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

TERT Gene

protein-coding   GIFtS: 73
GCID: GC05M001253

telomerase reverse transcriptase

 Explore 181 diseases affiliated with
TERT via our new
 Human Malady Compendium 
Biological research products
for TERT
    

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

Aliases
Telomerase Reverse Transcriptase1 2     EC 2.7.7.493 8
EST21 2 3 5     DKCA22
TCS11 2 3 5     DKCB42
TP21 2 3     PFBMFT12
TRT1 2 3     HTRT1
HEST23     HEST23
Telomerase Catalytic Subunit2 3     EC 2.7.78
Telomerase-Associated Protein 22 3     

External Ids:    HGNC: 117301   Entrez Gene: 70152   Ensembl: ENSG000001643627   OMIM: 1872705   UniProtKB: O147463   

Export aliases for TERT gene to outside databases

Previous GC identifers: GC05P001643 GC05M001282 GC05M001306


(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 TERT:
Telomerase is a ribonucleoprotein polymerase that maintains telomere ends by addition of the telomere repeat TTAGGG.
The enzyme consists of a protein component with reverse transcriptase activity, encoded by this gene, and an RNA
component which serves as a template for the telomere repeat. Telomerase expression plays a role in cellular
senescence, as it is normally repressed in postnatal somatic cells resulting in progressive shortening of telomeres.
Deregulation of telomerase expression in somatic cells may be involved in oncogenesis. Studies in mouse suggest that
telomerase also participates in chromosomal repair, since de novo synthesis of telomere repeats may occur at
double-stranded breaks. Alternatively spliced variants encoding different isoforms of telomerase reverse transcriptase
have been identified; the full-length sequence of some variants has not been determined. Alternative splicing at this
locus is thought to be one mechanism of regulation of telomerase activity. (provided by RefSeq, Jul 2008)

UniProtKB/Swiss-Prot: TERT_HUMAN, O14746
Function: Telomerase is a ribonucleoprotein enzyme essential for the replication of chromosome termini in most
eukaryotes. Active in progenitor and cancer cells. Inactive, or very low activity, in normal somatic cells. Catalytic
component of the teleromerase holoenzyme complex whose main activity is the elongation of telomeres by acting as a
reverse transcriptase that adds simple sequence repeats to chromosome ends by copying a template sequence within the
RNA component of the enzyme. Catalyzes the RNA-dependent extension of 3'-chromosomal termini with the 6-nucleotide
telomeric repeat unit, 5'-TTAGGG-3'. The catalytic cycle involves primer binding, primer extension and release of
product once the template boundary has been reached or nascent product translocation followed by further extension.
More active on substrates containing 2 or 3 telomeric repeats. Telomerase activity is regulated by a number of factors
including telomerase complex-associated proteins, chaperones and polypeptide modifiers. Modulates Wnt signaling. Plays
important roles in aging and antiapoptosis

summary for TERT:
Telomerase is a ribonucleoprotein composed of an internal telomerase RNA template (TERC) and the enzyme,
telomerase reverse transcriptase (TERT). Telomerase adds small repeat sequences of DNA (TTAGGG) to the end
of chromosomes - multiple repeats of this hexanucleotide sequence over a 5kb span are known as a telomere.
During normal cellular replication, telomeres are eroded and thus protect the coding sequences of the DNA.
The erosion of telomeric sequences is thought to form the basis of the cellular clock which eventually
signals for the cell to exit the cell cycle and undergo senescence. Expression of telomerase is low in most
normal cells although it is thought to be active in embryonic cells and some rapidly dividing cells of the
immune system. Overexpression of telomerase is key component of the transformation process in many malignant
cancer cells.

Gene Wiki entry for TERT (Telomerase reverse transcriptase)


(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_000005.9  NC_018916.1  NT_006576.16  
Regulatory elements:
   SABiosciences Regulatory transcription factor binding sites in the TERT gene promoter:
         Egr-3   AP-1   Sp1   p53   STAT3   
         Other transcription factors

Browse SwitchGear Promoter luciferase reporter plasmids
   Search SABiosciences Chromatin IP Primers for TERT

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


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

Entrez Gene cytogenetic band: 5p15.33   Ensembl cytogenetic band:  5p15.33   HGNC cytogenetic band: 5p15.33

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

GeneLoc information about chromosome 5         GeneLoc Exon Structure

GeneLoc location for GC05M001253:  view genomic region     (about GC identifiers)

