T (brachyury, T-box transcription factor T) - Rat Genome Database

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Gene: T (brachyury, T-box transcription factor T) Mus musculus
Analyze
Symbol: T
Name: brachyury, T-box transcription factor T
RGD ID: 1320870
MGI Page MGI
Description: Enables DNA-binding transcription factor activity, RNA polymerase II-specific; RNA polymerase II cis-regulatory region sequence-specific DNA binding activity; and RNA polymerase II-specific DNA-binding transcription factor binding activity. Involved in cardiac muscle cell myoblast differentiation; negative regulation of transcription by RNA polymerase II; and positive regulation of transcription by RNA polymerase II. Acts upstream of or within several processes, including chordate embryonic development; circulatory system development; and embryonic morphogenesis. Located in cytoplasm and nucleus. Part of chromatin. Is expressed in several structures, including egg cylinder; embryo mesenchyme; future spinal cord; genitourinary system; and mesoderm. Human ortholog(s) of this gene implicated in neural tube defect. Orthologous to human TBXT (T-box transcription factor T).
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: B; Bra; brachyury; brachyury protein; brachyury-like 2; brachyury-like 3; cou; D17Mit170; Low; low ratio; Lr; me75; T-box transcription factor T; T1; Tbxt; Tl2; Tl3
RGD Orthologs
Human
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Latest Assembly: GRCm39 - Mouse Genome Assembly GRCm39
Position:
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39178,653,255 - 8,661,328 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl178,653,255 - 8,661,328 (+)EnsemblGRCm39 Ensembl
GRCm38178,434,423 - 8,442,496 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl178,434,423 - 8,442,496 (+)EnsemblGRCm38mm10GRCm38
MGSCv37178,627,288 - 8,635,361 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36178,272,597 - 8,280,670 (+)NCBIMGSCv36mm8
Celera178,480,245 - 8,488,318 (+)NCBICelera
Cytogenetic Map17A1NCBI
cM Map174.92NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
chromatin  (IBA,IDA,IMP,ISO)
cytoplasm  (IDA)
nucleoplasm  (ISO,TAS)
nucleus  (IBA,IDA,ISO)

