  EPDNEW_H1264  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38191,878,135 - 91,878,195EPDNEW
RGD ID:6856196
Promoter ID:EPDNEW_H1263
Type:initiation region
Name:TGFBR3_1
Description:transforming growth factor beta receptor 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1262  EPDNEW_H1264  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38191,886,121 - 91,886,181EPDNEW
RGD ID:6856198
Promoter ID:EPDNEW_H1264
Type:initiation region
Name:TGFBR3_2
Description:transforming growth factor beta receptor 3
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H1262  EPDNEW_H1263  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38191,906,305 - 91,906,365EPDNEW
RGD ID:6786984
Promoter ID:HG_KWN:3611
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   Lymphoblastoid
Transcripts:OTTHUMT00000027976
Position:
Human AssemblyChrPosition (strand)Source
Build 36191,950,691 - 91,951,357 (-)MPROMDB
RGD ID:6786985
Promoter ID:HG_KWN:3615
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:NM_003243,   OTTHUMT00000027973,   OTTHUMT00000027974,   UC001DOI.1
Position:
Human AssemblyChrPosition (strand)Source
Build 36192,123,849 - 92,124,349 (-)MPROMDB

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
NM_001195684.1(TGFBR3):c.-114+4569G>T single nucleotide variant Lung cancer [RCV000091043] Chr1:91895068 [GRCh38]
Chr1:92360625 [GRCh37]
Chr1:1p22.1
uncertain significance
GRCh38/hg38 1p22.1(chr1:91811903-92334237)x3 copy number gain See cases [RCV000051524] Chr1:91811903..92334237 [GRCh38]
Chr1:92277460..92799794 [GRCh37]
Chr1:92050048..92572382 [NCBI36]
Chr1:1p22.1
uncertain significance
GRCh38/hg38 1p31.1-13.3(chr1:72661709-107456880)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051825]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000051825]|See cases [RCV000051825] Chr1:72661709..107456880 [GRCh38]
Chr1:73127392..107999502 [GRCh37]
Chr1:72899980..107801025 [NCBI36]
Chr1:1p31.1-13.3
pathogenic
NM_003243.5(TGFBR3):c.385-20C>T single nucleotide variant Familial thoracic aortic aneurysm and aortic dissection [RCV000660324] Chr1:91734979 [GRCh38]
Chr1:92200536 [GRCh37]
Chr1:1p22.1
likely benign
NM_003243.5(TGFBR3):c.1076-16CTT[2] microsatellite Connective tissue disease [RCV000680616]|Familial thoracic aortic aneurysm and aortic dissection [RCV000660327] Chr1:91720238..91720240 [GRCh38]
Chr1:92185795..92185797 [GRCh37]
Chr1:1p22.1
likely benign
NM_003243.5(TGFBR3):c.453G>A (p.Arg151=) single nucleotide variant Familial thoracic aortic aneurysm and aortic dissection [RCV000660325] Chr1:91734891 [GRCh38]
Chr1:92200448 [GRCh37]
Chr1:1p22.1
likely benign
NM_003243.5(TGFBR3):c.2329C>T (p.Pro777Ser) single nucleotide variant Familial thoracic aortic aneurysm and aortic dissection [RCV000660328] Chr1:91698089 [GRCh38]
Chr1:92163646 [GRCh37]
Chr1:1p22.1
likely benign
NM_003243.5(TGFBR3):c.55A>G (p.Thr19Ala) single nucleotide variant Familial thoracic aortic aneurysm and aortic dissection [RCV000660323]|not provided [RCV000893090] Chr1:91861477 [GRCh38]
Chr1:92327034 [GRCh37]
Chr1:1p22.1
benign|likely benign
NM_003243.5(TGFBR3):c.765T>A (p.Asp255Glu) single nucleotide variant Familial thoracic aortic aneurysm and aortic dissection [RCV000660326] Chr1:91727779 [GRCh38]
Chr1:92193336 [GRCh37]
Chr1:1p22.1
uncertain significance
NM_003243.5(TGFBR3):c.2519C>T (p.Thr840Met) single nucleotide variant Infertility [RCV001327953]|Malignant tumor of prostate [RCV000149145] Chr1:91683776 [GRCh38]
Chr1:92149333 [GRCh37]
Chr1:1p22.1
uncertain significance
GRCh38/hg38 1p31.1-21.1(chr1:83457325-104273917)x3 copy number gain See cases [RCV000135654] Chr1:83457325..104273917 [GRCh38]
Chr1:83923008..104816539 [GRCh37]
Chr1:83695596..104618062 [NCBI36]
Chr1:1p31.1-21.1
pathogenic
GRCh38/hg38 1p22.1(chr1:91626400-92362203)x3 copy number gain See cases [RCV000135598] Chr1:91626400..92362203 [GRCh38]
Chr1:92091957..92827760 [GRCh37]
Chr1:91864545..92600348 [NCBI36]
Chr1:1p22.1
uncertain significance
GRCh37/hg19 1p36.12-12(chr1:20608823-120546301)x3 copy number loss not provided [RCV000762767] Chr1:20608823..120546301 [GRCh37]
Chr1:1p36.12-12
likely benign
GRCh37/hg19 1p22.1(chr1:92241399-92656121)x3 copy number gain not provided [RCV000487655] Chr1:92241399..92656121 [GRCh37]
Chr1:1p22.1
uncertain significance
GRCh37/hg19 1p31.1-22.1(chr1:72044544-92505091)x1 copy number loss See cases [RCV000510161] Chr1:72044544..92505091 [GRCh37]
Chr1:1p31.1-22.1
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 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44
pathogenic
GRCh37/hg19 1p22.1(chr1:92064829-92836061)x3 copy number gain not provided [RCV000684600] Chr1:92064829..92836061 [GRCh37]
Chr1:1p22.1
uncertain significance