Start:
1,253,262 bp from pter      End:
1,295,184 bp from pter
Size:
41,923 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: TERT_HUMAN, O14746 (See protein sequence)
Recommended Name: Telomerase reverse transcriptase  
Size: 1132 amino acids; 126997 Da
Subunit: Homodimer; dimerization is required to produce a functional complex. Oligomer; can form oligomers in the
absence of the telomerase RNA template component (TERC). Catalytic subunit of the telomerase holoenzyme complex
composed minimally of TERT and TERC. The telomerase complex is composed of TERT, DKC1, WDR79/TCAB1, NOP10, NHP2, GAR1,
TEP1, EST1A, POT1 and a telomerase RNA template component (TERC). The molecular chaperone HSP90/P23 complex is
required for correct assembly and stabilization of the active telomerase. Interacts directly with HSP90A and PTGES3.
Interacts with HSPA1A; the interaction occurs in the absence of TERC and dissociates once the complex has formed.
Interacts with RAN; the interaction promotes nuclear export of TERT. Interacts with XPO1. Interacts with PTPN11; the
interaction retains TERT in the nucleus. Interacts with NCL (via RRM1 and C-terminal RRM4/Arg/Gly-rich domains); the
interaction is important for nucleolar localization of TERT. Interacts with SMARCA4 (via the bromodomain); the
interaction regulates Wnt-mediated signaling. Interacts with MCRS1 (isoform MCRS2); the interaction inhibits in vitro
telomerase activity. Interacts with PIF1; the interaction has no effect on the elongation activity of TERT. Interacts
with PML; the interaction recruits TERT to PML bodies and inhibits telomerase activity. Interacts with GNL3L (By
similarity)
Subcellular location: Nucleus, nucleolus. Nucleus, nucleoplasm. Nucleus. Chromosome, telomere. Cytoplasm. Nucleus, PML
body. Note=Shuttling between nuclear and cytoplasm depends on cell cycle, phosphorylation states, transformation and
DNA damage. Diffuse localization in the nucleoplasm. Enriched in nucleoli of certain cell types. Translocated to the
cytoplasm via nuclear pores in a CRM1/RAN-dependent manner involving oxidative stress-mediated phosphorylation at
Tyr-707. Dephosphorylation at this site by SHP2 retains TERT in the nucleus. Translocated to the nucleus by
phosphorylation by AKT
1 PDB 3D structure from and Proteopedia for TERT:
2BCK (3D)    
Secondary accessions: O14783 Q2XS35 Q8N6C3 Q8NG46
Alternative splicing: 3 isoforms:  O14746-1   O14746-2   O14746-3   (May be produced at very low levels due to a premature stop codon in the mRNA, leading to nonsense-mediated mRNA decay. No experimental confirmation available)

Explore the universe of human proteins at neXtProt for TERT: NX_O14746

Post-translational modifications:

  • Ubiquitinated, leading to proteasomal degradation1
  • Phosphorylation at Tyr-707 under oxidative stress leads to translocation of TERT to the cytoplasm and reduces its
  • antiapoptotic activity. Dephosphorylated by SHP2/PTPN11 leading to nuclear retention. Phosphorylation by the AKT
    pathway promotes nuclear location1
  • View modification sites using PhosphoSitePlus2
  • View neXtProt modification sites for NX_O14746

  • 4/7 DME Specific Peptides for TERT (O14746) (see all 7)
     LRELSEAE  LVAQCLVC  LFLDLQVN  RYWQMRPLF 

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

    REFSEQ proteins (2 alternative transcripts): 
    NP_001180305.1  NP_937983.2  

    ENSEMBL proteins: 
     ENSP00000309572   ENSP00000425003   ENSP00000334346   ENSP00000426042   ENSP00000296820  
    Reactome Protein details: O14746
    Human Recombinant Protein Products: 
    Browse Purified and Recombinant Proteins at EMD Millipore
    Browse R&D Systems for human recombinant proteins
    Browse recombinant and purified proteins available from Enzo Life Sciences
    Browse OriGene full length recombinant human proteins expressed in human HEK293 cells
    OriGene Protein Over-expression Lysate: TERT
    OriGene Custom Protein Services for TERT 
    GenScript Custom Purified and Recombinant Proteins Services for TERT
    Novus Biologicals TERT Lysate
    Browse Sino Biological Recombinant Proteins
    Browse ProSpec Recombinant Proteins
    Uscn Proteins for TERT

    Gene Ontology (GO): 5/8 cellular component terms (GO ID links to tree view) (see all 8):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000781chromosome, telomeric region IC12135483
    GO:0000783nuclear telomere cap complex IC15632080
    GO:0005634nucleus ----
    GO:0005654nucleoplasm TAS--
    GO:0005697telomerase holoenzyme complex IDA12135483


    TERT for ontologies           About GeneDecksing



    TERT Antibody Products: 
    EMD Millipore Mono- and Polyclonal Antibodies for the study of TERT
    R&D Systems Antibodies for TERT
    OriGene Antibodies (see all 3): TERT
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    Abcam antibodies for TERT 
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    ThermoFisher Antibody for TERT