Phenotype Annotations     Click to see Annotation Detail View

Mammalian Phenotype
abnormal allantois morphology  (IAGP)
abnormal axial mesoderm morphology  (IAGP)
abnormal bone ossification  (IAGP)
abnormal cervical atlas morphology  (IAGP)
abnormal cervical vertebrae morphology  (IAGP)
abnormal colon morphology  (IAGP)
abnormal dorsal aorta morphology  (IEA)
abnormal embryo development  (IAGP)
abnormal epidermal layer morphology  (IEA)
abnormal forelimb bud morphology  (IEA)
abnormal head shape  (IEA)
abnormal heart looping  (IAGP)
abnormal heart tube morphology  (IAGP)
abnormal limb bud morphology  (IAGP)
abnormal lumbar vertebrae morphology  (IAGP)
abnormal mesoderm development  (IAGP)
abnormal nervous system development  (IEA)
abnormal neural fold formation  (IAGP)
abnormal neural tube morphology  (IAGP)
abnormal notochord morphology  (IAGP)
abnormal nucleus pulposus morphology  (IAGP)
abnormal odontoid process morphology  (IAGP)
abnormal pelvic girdle bone morphology  (IEA)
abnormal pericardial cavity morphology  (IEA)
abnormal placenta development  (IEA)
abnormal posterior primitive streak morphology  (IAGP)
abnormal prechordal plate morphology  (IAGP)
abnormal primitive streak formation  (IAGP)
abnormal roof plate morphology  (IAGP)
abnormal rostral-caudal axis patterning  (IAGP)
abnormal rostral-caudal body axis extension  (IEA)
abnormal sacral vertebrae morphology  (IAGP)
abnormal somite development  (IAGP)
abnormal spinal cord morphology  (IAGP)
abnormal tail bud morphology  (IAGP)
abnormal tail development  (IEA)
abnormal tail morphology  (IAGP)
abnormal thoracic vertebrae morphology  (IEA)
abnormal vertebrae morphology  (IAGP)
abnormal vertebral arch development  (IAGP)
abnormal vertebral body development  (IAGP)
abnormal vertebral body morphology  (IAGP)
absent allantois  (IAGP)
absent anus  (IEA)
absent caudal vertebrae  (IEA)
absent forelimb buds  (IAGP)
absent hindlimb buds  (IAGP)
absent notochord  (IAGP)
absent primitive node  (IAGP)
absent sacral vertebrae  (IEA)
absent somites  (IAGP)
absent tail  (IAGP)
absent tail bud  (IAGP)
absent vertebrae  (IAGP)
absent vertebral arch  (IEA)
absent vertebral body  (IAGP)
bleb  (IEA)
caudal body truncation  (IAGP)
cervical vertebral fusion  (IAGP)
curly tail  (IAGP)
decreased body size  (IAGP)
decreased caudal vertebrae number  (IAGP)
decreased embryo size  (IEA)
decreased litter size  (IEA)
decreased presacral vertebrae number  (IAGP)
decreased rib number  (IAGP)
decreased survivor rate  (IAGP)
decreased ventral ectodermal ridge size  (IAGP)
delayed heart development  (IEA)
distended pericardium  (IAGP)
distended urinary bladder  (IAGP)
edema  (IAGP)
embryonic growth arrest  (IAGP)
embryonic growth retardation  (IAGP)
embryonic lethality  (IAGP)
embryonic lethality between implantation and somite formation, complete penetrance  (IAGP)
embryonic lethality between somite formation and embryo turning, complete penetrance  (IAGP)
embryonic lethality during organogenesis, complete penetrance  (IAGP)
embryonic lethality during organogenesis, incomplete penetrance  (IAGP)
embryonic lethality, complete penetrance  (IAGP)
failure of heart looping  (IAGP)
failure of initiation of embryo turning  (IAGP)
fusion of vertebral arches  (IAGP)
head tilt  (IAGP)
hemopericardium  (IEA)
hemorrhage  (IEA)
hindlimb paralysis  (IAGP)
incomplete caudal neuropore closure  (IAGP)
incomplete embryo turning  (IAGP)
incomplete somite formation  (IAGP)
kinked neural tube  (IAGP)
kinked tail  (IAGP)
male infertility  (IAGP)
meningocele  (IAGP)
meningomyelocele  (IEA)
neonatal lethality, incomplete penetrance  (IAGP)
no abnormal phenotype detected  (IAGP)
notochord degeneration  (IEA)
open neural tube  (IAGP)
perinatal lethality, incomplete penetrance  (IAGP)
postnatal lethality  (IAGP)
postnatal lethality, complete penetrance  (IAGP)
prenatal lethality  (IEA)
prenatal lethality, complete penetrance  (IEA)
preweaning lethality, incomplete penetrance  (IEA)
reduced male fertility  (IAGP)
rib fusion  (IAGP)
short ribs  (IAGP)
short tail  (IAGP)
spina bifida occulta  (IAGP)
split notochord  (IAGP)
thin tail  (IAGP)
thoracic vertebral fusion  (IAGP)
transmission ratio distortion  (IAGP)
vertebral fusion  (IAGP)
vestigial tail  (IEA)
References

References - curated
# Reference Title Reference Citation
1. MGDs mouse GO annotations MGD data from the GO Consortium
2. MGD IEA MGD IEA
3. OMIM Disease Annotation Pipeline OMIM Disease Annotation Pipeline
4. Mouse MP Annotation Import Pipeline RGD automated import pipeline
5. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
6. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
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PMID:26809587   PMID:26969725   PMID:26975355   PMID:27006501   PMID:27026076   PMID:27061115   PMID:27217206   PMID:27226536   PMID:27239041   PMID:27256596   PMID:27292645   PMID:27297885  
PMID:27369076   PMID:27411055   PMID:27453501   PMID:27466203   PMID:27515175   PMID:27521049   PMID:27586544   PMID:27713415   PMID:27760115   PMID:27870829   PMID:27881714   PMID:27894818  
PMID:27930333   PMID:28009287   PMID:28087629   PMID:28174238   PMID:28182636   PMID:28188179   PMID:28196692   PMID:28254784   PMID:28322735   PMID:28389228   PMID:28445719   PMID:28565025  
PMID:28619992   PMID:28826820   PMID:28839193   PMID:28854362   PMID:28875501   PMID:28882402   PMID:29084802   PMID:29138255   PMID:29141987   PMID:29168693   PMID:29203676   PMID:29378823  
PMID:29412136   PMID:29467473   PMID:29618843   PMID:29636380   PMID:29915126   PMID:29964027   PMID:30026265   PMID:30061166   PMID:30189017   PMID:30201686   PMID:30297839   PMID:30380057  
PMID:30446626   PMID:30530745   PMID:30592646   PMID:30661984   PMID:30842446   PMID:30940539   PMID:30959515   PMID:31092598   PMID:31107948   PMID:31143371   PMID:31189761   PMID:31232685  
PMID:31235634   PMID:31260508   PMID:31276560   PMID:31301300   PMID:31371508   PMID:31597657   PMID:31792383   PMID:31794640   PMID:31909538   PMID:31950080   PMID:32156757   PMID:32296071  
PMID:32376682   PMID:32439762   PMID:32450229   PMID:32521258   PMID:32523119   PMID:32541007   PMID:32579954   PMID:32597756   PMID:32628936   PMID:32855167   PMID:33051257   PMID:33184218  
PMID:33230114   PMID:33247143   PMID:33308481   PMID:33420489   PMID:33454424   PMID:33929320   PMID:33951437   PMID:33999917   PMID:34168324   PMID:34256037   PMID:34446717   PMID:34601382  
PMID:34671097   PMID:34672258   PMID:34679163   PMID:34686326   PMID:34769078   PMID:34822716   PMID:34887431   PMID:35017475   PMID:35177595   PMID:35276131   PMID:35297517   PMID:35440748  
PMID:35514236   PMID:35608036   PMID:35726782   PMID:35876795   PMID:35950911   PMID:35988542   PMID:35998584   PMID:36007540   PMID:36123354   PMID:36142249   PMID:36154671   PMID:36197846  
PMID:36517595   PMID:36717694   PMID:36913092   PMID:37012455   PMID:37024462   PMID:37080203   PMID:37163450   PMID:37217538   PMID:37315133   PMID:37390294   PMID:37414952   PMID:37633271  
PMID:37709743   PMID:37761995   PMID:37852970   PMID:37940010   PMID:38110169   PMID:38345319   PMID:38418917  


