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Category   Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21
GIFtS

T Gene

protein-coding   GIFtS: 57
GCID: GC06M166541

T, brachyury homolog (mouse)

(Previous name: T brachyury (mouse) homolog )
 Explore 51 diseases affiliated with
T via our new
 Human Malady Compendium 
Biological research products
for T
    

(According to 1HGNC, 2Entrez Gene,
3UniProtKB/Swiss-Prot, 4UniProtKB/TrEMBL, 5OMIM, 6GeneLoc, 7Ensembl, 8DME, 9miRBase, and/or 10fRNAdb)
About This Section

Aliases
T, Brachyury Homolog (Mouse)1 2     Brachyury Protein2
Protein T2 3     T Brachyury Homolog2
T Brachyury (Mouse) Homolog1     TF5
TFT2     

External Ids:    HGNC: 115151   Entrez Gene: 68622   Ensembl: ENSG000001644587   OMIM: 6013975   UniProtKB: O151783   

Export aliases for T gene to outside databases

Previous GC identifers: GC06M165924 GC06M166444 GC06M166481 GC06M166482 GC06M164037


(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for T:
The protein encoded by this gene is an embryonic nuclear transcription factor that binds to a specific DNA element, the
palindromic T-site. It binds through a region in its N-terminus, called the T-box, and effects transcription of genes
required for mesoderm formation and differentiation. The protein is localized to notochord-derived cells. Two
transcript variants encoding different isoforms have been found for this gene. (provided by RefSeq, Jul 2012)

UniProtKB/Swiss-Prot: BRAC_HUMAN, O15178
Function: Involved in the transcriptional regulation of genes required for mesoderm formation and differentiation.
Binds to a palindromic site (called T site) and activates gene transcription when bound to such a site

Gene Wiki entry for T (Brachyury)


(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section
RefSeq DNA sequence:
NC_000006.11  NC_018917.1  NT_025741.15  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the T gene promoter:
         SREBP-1c   p300   Pax-2a   HNF-4alpha2   C/EBPalpha   SREBP-1b   HNF-4alpha1   SREBP-1a   
         Other transcription factors

SwitchGear Promoter luciferase reporter plasmidT promoter sequence
   Search SABiosciences Chromatin IP Primers for T

Epigenetics:
QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat T


Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 6q27   Ensembl cytogenetic band:  6q27   HGNC cytogenetic band: 6q27

T Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
T gene location

GeneLoc information about chromosome 6         GeneLoc Exon Structure

GeneLoc location for GC06M166541:  view genomic region     (about GC identifiers)

Start:
166,571,086 bp from pter      End:
166,582,188 bp from pter
Size:
11,103 bases      Orientation:
minus strand

(According to 1UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to 2PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: BRAC_HUMAN, O15178 (See protein sequence)
Recommended Name: Brachyury protein  
Size: 435 amino acids; 47443 Da
Subunit: Monomer (By similarity)
Subcellular location: Nucleus
Secondary accessions: E7ERD6 Q4KMP4
Alternative splicing: 2 isoforms:  O15178-1   O15178-2   (No experimental confirmation available)

Explore the universe of human proteins at neXtProt for T: NX_O15178

Post-translational modifications:

  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_O15178

  • T Protein expression data from MOPED and PaxDb:    About this image 
    Estimated protein expression log10 (pmol).

    REFSEQ proteins (2 alternative transcripts): 
    NP_001257413.1  NP_003172.1  

    ENSEMBL proteins: 
     ENSP00000296946   ENSP00000355836   ENSP00000355841   ENSP00000453512  

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    Uscn Proteins for T

    Gene Ontology (GO): 4 cellular component terms (GO ID links to tree view):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000785chromatin ----
    GO:0000790nuclear chromatin IDA--
    GO:0005634nucleus ----
    GO:0005737cytoplasm IEA--


    T for ontologies           About GeneDecksing



    T Antibody Products: 
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    Uscn ELISAs and CLIAs for T


    (According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
    About This Section

    T for domains           About GeneDecksing

    4 InterPro domains/families:
     IPR001699 TF_T-box
     IPR008967 p53-like_TF_DNA-bd
     IPR002070 TF_Brachyury
     IPR018186 TF_T-box_CS

    Graphical View of Domain Structure for InterPro Entry O15178

    ProtoNet protein and cluster: O15178

    2 Blocks protein families:
    IPB001699 Transcription factor
    IPB002070 Brachyury protein family signature


    UniProtKB/Swiss-Prot: BRAC_HUMAN, O15178
    Similarity: Contains 1 T-box DNA-binding domain


    (According to 1UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or 2DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
    bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
    About This Section

    Function Summary:

         UniProtKB/Swiss-Prot: BRAC_HUMAN, O15178
    Function: Involved in the transcriptional regulation of genes required for mesoderm formation and differentiation.
    Binds to a palindromic site (called T site) and activates gene transcription when bound to such a site

         Genatlas biochemistry entry for T:
    murine T-box gene Tbx (T,brachyury) homolog,expressed in cells derived from the notochord,crucial for mesoderm
    formation,no evidence of association with neural tube defects (NTD) in Netherlands and U.K.