    Assay Products for TERT: 
    Browse Kits and Assays available from EMD Millipore
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    Browse OriGene Fluorogenic Cell Assay Kits
    Browse R&D Systems for biochemical assays
    GenScript Custom Assay Services for TERT
    Browse Enzo Life Sciences for kits & assays
    Uscn ELISAs and CLIAs for TERT


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

    TERT for domains           About GeneDecksing

    3 InterPro domains/families:
     IPR003545 Telomerase_RT
     IPR000477 RVT
     IPR021891 Telomerase_RBD

    Graphical View of Domain Structure for InterPro Entry O14746

    ProtoNet protein and cluster: O14746

    1 Blocks protein family: IPB003545 Telomere reverse transcriptase signature

    UniProtKB/Swiss-Prot: TERT_HUMAN, O14746
    Domain: The primer grip sequence in the RT domain is required for telomerase activity and for stable association with
    short telomeric primers
    Domain: The RNA-interacting domain 1 (RD1)/N-terminal extension (NTE) is required for interaction with the
    pseudoknot-template domain of each of TERC dimers. It contains anchor sites that bind primer nucleotides upstream of
    the RNA-DNA hybrid and is thus an essential determinant of repeat addition processivity
    Domain: The RNA-interacting domain 2 (RD2) is essential for both interaction with the CR4-CR5 domain of TERC and for
    DNA synthesis
    Similarity: Belongs to the reverse transcriptase family. Telomerase subfamily
    Similarity: Contains 1 reverse transcriptase 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: TERT_HUMAN, O14746
    Function: Telomerase is a ribonucleoprotein enzyme essential for the replication of chromosome termini in most
    eukaryotes. Active in progenitor and cancer cells. Inactive, or very low activity, in normal somatic cells. Catalytic
    component of the teleromerase holoenzyme complex whose main activity is the elongation of telomeres by acting as a
    reverse transcriptase that adds simple sequence repeats to chromosome ends by copying a template sequence within the
    RNA component of the enzyme. Catalyzes the RNA-dependent extension of 3'-chromosomal termini with the 6-nucleotide
    telomeric repeat unit, 5'-TTAGGG-3'. The catalytic cycle involves primer binding, primer extension and release of
    product once the template boundary has been reached or nascent product translocation followed by further extension.
    More active on substrates containing 2 or 3 telomeric repeats. Telomerase activity is regulated by a number of factors
    including telomerase complex-associated proteins, chaperones and polypeptide modifiers. Modulates Wnt signaling. Plays
    important roles in aging and antiapoptosis
    Catalytic activity: Deoxynucleoside triphosphate + DNA(n) = diphosphate + DNA(n+1)
    Induction: Activated by cytotoxic events and down-regulated during aging. In peripheral T-lymphocytes, induced By CD3
    and by PMA/ionomycin. Inhibited by herbimycin B

         Genatlas biochemistry entry for TERT:
    telomerase,catalytic subunit,yeast Est2 homolog,100kDa,involved in telomere maintenance,putative up-regulated c-Myc
    target gene,protein activity deleted in cancer,repressed in normal tissues

    Enzyme Numbers (IUBMB): EC 2.7.7.491 2 EC 2.7.72

    miRNA
    Products:
        
    miRTarBase miRNAs that target TERT:
    hsa-mir-138 (MIRT003991)

    OriGene 3'-UTR Clone (see all 2): TERT
    Browse MicroRNA Expression Plasmids
    QIAGEN Custom miScript Target Protector blocks miRNA-binding site of human, mouse, rat TERT
    Search QIAGEN for miScript miRNA Assays for microRNAs that regulate TERT
    SwitchGear 3'UTR luciferase reporter plasmidTERT 3' UTR sequence
    Inhib. RNA
    Products:
        
    Browse for Gene Knock-down Tools from EMD Millipore
    OriGene 29mer shRNA kits in GFP-retroviral vector in human, mouse, rat for TERT (see all 7)
    OriGene shRNA RFP: TERT
    OriGene siRNA: TERT
    QIAGEN FlexiTube/FlexiPlate siRNA for gene silencing in human, mouse, rat TERT

    Gene Editing
    Products:
    DNA2.0 Custom Protein Engineering Service for TERT

    Clone
    Products:
         
    Browse Clones for the Expression of Recombinant Proteins Available from EMD Millipore
    OriGene Myc/DDK tagged cDNA clones in CMV expression vector in human, mouse, rat for TERT (see first 1)
    NM_001193376 (human cat#: RC231464)  NM_198253 (human cat#: RC217436)  NM_009354 (mouse cat#: MR226892)  NM_053423 (rat cat#: RR210889)  
    OriGene untagged cDNA clones in CMV expression vector in human, mouse, rat for TERT (see all 2)
    OriGene custom cloning services – gene synthesis, subcloning, mutagenesis, variant library, vector shuttling 
    GenScript: all cDNA clones in your preferred vector (see all 2): TERT (NM_198253)
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    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat TERT 