Genomics

Comparative Map Data
T
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39178,653,255 - 8,661,328 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl178,653,255 - 8,661,328 (+)EnsemblGRCm39 Ensembl
GRCm38178,434,423 - 8,442,496 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl178,434,423 - 8,442,496 (+)EnsemblGRCm38mm10GRCm38
MGSCv37178,627,288 - 8,635,361 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36178,272,597 - 8,280,670 (+)NCBIMGSCv36mm8
Celera178,480,245 - 8,488,318 (+)NCBICelera
Cytogenetic Map17A1NCBI
cM Map174.92NCBI
TBXT
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh386166,157,656 - 166,168,655 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl6166,157,656 - 166,168,700 (-)EnsemblGRCh38hg38GRCh38
GRCh376166,571,144 - 166,582,143 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 366166,491,076 - 166,502,121 (-)NCBINCBI36Build 36hg18NCBI36
Build 346166,541,496 - 166,552,542NCBI
Celera6167,310,712 - 167,321,757 (-)NCBICelera
Cytogenetic Map6q27NCBI
HuRef6164,037,863 - 164,048,876 (-)NCBIHuRef
CHM1_16166,835,290 - 166,846,303 (-)NCBICHM1_1
T2T-CHM13v2.06167,527,458 - 167,538,457 (-)NCBIT2T-CHM13v2.0
Tbxt
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8154,845,674 - 54,859,340 (-)NCBIGRCr8
mRatBN7.2152,298,104 - 52,309,813 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl152,298,099 - 52,305,864 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx152,999,608 - 53,007,373 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0158,991,427 - 58,999,192 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0153,075,196 - 53,082,961 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0152,887,067 - 52,900,691 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl152,887,067 - 52,894,832 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0154,139,554 - 54,147,385 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4146,937,223 - 46,944,988 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1146,940,188 - 46,947,933 (-)NCBI
Celera148,061,384 - 48,069,149 (-)NCBICelera
Cytogenetic Map1q12NCBI
Tbxt
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495543915,676,095 - 15,683,554 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495543915,675,680 - 15,683,542 (+)NCBIChiLan1.0ChiLan1.0
TBXT
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v25186,353,564 - 186,363,413 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan16184,249,368 - 184,259,217 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v06164,112,117 - 164,122,253 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.16169,095,723 - 169,106,595 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl6169,095,723 - 169,106,595 (-)Ensemblpanpan1.1panPan2
TBXT
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1154,183,495 - 54,192,331 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl154,183,153 - 54,192,352 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha154,970,966 - 54,979,790 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0154,360,266 - 54,369,833 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl154,360,928 - 54,369,833 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1154,257,349 - 54,266,189 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0154,107,519 - 54,116,264 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0154,733,858 - 54,742,687 (-)NCBIUU_Cfam_GSD_1.0
Tbxt
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404946148,774,775 - 148,782,886 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_00493648916,027,359 - 16,035,041 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_00493648916,027,359 - 16,035,041 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
TBXT
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl12,717,165 - 2,725,601 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.112,717,165 - 2,725,561 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.213,857,228 - 3,861,219 (+)NCBISscrofa10.2Sscrofa10.2susScr3
TBXT
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11393,854,086 - 93,864,910 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1393,855,534 - 93,864,507 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604065,656,160 - 65,666,958 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Tbxt
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462478513,058,444 - 13,066,719 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462478513,058,520 - 13,066,607 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in T
241 total Variants
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:538
Count of miRNA genes:382
Interacting mature miRNAs:449
Transcripts:ENSMUST00000074667, ENSMUST00000136922, ENSMUST00000177118
Prediction methods: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.


