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General Information



Gene_Symbol Gene_ID Gene_Name Chromosome Alias
TGFB2 7042 transforming growth factor, beta 2  1- 







  • Evidence
  • Gene
  • mRNA
  • CDS
  • Protein
  • PTM
  • Enzyme
  • PPi
  • Pathway
  • Structural
  • Domain
  • Ontology
  • SNP
  • Drug
  • External Links



Evidence Information


Pubmed ID Year Sample Information Techniques Mechanism Fold Change Remark
11166150   2001Cell line : -

Source : -

Sample Type : -

No. of Sample : -

Stage : -

-Up-regulation-Colon carcinoma progression is associated with gradual and significant increases in expression of TGF-beta1 and TGF-beta2 mRNA and proteins.

12209600   2002Cell line : -

Source : Charles River Breeding Laboratories (Montreal, Canada)

Sample Type : Weanling male F344 rats

No. of Sample : -

Stage : -

real time RT-PCR,ImmunohistochemistryUp-regulation--

16886611   2006Cell line : -

Source : Department of Pathology, Elpis Hospital, Athens, Greece.

Sample Type : Formalin-fixed paraffin-embedded tissue

No. of Sample : Formalin-fixed paraffin-embedded tissue from 49 cases of colon carcinoma.

Stage : Duke stageg A,B,C,D

ImmunohistochemistryUp-regulation- TGF-beta2 overexpression, due to the activation or deregulation of the TGF-fl signalling pathway. Inactivation of the TGF-beta gene occurs at an early stage of colorectal carcinogenesis, while inactivation of Smad4 is probably a late event.


Gene Details



NC_000001.10 (218518676..218617961)

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Gene Type protein coding
Gene Family Endogenous ligands
Description This gene encodes a member of the transforming growth factor beta (TGFB) family of cytokines, which are multifunctional peptides that regulate proliferation, differentiation, adhesion, migration, and other functions in many cell types by transducing their signal through combinations of transmembrane type I and type II receptors (TGFBR1 and TGFBR2) and their downstream effectors, the SMAD proteins. Disruption of the TGFB/SMAD pathway has been implicated in a variety of human cancers. The encoded protein is secreted and has suppressive effects of interleukin-2 dependent T-cell growth. Translocation t(1;7)(q41;p21) between this gene and HDAC9 is associated with Peters' anomaly, a congenital defect of the anterior chamber of the eye. The knockout mice lacking this gene show perinatal mortality and a wide range of developmental, including cardiac, defects. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Sep 2010]  
Chromosome 1
Location 1q41
Start 218518676  
End 218617961  
Strand +  
Gene Sequence

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Length 99286  
OMIM ID 190220   
HGNC ID HGNC:11768   
Unigene ID Hs.133379   
Ensembl ID ENSG00000092969   
PharmGKB ID PA36482   

mRNA Information


mRNA ID ?NM_001135599.2
Exon join(1..304,1966..2112,3328..3930)  
mRNA Sequence

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Length 1054  



CDS Information


   
Location 181..465
CDS Sequence

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CCDS ID CCDS1521.1



Protein Information


      
Protein IDNP_001129071.1
Protein Nametransforming growth factor, beta 2
Molecular Wt. (Da)47197
Protein Sequence

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Length 414  
Uniprot IDQ9UQC9
Ensembl Protein ID ENSP00000359596  



Post-translational Modification Information (Source : HPRD)


No matching records could be found.

Enzyme Information


No matching records could be found.

PPi Information


No STRING Network could be found.

                                                                                                         
Interactant Gene ID (Source: HPRD) Gene Symbol HPRD ID Ref Seq ID Technique References
351APP100NP_000475.1in vivo2119582   
650BMP2206NP_001191.1in vivo9493905   
1490CTGF412NP_001892.1in vivo10457363   
2022ENG565NP_001108225.1in vitro;in vivo12015308   
7040TGFB11821NP_000651.3in vivo11157754   
7046TGFBR11822NP_004603.1in vivo11157754   
7048TGFBR21823NP_001020018.1in vitro;in vivo810   655   311   157   754   


Pathway Information


                                                                                                                                                                        
Pathway Name Pathway ID
AGE-RAGE signaling pathway in diabetic complications hsa04933
Amoebiasis hsa05146
Cell cycle hsa04110
Chagas disease (American trypanosomiasis) hsa05142
Chronic myeloid leukemia hsa05220
Colorectal cancer hsa05210
Cytokine-cytokine receptor interaction hsa04060
Dilated cardiomyopathy hsa05414
Endocytosis hsa04144
FoxO signaling pathway hsa04068
Hepatitis B hsa05161
Hippo signaling pathway hsa04390
HTLV-I infection hsa05166
Hypertrophic cardiomyopathy (HCM) hsa05410
Inflammatory bowel disease (IBD) hsa05321
Leishmaniasis hsa05140
Malaria hsa05144
MAPK signaling pathway hsa04010
MicroRNAs in cancer hsa05206
Osteoclast differentiation hsa04380
Pancreatic cancer hsa05212
Pathways in cancer hsa05200
Proteoglycans in cancer hsa05205
Renal cell carcinoma hsa05211
Rheumatoid arthritis hsa05323
TGF-beta signaling pathway hsa04350
Toxoplasmosis hsa05145
Tuberculosis hsa05152


Structure Information


No matching records could be found.

Domain Information




ID Location Description
pfam00019314-414  TGF_beta
cl02510314-414  TGF_beta superfamily
smart00204317-414  TGFB
pfam0068820-225  TGFb_propeptide
cl0292820-225  TGFb_propeptide superfamily
PHA02913310-413  PHA02913


Ontology Information


   
HPRD ID14854
Molecular ClassGrowth factor
Molecular FunctionAuxiliary transport protein activity (GO:0015457)
Biological ProcessTransport (GO:0006810)  



SNP Information


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Drug Information


No matching records could be found.

External Links


                                 
ArrayExpressGO
ICGCGO
Cancer3DGO
COSMICGO
NCGGO
TSGeneGO
Tumor Gene Family of DatabasesGO
CCDBGO
G2SBCGO
Osteosarcoma DatabaseGO
RCDBGO