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    Search LifeMap BioReagents cell lines for TERT

    In Situ Assay
    Products:
       

     
    Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for TERT

    Gene Ontology (GO): 5/9 molecular function terms (GO ID links to tree view) (see all 9):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0003720telomerase activity IDA16043710
    GO:0003721telomeric template RNA reverse transcriptase activity TAS14991929
    GO:0003723RNA binding ----
    GO:0003964RNA-directed DNA polymerase activity ----
    GO:0005515protein binding IPI17237767


    TERT for ontologies           About GeneDecksing


    Animal Models:
         Mouse knock-outs for TERT: Terttm1Sear Terttm1Fish Terttm1Rdp Terttm1Yjc Terttm1Leah
         14 MGI mutant phenotypes (inferred from 8 alleles(MGI details for Tert):
     cellular  digestive/alimentary  endocrine/exocrine gland  growth/size  hematopoietic system 
     homeostasis/metabolism  immune system  mortality/aging  nervous system  normal 
     reproductive system  skeleton  taste/olfaction  tumorigenesis 

    TERT 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 - 5/14 super-pathways (see all 14About this table 
    See pathways by source

    Super-pathwaycontained gene-specific pathways
    1Meiotic Synapsis
    Chromosome Maintenance0.56
    Telomere Maintenance0.38
    2Telomere Extension By Telomerase
    Telomere Extension By Telomerase1.00
    3Cell Cycle
    Cell Cycle1.00
    4Telomere Extension by Telomerase
    Telomere Extension by Telomerase1.00
    514-3-3 and Regulation of BAD Activity
    14-3-3 and Regulation of BAD Activity1.00

    Pathway sources
    See GeneCards unified pathways
    Show all pathways

    3 Downloadable PowerPoint Slides of QIAGEN Pathway Central Maps for TERT
        Telomerase Components in Cell Signaling
    14-3-3 and Regulation of BAD Activity
    Telomere Extension by Telomerase

    5/7 BioSystems Pathways for TERT (see all 7
        Id Signaling Pathway
    IL-2 Signaling Pathway
    IL2 signaling events mediated by PI3K
    Regulation of Wnt-mediated beta catenin signaling and target gene transcription
    HIF-1-alpha transcription factor network

    5        Reactome Pathways for TERT
        Extension of Telomeres
    Telomere Maintenance
    Cell Cycle
    Chromosome Maintenance
    Telomere Extension By Telomerase



    TERT for pathways           About GeneDecksing

    Interactions:

        SABiosciences Gene Network CentralTM Interacting Genes and Proteins Network for TERT

    STRING Interaction Network Preview (showing 5 interactants - click image to see 25)

    5/93 Interacting proteins for TERT (O147461, 2, 3 ENSP000003095724) via UniProtKB, MINT, STRING, and/or I2D (see all 93)
    InteractantInteraction Details
    GeneCardExternal ID(s)
    UPF1Q929002, 3, ENSP000002628034MINT-8286561 MINT-8286551 MINT-8286579 I2D: score=1 STRING: ENSP00000262803
    AKT1P317492, 3, ENSP000002702024MINT-6742762 I2D: score=3 STRING: ENSP00000270202
    RUVBL1Q9Y2651, 3, ENSP000003182974EBI-1772203,EBI-353675 I2D: score=1 STRING: ENSP00000318297
    CIB1Q998283, ENSP000003338734I2D: score=2 STRING: ENSP00000333873
    MCRS1Q96EZ83, ENSP000003496404I2D: score=2 STRING: ENSP00000349640
    About this table

    Gene Ontology (GO): 5/7 biological process terms (GO ID links to tree view) (see all 7):    About this table

    GO IDQualified GO termEvidencePubMed IDs
    GO:0000723telomere maintenance TAS--
    GO:0006278RNA-dependent DNA replication ----
    GO:0007004telomere maintenance via telomerase TAS--
    GO:0022616DNA strand elongation IDA16043710
    GO:0032203telomere formation via telomerase IDA16043710


    TERT 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

    TERT for compounds           About GeneDecksing

    EMD Millipore small molecules for TERT:
    Small Molecule - inhibitor
    Enzo Life Sciences drugs & compounds for TERT

    Compounds for TERT available from Tocris Bioscience    About this table
    CompoundAction CAS #
    BIBR 1532Selective telomerase inhibitor[321674-73-1]
    CostunolideInhibitor of human telomerase activity[553-21-9]

