HCSGD entry for TEC


1. General information

Official gene symbolTEC
Entrez ID7006
Gene full nametec protein tyrosine kinase
Other gene symbolsPSCTK4
Links to Entrez GeneLinks to Entrez Gene

2. Neighbors in the network

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This gene isn't in Literature mining network.

3. Gene ontology annotation

Not in the Gene ontology

4. Expression levels in datasets

  • Meta-analysis result

p-value upp-value downFDR upFDR down
0.40029873490.89747645610.99999024731.0000000000

  • Individual experiment result
    ( "-" represent NA in the specific microarray platform )

Data sourceUp or downLog fold change
GSE11954Up0.0223233188
GSE13712_SHEARDown-0.0752829297
GSE13712_STATICDown-0.0583998726
GSE19018Up0.1059876326
GSE19899_A1Up0.0713944708
GSE19899_A2Up0.2314048903
PubMed_21979375_A1Down-0.2294047179
PubMed_21979375_A2Up0.1629026863
GSE35957Up0.1430953705
GSE36640Up0.0525224772
GSE54402Up0.1230488614
GSE9593Up0.0956841575
GSE43922Up0.0483945653
GSE24585Up0.1988685627
GSE37065Up0.3522576798
GSE28863_A1Down-0.2527065520
GSE28863_A2Up0.0816235996
GSE28863_A3Up0.0821020634
GSE28863_A4Up0.0210776889
GSE48662Down-0.0135981797

5. Regulation relationships with compounds/drugs/microRNAs

  • Compounds

Not regulated by compounds

  • Drugs

Not regulated by drugs

  • MicroRNAs

  • mirTarBase
No target information from mirTarBase
  • mirRecord
No target information from mirRecord

6. Text-mining results about the gene

Gene occurances in abstracts of cellular senescence-associated articles: 6 abstracts the gene occurs.


PubMed ID of the article

Sentenece the gene occurs

27173733H-2h4 mice develop autoimmune disease with extensive hyperplasia and proliferation of thyroid epithelial cells (TEC H/P) and fibrosis
27173733Splenic T cells from donors with severe TEC H/P transfer TEC H/P to SCID recipients
27173733Splenic T cells from donors with severe TEC H/P transfer TEC H/P to SCID recipients
27173733The goal of this study was to determine what factors control TEC H/P development/progression by examining T cells, markers of apoptosis, senescence and proliferation in thyroids of SCID recipients over time
27173733X, indicative of cellular senescence, when TEC H/P progressed and thyrocyte proliferation declined
26974507The purpose of this study was to elucidate the feasibility of LOT preparation on the chondrogenic differentiation of a scaffold-free tissue-engineered construct (TEC) derived from synovial mesenchymal stem cells (MSCs), construct whose feasibility for cartilage repair has been demonstrated in previous preclinical and clinical studies
26974507In addition, TEC prepared from human synovial MSCs under LOT conditions (5% O2; LOT-TEC) showed superior in vitro chondrogenic differentiation capacity compared to that prepared under the usual 20% O2 (normal oxygen tension [NOT]; NOT-TEC), with elevated glycosaminoglycan production and elevated levels of chondrogenic marker gene expression
24263106However, their collaborative role in the regulation of TEC homeostasis during thymic aging is largely unknown
24263106Blockade of TEC differentiation via conditional FoxN1 gene knockout accelerated the appearance of this phenotype to early middle age, whereas intrathymic infusion of exogenous FoxN1 cDNA into aged WT mice brought only a modest reduction in the proportion of TAp63(+) TECs, but an increase in DeltaNp63(+) TECs in the partially rejuvenated thymus
24263106Thus, TAp63 levels are positively correlated with TEC senescence but inversely correlated with expression of FoxN1 and FoxN1-regulated TEC differentiation
24263106Thus, TAp63 levels are positively correlated with TEC senescence but inversely correlated with expression of FoxN1 and FoxN1-regulated TEC differentiation
24263106Thereby, the p63-FoxN1 regulatory axis in regulation of postnatal TEC homeostasis has been revealed
16391858Increasing evidence indicates that tumor-derived endothelial cells (TEC) possess a distinct and unique phenotype in respect to normal endothelial cells and may be able to acquire resistance to drugs
16391858However, few functional studies are available on cultured TEC
16391858In the present study, we obtained TEC from human breast carcinomas and, to dispel the possibility of contaminating tumor cells, we established six different clones that we characterized at a functional level
16391858In addition, breast TEC, at variance to normal endothelial cells, were able to grow and to organize in the absence of serum in capillary-like structures on Matrigel that persisted up to one week
16391858These functional characteristics of breast TEC may be relevant for tumor angiogenesis and may indicate an increased pro-angiogenic activity of endothelial cells within the tumor
16391858Moreover, our data suggest that TEC might be more appropriate for screening antiangiogenic drugs than normal endothelial cells
9892847Thymulin is a Zn-bound nonapeptide produced by the thymic epithelial cells (TEC) whose secretion is modulated by growth hormone (GH), among others
9892847Supernatants from TEC lines also showed GH secretagogue activity
9818729Thymulin is a Zn-bound nonapeptide produced by the thymic epithelial cells (TEC) whose secretion is modulated by prolactin (PRL) and thyroid hormones, among other hormones
9818729Supernatants from TEC lines also showed PRL and TSH secretagogue activity
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