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    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for T

    Gene Ontology (GO): 5/11 molecular function terms (GO ID links to tree view) (see all 11):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000978RNA polymerase II core promoter proximal region sequence-specific DNA binding ISS--
    GO:0000980RNA polymerase II distal enhancer sequence-specific DNA binding IDA--
    GO:0000981sequence-specific DNA binding RNA polymerase II transcription factor activity ----
    GO:0001085RNA polymerase II transcription factor binding ISS--
    GO:0001102RNA polymerase II activating transcription factor binding IPI--


    T for ontologies           About GeneDecksing


    Animal Models:
         15/16 MGI mutant phenotypes (inferred from 35 alleles(MGI details for T) (see all 16):
     behavior/neurological  cardiovascular system  craniofacial  digestive/alimentary  embryogenesis 
     growth/size  homeostasis/metabolism  integument  limbs/digits/tail  mortality/aging 
     nervous system  no phenotypic analysis  normal  renal/urinary system  reproductive system 

    T for phenotypes           About GeneDecksing


    (Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to 1UniProtKB, 2MINT, 3I2D, and/or 4STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
    About This Section

    Unified GeneCards pathways  About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Wnt / Hedgehog / Notch
    Wnt / Hedgehog / Notch1.00
    2Selected targets of HNF1
    Selected targets of HNF11.00
    3Selected targets of Oct-3/4
    Selected targets of Oct-3/41.00
    4Regulation of Wnt-mediated beta catenin signaling and target gene transcription
    Regulation of Wnt-mediated beta catenin signaling and target gene transcription1.00
    5glycine cleavage
    glycine cleavage1.00

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    2 EMD Millipore Pathways for T
        Selected targets of Oct-3/4
    Selected targets of HNF1


    1 Cell Signaling Technology (CST) Pathway for T
        Wnt / Hedgehog / Notch

    2 BioSystems Pathways for T 
        glycine cleavage
    Regulation of Wnt-mediated beta catenin signaling and target gene transcription



    T for pathways           About GeneDecksing

    Interactions:

        Search SABiosciences Gene Network CentralTM Interacting Genes and Proteins Networks for T

    STRING Interaction Network Preview (showing 5 interactants - click image to see 6)

    5/6 Interacting proteins for T (ENSP000002969464) via UniProtKB, MINT, STRING, and/or I2D (see all 6)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    DLDENSP000002054024STRING: ENSP00000205402
    GLDCENSP000003707374STRING: ENSP00000370737
    LEF1ENSP000002651654STRING: ENSP00000265165
    OCA2ENSP000003466594STRING: ENSP00000346659
    CTNNB1ENSP000003444564STRING: ENSP00000344456
    About this table

    Gene Ontology (GO): 5/34 biological process terms (GO ID links to tree view) (see all 34):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000122negative regulation of transcription from RNA polymerase II promoter ISS--
    GO:0001570vasculogenesis IEA--
    GO:0001756somitogenesis IEA--
    GO:0001839neural plate morphogenesis IEA--
    GO:0001843neural tube closure IEA--


    T for ontologies           About GeneDecksing



    (Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
    About This Section
    Browse Small Molecules at EMD Millipore
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    Browse Tocris compounds for T
    Search CenterWatch for drugs/clinical trials and news about T / BRAC 

    (Secondary structures according to fRNAdb,
    GenBank/EMBL/DDBJ Accessions according to
    Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
    RefSeq according to Entrez Gene,
    DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
    exon structure from GeneLoc, alternative splicing isoforms according to ASD and/or ECgene,
    RNAi Products from EMD Millipore,
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    Tagged/untagged cDNA clones from OriGene, SwitchGear Genomics, GenScript, DNA2.0, Vector BioLabs, Primers from OriGene, SABiosciences, and/or QIAGEN )
    About This Section

    REFSEQ mRNAs for T gene (2 alternative transcripts): 
    NM_001270484.1  NM_003181.3  