    2 HMDB Compounds for TERT    About this table
    CompoundSynonyms CAS #PubMed Ids
    Phosphoric acidacide phosphorique (FRENCH) (see all 20)7664-38-2--
    Pyrophosphate(4-)Diphosphoric acid ion (see all 10)14000-31-8--
    10/50 Novoseek chemical compound relationships for TERT gene (see all 50)    About this table
    Compound   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    tin(2+) 59.3 7 12007281 (2), 11494028 (1), 19419704 (1), 18669893 (1)
    lipofectamine 36.4 1 17495775 (1)
    ganciclovir 26.4 4 19328781 (1), 15312323 (1), 17407070 (1), 19809268 (1)
    retinoic acid 25.4 12 12529350 (2), 15236314 (2), 12939463 (1), 14592454 (1) (see all 7)
    ly294002 24.5 2 16093915 (1)
    depsipeptide 22.8 2 17610380 (1), 15791453 (1)
    oligonucleotide 17.5 5 12838868 (1), 17991312 (1), 12519411 (1)
    cisplatin 16.5 4 11877097 (1), 17923759 (1), 19639202 (1), 11384107 (1)
    etoposide 14 3 12594176 (1), 11718848 (1)
    5-aza-2'deoxycytidine 13.9 2 15805278 (1)

    Search CenterWatch for drugs/clinical trials and news about TERT 

    (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,
    siRNAs from OriGene, QIAGEN, shRNA from OriGene, microRNA from QIAGEN,
    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 TERT gene (4 alternative transcripts): 
    NM_001193376.1  NM_198253.2  NM_198254.1  NM_198255.2  

    Unigene Cluster for TERT:

    Telomerase reverse transcriptase
    Hs.492203  [show with all ESTs]
    Unigene Representative Sequence: AF018167
    8 Ensembl transcripts including schematic representations, and UCSC links where relevant:
    ENST00000484238(uc003jbz.1 uc021xvz.1) ENST00000310581(uc003jcb.1 uc003jcc.1 uc003jca.1 uc003jcd.1 uc003jce.1)
    ENST00000460137 ENST00000334602 ENST00000503656 ENST00000508104 ENST00000522877
    ENST00000296820(uc021xwa.1 uc021xwb.1 uc021xwc.1)

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    Inhib. RNA
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    OriGene 29mer shRNA kits in GFP-retroviral vector in human, mouse, rat for TERT (see all 7)
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    OriGene siRNA: TERT
    QIAGEN FlexiTube/FlexiPlate siRNA for gene silencing in human, mouse, rat TERT
    Clone
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    DNA2.0 Custom Codon Optimized Gene Synthesis Service for TERT
    Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat TERT 
    Primer
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      QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat TERT
      QIAGEN QuantiFast Probe-based Assays in human, mouse, rat TERT

    Additional cDNA sequence: 

    AB085628.1 AF015950.1 AF018167.1 BC062321.1 JF896280.1 JF896281.1 JF896282.1 JF896283.1 
    JF896284.1 JF896285.1 JF896286.1 

    3 DOTS entries:

    DT.108983  DT.101961620  DT.40268927 

    24/29 AceView cDNA sequences (see all 29):

    AI824948 AX810036 AB086379 AX810038 NM_003219 AW276315 BC062321 NM_198253 
    NM_198254 AB085628 AB086950 NM_198255 AF015950 AW270031 AX810378 BE514070 
    AA311750 AF018167 AA811084 AX810043 AA281296 BM824748 BM453198 AA299878 

    GeneLoc Exon Structure

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

    ExUns: 1a · 1b ^ 2 ^ 3a · 3b ^ 4 ^ 5 ^ 6a · 6b ^ 7 ^ 8 ^ 9 ^ 10 ^ 11 ^ 12 ^ 13 ^ 14 ^ 15 ^ 16a · 16b
    SP1:                    -                                                                                                   
    SP2:                    -                                                           -                                       
    SP3:                    -                                   -     -                 -                                       
    SP4:                    -                       -           -     -                 -                                       
    SP5:                                                        -     -                                                         