GRCh37/hg19 1p22.2-22.1(chr1:91668330-93539185)x3 copy number gain not provided [RCV000684599] Chr1:91668330..93539185 [GRCh37]
Chr1:1p22.2-22.1
uncertain significance
NM_003243.5(TGFBR3):c.935T>C (p.Met312Thr) single nucleotide variant Connective tissue disease [RCV000680617]|not provided [RCV000881957] Chr1:91722095 [GRCh38]
Chr1:92187652 [GRCh37]
Chr1:1p22.1
benign|likely benign
NM_003243.5(TGFBR3):c.2027T>C (p.Phe676Ser) single nucleotide variant Connective tissue disease [RCV000680615] Chr1:91712382 [GRCh38]
Chr1:92177939 [GRCh37]
Chr1:1p22.1
uncertain significance
NM_003243.5(TGFBR3):c.477T>C (p.His159=) single nucleotide variant Connective tissue disease [RCV000680618] Chr1:91734867 [GRCh38]
Chr1:92200424 [GRCh37]
Chr1:1p22.1
likely benign
NM_003243.5(TGFBR3):c.466G>A (p.Gly156Arg) single nucleotide variant Connective tissue disease [RCV000680619] Chr1:91734878 [GRCh38]
Chr1:92200435 [GRCh37]
Chr1:1p22.1
likely benign
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 1p22.1(chr1:92234553-92632813)x3 copy number gain not provided [RCV000749065] Chr1:92234553..92632813 [GRCh37]
Chr1:1p22.1
benign
NM_003243.5(TGFBR3):c.405C>T (p.Val135=) single nucleotide variant not provided [RCV000927019] Chr1:91734939 [GRCh38]
Chr1:92200496 [GRCh37]
Chr1:1p22.1
likely benign
GRCh37/hg19 1p22.1(chr1:92188770-92385442)x1 copy number loss not provided [RCV000845920] Chr1:92188770..92385442 [GRCh37]
Chr1:1p22.1
uncertain significance
GRCh37/hg19 1p36.22-21.1(chr1:103343285-103455144)x3 copy number gain Global developmental delay [RCV000787285] Chr1:103343285..103455144 [GRCh37]
Chr1:1p36.22-21.1
uncertain significance
GRCh37/hg19 1p22.1(chr1:92035840-92263616)x1 copy number loss not provided [RCV000846004] Chr1:92035840..92263616 [GRCh37]
Chr1:1p22.1
uncertain significance
NM_003243.5(TGFBR3):c.1128C>T (p.Ile376=) single nucleotide variant not provided [RCV000953154] Chr1:91720178 [GRCh38]
Chr1:92185735 [GRCh37]
Chr1:1p22.1
benign
NM_003243.5(TGFBR3):c.464A>G (p.His155Arg) single nucleotide variant not provided [RCV000884968] Chr1:91734880 [GRCh38]
Chr1:92200437 [GRCh37]
Chr1:1p22.1
likely benign
NM_003243.5(TGFBR3):c.2293G>C (p.Gly765Arg) single nucleotide variant not provided [RCV000957783] Chr1:91698125 [GRCh38]
Chr1:92163682 [GRCh37]
Chr1:1p22.1
benign
NM_003243.5(TGFBR3):c.1647A>G (p.Gly549=) single nucleotide variant not provided [RCV001311638] Chr1:91716628 [GRCh38]
Chr1:92182185 [GRCh37]
Chr1:1p22.1
likely benign

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:11774 AgrOrtholog
COSMIC TGFBR3 COSMIC
Ensembl Genes ENSG00000069702 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000212355 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000359426 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000395975 UniProtKB/TrEMBL
  ENSP00000432638 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000433477 UniProtKB/TrEMBL
  ENSP00000434994 UniProtKB/TrEMBL
  ENSP00000436127 ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000212355 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000370399 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000417833 UniProtKB/TrEMBL
  ENST00000465892 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000525962 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000532540 UniProtKB/TrEMBL
  ENST00000533089 ENTREZGENE, UniProtKB/TrEMBL
GTEx ENSG00000069702 GTEx
HGNC ID HGNC:11774 ENTREZGENE
Human Proteome Map TGFBR3 Human Proteome Map
InterPro ZP_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZP_dom_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:7049 UniProtKB/Swiss-Prot
NCBI Gene 7049 ENTREZGENE
OMIM 600742 OMIM
Pfam Zona_pellucida UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA36487 PharmGKB
PRINTS ZPELLUCIDA UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE ZP_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ZP_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART SM00241 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0A8KWK3 ENTREZGENE, UniProtKB/TrEMBL
  E9PAW7_HUMAN UniProtKB/TrEMBL
  E9PKY4_HUMAN UniProtKB/TrEMBL
  E9PMG7_HUMAN UniProtKB/TrEMBL
  Q03167 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary A0AUW8 UniProtKB/Swiss-Prot
  A8K5N0 UniProtKB/Swiss-Prot
  B9EG88 UniProtKB/Swiss-Prot
  Q5T2T4 UniProtKB/Swiss-Prot
  Q5U731 UniProtKB/Swiss-Prot
  Q9UGI2 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-05-03 TGFBR3  transforming growth factor beta receptor 3    transforming growth factor beta receptor III  Symbol and/or name change 5135510 APPROVED
2015-11-10 TGFBR3  transforming growth factor beta receptor III    transforming growth factor, beta receptor III  Symbol and/or name change 5135510 APPROVED