QTLs in Region (GRCm39)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1357452Vtbt18_mvertebral trabecular bone trait 18 (mouse)Not determined17120975022Mouse
1302196Myaa1_mmodifier of Yaa 1 (mouse)Not determined17120975022Mouse
1357902Obq19_mobesity QTL 19 (mouse)Not determined17125662076Mouse
12910982Pifs2_mpeptide-induced fatal syndrome 2 (mouse)17126189355Mouse
1357743Lith3_mlithogenic gene 3 (mouse)Not determined17126194456Mouse
1301615Cfld3_mcystic fibrosis lung disease 3 (mouse)Not determined17127081639Mouse
1300613Pcyts4_mplasmacytoma susceptibility 4 (mouse)Not determined17127081639Mouse
1302100Circp2_mcircadian photosensitivity 2 (mouse)Not determined17129198453Mouse
12910527Nrq1a_mnoise-induced hearing loss resistant QTL 1a (mouse)17129198453Mouse
12910528Nrq1_mnoise-induced hearing loss resistant QTL 1 (mouse)17129198453Mouse
13524851Asrq8_macoustic startle response 8 (mouse)17131030170Mouse
10412276Leci2_mleukocyte endothelial cell interactions 2 (mouse)Not determined17334817537348299Mouse
1357680Idd23_minsulin dependent diabetes susceptibility 23 (mouse)Not determined17397489026401133Mouse
1300890Bhr3_mbronchial hyperresponsiveness 3 (mouse)Not determined17397489048866091Mouse
1301327Lmr7_mleishmaniasis resistance 7 (mouse)Not determined17485475227715939Mouse
4141215Mnic1_mmacronutrient intake, carbohydrate 1 (mouse)Not determined485475245670266Mouse
1300706Alan1_malloantigen response 1 (mouse)Not determined17485475246469702Mouse
1357789Kdnw3_mkidney weight 3 (mouse)Not determined17485475247885665Mouse
4141272Tfv1_mtotal food volume 1 (mouse)Not determined485475265637357Mouse
10043949Pbft7_mpercent body fat 7 (mouse)Not determined17689393640893936Mouse
4141608Phl1_mprogressive hearing loss 1 (mouse)Not determined17787584329487423Mouse
13824987Flal1_mfatty liver accumulation QTL 1, females only (mouse)17821883211218887Mouse
1301935Skull24_mskull morphology 24 (mouse)Not determined17858491442585149Mouse
1300787Cd8mts5_mCD8 memory T cell subset 5 (mouse)Not determined17858491442585149Mouse