    Unigene Cluster for T:

    T, brachyury homolog (mouse)
    Hs.389457  [show with all ESTs]
    Unigene Representative Sequence: NM_003181
    4 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000296946(uc003qut.1 uc003quu.1) ENST00000366871(uc003quv.1)
    ENST00000366876 ENST00000461348

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    Inhib. RNA
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    Additional cDNA sequence: 

    AJ001699.1 BC039877.1 BC098425.1 

    5 DOTS entries:

    DT.97837890  DT.97837889  DT.202766  DT.100737559  DT.75161871 

    24/48 AceView cDNA sequences (see all 48):

    NM_003181 BF512284 BU164583 BQ927155 BG490984 AW003327 BQ931406 BU192473 
    BG333106 BQ222875 AA994493 BC039877 BQ221790 BQ925830 BQ951069 BG332916 
    BQ420570 BU190437 AI001036 BQ422302 BF223613 AI797600 BQ430235 BQ221957 

    GeneLoc Exon Structure

    5 Alternative Splicing Database (ASD) splice patterns (SP) for T    About this scheme

    ExUns: 1a · 1b · 1c · 1d ^ 2a · 2b · 2c ^ 3a · 3b ^ 4 ^ 5 ^ 6 ^ 7a · 7b ^ 8 ^ 9a · 9b
    SP1:                          -     -                                         -     -                     
    SP2:                                                                                                      
    SP3:                                                                                                      
    SP4:                    -     -     -                                                                     
    SP5:                                                                                                      


    ECgene alternative splicing isoforms for T

    (RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
    PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
    About This Section

    T expression in normal human tissues (normalized intensities)
    See probesets specificity/sensitivity at GeneAnnot
    About this imageBioGPS
    CGAP TAG: TGAAGCAGCA

    Microarray
    RNAseq (Illumina Body Map)
    (100×FPKM)½
    SAGE (Serial Analysis of Gene Expression)

    About this image

    T expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    10/15 LifeMap In Vivo Development Anatomical Compartments/Cells (see all 15
    Tissue Anatomical Compartment CellCategory (developmental path)
    MesodermMesodermMesoderm CellsEarly Embryo, Mesoderm
    Primitive StreakAnterior Primitive StreakMesoderm Progenitor CellsEarly Embryo, Mesoderm
    Primitive StreakNotochordNotochord CellsCartilage
    Primitive StreakPosterior Primitive StreakHemangioblastsBlood, Endothelium
    Primitive StreakPosterior Primitive StreakMesoderm Progenitor CellsEarly Embryo, Mesoderm
    Primitive StreakPrimitive StreakPrimitive Streak CellsEarly Embryo
    EpiblastEpiblastPrimordial Germ Cell PrecursorsGerm Cells
    CartilageCervical Intervertebral DiscIntervertebral Disc Nucleus Pulposus CellsCartilage
    CartilageLumbar Intervertebral DiscIntervertebral Disc Nucleus Pulposus CellsCartilage
    CartilageSacral Intervertebral DiscIntervertebral Disc Nucleus Pulposus CellsCartilage
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization
    Stem Cell Differentiation: 10/37 LifeMap Cells (see all 37
    NameCategory
    Embryoid bodies (Generation and expan...)
    Mesoderm-like cells (Direct differentiati...)Mesoderm
    Primitive Streak Mesendoderm cells (Direct differentiati...)
    Early mesoderm cells (Generation of human ...)
    Primitive streak-like cells (Generation of primit...)
    Activin A-induced embryoid bodies (Mouse embryonic stem...)
    Mesendoderm embryoid bodies (Mouse embryonic stem...)
    Anterior foregut progenitor cells (Directed differentia...)
    Mesendoderm-like cells (A scalable, suspensi...)
    Mesendoderm-like cells (Generation of beta c...)

    See T Protein Expression from SPIRE MOPED and PaxDB
    Genevestigator expression for T

    SOURCE GeneReport for Unigene cluster: Hs.389457
        SABiosciences Expression via Pathway-Focused PCR Arrays including T: 
              Cell Lineage Identification in human mouse rat
              WNT Signaling Targets in human mouse rat
              Embryonic Stem Cells in human mouse rat
              Stem Cells in human mouse rat

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    (Orthologs according to 1,2HomoloGene (2older version, for species not in 1newer version), 3euGenes, 4SGD , 5MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or 6Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
    About This Section

    This gene was present in the common ancestor of animals.