    ECgene alternative splicing isoforms for TERT

    (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

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

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

    About this image

    TERT expression in embryonic tissues and stem cells
    Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine    About this table
    1 LifeMap In Vivo Development Anatomical Compartment/Cell 
    Tissue Anatomical Compartment CellCategory (developmental path)
    HeartEndocardiumEndocardial Tube CellsEndocardium
    Expression: Positive    Negative     Selective marker
    Experimental details: Curated     Microarrays     In-situ hybridization
    Stem Cell Differentiation: 10/13 LifeMap Cells (see all 13
    NameCategory
    Mesenchymal Precursor Cells (STRO-3 selected) (Adult Stem / Progenitor Cell)Bone
    Induced pluripotent stem cell line 201B6 (Induced Pluripotent Stem Cell)Early Embryo, Fibroblast
    Induced pluripotent stem cells (ALS patient) (Induced Pluripotent Stem Cell)Early Embryo, Fibroblast
    Line H1 (WA01) (Embryonic Stem Cell)Early Embryo, Inner Cell Mass
    Line H7 (WA07) (Embryonic Stem Cell)Early Embryo, Inner Cell Mass
    Endometrial regenerative cell (Adult Stem / Progenitor Cell)Reproductive System
    Ovarian tissue-dissociated cells (Primary Cell)Reproductive System
    Ovarian tissue-dissociated cells (human) (Primary Cell)Ovary, Reproductive System
    Line H9 (WA09) (Embryonic Stem Cell)Early Embryo, Inner Cell Mass
    Ddx4-positive cells (Oocyte formation by ...)

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

    SOURCE GeneReport for Unigene cluster: Hs.492203

    UniProtKB/Swiss-Prot: TERT_HUMAN, O14746
    Tissue specificity: Expressed at a high level in thymocyte subpopulations, at an intermediate level in tonsil
    T-lymphocytes, and at a low to undetectable level in peripheral blood T-lymphocytes

        SABiosciences Expression via Pathway-Focused PCR Arrays including TERT (see all 9): 
              Lung Cancer in human mouse rat
              Stem Cell Transcription Factors in human mouse rat
              Liver Cancer in human mouse rat
              Stem Cells in human mouse rat
              Cancer Drug Targets 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 eukaryotes.

    Orthologs for TERT gene from 7/15 species (see all 15)    About this table
    Organism Taxonomic
    classification
    Gene Description Human
    Similarity
    Orthology
    Type
    Details
    mouse
    (Mus musculus)
    Mammalia Tert1 , 5 telomerase reverse transcriptase1, 5 70.97(n)1
    64.53(a)1
      13 (40.12 cM)5
    217521  NM_009354.11  NP_033380.11 
     736270015 
    chicken
    (Gallus gallus)
    Aves TERT1 telomerase reverse transcriptase 56.89(n)
    52.89(a)
      420972  NM_001031007.1  NP_001026178.1 
    lizard
    (Anolis carolinensis)
    Reptilia TERT6
    --
    40(a)
    1 ↔ 1
    4(68148323-68189278)
    African clawed frog
    (Xenopus laevis)
    Amphibia tert-A2 telomerase reverse transcriptase 71.34(n)    AF212299.1 
    zebrafish
    (Danio rerio)
    Actinopterygii tert1 telomerase reverse transcriptase 47.95(n)
    37.75(a)
      796551  NM_001083866.1  NP_001077335.1 
    thale cress
    (Arabidopsis thaliana)
    eudicotyledons TERT1 telomerase reverse transcriptase 41.22(n)
    28.78(a)
      831548  NM_121691.3  NP_197187.1 
    rice
    (Oryza sativa)
    Liliopsida Os12g02931001 hypothetical protein 39.61(n)
    30.21(a)
      4352024  NM_001073142.1  NP_001066610.1 


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

    (Paralogs according to 1HomoloGene,
    2Ensembl, and 3SIMAP, Pseudogenes according to 4Pseudogene.org Build 68)
    About This Section
      --

    (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

    10/1293 NCBI SNPs in TERT are shown (see all 1293    About this table
    Genomic DataTranscription Related DataAllele Frequencies
    SNP IDValidClinical
    significance
    Chr 5 posSequence#AA
    Chg
    TypeMore#Allele
    freq
    PopTotal
    sample
    More
    ----------
    rs339546911,2
    C,F,non-pathogenic1255520(-) TTTCAC/TGCATG 4 H syn115Minor allele frequency- T:0.13MN NA NS EA EU 2214
    rs1994222881,2
    C,non-pathogenic1278864(-) CTCACA/GGAGGT 4 T syn10--------
    rs339636171,2
    C,F,non-pathogenic1279439(-) CGGGCC/TCAGGA 4 A syn112Minor allele frequency- T:0.01MN NS NA EA 830
    rs27360981,2
    C,F,A,H,non-pathogenic1294086(-) CACGCG/AGGCCC 4 /A syn1 ese319Minor allele frequency- A:0.21MN NS EA NA WA 3726
    rs357199401,2
    C,F,pathogenic1254594(-) GCGCCG/ACCGGC 4 /T /A mis18Minor allele frequency- A:0.01NS NA EU 1499
    rs1219186651,2
    Cpathogenic1264656(-) CGGAAC/GACAGT 3 N K int1 mis10--------
    rs1115767401,2
    Cpathogenic1266652(+) CAGCCC/TAAAAT 2 -- spa10--------
    rs1495668581,2
    Cpathogenic1278865(+) CCTCCG/ATGAGC 4 /T /M mis11Minor allele frequency- A:0.00NA 4552
    rs340947201,2
    C,pathogenic1293767(-) AGACGC/TACTGC 4 H Y mis16Minor allele frequency- T:0.00NS NA 192
    rs617481811,2
    C,F,pathogenic1294166(+) TTCGGC/TGGGTC 4 T A mis13Minor allele frequency- T:0.02NA EU 4097