Markers in Region
X51683  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38178,442,269 - 8,442,373UniSTSGRCm38
MGSCv37178,635,134 - 8,635,238UniSTSGRCm37
Celera178,488,091 - 8,488,195UniSTS
Cytogenetic Map17A1UniSTS
cM Map174.02UniSTS
Whitehead/MRC_RH1770.74UniSTS
T  
Mouse AssemblyChrPosition (strand)SourceJBrowse
MGSCv37178,634,462 - 8,634,784UniSTSGRCm37
MGSCv37178,628,251 - 8,629,062UniSTSGRCm37
MGSCv37178,635,064 - 8,635,327UniSTSGRCm37
MGSCv37178,629,003 - 8,629,893UniSTSGRCm37
Celera178,488,021 - 8,488,284UniSTS
Celera178,481,960 - 8,482,850UniSTS
Celera178,481,208 - 8,482,019UniSTS
Celera178,487,419 - 8,487,741UniSTS
Cytogenetic Map17A1UniSTS
cM Map174.02UniSTS
cM Map174.02UniSTS
cM Map174.02UniSTS
cM Map174.02UniSTS
cM Map174.02UniSTS
T  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map17A1UniSTS
T  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map17A1UniSTS
T  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map17A1UniSTS
T  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map17A1UniSTS
cM Map174.02UniSTS
T  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38178,436,138 - 8,437,028UniSTSGRCm38
MGSCv37178,629,003 - 8,629,893UniSTSGRCm37
Celera178,481,960 - 8,482,850UniSTS
Cytogenetic Map17A1UniSTS
cM Map174.02UniSTS
T  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38178,441,597 - 8,441,919UniSTSGRCm38
MGSCv37178,634,462 - 8,634,784UniSTSGRCm37
Celera178,487,419 - 8,487,741UniSTS
Cytogenetic Map17A1UniSTS
cM Map174.02UniSTS
T  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map17A1UniSTS
cM Map174.02UniSTS
T  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map17A1UniSTS
T  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38178,435,386 - 8,436,197UniSTSGRCm38
MGSCv37178,628,251 - 8,629,062UniSTSGRCm37
Celera178,481,208 - 8,482,019UniSTS
Cytogenetic Map17A1UniSTS
T  
Mouse AssemblyChrPosition (strand)SourceJBrowse
GRCm38178,442,199 - 8,442,462UniSTSGRCm38
MGSCv37178,635,064 - 8,635,327UniSTSGRCm37
Celera178,488,021 - 8,488,284UniSTS
Cytogenetic Map17A1UniSTS
T  
Mouse AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map17A1UniSTS


Expression


Sequence


RefSeq Acc Id: ENSMUST00000074667   ⟹   ENSMUSP00000074236
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl178,653,255 - 8,661,328 (+)Ensembl
GRCm38.p6 Ensembl178,434,423 - 8,442,496 (+)Ensembl
RefSeq Acc Id: ENSMUST00000136922   ⟹   ENSMUSP00000119581
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl178,653,757 - 8,655,824 (+)Ensembl
GRCm38.p6 Ensembl178,434,925 - 8,436,992 (+)Ensembl
RefSeq Acc Id: ENSMUST00000177118   ⟹   ENSMUSP00000135526
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39 Ensembl178,654,243 - 8,660,574 (+)Ensembl
GRCm38.p6 Ensembl178,435,411 - 8,441,742 (+)Ensembl
RefSeq Acc Id: NM_009309   ⟹   NP_033335
RefSeq Status: VALIDATED
Type: CODING
Position:
Mouse AssemblyChrPosition (strand)Source
GRCm39178,653,255 - 8,661,328 (+)NCBI
GRCm38178,434,423 - 8,442,496 (+)NCBI
MGSCv37178,627,288 - 8,635,361 (+)RGD
Celera178,480,245 - 8,488,318 (+)RGD
cM Map17 ENTREZGENE
Sequence:
RefSeq Acc Id: NP_033335   ⟸   NM_009309
- UniProtKB: P20293 (UniProtKB/Swiss-Prot),   Q78ZW9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSMUSP00000135526   ⟸   ENSMUST00000177118
RefSeq Acc Id: ENSMUSP00000074236   ⟸   ENSMUST00000074667
RefSeq Acc Id: ENSMUSP00000119581   ⟸   ENSMUST00000136922
Protein Domains
T-box

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-P20293-F1-model_v2 AlphaFold P20293 1-436 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene MGI:98472 AgrOrtholog
Ensembl Genes ENSMUSG00000062327 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENSMUST00000074667 ENTREZGENE
  ENSMUST00000074667.9 UniProtKB/Swiss-Prot
  ENSMUST00000136922.8 UniProtKB/TrEMBL
  ENSMUST00000177118.2 UniProtKB/TrEMBL
Gene3D-CATH 2.60.40.820 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
InterPro p53-like_TF_DNA-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  T-box_DNA-bd UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  T-box_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TF_Brachyury UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TF_T-box UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TF_T-box_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report mmu:20997 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
MGD MGI:98472 ENTREZGENE
NCBI Gene 20997 ENTREZGENE
PANTHER PTHR11267 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  T-BOX TRANSCRIPTION FACTOR T UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam T-box UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PhenoGen T PhenoGen
PRINTS BRACHYURY UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TBOX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE TBOX_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TBOX_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  TBOX_3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART TBOX UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF49417 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt D3Z1X4_MOUSE UniProtKB/TrEMBL
  H3BKU2_MOUSE UniProtKB/TrEMBL
  P20293 ENTREZGENE
  Q78ZW9 ENTREZGENE, UniProtKB/TrEMBL
  TBXT_MOUSE UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2017-11-16 brachyury, T-box transcription factor T    brachyury  Symbol and/or name change 5135510 APPROVED