    Orthologs for T gene from 6/21 species (see all 21)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    chicken
    (Gallus gallus)
    Aves T1 T, brachyury homolog (mouse) 81.13(n)
    80.93(a)
      395782  NM_204940.1  NP_990271.1 
    lizard
    (Anolis carolinensis)
    Reptilia T6
    MGA6
    --
    81(a)
    1(a)
    1 ↔ 1
    possible ortholog
    GL343461.1(590323-608045)
    1(41056654-41078608)
    African clawed frog
    (Xenopus laevis)
    Amphibia Xl.5142 Xenopus laevis brachyury (T) (Xbra) gene, complete cds less 76.01(n)    M77243.1 
    zebrafish
    (Danio rerio)
    Actinopterygii ntl2 no tail 78.83(n)   30399  NM_131162.1 
    fruit fly
    (Drosophila melanogaster)
    Insecta byn1 , 3 Malpighian tubule morphogenesis RNA
    polymerase II transcription factor less3
    brachyenteron1
    68(a)3
    56.98(n)1
    55.84(a)1
      68E33
    393491  NM_079307.11  NP_524031.11 
    worm
    (Caenorhabditis elegans)
    Secernentea tbx-83 Brachyury 42(a)
    (best of 2)
      III(10419228-10421240)   --


    ENSEMBL Gene Tree for T (if available)
    TreeFam Gene Tree for T (if available) 

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
    Paralogs for T gene
    TBX12  TBX222  TBX192  EOMES2  TBX22  TBX62  TBX212  TBX32  
    TBX202  TBX52  TBX102  TBX42  TBX152  TBR12  TBX182  
    14 SIMAP similar genes for T using alignment to 3 protein entries:     BRAC_HUMAN (see all proteins):
    TBX19    TBX6    TBX1    MGA    TBX18    TBX10
    TBX20    TBX5    TBX4    DKFZp762H2012    TBX2    EOMES
    TBR1    TBX21

    T for paralogs           About GeneDecksing


    2 Pseudogenes.org Pseudogenes for T
    PGOHUM00000244365 PGOHUM00000235170


    (SNPs/Variants according to the 1NCBI SNP Database, 2Ensembl, 3PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
    About This Section

    10/304 NCBI SNPs in T are shown (see all 304    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 6 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs31273271,2
    H--164037999(+) ACATTC/ATAGGG 2 -- ut31 ese34Minor allele frequency- A:0.00NS EA 420
    rs10560501,2
    C,F,H,--164038319(-) AGTAGC/TGGTGC 2 -- ut3110Minor allele frequency- T:0.06MN NS EA NA WA CSA 730
    rs798823411,2
    F,--164038368(+) GTGCCG/ATGTGC 2 -- ut311Minor allele frequency- A:0.04EA 120
    rs792531851,2
    F,--164039051(+) TCAGAG/ACTCAT 2 -- int11Minor allele frequency- A:0.02WA 118
    rs117584761,2
    C,F,H,--164039160(+) ggatcA/Ggctga 2 -- int15Minor allele frequency- G:0.29NA WA CSA 128
    rs58816821,2
    C,F,--164040167(+) CAATTG/-AATTC 2 -- int12Minor allele frequency- -:0.50NA CSA 4
    rs612623281,2
    --164040259(+) TTTGAA/GGTCAA 2 -- int10--------
    rs614324601,2
    --164040596(+) CGAAAC/TGATCT 2 -- int10--------
    rs767921231,2
    --164040792(+) ATAGCG/ACAGCT 2 -- int11Minor allele frequency- A:0.01NA 120
    rs787969051,2
    --164040935(+) CCACCC/TACAGG 2 -- int11Minor allele frequency- T:0.01NA 120

    HapMap Linkage Disequilibrium report for T (166571086 - 166582188 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
          Database of Genomic Variants (DGV) variations for T: --
    Human Gene Mutation Database (HGMD): T

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    (in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Novoseek, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
    About This Section

    T for disorders           About GeneDecksing

    OMIM gene information: 601397   
    OMIM disorders: 182940  
    UniProtKB/Swiss-Prot: BRAC_HUMAN, O15178
  • Genetic variations in T are associated with susceptibility to neural tube defects (NTD) [MIM:182940]. NTD are
  • common congenital malformations. Spina bifida, which results from malformations in the caudal region of the neural
    tube, is compatible with life but associated with significant morbidity, including lower limb paralysis
  • T is involved in susceptibility to the development of chordoma (CHDM) [MIM:215400]. Chordomas are rare,
  • clinically malignant tumors derived from notochordal remnants. They occur along the length of the spinal axis,
    predominantly in the sphenooccipital, vertebral and sacrococcygeal regions. They are characterized by slow growth,
    local destruction of bone, extension into adjacent soft tissues and rarely, distant metastatic spread.
    Note=Susceptibility to development of chordomas is due to a T gene duplication