    HapMap Linkage Disequilibrium report for TERT (1253262 - 1295184 bp)
    Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
    Database of Genomic Variants (DGV): 7 variations for TERT
         2 CNVs: 68962 68963
         5 Indels: 42566 27803 46774 27802 27805
    Human Gene Mutation Database (HGMD): TERT

    Locus Specific Mutation Databases (LSDB): TERT

    SABiosciences Cancer Mutation PCR Assays
    1 SABiosciences qBiomarker Copy Number PCR Array containing TERT:
    Oncogenes & Tumor Suppressor Genes 384HC
    QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing TERT
    DNA2.0 Custom Variant and Variant Library Synthesis for TERT

    (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

    TERT for disorders           About GeneDecksing

    OMIM gene information: 187270   
    OMIM disorders: 609135  178500  127550  
    UniProtKB/Swiss-Prot: TERT_HUMAN, O14746
  • Note=Activation of telomerase has been implicated in cell immortalization and cancer cell pathogenesis
  • Defects in TERT are associated with susceptibilty to aplastic anemia (AA) [MIM:609135]. AA is a rare disease
  • in which the reduction of the circulating blood cells results from damage to the stem cell pool in bone marrow. In
    most patients, the stem cell lesion is caused by an autoimmune attack. T-lymphocytes, activated by an endogenous or
    exogenous, and most often unknown antigenic stimulus, secrete cytokines, including IFN-gamma, which would in turn be
    able to suppress hematopoiesis
  • Note=Genetic variations in TERT are associated with coronary artery disease (CAD)
  • Defects in TERT are the cause of dyskeratosis congenita autosomal dominant type 2 (DKCA2) [MIM:613989]. A rare
  • multisystem disorder caused by defective telomere maintenance. It is characterized by progressive bone marrow failure,
    and the clinical triad of reticulated skin hyperpigmentation, nail dystrophy, and mucosal leukoplakia. Common but
    variable features include premature graying, aplastic anemia, low platelets, osteoporosis, pulmonary fibrosis, and
    liver fibrosis among others. Early mortality is often associated with bone marrow failure, infections, fatal pulmonary
    complications, or malignancy
  • Defects in TERT are the cause of pulmonary fibrosis, and/or bone marrow failure, telomere-related, type 1
  • (PFBMFT1) [MIM:614742]. A disease associated with shortened telomeres. Pulmonary fibrosis is the most common
    manifestation. Other manifestations include aplastic anemia due to bone marrow failure, hepatic fibrosis, and
    increased cancer risk, particularly myelodysplastic syndrome and acute myeloid leukemia. Phenotype, age at onset, and
    severity are determined by telomere length. infections, fatal pulmonary complications, or malignancy
  • Defects in TERT are the cause of dyskeratosis congenita autosomal recessive type 4 (DKCB4) [MIM:613989]. A
  • rare multisystem disorder caused by defective telomere maintenance. It is characterized by progressive bone marrow
    failure, and the clinical triad of reticulated skin hyperpigmentation, nail dystrophy, and mucosal leukoplakia. Common
    but variable features include premature graying, aplastic anemia, low platelets, osteoporosis, pulmonary fibrosis, and
    liver fibrosis among others. Early mortality is often associated with bone marrow failure, infections, fatal pulmonary
    complications, or malignancy
  • Defects in TERT are a cause of susceptibility to pulmonary fibrosis idiopathic (IPF) [MIM:178500]. Pulmonary
  • fibrosis is a lung disease characterized by shortness of breath, radiographically evident diffuse pulmonary
    infiltrates, and varying degrees of inflammation and fibrosis on biopsy. It results in acute lung injury with
    subsequent scarring and endstage lung disease

    20/181 diseases for TERT (see all 181):    About MalaCards
    cri-du-chat syndrome    dyskeratosis congenita autosomal dominant    dyskeratosis congenita    malignant peripheral nerve sheath tumor
    hoyeraal-hreidarsson syndrome    estrogen-receptor negative breast cancer    dyskeratosis congenita autosomal recessive    mixed ductal-endocrine carcinoma
    bowenoid papulosis    dyskeratosis    cervical intraepithelial neoplasia    pulmonary fibrosis
    squamous cell carcinoma    non-small cell lung carcinoma    aplastic anemia    nijmegen breakage syndrome
    laryngeal squamous cell carcinoma    gastroesophageal reflux disease    clear cell renal cell carcinoma    bile duct carcinoma