    20/51 diseases for T (see all 51):    About MalaCards
    neural tube defect    tropical spastic paraparesis    spastic paraparesis    abdominal aortic aneurysm
    clear cell renal cell carcinoma    cervical intraepithelial neoplasia    type 2 diabetes mellitus    aortic aneurysm
    autoimmune hemolytic anemia    hemolytic anemia    alopecia areata    genital herpes
    spina bifida    hairy cell leukemia    parachordoma    renal cell carcinoma
    allergic rhinitis    aplastic anemia    diabetes mellitus    myoepithelioma

    3 Novoseek disease relationships for T gene    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    colitis 22.3 1 17923080 (1), 11994418 (1)
    inflammation 18.4 3 19412181 (1), 17723218 (1), 15498029 (1)
    asthma 6.56 1 15604153 (1)

    Human Genome Epidemiology (HuGE) Navigator: T (0 documents)

    Export disorders for T gene to outside databases

    (in PubMed. Associations of this gene to articles via 1Entrez Gene, 2UniProtKB/Swiss-Prot, 3HGNC, 4GAD, 5PharmGKB, 6HMDB, 7DrugBank, 8UniProtKB/TrEMBL, 9 Novoseek, and/or 10fRNAdb)
    About This Section

    PubMed articles for T gene, integrated from 9 sources (see all 118):
    (articles sorted by number of sources associating them with T)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. The human homolog T of the mouse T(Brachyury) gene; gene structure, cDNA sequence, and assignment to chromosome 6q27. (PubMed id 8963900)1, 2, 3, 9 Edwards Y.H....Sowden J. (1996)
    2. T (brachyury) gene duplication confers major suscepti bility to familial chordoma. (PubMed id 19801981)1, 2 Yang X.R....Kelley M.J. (2009)
    3. The DNA sequence and analysis of human chromosome 6. (PubMed id 14574404)1, 2 Mungall A.J.... Beck S. (2003)
    4. The human T locus and spina bifida risk. (PubMed id 15449172)2, 9 Jensen L.E....Mitchell L.E. (2004)
    5. Genome-wide association identifies the T gene as a nov el asthma pharmacogenetic locus. (PubMed id 22538805)1 Tantisira K.G....Israel E. (2012)
    6. An integrated functional genomics approach identifies the regulatory network directed by brachyury (T) in chordoma. (PubMed id 22847733)1 Nelson A.C....Flanagan A.M. (2012)
    7. BRACHYURY confers cancer stem cell characteristics on colorectal cancer cells. (PubMed id 21365650)1 Sarkar D....Wakeman J.A. (2012)
    8. Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in women. (PubMed id 22589738)1 Fox C.S....Borecki I.B. (2012)
    9. Expression of brachyury in hemangioblastoma: potential use in differential diagnosis. (PubMed id 22446946)1 Barresi V....Barresi G. (2012)
    10. P63 does not regulate brachyury expression in human ch ordomas and osteosarcomas. (PubMed id 22007675)1 Pillay N....Flanagan A.M. (2011)

    (in PubMed, OMIM, and NCBI Bookshelf)
    About This Section
     ANDOR
    Aliases
    Disorders
    Free Text  

      Query String
    PubMed
    OMIM
    NCBI Bookshelf
      (Note: In FireFox, select the above section and copy using Ctrl-C)

    (According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
    About This Section
    Entrez Gene: 6862 HGNC: 11515 AceView: T Ensembl:ENSG00000164458 euGenes: HUgn6862
    ECgene: T H-InvDB: T

    (According to HUGE)
    About This Section
      --

    (According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
    Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
    About This Section
    NameDescription
    PharmGKB entry for T Pharmacogenomics, SNPs, Pathways

    (Patent information from GeneIP,
    Licensable technologies from WIS Yeda, Salk, Tufts,
    IP news from LifeMap Sciences, Inc.)
    About This Section
    Patent Information for T gene:
    Search GeneIP for patents involving T

    GeneCards and IP:
    Japan Patent Office Licenses GeneCards     European Patent Office Licenses GeneCards     Improving the IP Search



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    About This Section

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    GeneCards Homepage - Last full update: 18 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013

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