    2 diseases from the University of Copenhagen DISEASES database for TERT:
    Dyskeratosis congenita     Cancer

    10/95 Novoseek disease relationships for TERT gene (see all 95)    About this table

    Disease   -log (P-Val)   Hits   PubMed IDs for Articles with Shared Sentences (# sentences)
    dyskeratosis congenita 85 10 15885610 (2), 17454774 (1), 17468339 (1), 19415813 (1) (see all 9)
    dyskeratosis congenita, autosomal dominant 77.5 6 16247010 (1), 17392301 (1), 18460650 (1), 17875000 (1) (see all 5)
    cancer 73.1 215 20478107 (4), 11934015 (4), 14532739 (4), 19809268 (3) (see all 99)
    tumors 69.5 256 10973321 (5), 17130181 (5), 18204433 (5), 17656250 (4) (see all 99)
    hepatocellular carcinoma 57 32 19627485 (2), 18753050 (2), 11944954 (2), 15143919 (2) (see all 27)
    laryngeal squamous cell carcinoma 54.7 13 17592663 (2), 17219990 (2), 15823813 (2), 11911285 (2) (see all 8)
    anemia aplastic 47.6 12 15814878 (2), 15885610 (2), 17625368 (1), 17640862 (1) (see all 8)
    benign meningioma 47.2 2 17227292 (1), 17415213 (1)
    precancerous lesions 47 8 10429648 (2), 14716817 (2), 11906620 (1), 10779229 (1) (see all 5)
    premalignant 44.7 4 14575609 (1), 17581401 (1), 9620778 (1), 9731489 (1)

    GeneTests: TERT
    Familial Pulmonary Fibrosis

    Genetic Association Database (GAD): TERT
    Human Genome Epidemiology (HuGE) Navigator: TERT (64 documents)

    Export disorders for TERT 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 TERT gene, integrated from 9 sources (see all 1483):
    (articles sorted by number of sources associating them with TERT)
        Utopia: connect your pdf to the dynamic
    world of online information

    1. Mutations in TERT, the gene for telomerase reverse transcriptase, in aplastic anemia. (PubMed id 15814878)1, 2, 4, 9 Yamaguchi H.... Young N.S. (2005)
    2. Telomerase catalytic subunit homologs from fission yeast and human. (PubMed id 9252327)1, 2, 3 Nakamura T.M.... Cech T.R. (1997)
    3. Hydrogen peroxide triggers nuclear export of telomerase reverse transcriptase via Src kinase family-dependent phosphorylation of tyrosine 707. (PubMed id 12808100)1, 2, 9 Haendeler J....Dimmeler S. (2003)
    4. PML-IV functions as a negative regulator of telomeras e by interacting with TERT. (PubMed id 19567472)1, 2, 9 Oh W....Song J. (2009)
    5. Nuclear protein tyrosine phosphatase Shp-2 is one important negative regulator of nuclear export of telomerase reverse transcriptase. (PubMed id 18829466)1, 2, 9 Jakob S.... Haendeler J. (2008)
    6. Telomerase reverse-transcriptase homozygous mutations in autosomal recessive dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome. (PubMed id 17785587)1, 2, 9 Marrone A....Dokal I. (2007)
    7. Mutations in the reverse transcriptase component of telomerase (TERT) in patients with bone marrow failure. (PubMed id 15885610)1, 2, 9 Vulliamy T.J....Dokal I. (2005)
    8. Constitutional hypomorphic telomerase mutations in patients with acute myeloid leukemia. (PubMed id 19147845)1, 2, 9 Calado R.T.... Young N.S. (2009)
    9. Adult-onset pulmonary fibrosis caused by mutations in telomerase. (PubMed id 17460043)1, 2, 9 Tsakiri K.D.... Garcia C.K. (2007)
    10. Human telomerase contains evolutionarily conserved catalytic and structural subunits. (PubMed id 9389643)1, 2, 9 Harrington L.... Robinson M.O. (1997)

    (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: 7015 HGNC: 11730 AceView: TERT Ensembl:ENSG00000164362 euGenes: HUgn7015
    ECgene: TERT H-InvDB: TERT

    (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 TERT Pharmacogenomics, SNPs, Pathways
    ATLAS Chromosomes in Cancer entry for TERT Genetics and Cytogenetics in Oncology and Haematology
    NIEHS-SNPshttp://egp.gs.washington.edu/data/tert/

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

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



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